Esterases are hydrolase enzymes that catalyze the hydrolysis of ester bonds, converting esters into alcohols and acids, playing crucial roles in various biological processes including metabolism and detoxification.
Enzymes which catalyze the hydrolysis of carboxylic acid esters with the formation of an alcohol and a carboxylic acid anion.
Hydrolytic enzyme activity used as a histocytochemical test for the presence of esterases in tissue. Substrate used is 3-hydroxy-4'-nitro-2-naphthanilide chloroacetate (naphthol AS-D).
An enzyme that catalyzes the hydrolysis of CHOLESTEROL ESTERS and some other sterol esters, to liberate cholesterol plus a fatty acid anion.
An enzyme that catalyzes the conversion of acetate esters and water to alcohols and acetate. EC 3.1.1.6.
Carboxylesterase is a serine-dependent esterase with wide substrate specificity. The enzyme is involved in the detoxification of XENOBIOTICS and the activation of ester and of amide PRODRUGS.
A di-isopropyl-fluorophosphate which is an irreversible cholinesterase inhibitor used to investigate the NERVOUS SYSTEM.
"Esters are organic compounds that result from the reaction between an alcohol and a carboxylic acid, playing significant roles in various biological processes and often used in pharmaceutical synthesis."
An organophosphate cholinesterase inhibitor that is used as a pesticide.
The process of cleaving a chemical compound by the addition of a molecule of water.
An endogenous 105-kDa plasma glycoprotein produced primarily by the LIVER and MONOCYTES. It inhibits a broad spectrum of proteases, including the COMPLEMENT C1R and the COMPLEMENT C1S proteases of the CLASSICAL COMPLEMENT PATHWAY, and the MANNOSE-BINDING PROTEIN-ASSOCIATED SERINE PROTEASES. C1-INH-deficient individuals suffer from HEREDITARY ANGIOEDEMA TYPES I AND II.
Serum proteins that inhibit, antagonize, or inactivate COMPLEMENT C1 or its subunits.
A characteristic feature of enzyme activity in relation to the kind of substrate on which the enzyme or catalytic molecule reacts.
A triglyceride that is used as an antifungal agent.
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.
An aspect of cholinesterases.
An enzyme of the hydrolase class that catalyzes the reaction of triacylglycerol and water to yield diacylglycerol and a fatty acid anion. It is produced by glands on the tongue and by the pancreas and initiates the digestion of dietary fats. (From Dorland, 27th ed) EC 3.1.1.3.
A mixture of isomeric tritolyl phosphates. Used in the sterilization of certain surgical instruments and in many industrial processes.
Nitrophenols are organic compounds characterized by the presence of a nitro group (-NO2) attached to a phenol molecule, known for their potential use in chemical and pharmaceutical industries, but also recognized as environmental pollutants due to their toxicity and potential carcinogenicity.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
An enzyme inhibitor that inactivates IRC-50 arvin, subtilisin, and the fatty acid synthetase complex.
Electrophoresis in which a starch gel (a mixture of amylose and amylopectin) is used as the diffusion medium.
Swelling involving the deep DERMIS, subcutaneous, or submucosal tissues, representing localized EDEMA. Angioedema often occurs in the face, lips, tongue, and larynx.
Narrow pieces of material impregnated or covered with a substance used to produce a chemical reaction. The strips are used in detecting, measuring, producing, etc., other substances. (From Dorland, 28th ed)
The development by insects of resistance to insecticides.
An enzyme that catalyzes the hydrolysis of ACETYLCHOLINE to CHOLINE and acetate. In the CNS, this enzyme plays a role in the function of peripheral neuromuscular junctions. EC 3.1.1.7.
An aspect of cholinesterase (EC 3.1.1.8).
Polysaccharides consisting of xylose units.
Organic compounds that contain phosphorus as an integral part of the molecule. Included under this heading is broad array of synthetic compounds that are used as PESTICIDES and DRUGS.
The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH = log 1/2[1/(H+)], where (H+) is the hydrogen ion concentration in gram equivalents per liter of solution. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
The rate dynamics in chemical or physical systems.
Cholinesterases are a group of enzymes that catalyze the hydrolysis of acetylcholine and other choline esters, playing crucial roles in the termination of impulse transmission at cholinergic synapses and neuro-muscular junctions, and in the metabolism of certain drugs and toxic substances.
Naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position. They are often used in dyes and pigments, as antioxidants for rubber, fats, and oils, as insecticides, in pharmaceuticals, and in numerous other applications.
The extent to which an enzyme retains its structural conformation or its activity when subjected to storage, isolation, and purification or various other physical or chemical manipulations, including proteolytic enzymes and heat.
Pesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics.
A genus of fungi in the family Ophiostomataceae, order OPHIOSTOMATALES. Several species are the source of Dutch elm disease, which is spread by the elm bark beetle.
The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells.
Hydroxycinnamic acid and its derivatives. Act as activators of the indoleacetic acid oxidizing system, thereby producing a decrease in the endogenous level of bound indoleacetic acid in plants.
7-Hydroxycoumarins. Substances present in many plants, especially umbelliferae. Umbelliferones are used in sunscreen preparations and may be mutagenic. Their derivatives are used in liver therapy, as reagents, plant growth factors, sunscreens, insecticides, parasiticides, choleretics, spasmolytics, etc.
Electrophoresis in which a polyacrylamide gel is used as the diffusion medium.
Naphthalene derivatives containing the -CH2CCO2H radical at the 1-position, the 2-position, or both. Compounds are used as plant growth regulators to delay sprouting, exert weed control, thin fruit, etc.
Study of intracellular distribution of chemicals, reaction sites, enzymes, etc., by means of staining reactions, radioactive isotope uptake, selective metal distribution in electron microscopy, or other methods.
A group of enzymes that catalyze the hydrolysis of alpha- or beta-xylosidic linkages. EC 3.2.1.8 catalyzes the endo-hydrolysis of 1,4-beta-D-xylosidic linkages; EC 3.2.1.32 catalyzes the endo-hydrolysis of 1,3-beta-D-xylosidic linkages; EC 3.2.1.37 catalyzes the exo-hydrolysis of 1,4-beta-D-linkages from the non-reducing termini of xylans; and EC 3.2.1.72 catalyzes the exo-hydrolysis of 1,3-beta-D-linkages from the non-reducing termini of xylans. Other xylosidases have been identified that catalyze the hydrolysis of alpha-xylosidic bonds.

A review of the pharmacology, pharmacokinetics and behavioral effects of procaine in thoroughbred horses. (1/1604)

Since procaine has both local anaesthetic and central stimulant actions its presence in the blood or urine of racing horses is forbidden. After rapid intravenous injection of procaine HC1 (2.5 mg/Kg) in thoroughbred mares plasma levels of this drug fell rapidly (t 1/2 alpha = 5 min) and then more slowly (t 1/2 beta = 50.2 min). These kinetics were well fitted by a two compartment open model (Model I). This model gave an apparent Vdbeta for procaine in the horse of about 3,500 litres. Since procaine was about 45% bound to equine plasma protein this gives a true Vdbeta for procaine of about 6,500 litres. After subcutaneous injection of procaine HC1 (3.3 mg/Kg) plasma levels peaked at about 400 ng/ml and then declined with a half-life of about 75 minutes. These data were well fitted by Model I when this was modified to include simple first order absorption (K = 0.048 min-1) from the subcutaneous injection site (Model II). After intramuscular injection of procaine penicillin (33,000 I.U./Kg) plasma levels reached a peak at about 270 ng/ml and then declined with a half-life of about 9 hours. These data were approximately fitted by Model II assuming a first order rate constant for absorption of procaine of 0.0024 min-1. After intramuscular injection of procaine HC1 (10 mg/Kg) plasma levels of procaine peaked rapidly at about 600 ng/ml but thereafter declined slowly (+ 1/2 = 2 hours). A satisfactory pharmaco-kinetic model for this intramuscular data could not be developed. An approximation of these data was obtained by assuming the existence of two intramuscular drug compartments, one containing readily absorbable drug and the other poorly absorbable drug (Model III). After intra-articular administration of procaine (0.33 mg/Kg) plasma levels of this drug reached a peak at about 17 ng/ml and then declined with a half-life of about 2 hours. These data were not modelled.  (+info)

Polymorphism in a cyclic parthenogenetic species: Simocephalus serrulatus. (2/1604)

A survey of sixteen isozyme loci using electrophoretic techniques was conducted for three isolated natural populations and one laboratory population of the cyclic parthenogenetic species, Simocephalus serrulatus. The proportion of polymorphic loci (33%-60%) and the average number of heterozygous loci per individual (6%-23%) in the three natural populations were found to be comparable to those found in most sexually reproducing organisms. Detailed analyses were made for one of these populations using five polymorphic loci. The results indicated that (1) seasonal changes in genotypic frequencies took place, (2) apomicitic parthenogenesis does not lead to genetic homogeneity, and (3) marked gametic disequilibrium at these five loci was present in the population, indicating that selection acted on coadapted groups of genes.  (+info)

The role of gene splicing, gene amplification and regulation in mosquito insecticide resistance. (3/1604)

The primary routes of insecticide resistance in all insects are alterations in the insecticide target sites or changes in the rate at which the insecticide is detoxified. Three enzyme systems, glutathione S-transferases, esterases and monooxygenases, are involved in the detoxification of the four major insecticide classes. These enzymes act by rapidly metabolizing the insecticide to non-toxic products, or by rapidly binding and very slowly turning over the insecticide (sequestration). In Culex mosquitoes, the most common organophosphate insecticide resistance mechanism is caused by co-amplification of two esterases. The amplified esterases are differentially regulated, with three times more Est beta 2(1) being produced than Est alpha 2(1). Cis-acting regulatory sequences associated with these esterases are under investigation. All the amplified esterases in different Culex species act through sequestration. The rates at which they bind with insecticides are more rapid than those for their non-amplified counterparts in the insecticide-susceptible insects. In contrast, esterase-based organophosphate resistance in Anopheles is invariably based on changes in substrate specificities and increased turnover rates of a small subset of insecticides. The up-regulation of both glutathione S-transferases and monooxygenases in resistant mosquitoes is due to the effects of a single major gene in each case. The products of these major genes up-regulate a broad range of enzymes. The diversity of glutathione S-transferases produced by Anopheles mosquitoes is increased by the splicing of different 5' ends of genes, with a single 3' end, within one class of this enzyme family. The trans-acting regulatory factors responsible for the up-regulation of both the monooxygenase and glutathione S-transferases still need to be identified, but the recent development of molecular tools for positional cloning in Anopheles gambiae now makes this possible.  (+info)

An overview of the evolution of overproduced esterases in the mosquito Culex pipiens. (4/1604)

Insecticide resistance genes have developed in a wide variety of insects in response to heavy chemical application. Few of these examples of adaptation in response to rapid environmental change have been studied both at the population level and at the gene level. One of these is the evolution of the overproduced esterases that are involved in resistance to organophosphate insecticides in the mosquito Culex pipiens. At the gene level, two genetic mechanisms are involved in esterase overproduction, namely gene amplification and gene regulation. At the population level, the co-occurrence of the same amplified allele in distinct geographic areas is best explained by the importance of passive transportation at the worldwide scale. The long-term monitoring of a population of mosquitoes in southern France has enabled a detailed study to be made of the evolution of resistance genes on a local scale, and has shown that a resistance gene with a lower cost has replaced a former resistance allele with a higher cost.  (+info)

Isolation and complete covalent structure of liver microsomal paraoxonase. (5/1604)

Paraoxonase (PON1) is a serum esterase exclusively associated with high-density lipoproteins; it might confer protection against coronary artery disease by destroying pro-inflammatory oxidized lipids in oxidized low-density lipoproteins. Here I show that rabbit liver microsomes contain a PON analogue (MsPON) and report the isolation and complete covalent structure of MsPON. In detergent-solubilized microsomes, MsPON co-purifies with the microsomal triacylglycerol transfer protein (MTP) complex. MsPON was separated from the complex and purified to homogeneity under non-denaturing conditions. Automated sequence analysis of intact MsPON and peptides obtained from enzymic and chemical cleavages led to the elucidation of the complete covalent structure of MsPON. The protein is a single polypeptide consisting of 350 residues. The sequence of rabbit liver microsomal MsPON is 60% identical with that of rabbit serum PON1, and 84% identical with the sequence predicted by a human cDNA of unknown function, designated PON3. MsPON has a hydrophobic segment at the N-terminus that might serve to anchor the protein to the microsomal membrane or to the MTP complex. Unlike in the serum enzyme, two potential N-glycan acceptor sites in MsPON are not glycosylated. An absence of N-glycans was also indicated in the rabbit liver MTP. MsPON has a single free cysteine residue at position 38 and a disulphide bond between Cys-279 and Cys-348. The microsomal enzyme lacks three residues at the N-terminus that are present in the serum protein. MsPON lacks four residues at the C-terminus that are present in the rabbit serum protein but absent from human serum PON1. On the basis of the observation that MsPON displays a high degree of similarity with serum PON1, it is proposed that MsPON might have a function related to that of PON1 in serum high-density lipoprotein complexes.  (+info)

Lipoprotein-associated phospholipase A2, platelet-activating factor acetylhydrolase, generates two bioactive products during the oxidation of low-density lipoprotein: use of a novel inhibitor. (6/1604)

A novel and potent azetidinone inhibitor of the lipoprotein-associated phospholipase A2 (Lp-PLA2), i.e. platelet-activating factor acetylhydrolase, is described for the first time. This inhibitor, SB-222657 (Ki=40+/-3 nM, kobs/[I]=6. 6x10(5) M-1.s-1), is inactive against paraoxonase, is a poor inhibitor of lecithin:cholesterol acyltransferase and has been used to investigate the role of Lp-PLA2 in the oxidative modification of lipoproteins. Although pretreatment with SB-222657 did not affect the kinetics of low-density lipoprotein (LDL) oxidation by Cu2+ or an azo free-radical generator as determined by assay of lipid hydroperoxides (LOOHs), conjugated dienes and thiobarbituric acid-reacting substances, in both cases it inhibited the elevation in lysophosphatidylcholine content. Moreover, the significantly increased monocyte chemoattractant activity found in a non-esterified fatty acid fraction from LDL oxidized by Cu2+ was also prevented by pretreatment with SB-222657, with an IC50 value of 5.0+/-0.4 nM. The less potent diastereoisomer of SB-222657, SB-223777 (Ki=6.3+/-0.5 microM, kobs/[I]=1.6x10(4) M-1.s-1), was found to be significantly less active in both assays. Thus, in addition to generating lysophosphatidylcholine, a known biologically active lipid, these results demonstrate that Lp-PLA2 is capable of generating oxidized non-esterified fatty acid moieties that are also bioactive. These findings are consistent with our proposal that Lp-PLA2 has a predominantly pro-inflammatory role in atherogenesis. Finally, similar studies have demonstrated that a different situation exists during the oxidation of high-density lipoprotein, with enzyme(s) other than Lp-PLA2 apparently being responsible for generating lysophosphatidylcholine.  (+info)

Re-entering the translocon from the lumenal side of the endoplasmic reticulum. Studies on mutated carboxypeptidase yscY species. (7/1604)

Misfolded or unassembled secretory proteins are retained in the endoplasmic reticulum (ER) and subsequently degraded by the cytosolic ubiquitin-proteasome system. This requires their retrograde transport from the ER lumen into the cytosol, which is mediated by the Sec61 translocon. It had remained a mystery whether ER-localised soluble proteins are at all capable of re-entering the Sec61 channel de novo or whether a permanent contact of the imported protein with the translocon is a prerequisite for retrograde transport. In this study we analysed two new variants of the mutated yeast carboxypeptidase yscY, CPY*: a carboxy-terminal fusion protein of CPY* and pig liver esterase and a CPY* species carrying an additional glycosylation site at its carboxy-terminus. With these constructs it can be demonstrated that the newly synthesised CPY* chain is not retained in the translocation channel but reaches its ER lumenal side completely. Our data indicate that the Sec61 channel provides the essential pore for protein transport through the ER membrane in either direction; persistent contact with the translocon after import seems not to be required for retrograde transport.  (+info)

Activation of stimulus-specific serine esterases (proteases) in the initiation of platelet secretion. I. Demonstration with organophosphorus inhibitors. (8/1604)

The effect of organophosphorus inhibitors of serine esterases (proteases) on secretion from washed rabbit platelets was examined. Five noncytotoxic stimuli were employed: collagen, thrombin, heterologous anti-platelet antibody (in the absence of complement), rabbit C3 bound to zymosan, and platelet activating factor derived from antigen-stimulated, IgE-sensitized rabbit basophils. Diisoprophyl phosphofluoridate, three series of p-nitrophenyl ethyl phosphonates, and a series of cyclohexyl phenylalkylphosphonofluridates were all found to be inhibitory to the platelet secretion. These are irreversible inhibitors of serine proteases but in this system were only inhibitory if added to the platelets concurrently with the stimuli. Pretreatment of either the platelets or the stimuli with the inhibitors followed by washing, was without effect on the subsequent reaction. This suggested the involvement of stimulus-activatable serine proteases in the secretory process. The concept was supported by finding that nonphosphorylating phosphonates or hydrolyzed phosphonates or phosphonofluoridates were without inhibitory action. The effect of a series of phosphonates or phosphonoflouridates in inhibiting each stimulus exhibited a unique activity-structure profile. The demonstration of such unique profiles with four series of inhibitors for each of the five stimuli was interpreted as demonstrating that a specific activatable serine protease was involved in the platelet secretory response to each stimulus.  (+info)

Esterases are a group of enzymes that catalyze the hydrolysis of ester bonds in esters, producing alcohols and carboxylic acids. They are widely distributed in plants, animals, and microorganisms and play important roles in various biological processes, such as metabolism, digestion, and detoxification.

Esterases can be classified into several types based on their substrate specificity, including carboxylesterases, cholinesterases, lipases, and phosphatases. These enzymes have different structures and mechanisms of action but all share the ability to hydrolyze esters.

Carboxylesterases are the most abundant and diverse group of esterases, with a wide range of substrate specificity. They play important roles in the metabolism of drugs, xenobiotics, and lipids. Cholinesterases, on the other hand, specifically hydrolyze choline esters, such as acetylcholine, which is an important neurotransmitter in the nervous system. Lipases are a type of esterase that preferentially hydrolyzes triglycerides and plays a crucial role in fat digestion and metabolism. Phosphatases are enzymes that remove phosphate groups from various molecules, including esters, and have important functions in signal transduction and other cellular processes.

Esterases can also be used in industrial applications, such as in the production of biodiesel, detergents, and food additives. They are often produced by microbial fermentation or extracted from plants and animals. The use of esterases in biotechnology is an active area of research, with potential applications in biofuel production, bioremediation, and medical diagnostics.

Carboxylic ester hydrolases are a class of enzymes that catalyze the hydrolysis of ester bonds in carboxylic acid esters, producing alcohols and carboxylates. This group includes several subclasses of enzymes such as esterases, lipases, and thioesterases. These enzymes play important roles in various biological processes, including metabolism, detoxification, and signal transduction. They are widely used in industrial applications, such as the production of biodiesel, pharmaceuticals, and food ingredients.

Naphthol AS-D esterase is an enzyme that catalyzes the hydrolysis of Naphthol AS-D esters to produce phenol and naphthoic acids. It is commonly found in various tissues, including the liver, kidney, and intestine, and is used as a marker for neutrophil activation in diagnostic tests.

In medical terms, Naphthol AS-D esterase is often referred to as a "non-specific esterase" because it can hydrolyze various types of esters, not just those containing the Naphthol AS-D group. It is also known as "alkaline phosphatase" because it has optimal activity at alkaline pH levels and contains phosphate groups in its active site.

Naphthol AS-D esterase is often used in histological staining techniques to identify and differentiate various types of cells, such as neutrophils, monocytes, and macrophages, based on their enzymatic activity. The presence and intensity of the enzyme activity can provide valuable information about the type, location, and severity of inflammation or tissue damage in various pathological conditions.

A sterol esterase is an enzyme that catalyzes the hydrolysis of sterol esters, which are fatty acid esters of sterols (such as cholesterol) that are commonly found in lipoproteins and cell membranes. Sterol esterases play a crucial role in the metabolism of lipids by breaking down sterol esters into free sterols and free fatty acids, which can then be used in various biochemical processes.

There are several types of sterol esterases that have been identified, including:

1. Cholesteryl esterase (CE): This enzyme is responsible for hydrolyzing cholesteryl esters in the intestine and liver. It plays a critical role in the absorption and metabolism of dietary cholesterol.
2. Hormone-sensitive lipase (HSL): This enzyme is involved in the hydrolysis of sterol esters in adipose tissue, as well as other lipids such as triacylglycerols. It is regulated by hormones such as insulin and catecholamines.
3. Carboxylesterase (CES): This enzyme is a broad-specificity esterase that can hydrolyze various types of esters, including sterol esters. It is found in many tissues throughout the body.

Sterol esterases are important targets for drug development, as inhibiting these enzymes can have therapeutic effects in a variety of diseases, such as obesity, diabetes, and cardiovascular disease.

Acetylesterase is an enzyme that catalyzes the hydrolysis of acetyl esters into alcohol and acetic acid. This enzyme plays a role in the metabolism of various xenobiotics, including drugs and environmental toxins, by removing acetyl groups from these compounds. Acetylesterase is found in many tissues, including the liver, intestine, and blood. It belongs to the class of enzymes known as hydrolases, which act on ester bonds.

Carboxylesterase is a type of enzyme that catalyzes the hydrolysis of ester bonds in carboxylic acid esters, producing alcohol and carboxylate products. These enzymes are widely distributed in various tissues, including the liver, intestines, and plasma. They play important roles in detoxification, metabolism, and the breakdown of xenobiotics (foreign substances) in the body.

Carboxylesterases can also catalyze the reverse reaction, forming esters from alcohols and carboxylates, which is known as transesterification or esterification. This activity has applications in industrial processes and biotechnology.

There are several families of carboxylesterases, with different substrate specificities, kinetic properties, and tissue distributions. These enzymes have been studied for their potential use in therapeutics, diagnostics, and drug delivery systems.

I'm sorry for any confusion, but "Isoflurophate" does not appear to be a recognized term in medical or scientific literature. It is possible that there may be a spelling error or typo in the term you are looking for. If you meant "Isoflurane," which is a commonly used anesthetic in medical and surgical procedures, I can provide a definition for that.

Isoflurane: A volatile halogenated ether liquid used as an inhalational general anesthetic agent. It has a rapid onset and offset of action, making it useful for both induction and maintenance of anesthesia. Isoflurane is also known to have bronchodilatory properties, which can be beneficial in patients with reactive airway disease or asthma.

Esters are organic compounds that are formed by the reaction between an alcohol and a carboxylic acid. They are widely found in nature and are used in various industries, including the production of perfumes, flavors, and pharmaceuticals. In the context of medical definitions, esters may be mentioned in relation to their use as excipients in medications or in discussions of organic chemistry and biochemistry. Esters can also be found in various natural substances such as fats and oils, which are triesters of glycerol and fatty acids.

Paraoxon is the active metabolite of the organophosphate insecticide parathion. It functions as an acetylcholinesterase inhibitor, which means it prevents the breakdown of the neurotransmitter acetylcholine in the synaptic cleft. This leads to an accumulation of acetylcholine and overstimulation of cholinergic receptors, causing a variety of symptoms such as muscle weakness, increased salivation, sweating, lacrimation, nausea, vomiting, and potentially fatal respiratory failure.

Paraoxon is also used in research and diagnostic settings to measure acetylcholinesterase activity. It can be used to determine the degree of inhibition of this enzyme by various chemicals or toxins, including other organophosphate compounds.

Hydrolysis is a chemical process, not a medical one. However, it is relevant to medicine and biology.

Hydrolysis is the breakdown of a chemical compound due to its reaction with water, often resulting in the formation of two or more simpler compounds. In the context of physiology and medicine, hydrolysis is a crucial process in various biological reactions, such as the digestion of food molecules like proteins, carbohydrates, and fats. Enzymes called hydrolases catalyze these hydrolysis reactions to speed up the breakdown process in the body.

The Complement C1 Inhibitor protein, also known as C1-INH, is a protein involved in the regulation of the complement system and the contact system, which are parts of the immune system. The complement system helps to eliminate pathogens (e.g., bacteria, viruses) from the body, while the contact system helps to regulate blood coagulation and inflammation.

C1-INH works by inhibiting the activation of C1, an enzyme complex that is the first component of the classical complement pathway. By inhibiting C1, C1-INH prevents the activation of downstream components of the complement system, thereby helping to regulate the immune response and prevent excessive inflammation.

Deficiencies or dysfunction in the C1-INH protein can lead to a group of genetic disorders known as C1 inhibitor deficiency disorders, which include hereditary angioedema (HAE) and acquired angioedema (AAE). These conditions are characterized by recurrent episodes of swelling in various parts of the body, such as the face, hands, feet, and airway, which can be painful and potentially life-threatening if they affect the airway.

Complement C1 Inactivator proteins are a part of the complement system, which is a group of proteins in the blood that play a crucial role in the body's immune defense system. Specifically, Complement C1 Inactivator proteins are responsible for regulating the activation of the first component of the complement system, C1.

The complement system is activated in response to the presence of foreign substances such as bacteria or viruses in the body. The activation of C1 leads to a cascade of reactions that result in the destruction of the foreign substance. However, if this process is not properly regulated, it can lead to damage to the body's own cells and tissues.

Complement C1 Inactivator proteins help to prevent this by regulating the activation of C1. They do this by binding to and inhibiting the activity of C1, preventing it from initiating the complement cascade. A deficiency in Complement C1 Inactivator proteins can lead to a condition called hereditary angioedema, which is characterized by recurrent episodes of swelling in various parts of the body.

Substrate specificity in the context of medical biochemistry and enzymology refers to the ability of an enzyme to selectively bind and catalyze a chemical reaction with a particular substrate (or a group of similar substrates) while discriminating against other molecules that are not substrates. This specificity arises from the three-dimensional structure of the enzyme, which has evolved to match the shape, charge distribution, and functional groups of its physiological substrate(s).

Substrate specificity is a fundamental property of enzymes that enables them to carry out highly selective chemical transformations in the complex cellular environment. The active site of an enzyme, where the catalysis takes place, has a unique conformation that complements the shape and charge distribution of its substrate(s). This ensures efficient recognition, binding, and conversion of the substrate into the desired product while minimizing unwanted side reactions with other molecules.

Substrate specificity can be categorized as:

1. Absolute specificity: An enzyme that can only act on a single substrate or a very narrow group of structurally related substrates, showing no activity towards any other molecule.
2. Group specificity: An enzyme that prefers to act on a particular functional group or class of compounds but can still accommodate minor structural variations within the substrate.
3. Broad or promiscuous specificity: An enzyme that can act on a wide range of structurally diverse substrates, albeit with varying catalytic efficiencies.

Understanding substrate specificity is crucial for elucidating enzymatic mechanisms, designing drugs that target specific enzymes or pathways, and developing biotechnological applications that rely on the controlled manipulation of enzyme activities.

Triacetin is not a medical term, but it is a chemical compound with the formula C9H14O6. It is also known as glycerol triacetate and is an ester formed from glycerin and acetic acid. Triacetin is used in various applications including as a food additive, plasticizer, solvent, and in the manufacture of explosives.

In the medical field, triacetin has been studied for its potential therapeutic uses, such as a topical agent to enhance the penetration of drugs through the skin, and as an excipient in pharmaceutical formulations. However, it is not commonly used as a medication or treatment.

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.

Pseudocholinesterase, also known as butyrylcholinesterase or plasma cholinesterase, is an enzyme found in the blood plasma. It is responsible for breaking down certain types of drugs and muscle relaxants that are used during general anesthesia, such as succinylcholine and mivacurium.

Pseudocholinesterase deficiency can lead to prolonged neuromuscular blockade and difficulty in reversing the effects of these muscle relaxants, which can result in respiratory complications and other adverse effects during or after surgery. This deficiency can be inherited or acquired due to various factors such as liver disease, malnutrition, or exposure to certain chemicals.

It is important to test the patient's pseudocholinesterase levels before administering succinylcholine or mivacurium to ensure that they have adequate enzyme activity to metabolize these drugs properly.

Lipase is an enzyme that is produced by the pancreas and found in the digestive system of most organisms. Its primary function is to catalyze the hydrolysis of fats (triglycerides) into smaller molecules, such as fatty acids and glycerol, which can then be absorbed by the intestines and utilized for energy or stored for later use.

In medical terms, lipase levels in the blood are often measured to diagnose or monitor conditions that affect the pancreas, such as pancreatitis (inflammation of the pancreas), pancreatic cancer, or cystic fibrosis. Elevated lipase levels may indicate damage to the pancreas and its ability to produce digestive enzymes.

Tritolyl phosphates are not a medical term, but rather a class of industrial chemicals. They are organophosphate esters made from the reaction of toluene with phosphoric acid. These chemicals have various uses, including as plasticizers, flame retardants, and hydraulic fluids.

Exposure to high levels of tritolyl phosphates can cause irritation to the skin, eyes, and respiratory tract. However, they are not typically considered a significant health concern at the low levels encountered in most occupational or environmental settings. There is no known medical condition specifically associated with "tritolyl phosphates."

Nitrophenols are organic compounds that contain a hydroxyl group (-OH) attached to a phenyl ring (aromatic hydrocarbon) and one or more nitro groups (-NO2). They have the general structure R-C6H4-NO2, where R represents the hydroxyl group.

Nitrophenols are known for their distinctive yellow to brown color and can be found in various natural sources such as plants and microorganisms. Some common nitrophenols include:

* p-Nitrophenol (4-nitrophenol)
* o-Nitrophenol (2-nitrophenol)
* m-Nitrophenol (3-nitrophenol)

These compounds are used in various industrial applications, including dyes, pharmaceuticals, and agrochemicals. However, they can also be harmful to human health and the environment, as some nitrophenols have been identified as potential environmental pollutants and may pose risks to human health upon exposure.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

Phenylmethylsulfonyl Fluoride (PMSF) is not a medication or a treatment, but it is a chemical compound with the formula C8H9FO3S. It is commonly used in biochemistry and molecular biology research as a serine protease inhibitor.

Proteases are enzymes that break down other proteins by cleaving specific peptide bonds. Serine proteases are a class of proteases that use a serine residue in their active site to carry out the hydrolysis reaction. PMSF works by irreversibly modifying this serine residue, inhibiting the enzyme's activity.

PMSF is used in laboratory settings to prevent protein degradation during experiments such as protein purification or Western blotting. It is important to note that PMSF is highly toxic and must be handled with care, using appropriate personal protective equipment (PPE) and safety measures.

Electrophoresis, starch gel is a type of electrophoretic technique used in laboratory settings for the separation and analysis of large biomolecules such as DNA, RNA, and proteins. In this method, a gel made from cooked starch is used as the supporting matrix for the molecules being separated.

The sample containing the mixture of biomolecules is loaded onto the gel and an electric field is applied, causing the negatively charged molecules to migrate towards the positive electrode. The starch gel acts as a molecular sieve, with smaller molecules moving more quickly through the gel than larger ones. This results in the separation of the mixture into individual components based on their size and charge.

Once the separation is complete, the gel can be stained to visualize the separated bands. Different staining techniques are used depending on the type of biomolecule being analyzed. For example, proteins can be stained with dyes such as Coomassie Brilliant Blue or silver nitrate, while nucleic acids can be stained with dyes such as ethidium bromide.

Starch gel electrophoresis is a relatively simple and inexpensive technique that has been widely used in molecular biology research and diagnostic applications. However, it has largely been replaced by other electrophoretic techniques, such as polyacrylamide gel electrophoresis (PAGE), which offer higher resolution and can be automated for high-throughput analysis.

Angioedema is a medical condition characterized by rapid swelling of the skin, mucous membranes, and submucosal tissues. The swelling typically occurs in the face, lips, tongue, larynx, and extremities, and can also affect the gastrointestinal tract. Angioedema can be caused by a variety of factors, including allergic reactions, hereditary genetic mutations, and certain medications.

In medical terms, angioedema is defined as a self-limiting episode of localized edema in the deep dermis, subcutaneous tissue, or mucous membranes, characterized by well-circumscribed, nonpitting, nondependent swelling. The swelling can occur suddenly and may persist for up to 72 hours. In severe cases, angioedema can cause airway obstruction and be life-threatening if not treated promptly.

Angioedema can be classified into two main types: allergic or non-allergic. Allergic angioedema is caused by an immune response to an allergen, such as food, medication, or insect venom. Non-allergic angioedema can be further divided into several subtypes, including hereditary angioedema (HA), acquired angioedema (AAE), and drug-induced angioedema.

Hereditary angioedema is a rare genetic disorder caused by mutations in the C1 inhibitor gene, leading to uncontrolled activation of the complement system and increased production of bradykinin, a potent vasodilator. Acquired angioedema is similar to hereditary angioedema but occurs later in life and is associated with underlying medical conditions such as lymphoproliferative disorders or autoimmune diseases. Drug-induced angioedema can be caused by a variety of medications, including ACE inhibitors, angiotensin receptor blockers (ARBs), and nonsteroidal anti-inflammatory drugs (NSAIDs).

The diagnosis of angioedema is typically based on clinical presentation, medical history, and laboratory tests. Treatment depends on the underlying cause of the condition but may include antihistamines, corticosteroids, epinephrine, and medications that target the complement system or bradykinin pathway. In severe cases, hospitalization and intensive care may be necessary to manage airway obstruction and other complications.

Reagent strips, also known as diagnostic or test strips, are narrow pieces of plastic material that have been impregnated with chemical reagents. They are used in the qualitative or semi-quantitative detection of various substances, such as glucose, proteins, ketones, blood, and white blood cells, in body fluids like urine or blood.

Reagent strips typically contain multiple pad areas, each with a different reagent that reacts to a specific substance. To perform the test, a small amount of the fluid is applied to the strip, and the reaction between the reagents and the target substance produces a visible color change. The resulting color can then be compared to a standardized color chart to determine the concentration or presence of the substance.

Reagent strips are widely used in point-of-care testing, providing quick and convenient results for healthcare professionals and patients alike. They are commonly used for monitoring conditions such as diabetes (urine or blood glucose levels), urinary tract infections (leukocytes and nitrites), and kidney function (protein and blood).

Insecticide resistance is a genetic selection process in insect populations that allows them to survive and reproduce despite exposure to insecticides. It's the result of changes in the genetic makeup of insects, which can be caused by natural selection when insecticides are used repeatedly. Over time, this leads to the prevalence of genes that provide resistance to the insecticide, making the pest control methods less effective. Insecticide resistance is a significant challenge in public health and agriculture, as it can reduce the efficacy of interventions aimed at controlling disease-carrying insects or protecting crops from pests.

Acetylcholinesterase (AChE) is an enzyme that catalyzes the hydrolysis of acetylcholine (ACh), a neurotransmitter, into choline and acetic acid. This enzyme plays a crucial role in regulating the transmission of nerve impulses across the synapse, the junction between two neurons or between a neuron and a muscle fiber.

Acetylcholinesterase is located in the synaptic cleft, the narrow gap between the presynaptic and postsynaptic membranes. When ACh is released from the presynaptic membrane and binds to receptors on the postsynaptic membrane, it triggers a response in the target cell. Acetylcholinesterase rapidly breaks down ACh, terminating its action and allowing for rapid cycling of neurotransmission.

Inhibition of acetylcholinesterase leads to an accumulation of ACh in the synaptic cleft, prolonging its effects on the postsynaptic membrane. This can result in excessive stimulation of cholinergic receptors and overactivation of the cholinergic system, which may cause a range of symptoms, including muscle weakness, fasciculations, sweating, salivation, lacrimation, urination, defecation, bradycardia, and bronchoconstriction.

Acetylcholinesterase inhibitors are used in the treatment of various medical conditions, such as Alzheimer's disease, myasthenia gravis, and glaucoma. However, they can also be used as chemical weapons, such as nerve agents, due to their ability to disrupt the nervous system and cause severe toxicity.

Butyrylcholinesterase (BChE) is an enzyme that catalyzes the hydrolysis of esters of choline, including butyrylcholine and acetylcholine. It is found in various tissues throughout the body, including the liver, brain, and plasma. BChE plays a role in the metabolism of certain drugs and neurotransmitters, and its activity can be inhibited by certain chemicals, such as organophosphate pesticides and nerve agents. Elevated levels of BChE have been found in some neurological disorders, while decreased levels have been associated with genetic deficiencies and liver disease.

Xylans are a type of complex carbohydrate, specifically a hemicellulose, that are found in the cell walls of many plants. They are made up of a backbone of beta-1,4-linked xylose sugar molecules and can be substituted with various side groups such as arabinose, glucuronic acid, and acetyl groups. Xylans are indigestible by humans, but they can be broken down by certain microorganisms in the gut through a process called fermentation, which can produce short-chain fatty acids that have beneficial effects on health.

Organophosphorus compounds are a class of chemical substances that contain phosphorus bonded to organic compounds. They are used in various applications, including as plasticizers, flame retardants, pesticides (insecticides, herbicides, and nerve gases), and solvents. In medicine, they are also used in the treatment of certain conditions such as glaucoma. However, organophosphorus compounds can be toxic to humans and animals, particularly those that affect the nervous system by inhibiting acetylcholinesterase, an enzyme that breaks down the neurotransmitter acetylcholine. Exposure to these compounds can cause symptoms such as nausea, vomiting, muscle weakness, and in severe cases, respiratory failure and death.

Hydrogen-ion concentration, also known as pH, is a measure of the acidity or basicity of a solution. It is defined as the negative logarithm (to the base 10) of the hydrogen ion activity in a solution. The standard unit of measurement is the pH unit. A pH of 7 is neutral, less than 7 is acidic, and greater than 7 is basic.

In medical terms, hydrogen-ion concentration is important for maintaining homeostasis within the body. For example, in the stomach, a high hydrogen-ion concentration (low pH) is necessary for the digestion of food. However, in other parts of the body such as blood, a high hydrogen-ion concentration can be harmful and lead to acidosis. Conversely, a low hydrogen-ion concentration (high pH) in the blood can lead to alkalosis. Both acidosis and alkalosis can have serious consequences on various organ systems if not corrected.

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.

Cholinesterases are a group of enzymes that play an essential role in the nervous system by regulating the transmission of nerve impulses. They work by breaking down a type of chemical messenger called acetylcholine, which is released by nerves to transmit signals to other nerves or muscles.

There are two main types of cholinesterases: acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). AChE is found primarily in the nervous system, where it rapidly breaks down acetylcholine to terminate nerve impulses. BChE, on the other hand, is found in various tissues throughout the body, including the liver and plasma, and plays a less specific role in breaking down various substances, including some drugs and toxins.

Inhibition of cholinesterases can lead to an accumulation of acetylcholine in the synaptic cleft, which can result in excessive stimulation of nerve impulses and muscle contractions. This effect is exploited by certain medications used to treat conditions such as myasthenia gravis, Alzheimer's disease, and glaucoma, but can also be caused by exposure to certain chemicals or toxins, such as organophosphate pesticides and nerve agents.

Naphthols are chemical compounds that consist of a naphthalene ring (a polycyclic aromatic hydrocarbon made up of two benzene rings) substituted with a hydroxyl group (-OH). They can be classified as primary or secondary naphthols, depending on whether the hydroxyl group is directly attached to the naphthalene ring (primary) or attached through a carbon atom (secondary). Naphthols are important intermediates in the synthesis of various chemical and pharmaceutical products. They have been used in the production of azo dyes, antioxidants, and pharmaceuticals such as analgesics and anti-inflammatory agents.

Enzyme stability refers to the ability of an enzyme to maintain its structure and function under various environmental conditions, such as temperature, pH, and the presence of denaturants or inhibitors. A stable enzyme retains its activity and conformation over time and across a range of conditions, making it more suitable for industrial and therapeutic applications.

Enzymes can be stabilized through various methods, including chemical modification, immobilization, and protein engineering. Understanding the factors that affect enzyme stability is crucial for optimizing their use in biotechnology, medicine, and research.

Insecticides are substances or mixtures of substances intended for preventing, destroying, or mitigating any pest, including insects, arachnids, or other related pests. They can be chemical or biological agents that disrupt the growth, development, or behavior of these organisms, leading to their death or incapacitation. Insecticides are widely used in agriculture, public health, and residential settings for pest control. However, they must be used with caution due to potential risks to non-target organisms and the environment.

"Ophiostoma" is a genus of fungi that are often associated with trees and woody plants. Many species in this genus are able to cause diseases in trees, including the well-known Dutch Elm Disease, which is caused by the species Ophiostoma ulmi and Ophiostoma novo-ulmi. These fungi typically invade the sapwood of trees and can block the water-conducting vessels, leading to wilting and dieback of branches or even death of the entire tree in severe cases. The fungi produce specialized structures called perithecia, which contain asci (sexual spore-producing structures), and ascospores (sexual spores) are released from the perithecia to infect new trees. Some species of Ophiostoma can also be transported by bark beetles, which can carry the fungi into new trees and facilitate their spread.

Molecular cloning is a laboratory technique used to create multiple copies of a specific DNA sequence. This process involves several steps:

1. Isolation: The first step in molecular cloning is to isolate the DNA sequence of interest from the rest of the genomic DNA. This can be done using various methods such as PCR (polymerase chain reaction), restriction enzymes, or hybridization.
2. Vector construction: Once the DNA sequence of interest has been isolated, it must be inserted into a vector, which is a small circular DNA molecule that can replicate independently in a host cell. Common vectors used in molecular cloning include plasmids and phages.
3. Transformation: The constructed vector is then introduced into a host cell, usually a bacterial or yeast cell, through a process called transformation. This can be done using various methods such as electroporation or chemical transformation.
4. Selection: After transformation, the host cells are grown in selective media that allow only those cells containing the vector to grow. This ensures that the DNA sequence of interest has been successfully cloned into the vector.
5. Amplification: Once the host cells have been selected, they can be grown in large quantities to amplify the number of copies of the cloned DNA sequence.

Molecular cloning is a powerful tool in molecular biology and has numerous applications, including the production of recombinant proteins, gene therapy, functional analysis of genes, and genetic engineering.

Coumaric acids are a type of phenolic acid that are widely distributed in plants. They are found in various foods such as fruits, vegetables, and grains. The most common forms of coumaric acids are p-coumaric acid, o-coumaric acid, and m-coumaric acid.

Coumaric acids have been studied for their potential health benefits, including their antioxidant, anti-inflammatory, and antimicrobial properties. They may also play a role in preventing chronic diseases such as cancer and cardiovascular disease. However, more research is needed to fully understand the potential health benefits of coumaric acids.

It's worth noting that coumaric acids are not to be confused with warfarin (also known as Coumadin), a medication used as an anticoagulant. While both coumaric acids and warfarin contain a similar chemical structure, they have different effects on the body.

Umbelliferone is not a medical term, but a chemical compound that belongs to the class of coumarins. It can be found in various plants, including those from the family Apiaceae (also known as Umbelliferae), hence its name. Coumarins like umbelliferone have been studied for their potential pharmacological properties, such as anticoagulant, anti-inflammatory, and antimicrobial activities. However, they are not typically considered as a medical treatment on their own.

Electrophoresis, polyacrylamide gel (EPG) is a laboratory technique used to separate and analyze complex mixtures of proteins or nucleic acids (DNA or RNA) based on their size and electrical charge. This technique utilizes a matrix made of cross-linked polyacrylamide, a type of gel, which provides a stable and uniform environment for the separation of molecules.

In this process:

1. The polyacrylamide gel is prepared by mixing acrylamide monomers with a cross-linking agent (bis-acrylamide) and a catalyst (ammonium persulfate) in the presence of a buffer solution.
2. The gel is then poured into a mold and allowed to polymerize, forming a solid matrix with uniform pore sizes that depend on the concentration of acrylamide used. Higher concentrations result in smaller pores, providing better resolution for separating smaller molecules.
3. Once the gel has set, it is placed in an electrophoresis apparatus containing a buffer solution. Samples containing the mixture of proteins or nucleic acids are loaded into wells on the top of the gel.
4. An electric field is applied across the gel, causing the negatively charged molecules to migrate towards the positive electrode (anode) while positively charged molecules move toward the negative electrode (cathode). The rate of migration depends on the size, charge, and shape of the molecules.
5. Smaller molecules move faster through the gel matrix and will migrate farther from the origin compared to larger molecules, resulting in separation based on size. Proteins and nucleic acids can be selectively stained after electrophoresis to visualize the separated bands.

EPG is widely used in various research fields, including molecular biology, genetics, proteomics, and forensic science, for applications such as protein characterization, DNA fragment analysis, cloning, mutation detection, and quality control of nucleic acid or protein samples.

Naphthaleneacetic acids (NAAs) are a type of synthetic auxin, which is a plant hormone that promotes growth and development. Specifically, NAAs are derivatives of naphthalene, a polycyclic aromatic hydrocarbon, with a carboxylic acid group attached to one of the carbon atoms in the ring structure.

NAAs are commonly used in horticulture and agriculture as plant growth regulators. They can stimulate rooting in cuttings, promote fruit set and growth, and inhibit vegetative growth. NAAs can also be used in plant tissue culture to regulate cell division and differentiation.

In medical terms, NAAs are not typically used as therapeutic agents. However, they have been studied for their potential use in cancer therapy due to their ability to regulate cell growth and differentiation. Some research has suggested that NAAs may be able to inhibit the growth of certain types of cancer cells, although more studies are needed to confirm these findings and determine the safety and efficacy of NAAs as a cancer treatment.

Histochemistry is the branch of pathology that deals with the microscopic localization of cellular or tissue components using specific chemical reactions. It involves the application of chemical techniques to identify and locate specific biomolecules within tissues, cells, and subcellular structures. This is achieved through the use of various staining methods that react with specific antigens or enzymes in the sample, allowing for their visualization under a microscope. Histochemistry is widely used in diagnostic pathology to identify different types of tissues, cells, and structures, as well as in research to study cellular and molecular processes in health and disease.

Xylosidases are a group of enzymes that catalyze the hydrolysis of xylosides, which are glycosides with a xylose sugar. Specifically, they cleave the terminal β-1,4-linked D-xylopyranoside residues from various substrates such as xylooligosaccharides and xylan. These enzymes play an important role in the breakdown and metabolism of plant-derived polysaccharides, particularly hemicelluloses, which are a major component of plant biomass. Xylosidases have potential applications in various industrial processes, including biofuel production and animal feed manufacturing.

... acid Ester Leukocyte esterase Hemagglutinin esterase Nuclease Lipase Asymmetric ester hydrolysis with pig-liver esterase Enzyme ... An esterase is a hydrolase enzyme that splits esters into an acid and an alcohol in a chemical reaction with water called ... A wide range of different esterases exist that differ in their substrate specificity, their protein structure, and their ...
The enzyme 4-methyloxaloacetate esterase (EC 3.1.1.44) catalyzes the reaction oxaloacetate 4-methyl ester + H2O ⇌ {\ ...
C1 esterase inhibitor (C1-INH) is a protein found in the fluid part of your blood. It controls a protein called C1, which is ... C1 esterase inhibitor (C1-INH) is a protein found in the fluid part of your blood. It controls a protein called C1, which is ... C1 esterase inhibitor (C1-INH) is a protein found in the fluid part of your blood. It controls a protein called C1, which is ... Your health care provider will also measure the functional activity level of your C1 esterase inhibitor. Talk to your provider ...
cl28016 (PSSM ID: 421565): Conserved Protein Domain Family Hema_esterase,
... the first C1 Esterase Inhibitor (Human) for subcutaneous (under the skin) administration to prevent Hereditary Angioedema (HAE ... HAE, which is caused by having insufficient amounts of a plasma protein called C1-esterase inhibitor (or C1-INH), affects ... The U.S. Food and Drug Administration today approved Haegarda, the first C1 Esterase Inhibitor (Human) for subcutaneous (under ... FDA approves first subcutaneous C1 Esterase Inhibitor to treat rare genetic disease. * Share ...
Hypothetical esterase YJL068C. Timeline for Protein Hypothetical esterase YJL068C from c.69.1.34: Hypothetical esterase YJL068C ... Protein Hypothetical esterase YJL068C from c.69.1.34: Hypothetical esterase YJL068C first appeared in SCOP 1.71. *Protein ... Lineage for Protein: Hypothetical esterase YJL068C. *Root: SCOPe 2.08 *. Class c: Alpha and beta proteins (a/b) [51349] (148 ... Family c.69.1.34: Hypothetical esterase YJL068C [117714] (2 proteins). part of Pfam PF00756. ...
View mouse Pced1a Chr2:130259603-130266692 with: sequences, polymorphisms, proteins, references, function
Structures of Bacillus subtilis PdaA, a family 4 carbohydrate esterase, and a complex with N-acetyl-glucosamine.. Blair, D.E., ... Family 4 carbohydrate esterases deacetylate polymeric carbohydrate substrates such as chitin, acetyl xylan and peptidoglycan. ... Family 4 carbohydrate esterases deacetylate polymeric carbohydrate substrates such as chitin, acetyl xylan and peptidoglycan. ... The PdaA structure provides a template for interpreting the wealth of sequence data on family 4 carbohydrate esterases in a ...
About Cinryze® (C1 esterase inhibitor [human]). Cinryze is a highly purified, pasteurized and nanofiltered plasma-derived C1 ... ViroPharma And Halozyme Provide Update On Clinical Development Of Subcutaneous Cinryze® (C1 Esterase Inhibitor [Human]) With ... including C1 esterase inhibitor deficiency, treatment of seizures in children and adolescents, adrenal insufficiency (AI), and ... esterase inhibitor product. In the U.S., Cinryze is approved by the FDA for routine prophylaxis against angioedema attacks in ...
US-2009324574-A1 chemical patent summary.
Use of thermal imaging and the in situ technique to assess the impact of an inoculant with feruloyl esterase activity on the ... Use of thermal imaging and the in situ technique to assess the impact of an inoculant with feruloyl esterase activity on the ... Feruloyl esters limit the digestibility of forages, a constraint that may be overcome if additives with feruloyl esterase (FE) ... "Use of thermal imaging and the in situ technique to assess the impact of an inoculant with feruloyl esterase activity on the ...
Axon Medchem | Prime source supplier of high-value life science products, providing Axon Ligands™ for pharmaceutical research as world-wide recognized drug standards
CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity ...
Esterase activity of sediment core M21/3_MC409. PANGAEA, https://doi.org/10.1594/PANGAEA.400248, In supplement to: Pfannkuche, ... Pfannkuche, Olaf; Boetius, Antje; Lundgreen, Ulrich; Lochte, Karin; Thiel, Hjalmar (1999): Esterase activity of sediment core ...
MeJA esterase peptides could be identified as components of an esterase. For the identification of the MeJA esterase gene ... However MeJA esterase is not a highly specific enzyme. Enzyme kinetics of native MeJA esterase revealed a KM value of 14.7 ± ... MeJA esterase transcripts were present in all tomato plant tissues. High levels of MeJA esterase mRNA could be found in roots ... MeJA esterase coding sequence hybridized with two to seven cDNA fragments. It might be possible that MeJA esterase belongs to a ...
Furthermore, the role of the enzyme pectin methyl esterase (PME) on CH4 efflux potential was also examined. Different types of ... Effects of temperature, ultraviolet radiation and pectin methyl esterase on aerobic methane release from plant material.. Plant ... Effects of temperature, ultraviolet radiation and pectin methyl esterase on aerobic methane release from plant material ...
Twelve cases of follicular centroblastic/centrocytic malignant lymphoma were studied for acid non-specific esterase. The ... Distribution of T-lymphocytes in follicular lymphomas as revealed by acid alpha-naphthol acetate esterase. ... Distribution of T-lymphocytes in follicular lymphomas as revealed by acid alpha-naphthol acetate esterase. ...
... ... Cholesterol esterase (5 U/mg), Recombinant E. Coli (powder). ... Cholesterol esterase (5 U/mg), Recombinant E. Coli (powder). Form. Freeze dried powder. ...
The site of the esterase D gene to the often deleted region offers an objective means of deletion identification. The ... These findings emphasise the importance of measurements of esterase D in all patients with retinoblastoma, even those with an ... The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions. ... The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions. ...
... ... and its esterase property is analyzed via esterase enzymatic activity assay. ... HEF utilizes 9-O-acetylated sialic acids as its receptor and has both receptor binding and esterase activities, thus is a ... Here, we summarize the methods to evaluate the glycan-binding and esterase activities of HEF in vitro. The glycan-bind property ...
Two of the esterases characterized have activity of over two orders of magnitude higher than other members of the family, and ... Datasets supporting Characterisation of a New Family of Carboxyl Esterases with an OsmC domain. *Mai-Britt Jensen (Creator) ... A serine esterase from the psychrophilic bacterium Pseudoalteromonas arctica with a C-terminal OsmC-like domain was recently ... We determined the crystal structure of the esterase domain of the protein from Rhodothermus marinus and show that it conforms ...
title = "Pectic Esterases",. abstract = "Discussed are the pectin esterases. They comprise enzymes that hydrolyze the esters ... Pectic Esterases. / Benen, J.A.E.; van Alebeek, G.J.W.M.; Voragen, A.G.J. et al. Handbook of food enzymology. ed. / J.R. ... Benen, J. A. E., van Alebeek, G. J. W. M., Voragen, A. G. J., & Visser, J. (2003). Pectic Esterases. In J. R. Whitaker, A. G. J ... Pectic Esterases. Handbook of food enzymology. editor / J.R. Whitaker ; A.G.J. Voragen ; D.W.S. Wong. New York : Marcel Dekker ...
Novel Hybrid Esterase-Haloacid Dehalogenase Enzyme. Research output: Contribution to journal › Article › peer-review ...
In this work, an acetyl esterase was identified in the secretome of this strain by non-targeted proteomics, and classified in ... Identification of an acetyl esterase in the supernatant of the environmental strain Bacillus sp. HR21-6 ... Identification of an acetyl esterase in the supernatant of the environmental strain Bacillus sp. HR21-6. Biochimie, 198, 48-59. ... was performed to understand the role of different amino acids that are conserved among GDSL superfamily of esterases. Mutation ...
Retrieved from "http://www.cazypedia.org/index.php/Carbohydrate_Esterase_Family_13" ...
"Esterases" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... This graph shows the total number of publications written about "Esterases" by people in this website by year, and whether " ... Below are the most recent publications written about "Esterases" by people in Profiles. ...
... D Human. Esterase-D Human Recombinant fused with 20 amino acid His tag at N-terminus produced in E.Coli is a single, ... and having a molecular mass of 33.6kDa.The Esterase-D is purified by proprietary chromatographic techniques.. 10µg. 50µg. 1mg. ...
Esterase activity. Esterase activity was assayed using Nα-p-tosyl-L-arginine ester (TAME)116. The reaction mixture consisted of ... SVEVs presents amidolytic, caseinolytic and esterase activities. In order to further characterize the proteolytic activity of ...
The band (zone 1) esterase had approximately twice the molecular weight of the bands 1-4 esterases. 6. The kidney microsomes ... 4. The microsomal esterases were solubilised using Triton X-100. Sodium deoxycholate was almost as satisfactory and sonication ... 5. Five esterases were separated electrophoretically from the solubilised liver microsomes. They could be divided into two ... It was shown that this increase was due, mainly, to the presence of liver microsomal esterases. 12. After dosing with DDT (a ...
  • Our Cholesterol Esterase & Oxidase products can be used in both Biosensor and Clinical Chemistry applications. (bbisolutions.com)
  • Our Cholesterol Esterase is available from porcine pancreas (CE2) or Pseudomonas sp. (bbisolutions.com)
  • Others Cholesterol Esterase Grade I Cholesterol Esterase, Grade I For customers in the European Economic Area: Contains SVHC: octyl/nonylphenol ethoxylates. (roche.com)
  • 3.1.4.1.12.3 from Pseudomonas species, lyophilizate Cholesterol Esterase, Grade I custom fill CustomBiotech product. (roche.com)
  • SQ 11520857103 Not Available Reagents, kits en Use Cholesterol Esterase in diagnostic tests for the determination of cholesterol in combination with Cholesterol Oxidase, Catalog Nos. (roche.com)
  • The noncompetitive and competitive hydrolyses of (2R,4'R,8'R)-α-tocopheryl acetate (RRR-α-TOAc, the acetate of natural vitamin E) and (2S,4'R,8'R)-α-tocopheryl acetate (SRR-α-TOAc) catalyzed by crude and pure bovine cholesterol esterase (BCE) and crude and pure porcine cholesterol esterase (PCE) have been studied at 37 °C. These two CE's are catalytically active toward tocopheryl acetates only in the presence of bile salts. (canada.ca)
  • 7) The main objective of this study was to evaluate the in vitro cholesterol esterase inhibitory activity and in vivo antihyperlipidemic activity of Anisomeles malabarica leaf extract. (repository-tnmgrmu.ac.in)
  • BERINERT is a plasma-derived C1 Esterase Inhibitor (Human) indicated for the treatment of acute abdominal, facial, or laryngeal hereditary angioedema (HAE) attacks in adult and pediatric patients. (nih.gov)
  • C1 esterase inhibitor [human] is a serine proteinase inhibitor derived from human plasma that is used in treating hereditary angioedema. (nih.gov)
  • Various international consensus panels state that human plasma-derived C1 esterase inhibitor is considered to be the therapy of choice for both treatment and prophylaxis of maternal hereditary angioedema during lactation. (nih.gov)
  • Cost-utility analysis of Ruconest(®) (conestat alfa) compared to Berinert(®) P (human C1 esterase inhibitor) in the treatment of acute, life-threatening angioedema attacks in patients with hereditary angioedema. (nih.gov)
  • Administration of conestat alfa, human C1 esterase inhibitor and icatibant in the treatment of acute angioedema attacks in adults with hereditary angioedema due to C1 esterase inhibitor deficiency. (nih.gov)
  • Recombinant human C1 esterase inhibitor (Conestat alfa) for prophylaxis to prevent attacks in adult and adolescent patients with hereditary angioedema. (nih.gov)
  • HAEGARDA is a plasma-derived concentrate of C1 Esterase Inhibitor (Human) (C1-INH) indicated for routine prophylaxis to prevent Hereditary Angioedema (HAE) attacks in adolescent and adult patients. (globalrph.com)
  • Breastmilk levels of C1 esterase inhibitor have not been measured after exogenous administration in humans. (nih.gov)
  • The objectives of this study were to (i) establish the reference range and mean value for normal levels of C1- esterase inhibitor (C1 INH) during pregnancy , and (ii) investigate the association between C1 INH and uterine atony , as measured by blood loss at delivery. (bvsalud.org)
  • Hi, I have a problem to find to amino acid sequenes of following enzymes: -------------------------------------- lipase from Apergillus niger esterase from Horse liver esterase from Mucor miehei esterase from Porcine liver -------------------------------------- I have already tried a search with SWISS-PROT http://expasy.hcuge.ch/ without success. (bio.net)
  • Lipases/esterases with novel properties are always in demand due to the large number of synthetic reactions which these enzymes can possibly catalyze and for which enzymatic routes are currently not available [ 4 ]. (hindawi.com)
  • Glucuronoyl esterases (GEs) are microbial enzymes able to cleave covalent linkages between lignin and carbohydrates in the plant cell wall. (inrae.fr)
  • An esterase is a hydrolase enzyme that splits esters into an acid and an alcohol in a chemical reaction with water called hydrolysis. (wikipedia.org)
  • The enzyme 4-methyloxaloacetate esterase (EC 3.1.1.44) catalyzes the reaction oxaloacetate 4-methyl ester + H2O ⇌ {\displaystyle \rightleftharpoons } oxaloacetate + methanol This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. (wikipedia.org)
  • Conditions of enzyme production were optimized, which lead to 9 fold increase in the esterase yield. (hindawi.com)
  • The present work explored the possibility of using this novel isolate as a source of esterase active in polar organic solvents and for characterizing the enzyme for properties that are desirable for industrial esterases. (hindawi.com)
  • In the present study, we biochemically characterized a new enzyme with esterase activity that is a member of the α/β-hydrolase superfamily from a metagenomic library of dark soil in the Amazon. (usp.br)
  • This enzyme was named as Amazonian Dark Earth Esterase 1 (Ade1). (usp.br)
  • Through this study, thermophilic esterase enzyme was obtained using recombinant DNA technology and purified applying one-step His-Select HF nickel affinity gel. (iyte.edu.tr)
  • An unclassified carbohydrate esterase (FjoAcXE) was identified as a protein of unknown function from a polysaccharide utilization locus (PUL) otherwise comprising carbohydrate-active enzyme families known to target xylan. (biomedcentral.com)
  • Alpha naphthyl acetate esterase (ANAE) enzyme, found in atta flour, can be used to detect pesticides. (tku.edu.tw)
  • Neuropathy target esterase (NTE) is an integral membrane protein found predominantly in neurones. (le.ac.uk)
  • The molecular weight of the target esterase was found to be around 65 kilodaltons (kDa). (tku.edu.tw)
  • Histological staining techniques have revolutionized our understanding of cellular processes, and the α-Naphthyl Acetate Esterase (α-NAE) stain holds a significant place in this field. (pscientifics.com)
  • The α-Naphthyl Acetate Esterase (α-NAE) stain offers a fascinating glimpse into cellular esterase activity. (pscientifics.com)
  • Recombinant hemagglutinin-esterase of Bovine coronavirus strain L9 (amino acids 17 - 392). (european-virus-archive.com)
  • The purified recombinant esterase was immobilized efficiently by physical adsorption onto chitosan nanoparticles and effects of various immobilization conditions were investigated in details to develope highly cost-effective esterase as a biocatalyst to be utilized in biotechnological purposes. (iyte.edu.tr)
  • 1.0 mg/mL of recombinant esterase was immobilized on 1.5 mg chitosan nanoparticles for 30 min at 60C, pH 7.0 under 100 rpm stirring speed. (iyte.edu.tr)
  • Functional characterization of a new dark soil esterase from Amazon with hysterical behavior. (usp.br)
  • Characterization of Enterobacter cloacae and E. sakazakii by electrophoretic polymorphism of acid phosphatase, esterases, and glutamate, lactate and malate dehydrogenases. (nih.gov)
  • This study reports the discovery and characterization of the novel carbohydrate esterase, FjoAcXE. (biomedcentral.com)
  • HU, (2009) "Studies on the Purification and Characterization of Soybean Esterase, and Its Sensitivity to Organophosphate and Carbamate Pesticides" Agricultural Sciences in China 8(4): 455-463. (tku.edu.tw)
  • GEs are serine hydrolases found in carbohydrate esterase family 15 (CE15), which belongs to the large alpha/beta hydrolase superfamily. (inrae.fr)
  • en Hydrolase that splits fatty acids from sterols. (roche.com)
  • XAT contains a canonical Gly-Asp-Ser-Leu (GDSL) motif and is encoded by a member of the GDSL esterase/lipase gene family. (edu.au)
  • Serious arterial and venous thromboembolic (TE) events have been reported at the recommended dose of C1 Esterase Inhibitor (Human) products, including BERINERT, following administration in patients with HAE. (nih.gov)
  • isolated at the biotechnology division of CSIR-NIIST was found to produce esterase activity which was sustained at higher temperature and under high salt concentration. (hindawi.com)
  • 5] C. Hou, K. He, L. Yang, D. Huo, M. Yang, S. Huang, L. Zhang, and C. Shen, (2012) "Catalytic characteristics of plant-esterase from wheat flour" World Journal of Microbiology and Biotechnology 28(2): 541-548. (tku.edu.tw)
  • The aim of the current study was to evaluate the synergistic interactions between two termite metagenome-derived feruloyl esterases (FAE6 and FAE5) and endo-xylanases for the production of hydroxycinnamic acids and xylo-oligosaccharides (XOS) from model substrates, and untreated and pre-treated agricultural residues. (ru.ac.za)
  • Your health care provider will also measure the functional activity level of your C1 esterase inhibitor. (medlineplus.gov)
  • The purified esterase lost its thermo and halo tolerance but interestingly, retained 97% activity in methanol. (hindawi.com)
  • Link to all annotated objects annotated to retinyl-palmitate esterase activity. (planteome.org)
  • Link to all direct and indirect annotations to retinyl-palmitate esterase activity. (planteome.org)
  • FjoAcXE was shown to efficiently release acetyl groups from internal (2- O -MeGlc p A)3- O -acetyl-Xyl p structures, an activity that has been sought after but lacking in known carbohydrate esterases. (biomedcentral.com)
  • Moreover, FjoAcXE activity was not only restricted to GX, but also deacetylated (3- O -Ara f )2- O -acetyl-Xyl p of feruloylated xylooligomers, confirming the broad substrate range of this new carbohydrate esterase. (biomedcentral.com)
  • Esterase alteratons in the liver of dystrophic mice. (jax.org)
  • Tsuji S, Meier H. Esterase alteratons in the liver of dystrophic mice. (jax.org)
  • CINRYZE ® (C1 esterase inhibitor [human]) was the first FDA-approved preventive treatment that can start at age 6, helping to reduce HAE attacks earlier in life. (cinryze.com)
  • HAE can be treated with C1 esterase inhibitor concentrate (C1-INH), icatibant, and ecallantide. (chaen-rcah.ca)
  • A wide range of different esterases exist that differ in their substrate specificity, their protein structure, and their biological function. (wikipedia.org)
  • C1 esterase inhibitor (C1-INH) is a protein found in the fluid part of your blood. (medlineplus.gov)
  • Hydrolyzing phospholipids into a carboxylic acid and a lysophospholipid, the PLA1 and PLA2 (EC 3.1.1.4) esterases differentiate from PLC and PLD which are responsible for cleaving either sites of the phophonate bonds present in phospholipids. (axonmedchem.com)
  • Glucuronoyl esterase catalyze cleavage of ester-linked lignin-carbohydrate complexes (ester bonds between 4-O-methyl-D-glucuronic acid side residues of glucuronoxylans and lignin alcohols) and facilitate lignin degradation. (inrae.fr)
  • If you need more than just C1 Esterase Inhibitor, Functional lab test - add more tests one by one. (findlabtest.com)
  • C1 Esterase Inhibitor, Functional test cost minimal is in Jason Health (C1 Esterase Inhibitor, Functional) with price $88.00. (findlabtest.com)
  • The metabolic pathways involved include cytochrome P450 monooxygenases (CYP), esterases, and alcohol and aldehyde dehydrogenases. (cdc.gov)
  • Glucuronoyl esterases: diversity, properties and biotechnological potential. (inrae.fr)
  • Distinctive profiles of esterases from Klebsiella pneumoniae, K. oxytoca, Enterobacter aerogenes and E. gergovia]. (nih.gov)
  • Glucuronoyl esterases (GEs) belonging to the carbohydrate esterase family 15 (CE15) are involved in microbial degradation of lignocellulosic plant materials. (inrae.fr)
  • Detoxification Esterase StrH Initiates Strobilurin Fungicide Degradation in Hyphomicrobium sp. (usda.gov)
  • 7] J. Bao, C. Hou, M. Chen, J. Li, D. Huo, M. Yang, X. Luo, and Y. Lei, (2015) "Plant Esterase-Chitosan/Gold Nanoparticles-Graphene Nanosheet Composite-Based Biosensor for the Ultrasensitive Detection of Organophosphate Pesticides" Journal of Agricultural and Food Chemistry 63(47): 10319-10326. (tku.edu.tw)
  • TE events have also been reported following administration of a C1 Esterase Inhibitor (Human) product when used for unapproved indications at higher than recommended doses. (nih.gov)
  • The esterase-producing strain was isolated through an aerial sampling and was identified by molecular methods as Pseudozyma sp. (hindawi.com)
  • Esterases/lipases active in water miscible solvents are highly desired in biocatalysis where substrate solubility is limited and also when the solvent is desired as an acyl acceptor in transesterification reactions, as with the case of biodiesel production. (hindawi.com)
  • Spruce budworm (Choristoneura fumiferana) juvenile hormone esterase: hormonal regulation, developmental expression and cDNA cloning. (gc.ca)
  • Glucuronoyl esterases (GEs) (EC 3.1.1.117) catalyze the cleavage of ester-linked lignin-carbohydrate complexes that has high impact on the plant cell wall integrity. (inrae.fr)
  • The method uses sulfated alpha-cyclodextrin in the presence of Mg +2 , which forms complexes with apoB containing lipoproteins, and polyethylene glycol-coupled cholesteryl esterase and cholesterol oxidase for the HDL-cholesterol measurement. (cdc.gov)
  • The PC-Esterase family [ ( PUBMED:20056006 ) ] is comprised of Cas1p, the Homo sapiens C7orf58, Arabidopsis thaliana PMR5 and a group of plant freezing resistance/cold acclimatization proteins typified by Arabidopsis thaliana ESKIMO1 [ ( PUBMED:20657172 ) ( PUBMED:21408051 ) ], animal FAM55D proteins, and animal FAM113 proteins. (embl.de)
  • Reference range for C1-esterase inhibitor (C1 INH) in the third trimester of pregnancy. (bvsalud.org)

No images available that match "esterases"