A trihydroxy sugar alcohol that is an intermediate in carbohydrate and lipid metabolism. It is used as a solvent, emollient, pharmaceutical agent, and sweetening agent.
An enzyme that catalyzes the formation of glycerol 3-phosphate from ATP and glycerol. Dihydroxyacetone and L-glyceraldehyde can also act as acceptors; UTP and, in the case of the yeast enzyme, ITP and GTP can act as donors. It provides a way for glycerol derived from fats or glycerides to enter the glycolytic pathway. EC 2.7.1.30.
Any salt or ester of glycerophosphoric acid.
Glycerolphosphate Dehydrogenase is an enzyme (EC 1.1.1.8) that catalyzes the reversible conversion of dihydroxyacetone phosphate to glycerol 3-phosphate, using nicotinamide adenine dinucleotide (NAD+) as an electron acceptor in the process.
A ketotriose compound. Its addition to blood preservation solutions results in better maintenance of 2,3-diphosphoglycerate levels during storage. It is readily phosphorylated to dihydroxyacetone phosphate by triokinase in erythrocytes. In combination with naphthoquinones it acts as a sunscreening agent.
GLYCEROL esterified with FATTY ACIDS.
Reversibly catalyzes the oxidation of a hydroxyl group of sugar alcohols to form a keto sugar, aldehyde or lactone. Any acceptor except molecular oxygen is permitted. Includes EC 1.1.1.; EC 1.1.2. and EC 1.1.99.
A class of porins that allow the passage of WATER and other small molecules across CELL MEMBRANES.
GLYCEROL esterified with a single acyl (FATTY ACIDS) chain.
Substances that provide protection against the harmful effects of freezing temperatures.
A clear, colorless, viscous organic solvent and diluent used in pharmaceutical preparations.
The metabolic process of breaking down LIPIDS to release FREE FATTY ACIDS, the major oxidative fuel for the body. Lipolysis may involve dietary lipids in the DIGESTIVE TRACT, circulating lipids in the BLOOD, and stored lipids in the ADIPOSE TISSUE or the LIVER. A number of enzymes are involved in such lipid hydrolysis, such as LIPASE and LIPOPROTEIN LIPASE from various tissues.
A primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is used therapeutically in fluid and nutrient replacement.
An important intermediate in lipid biosynthesis and in glycolysis.
A colorless, odorless, viscous dihydroxy alcohol. It has a sweet taste, but is poisonous if ingested. Ethylene glycol is the most important glycol commercially available and is manufactured on a large scale in the United States. It is used as an antifreeze and coolant, in hydraulic fluids, and in the manufacture of low-freezing dynamites and resins.
Aquaporin 3 is an aquaglyceroporin that is expressed in the KIDNEY COLLECTING DUCTS and is constitutively localized at the basolateral MEMBRANE.
The rate dynamics in chemical or physical systems.
Compounds in which one or more of the three hydroxyl groups of glycerol are in ethereal linkage with a saturated or unsaturated aliphatic alcohol; one or two of the hydroxyl groups of glycerol may be esterified. These compounds have been found in various animal tissue.
Derivatives of propylene glycol (1,2-propanediol). They are used as humectants and solvents in pharmaceutical preparations.
Glyceraldehyde is a triose sugar, a simple monosaccharide (sugar) that contains three carbon atoms, with the molecular formula C3H6O3, and it exists in two structural forms, namely D-glyceraldehyde and L-glyceraldehyde, which are diastereomers of each other, and it is a key intermediate in several biochemical pathways, including glycolysis and gluconeogenesis.
Biosynthesis of GLUCOSE from nonhexose or non-carbohydrate precursors, such as LACTATE; PYRUVATE; ALANINE; and GLYCEROL.
FATTY ACIDS found in the plasma that are complexed with SERUM ALBUMIN for transport. These fatty acids are not in glycerol ester form.
Stable carbon atoms that have the same atomic number as the element carbon, but differ in atomic weight. C-13 is a stable carbon isotope.
A rather large group of enzymes comprising not only those transferring phosphate but also diphosphate, nucleotidyl residues, and others. These have also been subdivided according to the acceptor group. (From Enzyme Nomenclature, 1992) EC 2.7.
Salts and esters of the 10-carbon monocarboxylic acid-decanoic acid.
Any liquid or solid preparation made specifically for the growth, storage, or transport of microorganisms or other types of cells. The variety of media that exist allow for the culturing of specific microorganisms and cell types, such as differential media, selective media, test media, and defined media. Solid media consist of liquid media that have been solidified with an agent such as AGAR or GELATIN.
An enzyme that transfers acyl groups from acyl-CoA to glycerol-3-phosphate to form monoglyceride phosphates. It acts only with CoA derivatives of fatty acids of chain length above C-10. Also forms diglyceride phosphates. EC 2.3.1.15.
The pressure required to prevent the passage of solvent through a semipermeable membrane that separates a pure solvent from a solution of the solvent and solute or that separates different concentrations of a solution. It is proportional to the osmolality of the solution.
Propane is a colorless, odorless, and chemically simple hydrocarbon (C3H8), commonly used as a fuel for heating, cooking, and engines, which exists as a gas at room temperature but can be liquefied under pressure and stored in cylinders or tanks.
Organic, monobasic acids derived from hydrocarbons by the equivalent of oxidation of a methyl group to an alcohol, aldehyde, and then acid. Fatty acids are saturated and unsaturated (FATTY ACIDS, UNSATURATED). (Grant & Hackh's Chemical Dictionary, 5th ed)
Anaerobic degradation of GLUCOSE or other organic nutrients to gain energy in the form of ATP. End products vary depending on organisms, substrates, and enzymatic pathways. Common fermentation products include ETHANOL and LACTIC ACID.
An enzyme that catalyzes the dehydration of 1,2-propanediol to propionaldehyde. EC 4.2.1.28.
Bacterial polysaccharides that are rich in phosphodiester linkages. They are the major components of the cell walls and membranes of many bacteria.
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Liquids transforming into solids by the removal of heat.
Polyhydric alcohols having no more than one hydroxy group attached to each carbon atom. They are formed by the reduction of the carbonyl group of a sugar to a hydroxyl group.(From Dorland, 28th ed)
Lipids containing one or more phosphate groups, particularly those derived from either glycerol (phosphoglycerides see GLYCEROPHOSPHOLIPIDS) or sphingosine (SPHINGOLIPIDS). They are polar lipids that are of great importance for the structure and function of cell membranes and are the most abundant of membrane lipids, although not stored in large amounts in the system.
An analytical technique for resolution of a chemical mixture into its component compounds. Compounds are separated on an adsorbent paper (stationary phase) by their varied degree of solubility/mobility in the eluting solvent (mobile phase).
Chromatography on thin layers of adsorbents rather than in columns. The adsorbent can be alumina, silica gel, silicates, charcoals, or cellulose. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Triglycerides are the most common type of fat in the body, stored in fat cells and used as energy; they are measured in blood tests to assess heart disease risk, with high levels often resulting from dietary habits, obesity, physical inactivity, smoking, and alcohol consumption.
The property of objects that determines the direction of heat flow when they are placed in direct thermal contact. The temperature is the energy of microscopic motions (vibrational and translational) of the particles of atoms.
LIPOLYSIS of stored LIPIDS in the ADIPOSE TISSUE to release FREE FATTY ACIDS. Mobilization of stored lipids is under the regulation of lipolytic signals (CATECHOLAMINES) or anti-lipolytic signals (INSULIN) via their actions on the hormone-sensitive LIPASE. This concept does not include lipid transport.
Derivatives of ACETIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that contain the carboxymethane structure.
Salts and esters of the 12-carbon saturated monocarboxylic acid--lauric acid.
A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
Cellular processes in biosynthesis (anabolism) and degradation (catabolism) of CARBOHYDRATES.
Specialized connective tissue composed of fat cells (ADIPOCYTES). It is the site of stored FATS, usually in the form of TRIGLYCERIDES. In mammals, there are two types of adipose tissue, the WHITE FAT and the BROWN FAT. Their relative distributions vary in different species with most adipose tissue being white.
The process by which semen is kept viable outside of the organism from which it was derived (i.e., kept from decay by means of a chemical agent, cooling, or a fluid substitute that mimics the natural state within the organism).
Salts or esters of LACTIC ACID containing the general formula CH3CHOHCOOR.
A generic grouping for dihydric alcohols with the hydroxy groups (-OH) located on different carbon atoms. They are viscous liquids with high boiling points for their molecular weights.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
A genus of gram-negative, rod-shaped to ellipsoidal bacteria occurring singly or in pairs and found in flowers, soil, honey bees, fruits, cider, beer, wine, and vinegar. (From Bergey's Manual of Determinative Bacteriology, 9th ed)
A species of the genus SACCHAROMYCES, family Saccharomycetaceae, order Saccharomycetales, known as "baker's" or "brewer's" yeast. The dried form is used as a dietary supplement.
Cobamides are a class of compounds that function as cofactors in various enzymatic reactions, containing a corrin ring similar to vitamin B12, but with different substituents on the benzimidazole moiety, and can be found in certain bacteria and archaea.
A nitrogen-free class of lipids present in animal and particularly plant tissues and composed of one mole of glycerol and 1 or 2 moles of phosphatidic acid. Members of this group differ from one another in the nature of the fatty acids released on hydrolysis.
The concentration of osmotically active particles in solution expressed in terms of osmoles of solute per liter of solution. Osmolality is expressed in terms of osmoles of solute per kilogram of solvent.
Type species of the genus CLOSTRIDIUM, a gram-positive bacteria in the family Clostridiaceae. It is used as a source of PROBIOTICS.
The complete absence, or (loosely) the paucity, of gaseous or dissolved elemental oxygen in a given place or environment. (From Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)
A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances.
A nonreducing disaccharide composed of GLUCOSE and FRUCTOSE linked via their anomeric carbons. It is obtained commercially from SUGARCANE, sugar beet (BETA VULGARIS), and other plants and used extensively as a food and a sweetener.
An ethylene compound with two hydroxy groups (-OH) located on adjacent carbons. They are viscous and colorless liquids. Some are used as anesthetics or hypnotics. However, the class is best known for their use as a coolant or antifreeze.

Acute renal failure caused by nephrotoxins. (1/4138)

Renal micropuncture studies have greatly changed our views on the pathophysiology of acute renal failure caused by nephrotoxins. Formerly, this type of renal insufficiency was attributed to a direct effect of the nephrotoxins on tubule epithelial permeability. According to that theory, glomerular filtration was not greatly diminished, the filtrate formed being absorbed almost quantitatively and nonselectively across damaged tubule epithelium. Studies in a wide variety of rat models have now shown glomerular filtration to be reduced to a level which will inevitably cause renal failure in and of itself. Passive backflow of filtrate across tubular epithelium is either of minor degree or nonexistent even in models where frank tubular necrosis has occurred. This failure of filtration cannot be attributed to tubular obstruction since proximal tubule pressure is distinctly subnormal in most models studied. Instead, filtration failure appears best attributed to intrarenal hemodynamic alterations. While certain facts tend to incriminate the renin-angiotensin system as the cause of the hemodynamic aberrations, others argue to the contrary. The issue is underactive investigation.  (+info)

Dietary control of triglyceride and phospholipid synthesis in rat liver slices. (2/4138)

1. The effect of dietary manipulation on the synthesis of triglycerides and phospholipids was investigated by determining the incorporation of labeled long-chain fatty acid or glycerol into these lipids in liver slices derived from normally fed, fasted, and fat-free refed rats. 2. Triglyceride synthesis was affected markedly by the dietary regime of the animal; the lowest rates were measured with fasted rats, and the highest ones with fat-free refed rats. 3. In contrast to triglyceride synthesis, phospholipid synthesis occured at virtually constant rates regardless of the dietary conditions. 4. Addition of large amounts of fatty acid to the incubation mixture resulted in a marked stimulation of triglyceride synthesis, whereas phospholipid synthesis was affected to a much smaller extent. 5. These results indicate that the synthesis of triglycerides and that of phospholipids are controlled independently, and that the availability of fatty acid in the cell contributes to the control of triglyceride synthesis.  (+info)

Improved antibody detection by the use of range expansion and longer filter wavelength in a low ionic strength-protamine sulphate Auto-Analyzer system. (3/4138)

Range expansion, achieved by insertion of a variable resistance between the colorimeter and the recorder together with the use of 550 nm colorimeter filters, has resulted in markedly improved sensitivity for antibody detection, and improved sample identification, in a low ionic strength-protamine sulphate (LISPS) system. Range expansion also permits a lower concentration of red cells to be used, thus economizing on fully typed cells. Glycerol stored frozen cells were found to be only slightly less sensitive than fresh cells in this system.  (+info)

Isocitrate lyase of Ashbya gossypii--transcriptional regulation and peroxisomal localization. (4/4138)

The isocitrate lyase-encoding gene AgICL1 from the filamentous hemiascomycete Ashbya gossypii was isolated by heterologous complementation of a Saccharomyces cerevisiae icl1d mutant. The open reading frame of 1680 bp encoded a protein of 560 amino acids with a calculated molecular weight of 62584. Disruption of the AgICL1 gene led to complete loss of AgIcl1p activity and inability to grow on oleic acid as sole carbon source. Compartmentation of AgIcl1p in peroxisomes was demonstrated both by Percoll density gradient centrifugation and by immunogold labeling of ultrathin sections using specific antibodies. This fitted with the peroxisomal targeting signal AKL predicted from the C-terminal DNA sequence. Northern blot analysis with mycelium grown on different carbon sources as well as AgICL1 promoter replacement with the constitutive AgTEF promoter revealed a regulation at the transcriptional level. AgICL1 was subject to glucose repression, derepressed by glycerol, partially induced by the C2 compounds ethanol and acetate, and fully induced by soybean oil.  (+info)

Redundant systems of phosphatidic acid biosynthesis via acylation of glycerol-3-phosphate or dihydroxyacetone phosphate in the yeast Saccharomyces cerevisiae. (5/4138)

In the yeast Saccharomyces cerevisiae lipid particles harbor two acyltransferases, Gat1p and Slc1p, which catalyze subsequent steps of acylation required for the formation of phosphatidic acid. Both enzymes are also components of the endoplasmic reticulum, but this compartment contains additional acyltransferase(s) involved in the biosynthesis of phosphatidic acid (K. Athenstaedt and G. Daum, J. Bacteriol. 179:7611-7616, 1997). Using the gat1 mutant strain TTA1, we show here that Gat1p present in both subcellular fractions accepts glycerol-3-phosphate and dihydroxyacetone phosphate as a substrate. Similarly, the additional acyltransferase(s) present in the endoplasmic reticulum can acylate both precursors. In contrast, yeast mitochondria harbor an enzyme(s) that significantly prefers dihydroxyacetone phosphate as a substrate for acylation, suggesting that at least one additional independent acyltransferase is present in this organelle. Surprisingly, enzymatic activity of 1-acyldihydroxyacetone phosphate reductase, which is required for the conversion of 1-acyldihydroxyacetone phosphate to 1-acylglycerol-3-phosphate (lysophosphatidic acid), is detectable only in lipid particles and the endoplasmic reticulum and not in mitochondria. In vivo labeling of wild-type cells with [2-3H, U-14C]glycerol revealed that both glycerol-3-phosphate and dihydroxyacetone phosphate can be incorporated as a backbone of glycerolipids. In the gat1 mutant and the 1-acylglycerol-3-phosphate acyltransferase slc1 mutant, the dihydroxyacetone phosphate pathway of phosphatidic acid biosynthesis is slightly preferred as compared to the wild type. Thus, mutations of the major acyltransferases Gat1p and Slc1p lead to an increased contribution of mitochondrial acyltransferase(s) to glycerolipid synthesis due to their substrate preference for dihydroxyacetone phosphate.  (+info)

The PalkBFGHJKL promoter is under carbon catabolite repression control in Pseudomonas oleovorans but not in Escherichia coli alk+ recombinants. (6/4138)

The alk genes are located on the OCT plasmid of Pseudomonas oleovorans and encode an inducible pathway for the utilization of n-alkanes as carbon and energy sources. We have investigated the influence of alternative carbon sources on the induction of this pathway in P. oleovorans and Escherichia coli alk+ recombinants. In doing so, we confirmed earlier reports that induction of alkane hydroxylase activity in pseudomonads is subject to carbon catabolite repression. Specifically, synthesis of the monooxygenase component AlkB is repressed at the transcriptional level. The alk genes have been cloned into plasmid pGEc47, which has a copy number of about 5 to 10 per cell in both E. coli and pseudomonads. Pseudomonas putida GPo12 is a P. oleovorans derivative cured of the OCT plasmid. Upon introduction of pGEc47 in this strain, carbon catabolite repression of alkane hydroxylase activity was reduced significantly. In cultures of recombinant E. coli HB101 and W3110 carrying pGEc47, induction of AlkB and transcription of the alkB gene were no longer subject to carbon catabolite repression. This suggests that carbon catabolite repression of alkane degradation is regulated differently in Pseudomonas and in E. coli strains. These results also indicate that PalkBFGHJKL, the Palk promoter, might be useful in attaining high expression levels of heterologous genes in E. coli grown on inexpensive carbon sources which normally trigger carbon catabolite repression of native expression systems in this host.  (+info)

Characterization of the exopolygalacturonate lyase PelX of Erwinia chrysanthemi 3937. (7/4138)

Erwinia chrysanthemi 3937 secretes several pectinolytic enzymes, among which eight isoenzymes of pectate lyases with an endo-cleaving mode (PelA, PelB, PelC, PelD, PelE, PelI, PelL, and PelZ) have been identified. Two exo-cleaving enzymes, the exopolygalacturonate lyase, PelX, and an exo-poly-alpha-D-galacturonosidase, PehX, have been previously identified in other E. chrysanthemi strains. Using a genomic bank of a 3937 mutant with the major pel genes deleted, we cloned a pectinase gene identified as pelX, encoding the exopolygalacturonate lyase. The deduced amino acid sequence of the 3937 PelX is very similar to the PelX of another E. chrysanthemi strain, EC16, except in the 43 C-terminal amino acids. PelX also has homology to the endo-pectate lyase PelL of E. chrysanthemi but has a N-terminal extension of 324 residues. The transcription of pelX, analyzed by gene fusions, is dependent on several environmental conditions. It is induced by pectic catabolic products and affected by growth phase, oxygen limitation, nitrogen starvation, and catabolite repression. Regulation of pelX expression is dependent on the KdgR repressor, which controls almost all the steps of pectin catabolism, and on the global activator of sugar catabolism, cyclic AMP receptor protein. In contrast, PecS and PecT, two repressors of the transcription of most pectate lyase genes, are not involved in pelX expression. The pelX mutant displayed reduced pathogenicity on chicory leaves, but its virulence on potato tubers or Saintpaulia ionantha plants did not appear to be affected. The purified PelX protein has no maceration activity on plant tissues. Tetragalacturonate is the best substrate of PelX, but PelX also has good activity on longer oligomers. Therefore, the estimated number of binding subsites for PelX is 4, extending from subsites -2 to +2. PelX and PehX were shown to be localized in the periplasm of E. chrysanthemi 3937. PelX catalyzed the formation of unsaturated digalacturonates by attack from the reducing end of the substrate, while PehX released digalacturonates by attack from the nonreducing end of the substrate. Thus, the two types of exo-degrading enzymes appeared complementary in the degradation of pectic polymers, since they act on both extremities of the polymeric chain.  (+info)

Glucose kinetics during prolonged exercise in highly trained human subjects: effect of glucose ingestion. (8/4138)

1. The objectives of this study were (1) to investigate whether glucose ingestion during prolonged exercise reduces whole body muscle glycogen oxidation, (2) to determine the extent to which glucose disappearing from the plasma is oxidized during exercise with and without carbohydrate ingestion and (3) to obtain an estimate of gluconeogenesis. 2. After an overnight fast, six well-trained cyclists exercised on three occasions for 120 min on a bicycle ergometer at 50 % maximum velocity of O2 uptake and ingested either water (Fast), or a 4 % glucose solution (Lo-Glu) or a 22 % glucose solution (Hi-Glu) during exercise. 3. Dual tracer infusion of [U-13C]-glucose and [6,6-2H2]-glucose was given to measure the rate of appearance (Ra) of glucose, muscle glycogen oxidation, glucose carbon recycling, metabolic clearance rate (MCR) and non-oxidative disposal of glucose. 4. Glucose ingestion markedly increased total Ra especially with Hi-Glu. After 120 min Ra and rate of disappearance (Rd) of glucose were 51-52 micromol kg-1 min-1 during Fast, 73-74 micromol kg-1 min-1 during Lo-Glu and 117-119 micromol kg-1 min-1 during Hi-Glu. The percentage of Rd oxidized was between 96 and 100 % in all trials. 5. Glycogen oxidation during exercise was not reduced by glucose ingestion. The vast majority of glucose disappearing from the plasma is oxidized and MCR increased markedly with glucose ingestion. Glucose carbon recycling was minimal suggesting that gluconeogenesis in these conditions is negligible.  (+info)

Glycerol, also known as glycerine or glycerin, is a simple polyol (a sugar alcohol) with a sweet taste and a thick, syrupy consistency. It is a colorless, odorless, viscous liquid that is slightly soluble in water and freely miscible with ethanol and ether.

In the medical field, glycerol is often used as a medication or supplement. It can be used as a laxative to treat constipation, as a source of calories and energy for people who cannot eat by mouth, and as a way to prevent dehydration in people with certain medical conditions.

Glycerol is also used in the production of various medical products, such as medications, skin care products, and vaccines. It acts as a humectant, which means it helps to keep things moist, and it can also be used as a solvent or preservative.

In addition to its medical uses, glycerol is also widely used in the food industry as a sweetener, thickening agent, and moisture-retaining agent. It is generally recognized as safe (GRAS) by the U.S. Food and Drug Administration (FDA).

Glycerol kinase is an enzyme that plays a crucial role in the metabolism of glycerol, which is a simple carbohydrate. The enzyme catalyzes the conversion of glycerol to glycerol-3-phosphate by transferring a phosphate group from ATP to glycerol. This reaction is an essential step in the metabolic pathway that leads to the formation of glucose or other energy-rich compounds in the body.

There are two main forms of glycerol kinase found in humans, designated as GK1 and GK2. GK1 is primarily expressed in the liver, while GK2 is found in various tissues, including the brain, heart, and muscles. Deficiencies in glycerol kinase can lead to metabolic disorders such as hyperglycerolemia, which is characterized by high levels of glycerol in the blood.

Glycerophosphates are esters of glycerol and phosphoric acid. In the context of biochemistry and medicine, glycerophosphates often refer to glycerol 3-phosphate (also known as glyceraldehyde 3-phosphate or glycerone phosphate) and its derivatives.

Glycerol 3-phosphate plays a crucial role in cellular metabolism, particularly in the process of energy production and storage. It is an important intermediate in both glycolysis (the breakdown of glucose to produce energy) and gluconeogenesis (the synthesis of glucose from non-carbohydrate precursors).

In addition, glycerophosphates are also involved in the formation of phospholipids, a major component of cell membranes. The esterification of glycerol 3-phosphate with fatty acids leads to the synthesis of phosphatidic acid, which is a key intermediate in the biosynthesis of other phospholipids.

Abnormalities in glycerophosphate metabolism have been implicated in various diseases, including metabolic disorders and neurological conditions.

Glycerol-3-phosphate dehydrogenase (GPD) is an enzyme that plays a crucial role in the metabolism of glucose and lipids. It catalyzes the conversion of dihydroxyacetone phosphate (DHAP) to glycerol-3-phosphate (G3P), which is a key intermediate in the synthesis of triglycerides, phospholipids, and other glycerophospholipids.

There are two main forms of GPD: a cytoplasmic form (GPD1) and a mitochondrial form (GPD2). The cytoplasmic form is involved in the production of NADH, which is used in various metabolic processes, while the mitochondrial form is involved in the production of ATP, the main energy currency of the cell.

Deficiencies or mutations in GPD can lead to a variety of metabolic disorders, including glycerol kinase deficiency and congenital muscular dystrophy. Elevated levels of GPD have been observed in certain types of cancer, suggesting that it may play a role in tumor growth and progression.

Dihydroxyacetone (DHA) is a simple sugar that is used as an ingredient in many self-tanning products. When applied to the skin, DHA reacts with amino acids in the dead layer of the skin to temporarily darken the skin color. This process is known as the Maillard reaction, which is a chemical reaction between an amino acid and a sugar. The effect of DHA is limited to the uppermost layer of the skin and it does not provide any protection against sunburn or UV radiation. The tanning effect produced by DHA usually lasts for about 5-7 days.

It's important to note that while DHA is considered safe for external use, it should not be inhaled or ingested, as it can cause irritation and other adverse effects. Additionally, some people may experience skin irritation or allergic reactions to products containing DHA, so it's always a good idea to do a patch test before using a new self-tanning product.

Glycerides are esters formed from glycerol and one, two, or three fatty acids. They include monoglycerides (one fatty acid), diglycerides (two fatty acids), and triglycerides (three fatty acids). Triglycerides are the main constituents of natural fats and oils, and they are a major form of energy storage in animals and plants. High levels of triglycerides in the blood, also known as hypertriglyceridemia, can increase the risk of heart disease and stroke.

Sugar alcohol dehydrogenases (SADHs) are a group of enzymes that catalyze the interconversion between sugar alcohols and sugars, which involves the gain or loss of a pair of electrons, typically in the form of NAD(P)+/NAD(P)H. These enzymes play a crucial role in the metabolism of sugar alcohols, which are commonly found in various plants and some microorganisms.

Sugar alcohols, also known as polyols, are reduced forms of sugars that contain one or more hydroxyl groups instead of aldehyde or ketone groups. Examples of sugar alcohols include sorbitol, mannitol, xylitol, and erythritol. SADHs can interconvert these sugar alcohols to their corresponding sugars through a redox reaction that involves the transfer of hydrogen atoms.

The reaction catalyzed by SADHs is typically represented as follows:

R-CH(OH)-CH2OH + NAD(P)+ ↔ R-CO-CH2OH + NAD(P)H + H+

where R represents a carbon chain, and CH(OH)-CH2OH and CO-CH2OH represent the sugar alcohol and sugar forms, respectively.

SADHs are widely distributed in nature and have been found in various organisms, including bacteria, fungi, plants, and animals. These enzymes have attracted significant interest in biotechnology due to their potential applications in the production of sugar alcohols and other value-added products. Additionally, SADHs have been studied as targets for developing novel antimicrobial agents, as inhibiting these enzymes can disrupt the metabolism of certain pathogens that rely on sugar alcohols for growth and survival.

Aquaporins are a type of membrane protein that function as water channels, allowing the selective and efficient transport of water molecules across biological membranes. They play crucial roles in maintaining fluid homeostasis, regulating cell volume, and supporting various physiological processes in the body. In humans, there are 13 different aquaporin subtypes (AQP0 to AQP12) that have been identified, each with distinct tissue expression patterns and functions. Some aquaporins also facilitate the transport of small solutes such as glycerol and urea. Dysfunction or misregulation of aquaporins has been implicated in several pathological conditions, including neurological disorders, cancer, and water balance-related diseases.

Medical Definition of Monoglycerides:

Monoglycerides are types of glycerides that contain one molecule of fatty acid combined with a glycerol molecule through an ester linkage. They are often used as food additives, serving as emulsifiers to help blend together water and oil-based ingredients in foods such as baked goods, ice cream, and chocolate. Monoglycerides can also be found naturally in some foods, including certain vegetable oils.

In the context of human physiology, monoglycerides can serve as a source of energy and can also play a role in the absorption and transport of fatty acids in the body. However, they are not typically considered to be a major nutrient or component of the human diet.

Cryoprotective agents are substances that are used to protect biological material from damage during freezing and thawing. These agents work by reducing the amount of ice that forms in the cells, which can help to prevent the formation of damaging ice crystals. Commonly used cryoprotective agents include dimethyl sulfoxide (DMSO), glycerol, and ethylene glycol.

When biological material, such as cells or tissues, is cooled to very low temperatures for storage or transportation, the water in the cells can freeze and form ice crystals. These ice crystals can damage the cell membranes and other structures within the cell, leading to cell death. Cryoprotective agents help to prevent this by lowering the freezing point of the solution that the cells are stored in, which reduces the amount of ice that forms.

Cryoprotective agents are often used in the field of assisted reproductive technology (ART) to protect sperm, eggs, and embryos during freezing and thawing. They are also used in research settings to preserve cells and tissues for later use. It is important to note that while cryoprotective agents can help to reduce the amount of damage that occurs during freezing and thawing, they cannot completely prevent it. Therefore, it is important to carefully control the freezing and thawing process to minimize any potential harm to the biological material.

Propylene glycol is not a medical term, but rather a chemical compound. However, it does have various applications in the medical field. Medically, propylene glycol can be used as a:

1. Vehicle for intravenous (IV) medications: Propylene glycol helps dissolve drugs that are not water-soluble and allows them to be administered intravenously. It is used in the preparation of some IV medications, including certain antibiotics, antivirals, and chemotherapeutic agents.
2. Preservative: Propylene glycol acts as a preservative in various medical products, such as topical ointments, eye drops, and injectable solutions, to prevent bacterial growth and increase shelf life.
3. Humectant: In some medical devices and pharmaceutical formulations, propylene glycol is used as a humectant, which means it helps maintain moisture and prevent dryness in the skin or mucous membranes.

The chemical definition of propylene glycol (C3H8O2) is:

A colorless, nearly odorless, viscous liquid belonging to the alcohol family. It is a diol, meaning it contains two hydroxyl groups (-OH), and its molecular formula is C3H8O2. Propylene glycol is miscible with water and most organic solvents and has applications in various industries, including pharmaceuticals, food processing, cosmetics, and industrial manufacturing.

Lipolysis is the process by which fat cells (adipocytes) break down stored triglycerides into glycerol and free fatty acids. This process occurs when the body needs to use stored fat as a source of energy, such as during fasting, exercise, or in response to certain hormonal signals. The breakdown products of lipolysis can be used directly by cells for energy production or can be released into the bloodstream and transported to other tissues for use. Lipolysis is regulated by several hormones, including adrenaline (epinephrine), noradrenaline (norepinephrine), cortisol, glucagon, and growth hormone, which act on lipases, enzymes that mediate the breakdown of triglycerides.

Glucose is a simple monosaccharide (or single sugar) that serves as the primary source of energy for living organisms. It's a fundamental molecule in biology, often referred to as "dextrose" or "grape sugar." Glucose has the molecular formula C6H12O6 and is vital to the functioning of cells, especially those in the brain and nervous system.

In the body, glucose is derived from the digestion of carbohydrates in food, and it's transported around the body via the bloodstream to cells where it can be used for energy. Cells convert glucose into a usable form through a process called cellular respiration, which involves a series of metabolic reactions that generate adenosine triphosphate (ATP)—the main currency of energy in cells.

Glucose is also stored in the liver and muscles as glycogen, a polysaccharide (multiple sugar) that can be broken down back into glucose when needed for energy between meals or during physical activity. Maintaining appropriate blood glucose levels is crucial for overall health, and imbalances can lead to conditions such as diabetes mellitus.

Dihydroxyacetone Phosphate (DHAP) is a 3-carbon organic compound that plays a crucial role in the metabolic pathway called glycolysis. It is an intermediate molecule formed during the conversion of glucose into pyruvate, which ultimately produces energy in the form of ATP.

In the glycolytic process, DHAP is produced from glyceraldehyde 3-phosphate (G3P) in a reaction catalyzed by the enzyme triose phosphate isomerase. Then, DHAP is converted back to G3P in a subsequent step, which prepares it for further processing in the glycolytic pathway. This reversible conversion of DHAP and G3P helps maintain the equilibrium of the glycolytic process.

Apart from its role in energy metabolism, DHAP is also involved in other biochemical processes, such as the synthesis of glucose during gluconeogenesis and the formation of lipids in the liver.

Ethylene glycol is a colorless, odorless, syrupy liquid with a sweet taste, which makes it appealing to animals and children. It is commonly used in the manufacture of antifreeze, coolants, deicers, hydraulic brake fluids, solvents, and other industrial products. Ethylene glycol is also found in some household items such as certain types of wood stains, paints, and cosmetics.

Ingesting even small amounts of ethylene glycol can be harmful or fatal to humans and animals. It is metabolized by the body into toxic substances that can cause damage to the central nervous system, heart, kidneys, and other organs. Symptoms of ethylene glycol poisoning may include nausea, vomiting, abdominal pain, decreased level of consciousness, seizures, coma, acidosis, increased heart rate, low blood pressure, and kidney failure.

If you suspect that someone has ingested ethylene glycol, it is important to seek medical attention immediately. Treatment typically involves administering a medication called fomepizole or ethanol to inhibit the metabolism of ethylene glycol, as well as providing supportive care such as fluid replacement and dialysis to remove the toxic substances from the body.

Aquaporin 3 (AQP3) is a type of aquaglyceroporin, which is a subclass of aquaporins - water channel proteins that facilitate the transport of water and small solutes across biological membranes. AQP3 is primarily expressed in the epithelial cells of various tissues, including the skin, kidneys, and gastrointestinal tract.

In the skin, AQP3 plays a crucial role in maintaining skin hydration by facilitating water transport across the cell membrane. It also transports small neutral solutes like glycerol and urea, which contribute to skin moisturization and elasticity. In addition, AQP3 has been implicated in several physiological processes, such as wound healing, epidermal proliferation, and cutaneous sensory perception.

In the kidneys, AQP3 is involved in water reabsorption in the collecting ducts, helping to regulate body fluid homeostasis. In the gastrointestinal tract, it facilitates water absorption and secretion, contributing to maintaining proper hydration and electrolyte balance. Dysregulation of AQP3 has been associated with various pathological conditions, such as skin disorders, kidney diseases, and cancer.

In the context of medicine and pharmacology, "kinetics" refers to the study of how a drug moves throughout the body, including its absorption, distribution, metabolism, and excretion (often abbreviated as ADME). This field is called "pharmacokinetics."

1. Absorption: This is the process of a drug moving from its site of administration into the bloodstream. Factors such as the route of administration (e.g., oral, intravenous, etc.), formulation, and individual physiological differences can affect absorption.

2. Distribution: Once a drug is in the bloodstream, it gets distributed throughout the body to various tissues and organs. This process is influenced by factors like blood flow, protein binding, and lipid solubility of the drug.

3. Metabolism: Drugs are often chemically modified in the body, typically in the liver, through processes known as metabolism. These changes can lead to the formation of active or inactive metabolites, which may then be further distributed, excreted, or undergo additional metabolic transformations.

4. Excretion: This is the process by which drugs and their metabolites are eliminated from the body, primarily through the kidneys (urine) and the liver (bile).

Understanding the kinetics of a drug is crucial for determining its optimal dosing regimen, potential interactions with other medications or foods, and any necessary adjustments for special populations like pediatric or geriatric patients, or those with impaired renal or hepatic function.

Glyceryl ethers, also known as glycerol ethers or alkyl glycosides, are a class of compounds formed by the reaction between glycerol and alcohols. In the context of medical definitions, glyceryl ethers may refer to a group of naturally occurring compounds found in some organisms, including humans.

These compounds are characterized by an ether linkage between the glycerol molecule and one or more alkyl chains, which can vary in length. Glyceryl ethers have been identified as components of various biological tissues, such as lipid fractions of human blood and lung surfactant.

In some cases, glyceryl ethers may also be used as pharmaceutical excipients or drug delivery systems due to their unique physicochemical properties. For example, they can enhance the solubility and bioavailability of certain drugs, making them useful in formulation development. However, it is important to note that specific medical applications and uses of glyceryl ethers may vary depending on the particular compound and its properties.

Propylene glycol is not a medical term, but rather a chemical compound. Medically, it is classified as a humectant, which means it helps retain moisture. It is used in various pharmaceutical and cosmetic products as a solvent, preservative, and moisturizer. In medical settings, it can be found in topical creams, oral and injectable medications, and intravenous (IV) fluids.

The chemical definition of propylene glycol is:

Propylene glycol (IUPAC name: propan-1,2-diol) is a synthetic organic compound with the formula CH3CH(OH)CH2OH. It is a viscous, colorless, and nearly odorless liquid that is miscible with water, acetone, and chloroform. Propylene glycol is used as an antifreeze when mixed with water, as a solvent in the production of polymers, and as a moisturizer in various pharmaceutical and cosmetic products. It has a sweet taste and is considered generally recognized as safe (GRAS) by the U.S. Food and Drug Administration (FDA) for use as a food additive.

Glyceraldehyde is a triose, a simple sugar consisting of three carbon atoms. It is a clear, colorless, sweet-tasting liquid that is used as a sweetener and preservative in the food industry. In the medical field, glyceraldehyde is used in research and diagnostics, particularly in the study of carbohydrate metabolism and enzyme function.

Glyceraldehyde is also an important intermediate in the glycolytic pathway, which is a series of reactions that convert glucose into pyruvate, producing ATP and NADH as energy-rich compounds. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) is an enzyme that catalyzes the conversion of glyceraldehyde 3-phosphate to 1,3-bisphosphoglycerate in this pathway.

In addition, glyceraldehyde has been studied for its potential role in the development of diabetic complications and other diseases associated with carbohydrate metabolism disorders.

Gluconeogenesis is a metabolic pathway that occurs in the liver, kidneys, and to a lesser extent in the small intestine. It involves the synthesis of glucose from non-carbohydrate precursors such as lactate, pyruvate, glycerol, and certain amino acids. This process becomes particularly important during periods of fasting or starvation when glucose levels in the body begin to drop, and there is limited carbohydrate intake to replenish them.

Gluconeogenesis helps maintain blood glucose homeostasis by providing an alternative source of glucose for use by various tissues, especially the brain, which relies heavily on glucose as its primary energy source. It is a complex process that involves several enzymatic steps, many of which are regulated to ensure an adequate supply of glucose while preventing excessive production, which could lead to hyperglycemia.

Nonesterified fatty acids (NEFA), also known as free fatty acids (FFA), refer to fatty acid molecules that are not bound to glycerol in the form of triglycerides or other esters. In the bloodstream, NEFAs are transported while bound to albumin and can serve as a source of energy for peripheral tissues. Under normal physiological conditions, NEFA levels are tightly regulated by the body; however, elevated NEFA levels have been associated with various metabolic disorders such as insulin resistance, obesity, and type 2 diabetes.

Carbon isotopes are variants of the chemical element carbon that have different numbers of neutrons in their atomic nuclei. The most common and stable isotope of carbon is carbon-12 (^{12}C), which contains six protons and six neutrons. However, carbon can also come in other forms, known as isotopes, which contain different numbers of neutrons.

Carbon-13 (^{13}C) is a stable isotope of carbon that contains seven neutrons in its nucleus. It makes up about 1.1% of all carbon found on Earth and is used in various scientific applications, such as in tracing the metabolic pathways of organisms or in studying the age of fossilized materials.

Carbon-14 (^{14}C), also known as radiocarbon, is a radioactive isotope of carbon that contains eight neutrons in its nucleus. It is produced naturally in the atmosphere through the interaction of cosmic rays with nitrogen gas. Carbon-14 has a half-life of about 5,730 years, which makes it useful for dating organic materials, such as archaeological artifacts or fossils, up to around 60,000 years old.

Carbon isotopes are important in many scientific fields, including geology, biology, and medicine, and are used in a variety of applications, from studying the Earth's climate history to diagnosing medical conditions.

Phosphotransferases are a group of enzymes that catalyze the transfer of a phosphate group from a donor molecule to an acceptor molecule. This reaction is essential for various cellular processes, including energy metabolism, signal transduction, and biosynthesis.

The systematic name for this group of enzymes is phosphotransferase, which is derived from the general reaction they catalyze: D-donor + A-acceptor = D-donor minus phosphate + A-phosphate. The donor molecule can be a variety of compounds, such as ATP or a phosphorylated protein, while the acceptor molecule is typically a compound that becomes phosphorylated during the reaction.

Phosphotransferases are classified into several subgroups based on the type of donor and acceptor molecules they act upon. For example, kinases are a subgroup of phosphotransferases that transfer a phosphate group from ATP to a protein or other organic compound. Phosphatases, another subgroup, remove phosphate groups from molecules by transferring them to water.

Overall, phosphotransferases play a critical role in regulating many cellular functions and are important targets for drug development in various diseases, including cancer and neurological disorders.

Decanoates are a type of esterified form of certain drugs or medications, particularly in the case of testosterone. The decanoate ester is attached to the testosterone molecule to create a longer-acting formulation. Testosterone decanoate is a slow-release form of testosterone that is used as a replacement therapy for individuals who have low levels of natural testosterone. It is administered through intramuscular injection and has a duration of action of approximately 2-3 weeks.

Other medications may also be available in decanoate ester form, but testosterone decanoate is one of the most commonly used. As with any medication or treatment plan, it's important to consult with a healthcare provider to determine the best course of action based on individual needs and medical history.

Culture media is a substance that is used to support the growth of microorganisms or cells in an artificial environment, such as a petri dish or test tube. It typically contains nutrients and other factors that are necessary for the growth and survival of the organisms being cultured. There are many different types of culture media, each with its own specific formulation and intended use. Some common examples include blood agar, which is used to culture bacteria; Sabouraud dextrose agar, which is used to culture fungi; and Eagle's minimum essential medium, which is used to culture animal cells.

Glycerol-3-Phosphate O-Acyltransferase (GPAT) is an enzyme that plays a crucial role in the biosynthesis of triacylglycerols and phospholipids, which are major components of cellular membranes and energy storage molecules. The GPAT enzyme catalyzes the initial and rate-limiting step in the glycerolipid synthesis pathway, specifically the transfer of an acyl group from an acyl-CoA donor to the sn-1 position of glycerol-3-phosphate, forming lysophosphatidic acid (LPA). This reaction is essential for the production of various glycerolipids, including phosphatidic acid, diacylglycerol, and triacylglycerol. There are four isoforms of GPAT (GPAT1-4) in humans, each with distinct subcellular localizations and functions. Dysregulation of GPAT activity has been implicated in several pathological conditions, such as metabolic disorders, cardiovascular diseases, and cancers.

Osmotic pressure is a fundamental concept in the field of physiology and biochemistry. It refers to the pressure that is required to be applied to a solution to prevent the flow of solvent (like water) into it, through a semi-permeable membrane, when the solution is separated from a pure solvent or a solution of lower solute concentration.

In simpler terms, osmotic pressure is the force that drives the natural movement of solvent molecules from an area of lower solute concentration to an area of higher solute concentration, across a semi-permeable membrane. This process is crucial for maintaining the fluid balance and nutrient transport in living organisms.

The osmotic pressure of a solution can be determined by its solute concentration, temperature, and the ideal gas law. It is often expressed in units of atmospheres (atm), millimeters of mercury (mmHg), or pascals (Pa). In medical contexts, understanding osmotic pressure is essential for managing various clinical conditions such as dehydration, fluid and electrolyte imbalances, and dialysis treatments.

I'm sorry for any confusion, but "Propane" is not a medical term. It is a chemical compound commonly used as a fuel for heating, cooking, and engines. Propane is a gas at room temperature and pressure, but it can be liquefied under moderate pressure and stored in cylinders or tanks.

If you have any questions about a medical term or concept, I'd be happy to try to help answer those for you!

Fatty acids are carboxylic acids with a long aliphatic chain, which are important components of lipids and are widely distributed in living organisms. They can be classified based on the length of their carbon chain, saturation level (presence or absence of double bonds), and other structural features.

The two main types of fatty acids are:

1. Saturated fatty acids: These have no double bonds in their carbon chain and are typically solid at room temperature. Examples include palmitic acid (C16:0) and stearic acid (C18:0).
2. Unsaturated fatty acids: These contain one or more double bonds in their carbon chain and can be further classified into monounsaturated (one double bond) and polyunsaturated (two or more double bonds) fatty acids. Examples of unsaturated fatty acids include oleic acid (C18:1, monounsaturated), linoleic acid (C18:2, polyunsaturated), and alpha-linolenic acid (C18:3, polyunsaturated).

Fatty acids play crucial roles in various biological processes, such as energy storage, membrane structure, and cell signaling. Some essential fatty acids cannot be synthesized by the human body and must be obtained through dietary sources.

Fermentation is a metabolic process in which an organism converts carbohydrates into alcohol or organic acids using enzymes. In the absence of oxygen, certain bacteria, yeasts, and fungi convert sugars into carbon dioxide, hydrogen, and various end products, such as alcohol, lactic acid, or acetic acid. This process is commonly used in food production, such as in making bread, wine, and beer, as well as in industrial applications for the production of biofuels and chemicals.

Propanediol Dehydratase is not a medical term per se, but rather a biochemical term. It refers to an enzyme that catalyzes the conversion of 1,2-propanediol (also known as propylene glycol) into propionaldehyde and water in the metabolic pathway known as the glycerol/propanediol utilization (GUD) system.

The reaction catalyzed by Propanediol Dehydratase is:
(CH3)2CH(OH)CH2OH → CH3CH2CHO + H2O

This enzyme is found in certain bacteria and archaea that are capable of utilizing 1,2-propanediol as a carbon source for growth. Deficiency or absence of this enzyme can affect the metabolic capabilities of these microorganisms.

Teichoic acids are complex polymers of glycerol or ribitol linked by phosphate groups, found in the cell wall of gram-positive bacteria. They play a crucial role in the bacterial cell's defense against hostile environments and can also contribute to virulence by helping the bacteria evade the host's immune system. Teichoic acids can be either linked to peptidoglycan (wall teichoic acids) or to membrane lipids (lipoteichoic acids). They can vary in structure and composition among different bacterial species, which can have implications for the design of antibiotics and other therapeutics.

'Escherichia coli' (E. coli) is a type of gram-negative, facultatively anaerobic, rod-shaped bacterium that commonly inhabits the intestinal tract of humans and warm-blooded animals. It is a member of the family Enterobacteriaceae and one of the most well-studied prokaryotic model organisms in molecular biology.

While most E. coli strains are harmless and even beneficial to their hosts, some serotypes can cause various forms of gastrointestinal and extraintestinal illnesses in humans and animals. These pathogenic strains possess virulence factors that enable them to colonize and damage host tissues, leading to diseases such as diarrhea, urinary tract infections, pneumonia, and sepsis.

E. coli is a versatile organism with remarkable genetic diversity, which allows it to adapt to various environmental niches. It can be found in water, soil, food, and various man-made environments, making it an essential indicator of fecal contamination and a common cause of foodborne illnesses. The study of E. coli has contributed significantly to our understanding of fundamental biological processes, including DNA replication, gene regulation, and protein synthesis.

Medical definitions of water generally describe it as a colorless, odorless, tasteless liquid that is essential for all forms of life. It is a universal solvent, making it an excellent medium for transporting nutrients and waste products within the body. Water constitutes about 50-70% of an individual's body weight, depending on factors such as age, sex, and muscle mass.

In medical terms, water has several important functions in the human body:

1. Regulation of body temperature through perspiration and respiration.
2. Acting as a lubricant for joints and tissues.
3. Facilitating digestion by helping to break down food particles.
4. Transporting nutrients, oxygen, and waste products throughout the body.
5. Helping to maintain healthy skin and mucous membranes.
6. Assisting in the regulation of various bodily functions, such as blood pressure and heart rate.

Dehydration can occur when an individual does not consume enough water or loses too much fluid due to illness, exercise, or other factors. This can lead to a variety of symptoms, including dry mouth, fatigue, dizziness, and confusion. Severe dehydration can be life-threatening if left untreated.

"Freezing" is a term used in the medical field to describe a phenomenon that can occur in certain neurological conditions, most notably in Parkinson's disease. It refers to a sudden and temporary inability to move or initiate movement, often triggered by environmental factors such as narrow spaces, turning, or approaching a destination. This can increase the risk of falls and make daily activities challenging for affected individuals.

Freezing is also known as "freezing of gait" (FOG) when it specifically affects a person's ability to walk. During FOG episodes, the person may feel like their feet are glued to the ground, making it difficult to take steps forward. This can be very distressing and debilitating for those affected.

It is important to note that "freezing" has different meanings in different medical contexts, such as in the field of orthopedics, where it may refer to a loss of joint motion due to stiffness or inflammation. Always consult with a healthcare professional for accurate information tailored to your specific situation.

Sugar alcohols, also known as polyols, are carbohydrates that are chemically similar to sugar but have a different molecular structure. They occur naturally in some fruits and vegetables, but most sugar alcohols used in food products are manufactured.

The chemical structure of sugar alcohols contains a hydroxyl group (-OH) instead of a hydrogen and a ketone or aldehyde group, which makes them less sweet than sugar and have fewer calories. They are not completely absorbed by the body, so they do not cause a rapid increase in blood glucose levels, making them a popular sweetener for people with diabetes.

Common sugar alcohols used in food products include xylitol, sorbitol, mannitol, erythritol, and maltitol. They are often used as sweeteners in sugar-free and low-sugar foods such as candy, chewing gum, baked goods, and beverages.

However, consuming large amounts of sugar alcohols can cause digestive symptoms such as bloating, gas, and diarrhea, due to their partial absorption in the gut. Therefore, it is recommended to consume them in moderation.

Phospholipids are a major class of lipids that consist of a hydrophilic (water-attracting) head and two hydrophobic (water-repelling) tails. The head is composed of a phosphate group, which is often bound to an organic molecule such as choline, ethanolamine, serine or inositol. The tails are made up of two fatty acid chains.

Phospholipids are a key component of cell membranes and play a crucial role in maintaining the structural integrity and function of the cell. They form a lipid bilayer, with the hydrophilic heads facing outwards and the hydrophobic tails facing inwards, creating a barrier that separates the interior of the cell from the outside environment.

Phospholipids are also involved in various cellular processes such as signal transduction, intracellular trafficking, and protein function regulation. Additionally, they serve as emulsifiers in the digestive system, helping to break down fats in the diet.

Paper chromatography is a type of chromatography technique that involves the separation and analysis of mixtures based on their components' ability to migrate differently upon capillary action on a paper medium. This simple and cost-effective method utilizes a paper, typically made of cellulose, as the stationary phase. The sample mixture is applied as a small spot near one end of the paper, and then the other end is dipped into a developing solvent or a mixture of solvents (mobile phase) in a shallow container.

As the mobile phase moves up the paper by capillary action, components within the sample mixture separate based on their partition coefficients between the stationary and mobile phases. The partition coefficient describes how much a component prefers to be in either the stationary or mobile phase. Components with higher partition coefficients in the mobile phase will move faster and further than those with lower partition coefficients.

Once separation is complete, the paper is dried and can be visualized under ultraviolet light or by using chemical reagents specific for the components of interest. The distance each component travels from the origin (point of application) and its corresponding solvent front position are measured, allowing for the calculation of Rf values (retardation factors). Rf is a dimensionless quantity calculated as the ratio of the distance traveled by the component to the distance traveled by the solvent front.

Rf = (distance traveled by component) / (distance traveled by solvent front)

Paper chromatography has been widely used in various applications, such as:

1. Identification and purity analysis of chemical compounds in pharmaceuticals, forensics, and research laboratories.
2. Separation and detection of amino acids, sugars, and other biomolecules in biological samples.
3. Educational purposes to demonstrate the principles of chromatography and separation techniques.

Despite its limitations, such as lower resolution compared to high-performance liquid chromatography (HPLC) and less compatibility with volatile or nonpolar compounds, paper chromatography remains a valuable tool for quick, qualitative analysis in various fields.

Thin-layer chromatography (TLC) is a type of chromatography used to separate, identify, and quantify the components of a mixture. In TLC, the sample is applied as a small spot onto a thin layer of adsorbent material, such as silica gel or alumina, which is coated on a flat, rigid support like a glass plate. The plate is then placed in a developing chamber containing a mobile phase, typically a mixture of solvents.

As the mobile phase moves up the plate by capillary action, it interacts with the stationary phase and the components of the sample. Different components of the mixture travel at different rates due to their varying interactions with the stationary and mobile phases, resulting in distinct spots on the plate. The distance each component travels can be measured and compared to known standards to identify and quantify the components of the mixture.

TLC is a simple, rapid, and cost-effective technique that is widely used in various fields, including forensics, pharmaceuticals, and research laboratories. It allows for the separation and analysis of complex mixtures with high resolution and sensitivity, making it an essential tool in many analytical applications.

Triglycerides are the most common type of fat in the body, and they're found in the food we eat. They're carried in the bloodstream to provide energy to the cells in our body. High levels of triglycerides in the blood can increase the risk of heart disease, especially in combination with other risk factors such as high LDL (bad) cholesterol, low HDL (good) cholesterol, and high blood pressure.

It's important to note that while triglycerides are a type of fat, they should not be confused with cholesterol, which is a waxy substance found in the cells of our body. Both triglycerides and cholesterol are important for maintaining good health, but high levels of either can increase the risk of heart disease.

Triglyceride levels are measured through a blood test called a lipid panel or lipid profile. A normal triglyceride level is less than 150 mg/dL. Borderline-high levels range from 150 to 199 mg/dL, high levels range from 200 to 499 mg/dL, and very high levels are 500 mg/dL or higher.

Elevated triglycerides can be caused by various factors such as obesity, physical inactivity, excessive alcohol consumption, smoking, and certain medical conditions like diabetes, hypothyroidism, and kidney disease. Medications such as beta-blockers, steroids, and diuretics can also raise triglyceride levels.

Lifestyle changes such as losing weight, exercising regularly, eating a healthy diet low in saturated and trans fats, avoiding excessive alcohol consumption, and quitting smoking can help lower triglyceride levels. In some cases, medication may be necessary to reduce triglycerides to recommended levels.

Temperature, in a medical context, is a measure of the degree of hotness or coldness of a body or environment. It is usually measured using a thermometer and reported in degrees Celsius (°C), degrees Fahrenheit (°F), or kelvin (K). In the human body, normal core temperature ranges from about 36.5-37.5°C (97.7-99.5°F) when measured rectally, and can vary slightly depending on factors such as time of day, physical activity, and menstrual cycle. Elevated body temperature is a common sign of infection or inflammation, while abnormally low body temperature can indicate hypothermia or other medical conditions.

Lipid mobilization, also known as lipolysis, is the process by which fat cells (adipocytes) break down stored triglycerides into free fatty acids and glycerol, which can then be released into the bloodstream and used for energy by the body's cells. This process is regulated by hormones such as adrenaline, noradrenaline, glucagon, and cortisol, which activate enzymes in the fat cell that catalyze the breakdown of triglycerides. Lipid mobilization is an important physiological response to fasting, exercise, and stress, and plays a key role in maintaining energy homeostasis in the body.

Acetates, in a medical context, most commonly refer to compounds that contain the acetate group, which is an functional group consisting of a carbon atom bonded to two hydrogen atoms and an oxygen atom (-COO-). An example of an acetate is sodium acetate (CH3COONa), which is a salt formed from acetic acid (CH3COOH) and is often used as a buffering agent in medical solutions.

Acetates can also refer to a group of medications that contain acetate as an active ingredient, such as magnesium acetate, which is used as a laxative, or calcium acetate, which is used to treat high levels of phosphate in the blood.

In addition, acetates can also refer to a process called acetylation, which is the addition of an acetyl group (-COCH3) to a molecule. This process can be important in the metabolism and regulation of various substances within the body.

"Laureates" is not a medical term. However, if you are referring to "laurates" as a salt or ester of lauric acid, then here's the definition:

Laurates are organic compounds that contain a laurate group, which is the anion (negatively charged ion) derived from lauric acid. Lauric acid is a saturated fatty acid with a 12-carbon chain, and its anion has the chemical formula CH3(CH2)10COO-.

Laurates can be formed by reacting lauric acid with a base to form a salt (e.g., sodium laurate, potassium laurate) or by reacting it with an alcohol to form an ester (e.g., methyl laurate, ethyl laurate). These compounds have various applications in industry, including as surfactants, emulsifiers, and solubilizers in personal care products, cosmetics, and pharmaceuticals.

Lactic acid, also known as 2-hydroxypropanoic acid, is a chemical compound that plays a significant role in various biological processes. In the context of medicine and biochemistry, lactic acid is primarily discussed in relation to muscle metabolism and cellular energy production. Here's a medical definition for lactic acid:

Lactic acid (LA): A carboxylic acid with the molecular formula C3H6O3 that plays a crucial role in anaerobic respiration, particularly during strenuous exercise or conditions of reduced oxygen availability. It is formed through the conversion of pyruvate, catalyzed by the enzyme lactate dehydrogenase (LDH), when there is insufficient oxygen to complete the final step of cellular respiration in the Krebs cycle. The accumulation of lactic acid can lead to acidosis and muscle fatigue. Additionally, lactic acid serves as a vital intermediary in various metabolic pathways and is involved in the production of glucose through gluconeogenesis in the liver.

Carbohydrate metabolism is the process by which the body breaks down carbohydrates into glucose, which is then used for energy or stored in the liver and muscles as glycogen. This process involves several enzymes and chemical reactions that convert carbohydrates from food into glucose, fructose, or galactose, which are then absorbed into the bloodstream and transported to cells throughout the body.

The hormones insulin and glucagon regulate carbohydrate metabolism by controlling the uptake and storage of glucose in cells. Insulin is released from the pancreas when blood sugar levels are high, such as after a meal, and promotes the uptake and storage of glucose in cells. Glucagon, on the other hand, is released when blood sugar levels are low and signals the liver to convert stored glycogen back into glucose and release it into the bloodstream.

Disorders of carbohydrate metabolism can result from genetic defects or acquired conditions that affect the enzymes or hormones involved in this process. Examples include diabetes, hypoglycemia, and galactosemia. Proper management of these disorders typically involves dietary modifications, medication, and regular monitoring of blood sugar levels.

Adipose tissue, also known as fatty tissue, is a type of connective tissue that is composed mainly of adipocytes (fat cells). It is found throughout the body, but is particularly abundant in the abdominal cavity, beneath the skin, and around organs such as the heart and kidneys.

Adipose tissue serves several important functions in the body. One of its primary roles is to store energy in the form of fat, which can be mobilized and used as an energy source during periods of fasting or exercise. Adipose tissue also provides insulation and cushioning for the body, and produces hormones that help regulate metabolism, appetite, and reproductive function.

There are two main types of adipose tissue: white adipose tissue (WAT) and brown adipose tissue (BAT). WAT is the more common form and is responsible for storing energy as fat. BAT, on the other hand, contains a higher number of mitochondria and is involved in heat production and energy expenditure.

Excessive accumulation of adipose tissue can lead to obesity, which is associated with an increased risk of various health problems such as diabetes, heart disease, and certain types of cancer.

Semen preservation is the process of collecting, liquefying, testing, and storing semen samples for future use in assisted reproductive technologies (ART) such as artificial insemination (AI), in vitro fertilization (IVF), or intracytoplasmic sperm injection (ICSI). The semen sample is usually collected through masturbation, and then it is mixed with a cryoprotectant solution to prevent damage during the freezing and thawing process. After that, the sample is divided into straws or vials and frozen in liquid nitrogen tanks at temperatures below -196°C. Properly preserved semen can be stored for many years without significant loss of quality or fertility potential. Semen preservation is often recommended for men who are about to undergo medical treatments that may affect their sperm production or fertility, such as chemotherapy or radiation therapy, or for those who wish to postpone fatherhood for personal or medical reasons.

Lactates, also known as lactic acid, are compounds that are produced by muscles during intense exercise or other conditions of low oxygen supply. They are formed from the breakdown of glucose in the absence of adequate oxygen to complete the full process of cellular respiration. This results in the production of lactate and a hydrogen ion, which can lead to a decrease in pH and muscle fatigue.

In a medical context, lactates may be measured in the blood as an indicator of tissue oxygenation and metabolic status. Elevated levels of lactate in the blood, known as lactic acidosis, can indicate poor tissue perfusion or hypoxia, and may be seen in conditions such as sepsis, cardiac arrest, and severe shock. It is important to note that lactates are not the primary cause of acidemia (low pH) in lactic acidosis, but rather a marker of the underlying process.

Glycols are a type of organic compound that contain two hydroxyl (OH) groups attached to adjacent carbon atoms. They are colorless, odorless, and have a sweet taste. The most common glycols are ethylene glycol and propylene glycol. Ethylene glycol is widely used as an automotive antifreeze and in the manufacture of polyester fibers and resins, while propylene glycol is used as a food additive, in pharmaceuticals, and as a solvent in various industries. Glycols are also used as a coolant, humectant, and in the production of unsaturated polyester resins. Exposure to high levels of glycols can cause irritation to the eyes, skin, and respiratory tract, and ingestion can be harmful or fatal.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

"Gluconobacter" is a genus of gram-negative, aerobic bacteria that are capable of oxidizing various alcohols and sugars into their corresponding acids. These bacteria are often found in fruit, flowers, and sap, as well as in fermented foods and beverages. They are known for their ability to rapidly and efficiently oxidize glucose into gluconic acid, which gives them their name. Some species of Gluconobacter can also cause disease in humans, particularly in individuals with weakened immune systems. In medical contexts, Gluconobacter species may be associated with infections such as bacteremia, endocarditis, and peritonitis.

"Saccharomyces cerevisiae" is not typically considered a medical term, but it is a scientific name used in the field of microbiology. It refers to a species of yeast that is commonly used in various industrial processes, such as baking and brewing. It's also widely used in scientific research due to its genetic tractability and eukaryotic cellular organization.

However, it does have some relevance to medical fields like medicine and nutrition. For example, certain strains of S. cerevisiae are used as probiotics, which can provide health benefits when consumed. They may help support gut health, enhance the immune system, and even assist in the digestion of certain nutrients.

In summary, "Saccharomyces cerevisiae" is a species of yeast with various industrial and potential medical applications.

Cobamides are a class of compounds that are structurally related to vitamin B12 (cobalamin). They consist of a corrin ring, which is a large heterocyclic ring made up of four pyrrole rings, and a cobalt ion in the center. The lower axial ligand of the cobalt ion can be a variety of different groups, including cyano, hydroxo, methyl, or 5'-deoxyadenosyl groups.

Cobamides are involved in a number of important biological processes, including the synthesis of amino acids and nucleotides, the metabolism of fatty acids and cholesterol, and the regulation of gene expression. They function as cofactors for enzymes called cobamide-dependent methyltransferases, which transfer methyl groups (CH3) from one molecule to another.

Cobamides are found in a wide variety of organisms, including bacteria, archaea, and eukaryotes. In humans, the most important cobamide is vitamin B12, which is essential for the normal functioning of the nervous system and the production of red blood cells. Vitamin B12 deficiency can lead to neurological problems and anemia.

Phosphatidylglycerols are a type of glycerophospholipids, which are major components of biological membranes. They are composed of a glycerol backbone to which two fatty acid chains and a phosphate group are attached. In the case of phosphatidylglycerols, the phosphate group is linked to a glycerol molecule through an ester bond, forming a phosphoglyceride.

Phosphatidylglycerols are unique because they have an additional glycerol molecule attached to the phosphate group, making them more complex than other glycerophospholipids such as phosphatidylcholine or phosphatidylethanolamine. This additional glycerol moiety can be further modified by the addition of various headgroups, leading to the formation of different subclasses of phosphatidylglycerols.

In biological membranes, phosphatidylglycerols are often found in the inner leaflet of the mitochondrial membrane and play important roles in maintaining the structure and function of this organelle. They have also been implicated in various cellular processes such as membrane fusion, protein trafficking, and bacterial cell wall biosynthesis.

Osmolar concentration is a measure of the total number of solute particles (such as ions or molecules) dissolved in a solution per liter of solvent (usually water), which affects the osmotic pressure. It is expressed in units of osmoles per liter (osmol/L). Osmolarity and osmolality are related concepts, with osmolarity referring to the number of osmoles per unit volume of solution, typically measured in liters, while osmolality refers to the number of osmoles per kilogram of solvent. In clinical contexts, osmolar concentration is often used to describe the solute concentration of bodily fluids such as blood or urine.

'Clostridium butyricum' is a gram-positive, spore-forming, rod-shaped bacterium that is commonly found in the environment, including soil and water. It is also part of the normal gut microbiota in humans and animals. This organism produces butyric acid as one of its main fermentation products, hence the name 'butyricum'.

While 'Clostridium butyricum' can sometimes be associated with human diseases, particularly in individuals with weakened immune systems or underlying gastrointestinal disorders, it is also being investigated for its potential probiotic properties. Some studies suggest that certain strains of this bacterium may help prevent and treat various conditions, such as antibiotic-associated diarrhea, irritable bowel syndrome, and inflammatory bowel disease. However, more research is needed to confirm these findings and establish the safety and efficacy of 'Clostridium butyricum' as a probiotic.

Anaerobiosis is a state in which an organism or a portion of an organism is able to live and grow in the absence of molecular oxygen (O2). In biological contexts, "anaerobe" refers to any organism that does not require oxygen for growth, and "aerobe" refers to an organism that does require oxygen for growth.

There are two types of anaerobes: obligate anaerobes, which cannot tolerate the presence of oxygen and will die if exposed to it; and facultative anaerobes, which can grow with or without oxygen but prefer to grow in its absence. Some organisms are able to switch between aerobic and anaerobic metabolism depending on the availability of oxygen, a process known as "facultative anaerobiosis."

Anaerobic respiration is a type of metabolic process that occurs in the absence of molecular oxygen. In this process, organisms use alternative electron acceptors other than oxygen to generate energy through the transfer of electrons during cellular respiration. Examples of alternative electron acceptors include nitrate, sulfate, and carbon dioxide.

Anaerobic metabolism is less efficient than aerobic metabolism in terms of energy production, but it allows organisms to survive in environments where oxygen is not available or is toxic. Anaerobic bacteria are important decomposers in many ecosystems, breaking down organic matter and releasing nutrients back into the environment. In the human body, anaerobic bacteria can cause infections and other health problems if they proliferate in areas with low oxygen levels, such as the mouth, intestines, or deep tissue wounds.

The liver is a large, solid organ located in the upper right portion of the abdomen, beneath the diaphragm and above the stomach. It plays a vital role in several bodily functions, including:

1. Metabolism: The liver helps to metabolize carbohydrates, fats, and proteins from the food we eat into energy and nutrients that our bodies can use.
2. Detoxification: The liver detoxifies harmful substances in the body by breaking them down into less toxic forms or excreting them through bile.
3. Synthesis: The liver synthesizes important proteins, such as albumin and clotting factors, that are necessary for proper bodily function.
4. Storage: The liver stores glucose, vitamins, and minerals that can be released when the body needs them.
5. Bile production: The liver produces bile, a digestive juice that helps to break down fats in the small intestine.
6. Immune function: The liver plays a role in the immune system by filtering out bacteria and other harmful substances from the blood.

Overall, the liver is an essential organ that plays a critical role in maintaining overall health and well-being.

Sucrose is a type of simple sugar, also known as a carbohydrate. It is a disaccharide, which means that it is made up of two monosaccharides: glucose and fructose. Sucrose occurs naturally in many fruits and vegetables and is often extracted and refined for use as a sweetener in food and beverages.

The chemical formula for sucrose is C12H22O11, and it has a molecular weight of 342.3 g/mol. In its pure form, sucrose is a white, odorless, crystalline solid that is highly soluble in water. It is commonly used as a reference compound for determining the sweetness of other substances, with a standard sucrose solution having a sweetness value of 1.0.

Sucrose is absorbed by the body through the small intestine and metabolized into glucose and fructose, which are then used for energy or stored as glycogen in the liver and muscles. While moderate consumption of sucrose is generally considered safe, excessive intake can contribute to weight gain, tooth decay, and other health problems.

Ethylene glycols are a class of synthetic chemical compounds that are commonly used as automotive antifreeze, de-icing agents, and as raw materials in the manufacture of polyester fibers and resins. The two most common types of ethylene glycol are ethylene glycol monoethyl ether (also known as ethylene glycol monomethyl ether or EGME) and diethylene glycol (DEG).

Ethylene glycols are colorless, odorless liquids with a sweet taste. They are highly toxic to humans and animals if ingested, inhaled, or absorbed through the skin. Exposure can cause a range of symptoms, including nausea, vomiting, abdominal pain, dizziness, confusion, seizures, coma, and even death.

In medical terms, ethylene glycols are often referred to as "toxic alcohols" or "antifreeze poisoning" when they cause toxicity in humans. Treatment typically involves supportive care, such as fluid replacement and kidney dialysis, as well as the use of specific antidotes, such as fomepizole or ethanol, to prevent further absorption and metabolism of the toxic alcohol.

... kinase ATP ADP Glycerol-3-phosphate Glycerol-3-phosphate dehydrogenase NAD+ NADH NAD+ NADH Dihydroxyacetone ... An oxidation of glycerol affords mesoxalic acid. Dehydrating glycerol affords hydroxyacetone. Glycerol is used as fill for ... Glycerol is mainly metabolized in the liver. Glycerol injections can be used as a simple test for liver damage, as its rate of ... glycerol 3-phosphate is obtained from dihydroxyacetone phosphate with the enzyme glycerol-3-phosphate dehydrogenase. Glycerol ...
... catalyzes the transfer of a phosphate from ATP to glycerol thus forming glycerol 3-phosphate: ATP + glycerol ... sn-glycerol 3-phosphate Adipocytes lack glycerol kinase so they cannot metabolize the glycerol produced during triacyl glycerol ... This glycerol is instead shuttled to the liver via the blood where it is: Phosphorylated by glycerol kinase to glycerol 3- ... Glycerol Kinase Glycerol+Kinase at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Selwood T, Jaffe EK ( ...
... may refer to: Glycerol 1-phosphate Glycerol 2-phosphate Glycerol 3-phosphate This set index article lists ...
In enzymology, a glycerol dehydratase (EC 4.2.1.30) catalyzes the chemical reaction glycerol ⇌ {\displaystyle \ ... Forage RG, Foster MA (1982). "Glycerol fermentation in Klebsiella pneumoniae: functions of the coenzyme B12-dependent glycerol ... Other names in common use include glycerol dehydrase, and glycerol hydro-lyase. This enzyme participates in glycerolipid ... Schneider Z, Larsen EG, Jacobson G, Johnson BC, Pawelkiewicz J (1970). "Purification and properties of glycerol dehydrase". J. ...
Chemically it is the glycerol ester of stearic acid. It is also used as hydration powder in exercise formulas Glycerol ... and glycerol. Glycerol monostearate occurs naturally in the body as a product of the breakdown of fats by pancreatic lipase. It ... the enantiomeric pair of 1-glycerol monostearate and 2-glycerol monostearate. Typically these are encountered as a mixture as ... Glycerol monostearate, commonly known as GMS, is a monoglyceride commonly used as an emulsifier in foods. It takes the form of ...
... , sold under the brand name Ravicti, is a medication used in the treatment of certain inborn urea cycle ... glycerol phenylbutyrate liquid". DailyMed. 13 September 2021. Archived from the original on 3 May 2023. Retrieved 4 July 2023 ...
... (EC 1.1.1.6, also known as NAD+-linked glycerol dehydrogenase, glycerol: NAD+ 2-oxidoreductase, GDH, ... As a catalyst for the conversion of glycerol to glycerone, glycerol dehydrogenase is one such enzyme being investigated for ... Glycerol dehydrogenase (NADP+) Glycerol dehydrogenase (acceptor) Notes Mallinder, Phillip R.; Pritchard, Andrew; Moir, Anne ( ... Encoded by the gene gldA, the enzyme glycerol dehydrogenase, GlyDH catalyzes the oxidation of glycerol to glycerone. Unlike ...
Other names in common use include α-glycerophosphatase, α-glycerol phosphatase, glycerol 3-phosphatase, glycerol-3-phosphate ... The enzyme glycerol-1-phosphatase (EC 3.1.3.21) catalyzes the reaction glycerol 1-phosphate + H2O ⇌ {\displaystyle \ ... 2 February 2001). "The Yeast Glycerol 3-Phosphatases Gpp1p and Gpp2p Are Required for Glycerol Biosynthesis and Differentially ... "Disruption of a gene encoding glycerol 3-phosphatase from Candida albicans impairs intracellular glycerol accumulation-mediated ...
CoA Glycerol-1-phosphatase catalyzes the hydrolysis of glycerol 3-phosphate to regenerate glycerol, allowing glycerol ... Glycerol 1-phosphate, sometimes called as D-glycerol 3-phosphate, is the enantiomer of glycerol 3-phosphate. Most higher ... The Glycerol 3-phosphate shuttle is an emergency back-up system to supply neurons' demand of energy. Glycerol-3-phosphate was ... From a historical reason, it is also known as L-glycerol 3-phosphate, D-glycerol 1-phosphate, L-α-glycerophosphoric acid. ...
In enzymology, a CDP-glycerol diphosphatase (EC 3.6.1.16) is an enzyme that catalyzes the chemical reaction CDP-glycerol + H2O ... the two substrates of this enzyme are CDP-glycerol and H2O, whereas its two products are CMP and sn-glycerol 3-phosphate. This ... The systematic name of this enzyme class is CDP-glycerol phosphoglycerohydrolase. Other names in common use include CDP- ... glycerol pyrophosphatase, and cytidine diphosphoglycerol pyrophosphatase. This enzyme participates in glycerophospholipid ...
... is the conjugate base of phosphoric ester of glycerol. It is commonly known as β-glycerophosphate or BGP. ... Unlike glycerol 1-phosphate and glycerol 3-phosphate, this isomer is not chiral. It is also less common. β-Glycerophosphate is ...
Other names in common use include PPi-glycerol phosphotransferase, and pyrophosphate-glycerol phosphotransferase. Stetten MR ( ... glycerol 1-phosphate Thus, the two substrates of this enzyme are diphosphate and glycerol, whereas its two products are ... In enzymology, a diphosphate-glycerol phosphotransferase (EC 2.7.1.79) is an enzyme that catalyzes the chemical reaction ... The systematic name of this enzyme class is diphosphate:glycerol 1-phosphotransferase. ...
The enzyme glycerol-2-phosphatase (EC 3.1.3.19) catalyzes the reaction glycerol 2-phosphate + H2O ⇌ {\displaystyle \ ... The systematic name is glycerol-2-phosphate phosphohydrolase. Other names in common use include β-glycerophosphatase, β- ... rightleftharpoons } glycerol + phosphate This enzyme belongs to the family of hydrolases, specifically those acting on ...
It catalyzes the transfer of a phosphate group from an ATP to a glycerol molecule forming glycerol (3) phosphate. Then glycerol ... The enzyme glycerol kinase is encoded by the X-chromosome in humans. It acts as a catalyst in the phosphorylation of glycerol ... Glycerol Kinase Deficiency causes the condition known as hyperglycerolemia, an accumulation of glycerol in the blood and urine ... However, when suffering from a glycerol kinase deficiency many of the glycerol molecules released into the bloodstream end up ...
... to glycerol 3-phosphate (1) by oxidizing one molecule of NADH to NAD+ as in the following reaction: Glycerol-3-phosphate is ... The glycerol-3-phosphate shuttle is a mechanism used in skeletal muscle and the brain that regenerates NAD+ from NADH, a by- ... Either the glycerol-3-phosphate shuttle pathway or the malate-aspartate shuttle pathway, depending on the tissue of the ... The glycerol phosphate shuttle was first characterized as a major route of mitochondrial hydride transport in the flight ...
In enzymology, a CDP-glycerol glycerophosphotransferase (EC 2.7.8.12) is an enzyme that catalyzes the chemical reaction CDP- ... The systematic name of this enzyme class is CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase. Other names in ... teichoic acid glycerol transferase, glycerophosphate synthetase, and CGPTase. BURGER MM, GLASER L (1964). "THE SYNTHESIS OF ... the two substrates of this enzyme are CDP-glycerol and (glycerophosphate)n, whereas its two products are CMP and ( ...
In enzymology, a glycerol dehydrogenase (acceptor) (EC 1.1.99.22) is an enzyme that catalyzes the chemical reaction glycerol + ... The systematic name of this enzyme class is glycerol:acceptor 1-oxidoreductase. This enzyme is also called glycerol:(acceptor) ... the two substrates of this enzyme are glycerol and acceptor, whereas its two products are glycerone and reduced acceptor. This ... purification and properties of membrane-bound glycerol dehydrogenase from Gluconobacter industrius". Agric. Biol. Chem. 49 (4 ...
In enzymology, a glycerol 2-dehydrogenase (NADP+) (EC 1.1.1.156) is an enzyme that catalyzes the chemical reaction glycerol + ... The systematic name of this enzyme class is glycerol:NADP+ 2-oxidoreductase (glycerone-forming). Other names in common use ... and glycerol 2-dehydrogenase (NADP+). This enzyme participates in glycerolipid metabolism. Ben-Amotz A, Avron M (1973). "NADP ... NADP+ ⇌ {\displaystyle \rightleftharpoons } glycerone + NADPH + H+ Thus, the two substrates of this enzyme are glycerol and ...
Older terms for glycerol-3-phosphate dehydrogenase include alpha glycerol-3-phosphate dehydrogenase (alphaGPDH) and ... Enhanced GPDH activity, particularly GPD2, leads to an increase in glycerol production. Since glycerol is a main subunit in ... substrate pages: glycerol 3-phosphate, dihydroxyacetone phosphate related topics: glycerol phosphate shuttle, creatine kinase, ... to sn-glycerol 3-phosphate. Glycerol-3-phosphate dehydrogenase serves as a major link between carbohydrate metabolism and lipid ...
... lipids (GDGTs) are a class of membrane lipids synthesized by archaea and some bacteria, ... Rattray, Jayne E.; Smittenberg, Rienk H. (2020). "Separation of Branched and Isoprenoid Glycerol Dialkyl Glycerol Tetraether ( ... "Archaeal and Bacterial Glycerol Dialkyl Glycerol Tetraether Lipids in Hot Springs of Yellowstone National Park". Applied and ... "The organic geochemistry of glycerol dialkyl glycerol tetraether lipids: A review". Organic Geochemistry. 54: 19-61. doi: ...
... is formally the cyclic ester of carbonic acid with glycerol and has aroused great interest as a possible ... Glycerol-1,2-carbonate Sigma-Aldrich Co., product no. {{{id}}}. Entry from Glycerol-1,2-carbonate from TCI Europe, retrieved on ... K. Lanjekar, V.R. Rathod (2013). Utilization of glycerol for the production of glycerol carbonate through greener route. J. ... F.S.H. Simanjuntak (2011). CaO-catalyzed synthesis of glycerol carbonate from glycerol and dimethyl carbonate: Isolation and ...
Other names in common use include glycerol phosphate oxidase, glycerol-1-phosphate oxidase, glycerol phosphate oxidase, L-alpha ... In enzymology, a glycerol-3-phosphate oxidase (EC 1.1.3.21) is an enzyme that catalyzes the chemical reaction sn-glycerol 3- ... Gancedo C, Gancedo JM, Sols A (1968). "Glycerol metabolism in yeasts. Pathways of utilization and production". Eur. J. Biochem ... The systematic name of this enzyme class is sn-glycerol-3-phosphate:oxygen 2-oxidoreductase. ...
CDP-glycerol Thus, the two substrates of this enzyme are CTP and sn-glycerol 3-phosphate, whereas its two products are ... sn-glycerol-3-phosphate cytidylyltransferase. Other names in common use include CDP-glycerol pyrophosphorylase, cytidine ... In enzymology, a glycerol-3-phosphate cytidylyltransferase (EC 2.7.7.39) is an enzyme that catalyzes the chemical reaction CTP ... Shaw DR (February 1962). "Pyrophosphorolysis and enzymic synthesis of cytidine diphosphate glycerol and cytidine diphosphate ...
Creighton TE, Yanofsky C (1966). "Indole-3-glycerol phosphate synthetase of Escherichia coli, an enzyme of the tryptophan ... The enzyme indole-3-glycerol-phosphate synthase (IGPS) (EC 4.1.1.48) catalyzes the chemical reaction 1-(2-carboxyphenylamino)-1 ... glycerol-3-phosphate-forming]. Other names in common use include indoleglycerol phosphate synthetase, indoleglycerol phosphate ... D-ribulose 5-phosphate ⇌ {\displaystyle \rightleftharpoons } 1-C-(indol-3-yl)-glycerol 3-phosphate + CO2 + H2O This enzyme ...
... glycerol phosphate), whereas its two products are UDP and O-(alpha-D-glucosyl)poly(glycerol phosphate). This enzyme belongs to ... glycerol phosphate) ⇌ {\displaystyle \rightleftharpoons } UDP + O-(alpha-D-glucosyl)poly(glycerol phosphate) Thus, the two ... The systematic name of this enzyme class is UDP-glucose:poly(glycerol-phosphate) alpha-D-glucosyltransferase. Other names in ... In enzymology, a poly(glycerol-phosphate) alpha-glucosyltransferase (EC 2.4.1.52) is an enzyme that catalyzes the chemical ...
The encoded cytosolic protein and mitochondrial glycerol-3-phosphate dehydrogenase also form a glycerol phosphate shuttle that ... Glycerol-3-phosphate dehydrogenase 1 is a protein that in humans is encoded by the GPD1 gene. This gene encodes a member of the ... Ou X, Ji C, Han X, Zhao X, Li X, Mao Y, Wong LL, Bartlam M, Rao Z (2006). "Crystal structures of human glycerol 3-phosphate ... "Entrez Gene: Glycerol-3-phosphate dehydrogenase 1". Retrieved 2017-03-23. Gudayol M, Vidal J, Usac EF, Morales A, Fabregat ME, ...
Glycerol-3-phosphate dehydrogenase may refer to: Glycerol-3-phosphate dehydrogenase, an enzyme (EC 1.1.1.8) with systematic ... NAD+ 2-oxidoreductase Glycerol-3-phosphate dehydrogenase (NAD(P)+), an enzyme (EC 1.1.1.94) with systematic name sn-glycerol-3- ... phosphate:NAD(P)+ 2-oxidoreductase Glycerol-3-phosphate dehydrogenase (quinone), an enzyme (EC 1.1.5.3) with systematic name sn ... glycerol 3-phosphate:quinone oxidoreductase This set index page lists enzyme articles associated with the same name. If an ...
The gene encoding glycerol-1-phosphate dehydrogenase has been detected in all the archaeal species and has not been found in ... sn-glycerol 1-phosphate produced by this enzyme is the most fundamental difference by which Archaea and bacteria are ... The enzyme sn-glycerol-1-phosphate dehydrogenase, usually having 394 amino acids, was also identified in bacteria. More than ... The systematic name of this enzyme class is sn-glycerol-1-phosphate:NAD(P)+ 2-oxidoreductase. This enzyme is also called ...
The enzyme indole-3-glycerol-phosphate lyase (EC 4.1.2.8) catalyzes the chemical reaction (1S,2R)-1-C-(indol-3-yl)glycerol 3- ... indole-3-glycerol phosphate lyase, IGL, BX1, (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate, and D-glyceraldehyde-3-phosphate- ... The systematic name of this enzyme class is (1S,2R)-1-C-(indol-3-yl)glycerol-3-phosphate D-glyceraldehyde-3-phosphate-lyase ( ... indole glycerol phosphate hydrolase, indole synthase, indole-3-glycerolphosphate D-glyceraldehyde-3-phosphate-lyase, ...
... glycerol + D-glucose 6-phosphate Thus, the two substrates of this enzyme are sn-glycerol 3-phosphate and D-glucose, whereas its ... In enzymology, a glycerol-3-phosphate-glucose phosphotransferase (EC 2.7.1.142) is an enzyme that catalyzes the chemical ... The systematic name of this enzyme class is sn-glycerol-3-phosphate:D-glucose 6-phosphotransferase. Kiaira JK, Njogu RM (1989 ... "Evidence for glycerol 3-phosphate:glucose transphosphorylase activity in bloodstream Trypanosoma brucei brucei". Int. J. ...
sn-Glycerol 1-phosphate is the conjugate base of a phosphoric ester of glycerol. It is a component of ether lipids, which are ... Glycerol 1-phosphate is synthesized by reducing dihydroxyacetone phosphate (DHAP), a glycolysis intermediate, with sn-glycerol- ... DHAP and thus glycerol 1-phosphate is also possible to be synthesized from amino acids and citric acid cycle intermediates via ... NAD(P)H + H+ → + NAD(P)+ Glycerol 1-phosphate is a starting material for de novo synthesis of ether lipids, such as those ...
loge of Glycerol vapor pressure. Uses formula: log e ⁡ P k P a = {\displaystyle \scriptstyle \log _{e}P_{kPa}=} A × l n ( T ... This page provides supplementary chemical data on glycerol. The handling of this chemical may incur notable safety precautions ... Freezing Points of Glycerine-Water Solutions Dow Chemical Lane, Leonard B. (September 1925). "Freezing Points of Glycerol and ... Segur, J. B.; Oberstar, H. E. (1951). "Viscosity of Glycerol and Its Aqueous Solutions". Industrial & Engineering Chemistry. 43 ...
In enzymology, a glycerol dehydrogenase (NADP+) (EC 1.1.1.72) is an enzyme that catalyzes the chemical reaction glycerol + ... The systematic name of this enzyme class is glycerol:NADP+ oxidoreductase. This enzyme is also called glycerol dehydrogenase ( ... Kormann AW, Hurst RO, Flynn TG (1972). "Purification and properties of an NADP+-dependent glycerol dehydrogenase from rabbit ... Toews CJ (1967). "The kinetics and reaction mechanism of the nicotinamide-adinine dinucleotide phosphate-specific glycerol ...
Its reaction with glycerol (commonly known as glycerin or glycerine) (C3H5(OH)3) is highly exothermic, resulting rapidly in a ... A depression is made at the center of the permanganate powder and glycerol liquid is added to it. The white smoke-like vapor ... "Glycerol and KMnO4". University of Washington Department of Chemistry. Retrieved May 26, 2019. Ernest, Z. (April 16, 2014). " ... "Oxidation of glycerol by potassium permanganate". Chemedxchange. Retrieved May 26, 2019. Summerlin, L. R. (1988). Chemical ...
To make the glycerol ester of wood rosin, refined wood rosin is reacted with glycerin to produce the glycerol ester. Glycerol ... Glycerol ester of wood rosin (or gum rosin), also known as glyceryl abietate or ester gum, is an oil-soluble food additive (E ... Glycerol ester of wood rosin Standard Terminology Relating to Pine Chemicals, Including Tall Oil and Related Products ( ... and its name may be shortened in the ingredient list as glycerol ester of rosin. It is also used as an ingredient in the ...
Glycerol Glycerol kinase ATP ADP Glycerol-3-phosphate Glycerol-3-phosphate dehydrogenase NAD+ NADH NAD+ NADH Dihydroxyacetone ... An oxidation of glycerol affords mesoxalic acid. Dehydrating glycerol affords hydroxyacetone. Glycerol is used as fill for ... Glycerol is mainly metabolized in the liver. Glycerol injections can be used as a simple test for liver damage, as its rate of ... glycerol 3-phosphate is obtained from dihydroxyacetone phosphate with the enzyme glycerol-3-phosphate dehydrogenase. Glycerol ...
Glycerol alters the hygroscopic property of gelatin and its permeability to water vapour.. Glycerol Gelatin or glycerine jelly ... Prepared with gelatin, glycerol and phenol. Very similar in composition to Kaiser′s glycerol jelly. ... Glycerol Gelatin has been used for mounting endometrial tissue. and pancreatic sections. for microscopic examination. It has ...
Knorr, W.; Spiteller, G., Simple method for the analysis of glycerol enol ethers derived from plasmalogens in complex lipid ... Glycerol, 2,3-dimethyl, 1-octadecanoate. *Formula: C23H46O4 ...
Glycerol,Protol,Trihydroxylpropane; find Sigma-Aldrich-104095 MSDS, related peer-reviewed papers, technical documents, similar ... Glycerol - for fluorescence microscopy is used as a mounting medium for stained histology specimens (e.g. toluidine blue stain ... Glycerol for fluorescence (microscopy); Synonyms: 1,2,3-Propanetriol,Glycerin, ...
Predicted to be involved in glycerol catabolic process and glycerol-3-phosphate metabolic process. Predicted to be part of ... PLN02464; glycerol-3-phosphate dehydrogenase. cd00051. Location:628 → 685. EFh; EF-hand, calcium binding motif; A diverse ... putative glycerol-3-phosphate dehydrogenase, mitochondrial. Primary source. WormBase:WBGene00012031 Locus tag. CELE_T25G3.4 See ... enables sn-glycerol-3-phosphate:ubiquinone-8 oxidoreductase activity IEA Inferred from Electronic Annotation. more info ...
1-tetradecanoyl-sn-glycero-3-phospho-(1-sn-glycerol)(1−) (CHEBI:72826) is a 1-acyl-sn-glycero-3-phospho-(1-sn-glycerol)(1−) ( ... CHEBI:72826 - 1-tetradecanoyl-sn-glycero-3-phospho-(1-sn-glycerol)(1−). Main. ChEBI Ontology. Automatic Xrefs. Reactions. ... 1-tetradecanoyl-sn-glycero-3-phospho-(1-sn-glycerol) (CHEBI:73092) is conjugate acid of 1-tetradecanoyl-sn-glycero-3-phospho-( ... 1-tetradecanoyl-sn-glycero-3-phospho-(1-sn-glycerol)(1−) (CHEBI:72826) is conjugate base of 1-tetradecanoyl-sn-glycero-3- ...
Glycerol phenylbutyrate is used together with a proper diet and supplements to lower high levels of ammonia in the blood caused ...
Glycerol is a naturally occurring substance found in skin that locks in moisture and hydrates skin when applied topically. ...
Glycerol Monolaurate (GML) is a naturally occurring fatty acid widely utilized in food, cosmetics, and homeopathic supplements ... How to cite this article: Zhang, M. S. et al. Glycerol Monolaurate (GML) inhibits human T cell signaling and function by ... Glycerol monolaurate inhibits Candida and Gardnerella vaginalis in vitro and in vivo but not Lactobacillus. Antimicrobial ... Glycerol Monolaurate (GML) inhibits human T cell signaling and function by disrupting lipid dynamics. *Michael S. Zhang1, ...
On Jun 25, 9:33 pm, Kanchanadevi k ,kde... from gmail.com, wrote: , Hi all , , I want to revive bacterial culture from glycerol ... 70%) stock stored in -20 , for two years , I tried by inoculating glycerol stock in nutrient agar plate and nutrient , broth. , ... what is other possible way to revive the culture from glycerol stock? , , Thank you so much , -- What is the organism? Does it ... Previous message: [Microbiology] doubt in reviving bacterial culture from glycerol stock * Messages sorted by: [ date ] [ ...
J:243852 Zhang D, et al., Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5. Proc Natl ...
Two studies were performed to evaluate the influence of glycerol on the recovery of damaged stratum corneum barrier function. ... Significant differences between glycerol open vs. untreated and glycerol occluded vs. untreated were observed at day 3. Stratum ... Stratum corneum hydration showed highest values in the glycerol treated sites after 3 days of treatment. Glycerol creates a ... Glycerol accelerates recovery of barrier function in vivo Acta Derm Venereol. 1999 Nov;79(6):418-21. doi: 10.1080/ ...
V/V GLYCEROL 1ML   at Fishersci.com ... HR2-428-62/Additive Screen 62 (F02), 1.0 ml - 30% v/v Glycerol ...
In 20 smokers who switched to a new type of virtually tar free cigarette for three days, average nicotine intake was reduced by 44%, carbon monoxide intake increased by 19%, while estimated tar intake was reduced by about 90%. Such cigarettes pose substantially less risk of cancer and chronic obstructive lung disease than conventional cigarettes, and their acceptability and safety could be improved by increasing nicotine yield, reducing carbon monoxide yield, and improving the flavour.. ...
Shop Switch Nutrition Glycerol at ASN - a leading supplement retailer in Australia. Same day dispatch & FREE shipping over $150 ... Decrease quantity for Switch Nutrition Glycerol Increase quantity for Switch Nutrition Glycerol ... Glycerol is a naturally occurring sugar and plays a role in supporting cellular hydration. Improved hydration is key to ... Love smashing PBs? Putting your muscles through warfare to build the sickest pump in the gym? Consider adding glycerol to your ...
Protein target information for Glycerol kinase (Haemophilus influenzae Rd KW20). Find diseases associated with this biological ...
The chemical reactions and pathways involving glycerol-3-phosphate, a phosphoric monoester of glycerol. ... glycerol kinase. involved_in. ISO. IBA. (PMID:8651297). PMID:21873635. RGD. PMID:8651297 PMID:21873635. RGD:13792537. NCBI chr ... glycerol kinase. involved_in. IEA. GO_REF:0000002. InterPro. GO_REF:0000002. NCBI chr X:50,162,089...50,238,707 Ensembl chr X: ... glycerol-3-phosphate acyltransferase 3. involved_in. ISO. (MGI:6467919,PMID:11003606). RGD. PMID:11003606. MGI:6467919. NCBI ...
Use Dichloran-Glycerol 18% (DG18) (ISO) Agar Base for the enumeration and isolation of xenophilic molds from dried and semi- ... Dichloran-Glycerol (DG18) (ISO) Agar is a dehydrated culture medium formulated according to BS ISO 21527-2: 2008 Microbiology ... The formulation contains glycerol at 18% (w/w) which lowers the water activity (aW) from 0.999 to 0.95. ... Isolate and enumerate yeasts and molds associated with food spoilage with Thermo Scientific™ Oxoid™ Dichloran-Glycerol 18% ( ...
Crystal Structure of the Mycobacterium tuberculosis Indole-3-glycerol phosphate synthase (TrpC) in apo form ... Indole-3-glycerol phosphate synthase. A. 272. Mycobacterium tuberculosis. Mutation(s): 0 Gene Names: MT1646, MTCY01B2.03, trpC ... Small-molecule scaffolds for Mycobacterium tuberculosis Indole Glycerol Phosphate Synthase (IGPS) inhibitors identified by high ... Crystal Structure of the Mycobacterium tuberculosis Indole-3-glycerol phosphate synthase (TrpC) in apo form. *PDB DOI: https:// ...
Glycerol*Lactic Acid*Methylparaben*Paraffin Liquid Light*Paraffin Soft White*PEG-100*Propylparaben*Sodium Lactate*Sodium ... Balsam; Topical; Cetearyl Alcohol; Glycerol; Lactic Acid; Methylparaben; Paraffin Liquid Light; Paraffin Soft White; PEG-100; ...
... conversion to glycerol carbonate (GlyC). The biocatalyst characteristics for both designs (EIMP and CLEMPA) were evaluated ... The biocatalysts were prepared using lipase enzyme from Aspergillus niger for catalyzing the glycerol (Gly) ... Biocatalytic designs for the conversion of renewable glycerol into glycerol carbonate as a value-added product. * Madalina ... "Biocatalytic designs for the conversion of renewable glycerol into glycerol carbonate as a value-added product" Open Chemistry ...
Glycerol 3-phosphate. Description. Glycerol 3-phosphate is a chemical intermediate in the glycolysis metabolic pathway. It is ... Glycerol 3-phospate may then be converted by dehydrogenation to dihydroxyacetone phosphate (DHAP) by the enzyme glycerol-3- ... Glycerol 3-phosphate is produced from glycerol, the triose sugar backbone of triglycerides and glycerophospholipids, by the ... Glycerol 3-phosphate + a quinone → Dihydroxyacetone phosphate + a quinol. details. Glycerol 3-phosphate + FAD → ...
Combine Comfrey Glycerol Extract with Arnica Tincture and Eyebright Tincture along with some Witch Hazel Water when making eye ... Comfrey has a synergy with all forms of calendula so add Comfrey Glycerol Extract to a cream or lotion that uses Calendula Oil ... The individual materials that make up Comfrey Glycerol Extract are listed on the Cosmetic Ingredient Database (Cosing) here. ... Comfrey Glycerol Extract is a beige/yellow to dark brown, clear liquid. ...
Supported by the increasing sustainable awareness, glycerol carbonate has gained much interest over the last 20 years because ... reactivity and applications of glycerol carbonate (glycerine carbonate or 4-hydroxymethyl-2-oxo-1,3-dioxolane) are discussed ... glycerol. . Numerous synthesis pathways for this molecule were identified, some of them very promising and on the verge of ... Glycerol carbonate as a versatile building block for tomorrow: synthesis, reactivity, properties and applications M. O. Sonnati ...
There has been growing interest in the potential for converting glycerol-a relatively large (about 10 wt %) byproduct of the ... One-step process under mild conditions for conversion of glycerol to solketal, STBE fuel additives 26 January 2016 There has ... In a paper in the journal Fuel, they report a continuous, one-step process for the quantitative conversion of glycerol into a ... Zeolite-BEA converts glycerol completely into a mixture of solketal and solketal tert-butyl ether (STBE). ...
The sugar alcohol known as glycerol only sounds intimidating, but its all around us in the things we use every day from our ... What Else Can Glycerol Do for Skin?. When reading labels for your products, if you see "glycerol" or "glycerin," thats a win ... Glycerol Protects your skin. Often, glycerol is the wonder ingredient in many pharmaceutical-grade creams that your doctor may ... Glycerol Prevents moisture from escaping. Not only does glycerol restore hydration, but it also prevents it from depleting. ...
In this study, we show that expression of glycerol-3-phosphate acyltransferase 1 ( … ... In this study, we show that expression of glycerol-3-phosphate acyltransferase 1 (GPAT1; Gpam), a rate-limiting enzyme of ... Role of DNA methylation in the regulation of lipogenic glycerol-3-phosphate acyltransferase 1 gene expression in the mouse ...
Background Glycerol monolaurate (GML), a 12 carbon fatty acid monoester, inhibits Staphylococcus aureus growth and exotoxin ... Glycerol Is the Subject Area "Glycerol" applicable to this article? Yes. No. ...
Polyhydroxyalkanoates (PHA) production from fermented crude glycerol: Study on the conversion of 1,3-propanediol to PHA in ...
  • 1. The metabolism of glycerol by isolated rat-kidney tubules was investigated. (portlandpress.com)
  • Lactobacillus reuteri, a heterofermentative bacterium, metabolizes glycerol via a Pdu (propanediol-utilization) pathway involving dehydration to 3-hydroxypropionaldehyde (3-HPA) followed by reduction to 1,3-propandiol (1,3-PDO) with concomitant generation of an oxidized cofactor, NAD+ that is utilized to maintain cofactor balance required for glucose metabolism and even for oxidation of 3-HPA by a Pdu oxidative branch to 3-hydroxypropionic acid (3-HP). (lu.se)
  • Notably, it was demonstrated that PduQ is more active in generating NAD+ during glycerol metabolism within the microcompartment by resting cells, while ADH7 functions to balance NAD+/NADH by converting 3-HPA to 1,3-PDO outside the microcompartment in the growing cells. (lu.se)
  • Elimination Metabolism Upon oral administration, pancreatic lipases hydrolyze RAVICTI (i.e., glycerol phenylbutyrate), and release PBA. (clustermed.info)
  • Overview of Fatty Acid and Glycerol Metabolism Disorders Fatty acids are the preferred energy source for the heart and an important energy source for skeletal muscle during prolonged exertion. (msdmanuals.com)
  • Symptoms of glycerol metabolism disorders begin at any age and are usually accompanied by acidosis, hypoglycemia, and elevated blood and urine levels of glycerol. (msdmanuals.com)
  • Diagnosis of glycerol metabolism disorders is by detecting an elevated level of glycerol in serum and urine and is confirmed by DNA analysis. (msdmanuals.com)
  • Glycerol metabolism disorder treatment is with a low-fat diet, but glucocorticoid replacement is critical for patients with adrenal hypoplasia. (msdmanuals.com)
  • A specific experiment is reported, starting from an initial volume of 4 mL of liquid mixture methanol + glycerol (methanol/glycerol molar ratio 30), where, with a stepwise addition of CO2, diverse fluid phase phenomena were detected, such as VLE, Critical Point, VLLE, VLLLE, LLE and LE. (aston.ac.uk)
  • Under an optimum glycerol-to-DBT molar ratio, the DBT biodegradation rate constants increased up to 18-fold and enhanced DBT biodegradation by 25%-30% at day 1 relative to cultivation with DBT alone. (cdc.gov)
  • Glycerol is generally obtained from plant and animal sources where it occurs in triglycerides, esters of glycerol with long-chain carboxylic acids. (wikipedia.org)
  • Glycerol from triglycerides is produced on a large scale, but the crude product is of variable quality, with a low selling price of as low as US$0.02-0.05 per kilogram in 2011. (wikipedia.org)
  • Crude glycerol from the hydrolysis of triglycerides can be purified by treatment with activated carbon to remove organic impurities, alkali to remove unreacted glycerol esters, and ion exchange to remove salts. (wikipedia.org)
  • Both biocatalytic models were successfully used to prepare GlyC from "crude" glycerol collected directly from the biodiesel process (e.g. 49% Gly conversion with 91% GlyC selectivity for EIMP and 70% Gly conversion with 80% GlyC selectivity for CLEMPA). (degruyter.com)
  • Glycerol phenylbutyrate is used together with a proper diet and supplements to lower high levels of ammonia in the blood caused by urea cycle disorders. (mayoclinic.org)
  • Glycerol Phenylbutyrate Oral Liquid is also known as Ravicti. (clustermed.info)
  • What's The Definition Of The Medical Condition Glycerol Phenylbutyrate Oral Liquid? (clustermed.info)
  • In healthy subjects, intact glycerol phenylbutyrate was detected in plasma. (clustermed.info)
  • While the study was inconclusive, the incomplete hydrolysis of glycerol phenylbutyrate cannot be ruled out. (clustermed.info)
  • Intact glycerol phenylbutyrate was not detectable in plasma in patients with UCDs. (clustermed.info)
  • Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders. (bvsalud.org)
  • Glycerol phenylbutyrate (GPB) is safe and effective in reducing ammonia levels in patients with UCD above 2 months of age. (bvsalud.org)
  • The hydrolysis, saponification, or transesterification of these triglycerides produces glycerol as well as the fatty acid derivative: Triglyceride 3 NaOH / H2O Δ 3 × soap 3 × glycerol Triglycerides can be saponified with sodium hydroxide to give glycerol and fatty sodium salt or soap. (wikipedia.org)
  • Glycerol Monolaurate (GML) is a naturally occurring fatty acid widely utilized in food, cosmetics, and homeopathic supplements. (nature.com)
  • There has been growing interest in the potential for converting glycerol-a relatively large (about 10 wt %) byproduct of the conventional production of biodiesel (fatty acid methyl esters)-into solketal (2,2-dimethyl 1,3-dioxalane-4-methanol) for use as an oxygenated fuel additive or diesel combustion promoter. (greencarcongress.com)
  • The metabolites of note included small fatty acids such as decanoic and octanoic acid, amino acids such as serine and 1H-indole-3-acetic acid, and sugar derivatives such as glycerol. (medscape.com)
  • The formulation contains glycerol at 18% (w/w) which lowers the water activity (aW) from 0.999 to 0.95. (thermofisher.com)
  • It also contains glycerol or propylene glycol (PEG), which looks like smoke when you exhale. (medlineplus.gov)
  • Glycerol Kinase Deficiency occurs when the glycerol kinase gene which is found on the locus Xp21 of the X chromosome, is deleted or mutated (changed). (metabolicsupportuk.org)
  • When someone suffers from glycerol kinase deficiency, many of the glycerol molecules that are released into the bloodstream do not get converted to DHAP (dihydroxyacetone phosphate) like they should be because there is not enough of the enzyme to catalyse (cause or accelerate a reaction) all the reactions that are meant to occur. (metabolicsupportuk.org)
  • Glycerol Kinase Deficiency is an inherited condition. (metabolicsupportuk.org)
  • Thus, patients with glycerol kinase deficiency may have one or more of these disease entities. (msdmanuals.com)
  • Predicted to be part of glycerol-3-phosphate dehydrogenase complex. (nih.gov)
  • Orthologous to human GPD2 (glycerol-3-phosphate dehydrogenase 2). (nih.gov)
  • Glycerol 3-phospate may then be converted by dehydrogenation to dihydroxyacetone phosphate (DHAP) by the enzyme glycerol-3-phosphate dehydrogenase. (hmdb.ca)
  • Chlorine-free processes from propylene include the synthesis of glycerol from acrolein and propylene oxide. (wikipedia.org)
  • The synthesis, reactivity and applications of glycerol carbonate (glycerine carbonate or 4-hydroxymethyl-2-oxo-1,3-dioxolane ) are discussed and reviewed. (rsc.org)
  • A kinetic model of the glycerol synthesis pathway has been constructed. (fairdomhub.org)
  • The studies indicated that glycerol enhances DBT biodegradation via increased RL synthesis and bacterial growth. (cdc.gov)
  • Glycerol (/ˈɡlɪsərɒl/), also called glycerine or glycerin, is a simple triol compound. (wikipedia.org)
  • Glycerol Gelatin or glycerine jelly medium is an aqueous slide mounting media, used for mounting samples in microscopy and histology. (sigmaaldrich.com)
  • Similar experiments were conducted involving the same device for injection of 100%, 50% and 25% glycerol-water mixtures with trace amounts of rhodamine. (spie.org)
  • Vapour-liquid equilibrium of CO(2) + [0.00871 glycerol + 0.99129 (ethanol or 1-propanol or 1-butanol)] mixtures was measured at the temperatures of 313.15 K and 333.15 K, and close to the critical line, at pressures up to 12 MPa. (unl.pt)
  • On the liquid side, the bubble points measured for these ternary mixtures follow closely the behaviour of VLE reported by several authors for the corresponding binary mixtures without glycerol. (unl.pt)
  • The glycerol backbone is found in lipids known as glycerides. (wikipedia.org)
  • Glycerol 3-phosphate is produced from glycerol, the triose sugar backbone of triglycerides and glycerophospholipids, by the enzyme glycerol kinase. (hmdb.ca)
  • Upon oral ingestion, PBA is released from the glycerol backbone in the gastrointestinal tract by lipases. (clustermed.info)
  • The biocatalysts were prepared using lipase enzyme from Aspergillus niger for catalyzing the glycerol (Gly) conversion to glycerol carbonate (GlyC). (degruyter.com)
  • Glycerol has a caloric density similar to table sugar, but a lower glycemic index and different metabolic pathway within the body. (wikipedia.org)
  • Glycerol 3-phosphate is a chemical intermediate in the glycolysis metabolic pathway. (hmdb.ca)
  • The Pdu pathway is operative inside Pdu microcompartment that encapsulates different enzymes and cofactors involved in metabolizing glycerol or 1,2-propanediol, and protects the cells from the toxic effect of the aldehyde intermediate. (lu.se)
  • fumigatus and high-osmolarity glycerol (HOG) pathway MAPK mutants upon cell wall damage. (bath.ac.uk)
  • This investigation aims to gain a clearer understanding of and to quantify the extent to which parameters of the pathway affect glycerol flux in S. cerevisiae. (fairdomhub.org)
  • Predicted to be involved in glycerol catabolic process and glycerol-3-phosphate metabolic process. (nih.gov)
  • many patients with this deficiency also have a chromosomal deletion that extends beyond the glycerol kinase gene into the contiguous gene region, which contains the genes for congenital adrenal hypoplasia and Duchenne muscular dystrophy. (msdmanuals.com)
  • Supported by the increasing sustainable awareness, glycerol carbonate has gained much interest over the last 20 years because of its versatile reactivity and as a way to valorize waste glycerol . (rsc.org)
  • GKD is diagnosed through specialised blood and urine tests to find the amount of glycerol present. (metabolicsupportuk.org)
  • Directly after glycerol administration, δ13C-values were similar to the isotope ratio of the administered glycerol. (wada-ama.org)
  • In a paper in the journal Fuel , they report a continuous, one-step process for the quantitative conversion of glycerol into a mixture of ethers under mild conditions (atmospheric pressure and temperatures of 40-70 °C) over a zeolite BEA catalyst. (greencarcongress.com)
  • The observed effects were based on the modulation of barrier repair and were not biased by the humectant effect of glycerol. (nih.gov)
  • The chemical reactions and pathways involving glycerol-3-phosphate, a phosphoric monoester of glycerol. (mcw.edu)
  • Because of its three hydroxyl groups, glycerol is miscible with water and is hygroscopic in nature. (wikipedia.org)
  • Glycerol alters the hygroscopic property of gelatin and its permeability to water vapour. (sigmaaldrich.com)
  • Isolate and enumerate yeasts and molds associated with food spoilage with Thermo Scientific™ Oxoid™ Dichloran-Glycerol 18% (DG18) (ISO) Agar Base while adhering to BS ISO 21527-2:2008. (thermofisher.com)
  • Use Dichloran-Glycerol 18% (DG18) (ISO) Agar Base for the enumeration and isolation of xenophilic molds from dried and semi-dried foods like spices, dried fruits, confectionery, cereals, nuts, dried meat, and fish products. (thermofisher.com)
  • Exogenously administered glycerol is excreted in the urine so that the detection of the misuse of glycerol is possible in theory. (wada-ama.org)
  • Further, a suitable IRMS-method was developed to measure δ13C-values of glycerol in urine. (wada-ama.org)
  • It was projected in 2006 that by 2020, production would be six times more than demand, creating an excess of glycerol as a byproduct of biofuel production. (wikipedia.org)
  • 4. The results are discussed in relation to the observation that indomethacin increases the severity of glycerol-induced acute renal failure. (portlandpress.com)
  • Switch Nutrition uses GlycerPump® 65% Glycerol Powder, delivering a 3000mg dose that can improve your overall performance. (australiansportsnutrition.com.au)
  • In order to contribute to the development of urinary threshold levels for the misuse of glycerol, two placebo-controlled application studies (glycerol dose: 1 g/kg body weight) were performed at rest and in combination with exercise. (wada-ama.org)
  • 2. Indomethacin, at a concentration of 0.1 mmol/l, markedly inhibited the utilization of glycerol and its conversion into glucose and CO 2 . (portlandpress.com)
  • A correlation of the results obtained for the CO(2) + glycerol + ethanol mixture with the Peng-Robinson equation of state, admitting quasi-binary behaviour, equally yields good agreement on the liquid side, and significant deviations on the vapour side. (unl.pt)
  • Glycerol, a major by-product of ethanol fermentation by Saccharomyces cerevisiae, is of significant importance to the wine, beer, and ethanol production industries. (fairdomhub.org)
  • Therefore it is necessary to establish threshold values for urinary glycerol concentrations because glycerol may also be of endogenous origin or may be taken up from other exogenous sources. (wada-ama.org)
  • However, glycerol plasma concentrations can also be elevated during fasting and endurance exercise. (wada-ama.org)
  • For the development of urinary threshold levels we intend to perform a) application studies of glycerol at rest and during exercise, b) to assess urinary glycerol excretion due to fasting and exercise and c) to determine reference values for urinary glycerol concentrations in normal doping control samples. (wada-ama.org)
  • There was a rapid increase in urinary glycerol and maximum concentrations (50000-60000 µg/mL) were observed 2.5 to 4 h after the administration. (wada-ama.org)
  • After 18 h of food deprivation followed by 90 minutes of endurance exercise, highly elevated plasma glycerol concentrations were observed but urinary glycerol concentrations were only slightly increased (maximum concentration: 50.5 µg/mL). (wada-ama.org)
  • In 516 randomly selected routine doping control samples, it was confirmed that urinary concentrations are slightly higher in in-competition than in out-of-competition samples, but in all samples urinary glycerol concentrations remained below 200 µg/mL. (wada-ama.org)
  • The phase behaviour of the system CO2 + methanol + glycerol has been studied at low concentrations of this tri-alcohol. (aston.ac.uk)
  • Stratum corneum hydration showed significantly higher values in the sites treated with glycerol+occlusion, compared with all other sites. (nih.gov)
  • Stratum corneum hydration showed highest values in the glycerol treated sites after 3 days of treatment. (nih.gov)
  • As the glycerol-induced recovery of barrier function and stratum corneum hydration were observed even 7 days after the end of treatment, glycerol can be regarded as a barrier stabilizing and moisturizing compound. (nih.gov)
  • Switch Nutrition's patented highly bioavailable glycerol formula containing GlycerPump®, which is designed to support enhanced pumps, cell hydration, performance, endurance, and recovery. (australiansportsnutrition.com.au)
  • Glycerol is a naturally occurring sugar and plays a role in supporting cellular hydration. (australiansportsnutrition.com.au)
  • Glycerol helps to support hydration, aid muscle recovery, support athletic performance, and increase muscle cell volume. (australiansportsnutrition.com.au)
  • While intoxication as a result of excessive glycerol consumption is rare and its symptoms generally mild, occasional reports of hospitalization have occurred. (wikipedia.org)
  • Glycerol is a mild neurolytic agent used for treating trigeminal neuralgia but may cause perineural damage. (medscape.com)
  • Because of the large-scale production of biodiesel from fats, where glycerol is a waste product, the market for glycerol is depressed. (wikipedia.org)
  • Semen samples chosen as suitable for being frozen were extended 1:1 (semen/extender) by Tris extender containing 20% egg yolk without glycerol [Tris (hydroxymethyl-aminomethane) (2.40 g) - fructose (1.00 g) - citric acid (1.30 g) osmolarity: 285 mOsmol/kg] at +26 ºC. (tubitak.gov.tr)
  • Comfrey Glycerol Extract is a beige/yellow to dark brown, clear liquid. (aromantic.co.uk)
  • Furthermore, there are natural sources of glycerol such as foodstuff (e.g. wine) and over-the-counter drugs. (wada-ama.org)
  • Also, little is known about urinary glycerol following prolonged fasting, endurance exercise or the intake of glycerol-rich foods or drugs. (wada-ama.org)
  • In addition, glycerol may also occur endogenously during increased lipolysis and it can also be ingested from foodstuff or drugs. (wada-ama.org)
  • 2008) can be used to identify athletes, who have misused glycerol in relevant amounts. (wada-ama.org)
  • If you're looking to improve your muscle pumps, performance, and endurance, consider adding glycerol to your stack. (australiansportsnutrition.com.au)
  • By adding Switch Nutrition Glycerol to your supplement stack, this formula can help you improve endurance, recover quicker, and heighten workout intensity. (australiansportsnutrition.com.au)
  • Significant differences between glycerol open vs. untreated and glycerol occluded vs. untreated were observed at day 3. (nih.gov)
  • In study 2 a faster barrier repair was seen in glycerol-treated sites, with significant differences against untreated and base-treated sites 7 days after the end of the treatment. (nih.gov)
  • Glycerol and water are used to preserve certain types of plant leaves. (wikipedia.org)
  • In study 1 a faster barrier repair (transepidermal water loss) was monitored in glycerol-treated sites. (nih.gov)
  • Glycerol is best taken with water or a carbohydrate/electrolyte drink. (australiansportsnutrition.com.au)
  • Combine Comfrey Glycerol Extract with Arnica Tincture and Eyebright Tincture along with some Witch Hazel Water when making eye creams. (aromantic.co.uk)
  • In sports glycerol is typically used in high doses in combination with excess fluid in order to increase total body water. (wada-ama.org)
  • acids, soapstock, and glycerol water. (scirp.org)