A genus of gram-negative, facultatively anaerobic, rod-shaped bacteria that is not known to be pathogenic for man, animals, or plants. Its organisms are spoilers for beers and ciders and in sweet English ciders they are the causative agents of a secondary fermentation known as "cider sickness." The species Z. mobilis is used for experiments in molecular genetic studies.
Catalyzes the decarboxylation of an alpha keto acid to an aldehyde and carbon dioxide. Thiamine pyrophosphate is an essential cofactor. In lower organisms, which ferment glucose to ethanol and carbon dioxide, the enzyme irreversibly decarboxylates pyruvate to acetaldehyde. EC 4.1.1.1.
A large group of facultatively anaerobic, rod-shaped bacteria that show up as pink (negative) when treated by the gram-staining method.
A class of enzymes that catalyzes the phosphorylation of fructose in the presence of ATP. EC 2.7.1.-.
The coenzyme form of Vitamin B1 present in many animal tissues. It is a required intermediate in the PYRUVATE DEHYDROGENASE COMPLEX and the KETOGLUTARATE DEHYDROGENASE COMPLEX.
A large group of anaerobic bacteria which show up as pink (negative) when treated by the Gram-staining method.
Bacteria which lose crystal violet stain but are stained pink when treated by Gram's method.
A zinc-containing enzyme which oxidizes primary and secondary alcohols or hemiacetals in the presence of NAD. In alcoholic fermentation, it catalyzes the final step of reducing an aldehyde to an alcohol in the presence of NADH and hydrogen.
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.
A clear, colorless liquid rapidly absorbed from the gastrointestinal tract and distributed throughout the body. It has bactericidal activity and is used often as a topical disinfectant. It is widely used as a solvent and preservative in pharmaceutical preparations as well as serving as the primary ingredient in ALCOHOLIC BEVERAGES.
A colorless, flammable liquid used in the manufacture of acetic acid, perfumes, and flavors. It is also an intermediate in the metabolism of alcohol. It has a general narcotic action and also causes irritation of mucous membranes. Large doses may cause death from respiratory paralysis.
Polysaccharides composed of D-fructose units.
The functional hereditary units of BACTERIA.
Microbial, plant, or animal cells which are immobilized by attachment to solid structures, usually a column matrix. A common use of immobilized cells is in biotechnology for the bioconversion of a substrate to a particular product. (From Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)
Xylose is a monosaccharide, a type of sugar, that is commonly found in woody plants and fruits, and it is used in medical testing to assess the absorptive capacity of the small intestine.
The dry cells of any suitable strain of SACCHAROMYCES CEREVISIAE or CANDIDA. It can be obtained as a by-product from the brewing of beer or by growing on media not suitable for beer production. Dried yeast serves as a source of protein and VITAMIN B COMPLEX.
A genus known for fibers obtained from their leaves: sisal from A. sisalana, henequen from A. fourcroyoides and A. cantala, or Manila-Maguey fiber from A. cantala. Some species provide a sap that is fermented to an intoxicating drink, called pulque in Mexico. Some contain agavesides.
Enzymes that catalyze the dehydrogenation of GLYCERALDEHYDE 3-PHOSPHATE. Several types of glyceraldehyde-3-phosphate-dehydrogenase exist including phosphorylating and non-phosphorylating varieties and ones that transfer hydrogen to NADP and ones that transfer hydrogen to NAD.

Aspartate-27 and glutamate-473 are involved in catalysis by Zymomonas mobilis pyruvate decarboxylase. (1/129)

Zymomonas mobilis pyruvate decarboxylase (EC 4.1.1.1) was subjected to site-directed mutagenesis at two acidic residues near the thiamin diphosphate cofactor in the active site. Asp-27 was changed to Glu or Asn, and Glu-473 was mutated to Asp (E473D) or Gln (E473Q). Each mutant protein was purified to near-homogeneity, and the kinetic and cofactor-binding properties were compared with those of the wild-type protein. Despite the very conservative nature of these alterations, all mutants had a very low, but measurable, specific activity ranging from 0.025% (E473Q) to 0.173% (E473D) of the wild type. With the exception of E473Q, the mutants showed small decreases in the affinity for thiamin diphosphate, and binding of the second cofactor (Mg2+) was also weakened somewhat. With E473Q, both cofactors seemed to be very tightly bound so that they were not removed by the treatment that was effective for the wild-type enzyme and other mutant forms. All mutants showed minor changes in the Km for substrate, but these alterations did not account for the low activities. These low specific activities, accompanied by little change in the Km for pyruvate, are consistent with a quantitative model of the catalytic cycle in which the main effect of the mutations is to slow the decarboxylation step with a minor change in the rate constant for pyruvate binding.  (+info)

Bacterial proteins carrying twin-R signal peptides are specifically targeted by the delta pH-dependent transport machinery of the thylakoid membrane system. (2/129)

Glucose-fructose oxidoreductase (GFOR), a periplasmic protein of Zymomonas mobilis, is synthesized as a precursor polypeptide with a twin-R signal peptide for Sec-independent protein export in bacteria. In higher plant chloroplasts, twin-R signal peptides are specific targeting signals for the Sec-independent delta pH pathway of the thylakoid membrane system. In agreement with the assumed common phylogenetic origin of the two protein transport mechanisms, GFOR can be efficiently translocated by the delta pH-dependent pathway when analyzed with isolated thylakoid membranes. Transport is sensitive to the ionophore nigericin and competes with specific substrates for the delta pH-dependent transport route. In contrast, neither sodium azide nor enzymatic destruction of the nucleoside triphosphates in the assays affects thylakoid transport of GFOR indicating that the Sec apparatus is not involved in this process. Mutagenesis of the twin-R motif in the GFOR signal peptide prevents membrane translocation of the protein emphasizing the importance of these residues for the transport process.  (+info)

Enhancement of expression and apparent secretion of Erwinia chrysanthemi endoglucanase (encoded by celZ) in Escherichia coli B. (3/129)

Escherichia coli B has been engineered as a biocatalyst for the conversion of lignocellulose into ethanol. Previous research has demonstrated that derivatives of E. coli B can produce high levels of Erwinia chrysanthemi endoglucanase (encoded by celZ) as a periplasmic product and that this enzyme can function with commercial fungal cellulase to increase ethanol production. In this study, we have demonstrated two methods that improve celZ expression in E. coli B. Initially, with a low-copy-number vector, two E. coli glycolytic gene promoters (gap and eno) were tested and found to be less effective than the original celZ promoter. By screening 18,000 random fragments of Zymomonas mobilis DNA, a surrogate promoter was identified which increased celZ expression up to sixfold. With this promoter, large polar inclusion bodies were clearly evident in the periplasmic space. Sequencing revealed that the most active surrogate promoter is derived from five Sau3A1 fragments, one of which was previously sequenced in Z. mobilis. Visual inspection indicated that this DNA fragment contains at least five putative promoter regions, two of which were confirmed by primer extension analysis. Addition of the out genes from E. chrysanthemi EC16 caused a further increase in the production of active enzyme and facilitated secretion or release of over half of the activity into the extracellular environment. With the most active construct, of a total of 13,000 IU of active enzyme per liter of culture, 7,800 IU was in the supernatant. The total active endoglucanase was estimated to represent 4 to 6% of cellular protein.  (+info)

The efficient export of NADP-containing glucose-fructose oxidoreductase to the periplasm of Zymomonas mobilis depends both on an intact twin-arginine motif in the signal peptide and on the generation of a structural export signal induced by cofactor binding. (4/129)

The periplasmic, NADP-containing glucose-fructose oxidoreductase of the gram-negative bacterium Zymomonas mobilis belongs to a class of redox cofactor-dependent enzymes which are exported with the aid of a signal peptide containing a so-called twin-arginine motif. In this paper we show that the replacement of one or both arginine residues results in drastically reduced translocation of glucose-fructose oxidoreductase to the periplasm, showing that this motif is essential. Mutant proteins which, in contrast to wild-type glucose-fructose oxidoreductase, bind NADP in a looser and dissociable manner, were severely affected in the kinetics of plasma membrane translocation. These results strongly suggest that the translocation of glucose-fructose oxidoreductase into the periplasm uses a Sec-independent apparatus which recognizes, as an additional signal, a conformational change in the structure of the protein, most likely triggered by cofactor binding. Furthermore, these results suggest that glucose-fructose oxidoreductase is exported in a folded form. A glucose-fructose oxidoreductase:beta-galactosidase fusion protein is not lethal to Z. mobilis cells and leads to the accumulation of the cytosolic preform of wild-type glucose-fructose oxidoreductase expressed in trans but not of a typical Sec-substrate (OmpA), indicating that the glucose-fructose oxidoreductase translocation apparatus can be blocked without interfering with the export of essential proteins via the Sec pathway.  (+info)

Mutagenesis and crystallographic studies of Zymomonas mobilis tRNA-guanine transglycosylase to elucidate the role of serine 103 for enzymatic activity. (5/129)

The tRNA modifying enzyme tRNA-guanine transglycosylase (TGT) is involved in the exchange of guanine in the first position of the anticodon with preQ1 as part of the biosynthesis of the hypermodified base queuine (Q). Mutation of Ser90 to an alanine in Escherichia coli TGT leads to a dramatic reduction of enzymatic activity (Reuter, K. et al. (1994) Biochemistry 33, 7041-7046). To further clarify the role of this residue in the catalytic center, we have mutated the corresponding Ser103 of the crystallizable Zymomonas mobilis TGT into alanine. The crystal structure of a TGT(S103A)/preQ1 complex combined with biochemical data presented in this paper suggest that Ser103 is essential for substrate orientation in the TGT reaction.  (+info)

A Zymomonas mobilis mutant with delayed growth on high glucose concentrations. (6/129)

Exponentially growing cells of Zymomonas mobilis normally exhibit a lag period of up to 3 h when transferred from 0.11 M (2%) to 0.55 M (10%) glucose liquid medium. A mutant of Z. mobilis (CU1Rif2), fortuitously isolated, showed more than a 20-h lag period when grown under the same conditions, whereas on 0.55 M glucose solid medium, it failed to grow. The growth of CU1Rif2 on elevated concentrations of other fermentable (0.55 M sucrose or fructose) or nonfermentable (0.11 M glucose plus 0.44 M maltose or xylose) sugars appeared to be normal. Surprisingly, CU1Rif2 cells grew without any delay on 0.55 M glucose on which wild-type cells had been incubated for 3 h and removed at the beginning of their exponential phase. This apparent preconditioning was not observed with medium obtained from wild-type cells grown on 0.11 M glucose and supplemented to 0.55 M after removal of the wild-type cells. Undelayed growth of CU1Rif2 on 0.55 M glucose previously conditioned by the wild type was impaired by heating or protease treatment. It is suggested that in Z. mobilis, a diffusible proteinaceous heat-labile factor, transitionally not present in 0.55 M glucose CU1Rif2 cultures, triggers growth on 0.55 M glucose. Biochemical analysis of glucose uptake and glycolytic enzymes implied that glucose assimilation was not directly involved in the phenomenon. By use of a wild-type Z. mobilis genomic library, a 4.5-kb DNA fragment which complemented in low copy number the glucose-defective phenotype as well as glucokinase and glucose uptake of CU1Rif2 was isolated. This fragment carries a gene cluster consisting of four putative coding regions, encoding 167, 167, 145, and 220 amino acids with typical Z. mobilis codon usage, -35 and -10 promoter elements, and individual Shine-Dalgarno consensus sites. However, strong homologies were not detected in a BLAST2 (EMBL-Heidelberg) computer search with known protein sequences.  (+info)

Chromosomal integration of heterologous DNA in Escherichia coli with precise removal of markers and replicons used during construction. (7/129)

A set of vectors which facilitates the sequential integration of new functions into the Escherichia coli chromosome by homologous recombination has been developed. These vectors are based on plasmids described by Posfai et al. (J. Bacteriol. 179:4426-4428, 1997) which contain conditional replicons (pSC101 or R6K), a choice of three selectable markers (ampicillin, chloramphenicol, or kanamycin), and a single FRT site. The modified vectors contain two FRT sites which bracket a modified multiple cloning region for DNA insertion. After integration, a helper plasmid expressing the flippase (FLP) recombinase allows precise in vivo excision of the replicon and the marker used for selection. Sites are also available for temporary insertion of additional functions which can be subsequently deleted with the replicon. Only the DNA inserted into the multiple cloning sites (passenger genes and homologous fragment for targeting) and a single FRT site (68 bp) remain in the chromosome after excision. The utility of these vectors was demonstrated by integrating Zymomonas mobilis genes encoding the ethanol pathway behind the native chromosomal adhE gene in strains of E. coli K-12 and E. coli B. With these vectors, a single antibiotic selection system can be used repeatedly for the successive improvement of E. coli strains with precise deletion of extraneous genes used during construction.  (+info)

Probing the location and function of the conserved histidine residue of phosphoglucose isomerase by using an active site directed inhibitor N-bromoacetylethanolamine phosphate. (8/129)

Phosphoglucose isomerase (EC 5.3.1.9) catalyzes the interconversion of D-glucopyranose-6-phosphate and D-fructofuranose-6-phosphate by promoting an intrahydrogen transfer between C1 and C2. A conserved histidine exists throughout all phosphoglucose isomerases and was hypothesized to be the base catalyzing the isomerization reaction. In the present study, this conserved histidine, His311, of the enzyme from Bacillus stearothermophilus was subjected to mutational analysis, and the mutational effect on the inactivation kinetics by N-bromoacetylethanolamine phosphate was investigated. The substitution of His311 with alanine, asparagine, or glutamine resulted in the decrease of activity, in k(cat)/K(M), by a factor of 10(3), indicating the importance of this residue. N-bromoacetylethanolamine phosphate inactivated irreversibly the activity of wild-type phosphoglucose isomerase; however, His311 --> Ala became resistant to this inhibitor, indicating that His311 is located in the active site and is responsible for the inactivation of the enzyme by this active site-directed inhibitor. The pKa of His311 was estimated to be 6.31 according to the pH dependence of the inactivation. The proximity of this value with the pKa value of 6.35, determined from the pH dependence of k(cat)/K(M), supports a role of His311 as a general base in the catalysis.  (+info)

"Zymomonas" is a genus of Gram-negative, facultatively anaerobic bacteria that are commonly found in sugar-rich environments such as fruit and flower nectar. The most well-known species in this genus is Zymomonas mobilis, which has attracted significant interest in the field of biofuels research due to its ability to efficiently ferment sugars into ethanol.

Zymomonas bacteria are unique in their metabolism and possess a number of unusual features, including a highly streamlined genome, a single polar flagellum for motility, and the ability to survive and grow at relatively high temperatures and ethanol concentrations. These characteristics make Zymomonas an attractive candidate for industrial applications, particularly in the production of biofuels and other bioproducts.

In addition to their potential industrial uses, Zymomonas bacteria have also been implicated in certain human diseases, particularly in individuals with weakened immune systems or underlying medical conditions. However, such cases are relatively rare, and the overall impact of Zymomonas on human health is still not well understood.

Pyruvate decarboxylase is an enzyme that plays a crucial role in the cellular process of fermentation and gluconeogenesis. In medical and biochemical terms, pyruvate decarboxylase is defined as:

"An enzyme (EC 4.1.1.1) that catalyzes the decarboxylation of pyruvate to form acetaldehyde and carbon dioxide in the presence of thiamine pyrophosphate (TPP) as a cofactor. This reaction occurs during anaerobic metabolism, such as alcohol fermentation in yeast or bacteria, and helps to generate ATP and NADH for the cell's energy needs."

In humans, pyruvate decarboxylase is primarily found in the liver and kidneys, where it participates in gluconeogenesis – the process of generating new glucose molecules from non-carbohydrate precursors. The enzyme's activity is essential for maintaining blood glucose levels during fasting or low-carbohydrate intake.

Deficiencies in pyruvate decarboxylase can lead to metabolic disorders, such as pyruvate decarboxylase deficiency (PDC deficiency), which is characterized by lactic acidosis, developmental delays, and neurological issues. Proper diagnosis and management of these conditions often involve monitoring enzyme activity and glucose metabolism.

'Gram-Negative Facultatively Anaerobic Rods' is a term that refers to a specific group of bacteria. Here's a breakdown of the term:

1. **Gram-Negative**: This refers to the bacterial cell wall's reaction to Gram staining, a common laboratory test used to classify bacteria based on their structural differences. Gram-negative bacteria do not retain the crystal violet stain used in this process, instead taking up the counterstain (usually a pink or red dye like safranin), which makes them appear pink or red under a microscope.

2. **Facultatively Anaerobic**: This indicates that the bacteria can grow and reproduce both in the presence and absence of molecular oxygen (O2). They have the ability to switch their metabolism based on the availability of oxygen, making them versatile in different environments.

3. **Rods**: This term describes the shape of these bacteria. Rod-shaped bacteria are also known as bacilli. Their elongated form is one of several shapes bacteria can take, along with spherical (cocci) and spiral (spirochetes).

In summary, 'Gram-Negative Facultatively Anaerobic Rods' defines a group of rod-shaped bacteria that do not retain crystal violet during Gram staining (Gram-negative), and can grow with or without oxygen (facultatively anaerobic). Examples of such bacteria include Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis.

Fructokinase is an enzyme that phosphorylates fructose into fructose-1-phosphate in the metabolism of dietary sugars. It plays a crucial role in fructose metabolism, particularly in the liver, kidneys, and intestines. In humans, there are several isoforms of fructokinase, including ketohexokinase (KHK-A and KHK-C) and liver fructokinase (KHK-B). Disorders in fructose metabolism, such as hereditary fructose intolerance, can result from mutations in the gene encoding for fructokinase.

Thiamine pyrophosphate (TPP) is the active form of thiamine (vitamin B1) that plays a crucial role as a cofactor in various enzymatic reactions, particularly in carbohydrate metabolism. TPP is essential for the functioning of three key enzymes: pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and transketolase. These enzymes are involved in critical processes such as the conversion of pyruvate to acetyl-CoA, the oxidative decarboxylation of alpha-ketoglutarate in the Krebs cycle, and the pentose phosphate pathway, which is important for generating reducing equivalents (NADPH) and ribose sugars for nucleotide synthesis. A deficiency in thiamine or TPP can lead to severe neurological disorders, including beriberi and Wernicke-Korsakoff syndrome, which are often observed in alcoholics due to poor nutrition and impaired thiamine absorption.

Gram-negative anaerobic bacteria are a type of bacteria that do not require oxygen to grow and are characterized by their cell wall structure, which does not retain crystal violet dye in the Gram staining procedure. This is because they lack a thick peptidoglycan layer in their cell walls, which is typically stained dark purple in Gram-positive bacteria. Instead, gram-negative bacteria have an outer membrane that contains lipopolysaccharides (LPS), which can be toxic to human cells and contribute to the pathogenicity of these organisms.

Examples of gram-negative anaerobic bacteria include Bacteroides fragilis, Prevotella species, and Porphyromonas species. These bacteria are commonly found in the human mouth, gastrointestinal tract, and genitourinary tract, and can cause a variety of infections, including abscesses, wound infections, and bacteremia.

It's important to note that while gram-negative anaerobic bacteria do not require oxygen to grow, some may still tolerate or even prefer oxygen-rich environments. Therefore, the term "anaerobe" can be somewhat misleading when used to describe these organisms.

Gram-negative bacteria are a type of bacteria that do not retain the crystal violet stain used in the Gram staining method, a standard technique used in microbiology to classify and identify different types of bacteria based on their structural differences. This method was developed by Hans Christian Gram in 1884.

The primary characteristic distinguishing Gram-negative bacteria from Gram-positive bacteria is the composition and structure of their cell walls:

1. Cell wall: Gram-negative bacteria have a thin peptidoglycan layer, making it more susceptible to damage and less rigid compared to Gram-positive bacteria.
2. Outer membrane: They possess an additional outer membrane that contains lipopolysaccharides (LPS), which are endotoxins that can trigger strong immune responses in humans and animals. The outer membrane also contains proteins, known as porins, which form channels for the passage of molecules into and out of the cell.
3. Periplasm: Between the inner and outer membranes lies a compartment called the periplasm, where various enzymes and other molecules are located.

Some examples of Gram-negative bacteria include Escherichia coli (E. coli), Pseudomonas aeruginosa, Klebsiella pneumoniae, Salmonella enterica, Shigella spp., and Neisseria meningitidis. These bacteria are often associated with various infections, such as urinary tract infections, pneumonia, sepsis, and meningitis. Due to their complex cell wall structure, Gram-negative bacteria can be more resistant to certain antibiotics, making them a significant concern in healthcare settings.

Alcohol dehydrogenase (ADH) is a group of enzymes responsible for catalyzing the oxidation of alcohols to aldehydes or ketones, and reducing equivalents such as NAD+ to NADH. In humans, ADH plays a crucial role in the metabolism of ethanol, converting it into acetaldehyde, which is then further metabolized by aldehyde dehydrogenase (ALDH) into acetate. This process helps to detoxify and eliminate ethanol from the body. Additionally, ADH enzymes are also involved in the metabolism of other alcohols, such as methanol and ethylene glycol, which can be toxic if allowed to accumulate in the body.

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.

Ethanol is the medical term for pure alcohol, which is a colorless, clear, volatile, flammable liquid with a characteristic odor and burning taste. It is the type of alcohol that is found in alcoholic beverages and is produced by the fermentation of sugars by yeasts.

In the medical field, ethanol is used as an antiseptic and disinfectant, and it is also used as a solvent for various medicinal preparations. It has central nervous system depressant properties and is sometimes used as a sedative or to induce sleep. However, excessive consumption of ethanol can lead to alcohol intoxication, which can cause a range of negative health effects, including impaired judgment, coordination, and memory, as well as an increased risk of accidents, injuries, and chronic diseases such as liver disease and addiction.

Acetaldehyde is a colorless, volatile, and flammable liquid with a pungent odor. It is the simplest aldehyde, with the formula CH3CHO. Acetaldehyde is an important intermediate in the metabolism of alcohol and is produced by the oxidation of ethanol by alcohol dehydrogenase. It is also a naturally occurring compound that is found in small amounts in various foods and beverages, such as fruits, vegetables, and coffee.

Acetaldehyde is a toxic substance that can cause a range of adverse health effects, including irritation of the eyes, nose, and throat, nausea, vomiting, and headaches. It has been classified as a probable human carcinogen by the International Agency for Research on Cancer (IARC). Long-term exposure to acetaldehyde has been linked to an increased risk of certain types of cancer, including cancers of the oral cavity, esophagus, and liver.

Fructans are a type of carbohydrate known as oligosaccharides, which are made up of chains of fructose molecules. They are found in various plants, including wheat, onions, garlic, and artichokes. Some people may have difficulty digesting fructans due to a lack of the enzyme needed to break them down, leading to symptoms such as bloating, diarrhea, and stomach pain. This condition is known as fructan intolerance or fructose malabsorption. Fructans are also considered a type of FODMAP (Fermentable Oligosaccharides, Disaccharides, Monosaccharides, and Polyols), which are short-chain carbohydrates that can be poorly absorbed by the body and may cause digestive symptoms in some individuals.

A bacterial gene is a segment of DNA (or RNA in some viruses) that contains the genetic information necessary for the synthesis of a functional bacterial protein or RNA molecule. These genes are responsible for encoding various characteristics and functions of bacteria such as metabolism, reproduction, and resistance to antibiotics. They can be transmitted between bacteria through horizontal gene transfer mechanisms like conjugation, transformation, and transduction. Bacterial genes are often organized into operons, which are clusters of genes that are transcribed together as a single mRNA molecule.

It's important to note that the term "bacterial gene" is used to describe genetic elements found in bacteria, but not all genetic elements in bacteria are considered genes. For example, some DNA sequences may not encode functional products and are therefore not considered genes. Additionally, some bacterial genes may be plasmid-borne or phage-borne, rather than being located on the bacterial chromosome.

"Immobilized cells" is a term used in biotechnology and cell biology to describe situations where living cells are confined or restricted in their movement within a defined space. This can be achieved through various methods such as entrapment within a gel, adsorption onto a surface, or encapsulation within a semi-permeable membrane. The immobilization of cells allows for their repeated use in biochemical reactions, such as fermentation or waste treatment, while also providing stability and ease of separation from the reaction products. Additionally, immobilized cells can be used to study cellular processes and functions under controlled conditions.

Xylose is a type of sugar that is commonly found in plants and wood. In the context of medical definitions, xylose is often used in tests to assess the function of the small intestine. The most common test is called the "xylose absorption test," which measures the ability of the small intestine to absorb this sugar.

In this test, a patient is given a small amount of xylose to drink, and then several blood and/or urine samples are collected over the next few hours. The amount of xylose that appears in these samples is measured and used to determine how well the small intestine is absorbing nutrients.

Abnormal results on a xylose absorption test can indicate various gastrointestinal disorders, such as malabsorption syndromes, celiac disease, or bacterial overgrowth in the small intestine.

Dried yeast, in a medical context, typically refers to the inactive form of Saccharomyces cerevisiae, a type of yeast that has been dried and used as a dietary supplement. It contains proteins, B vitamins, and minerals. When rehydrated and consumed, it can help with digestion by providing live yeast cells to the gut flora. However, it is not a source of viable probiotics, as the drying process typically kills the yeast cells. It's important to note that overconsumption may lead to bloating, gas, and other digestive discomforts in some individuals.

'Agave' is a genus of plants, primarily found in hot and dry regions of the Americas. It is not a medical term or concept. Agave plants are known for their rosette-shaped arrangement of stiff, sharp leaves, and many species produce a tall flowering stalk after several years of growth. Some agave species are cultivated for the production of various products, such as tequila, a distilled beverage made from the blue agave plant (Agave tequilana), and agave nectar or syrup, derived from several different species.

While not directly related to medical terminology, it is worth noting that some agave species have been used in traditional medicine for various purposes, such as treating skin conditions, wounds, or digestive issues. However, these uses are not well-studied and should not be considered a substitute for evidence-based modern medical treatments.

Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an enzyme that plays a crucial role in the metabolic pathway of glycolysis. Its primary function is to convert glyceraldehyde-3-phosphate (a triose sugar phosphate) into D-glycerate 1,3-bisphosphate, while also converting nicotinamide adenine dinucleotide (NAD+) into its reduced form NADH. This reaction is essential for the production of energy in the form of adenosine triphosphate (ATP) during cellular respiration. GAPDH has also been implicated in various non-metabolic processes, including DNA replication, repair, and transcription regulation, due to its ability to interact with different proteins and nucleic acids.

Ethanol fermentation technology-Zymomonas mobilis Zymomonas mobilis ZM4 genome page Type strain of Zymomonas mobilis at BacDive ... LPSN entry for Zymomonas Rogers P; Lee K; Skotnicki M; Tribe D (1982). Microbial reactions: Ethanol Production by Zymomonas ... Zymomonas is an unwanted waterborn bacteria in beer, creating an estery-sulfury flavor due to the production of acetaldehyde ... Zymomonas have not been reported in lager breweries due to the low temperatures (8-12 °C) and stringent carbohydrate ...
Another flexible region at the active site of an inositol monophosphatase from Zymomonas mobilis ... Zymomonas mobilis subsp. mobilis ZM4 = ATCC 31821. Mutation(s): 0 Gene Names: ZMO1518. EC: 3.1.3.25. ... Crystal structure of cbbF from Zymomonas mobilis and its functional implication. Hwang, H.J., Park, S.Y., Kim, J.S.. (2014) ... Find proteins for Q5NMB8 (Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4)) ...
Zymomonas mobilis is a bacterium that produces ethanol from glucose at up to 97% of theoretical efficiency on a carbon basis. ... Zymomonas mobilis is a bacterium that produces ethanol from glucose at up to 97% of theoretical efficiency on a carbon basis. ... Wild-type Zymomonas mobilis subsp. mobilis ZM4 (ATCC 31821) and the plasmid pRL814 were obtained from Dr. Robert Landick. ... Dawes, E. A., Ribbons, D. W., and Large, P. J. (1966). The route of ethanol formation in Zymomonas mobilis. Biochem. J. 98, 795 ...
The transcriptomes of Zymomonas mobilis 2032 were captured during the fermentation of ammonia fiber expansion (AFEX)-pretreated ... Transcriptomic Data Sets for Zymomonas mobilis 2032 during Fermentation of Ammonia Fiber Expansion (AFEX)-Pretreated Corn ... Transcriptomic Data Sets for Zymomonas mobilis 2032 during Fermentation of Ammonia Fiber Expansion (AFEX)-Pretreated Corn ...
Xylose utilizing zymomonas mobilis with improved ethanol production in biomass hydrolysate medium Patent Caimi, Perry G; Hitz, ... Xylose-utilizing, ethanol producing strains of Zymomonas mobilis with improved performance in medium comprising biomass ...
Zymomonas mobilis produces near theoretical yields of ethanol and recombinant strains are candidate industrial microorganisms. ... Yang, S., Pelletier, D.A., Lu, TY.S. et al. The Zymomonas mobilis regulator hfq contributes to tolerance against multiple ... Kalnenieks U, Galinina N, Toma MM, Pickford JL, Rutkis R, Poole RK: Respiratory behaviour of a Zymomonas mobilis adhB::kan(r) ... The Zymomonas mobilis regulator hfq contributes to tolerance against multiple lignocellulosic pretreatment inhibitors. *Shihui ...
Open the PDF for Release of Cell-Free Ice Nucleators from Three Recombinant Ice + ,span class=search-highlight,Zymomonas,/ ... Open the PDF for Analysis of the Respiratory Chain in Ethanologenic ,span class=search-highlight,Zymomonas,/span, ,span class ... Analysis of the Respiratory Chain in Ethanologenic Zymomonas mobilis with a Cyanide-Resistant bd -Type Ubiquinol Oxidase as the ... Release of Cell-Free Ice Nucleators from Three Recombinant Ice + Zymomonas mobilis Strains ...
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Improving fermentation performance of recombinant Zymomonas in acetic acid-containing media.. Lawford, H G; Rousseau, J D. Appl ... Ácido Acético/farmacologia Celulose/química Zymomonas/fisiologia Biomassa Meios de Cultura Etanol/química Fermentação/efeitos ... dos fármacos Glucose/química Concentração de Íons de Hidrogênio Xilose/química Zymomonas/efeitos dos fármacos Zymomonas/ ... process that uses a proprietary metabolically engineered strain of Zymomonas mobilis that can coferment glucose and xylose. ...
Ethanol production by zymomonas mobilis NRRL B-806 from enzymatic hydrolysates of eucalyptus globulus. In: Revista Mexicana de ... Ethanol production by zymomonas mobilis NRRL B-806 from enzymatic hydrolysates of eucalyptus globulus. Translated title of the ... Ethanol production by zymomonas mobilis NRRL B-806 from enzymatic hydrolysates of eucalyptus globulus. / Morales-Martínez, T. K ... Ethanol production by zymomonas mobilis NRRL B-806 from enzymatic hydrolysates of eucalyptus globulus. Revista Mexicana de ...
Production of bioethanol after hydrolysis of lignocellulosic biomass into sugars using zymomonas mobilis and saccharomyces ...
Zymomonas / enzymology * Zymomonas / genetics Substances * Codon * DNA, Bacterial * Protein Sorting Signals * Alcohol ...
Under anaerobic conditions, Zymomonas transforms 45 percent of the glucose to ethanol and carbon dioxide. It also produces some ... cerevisiae, and Zymomonas mobilis.. The heterofermentative Leuconostoc plays the essential role of producing dextrans, which ...
Lactic acid bacteria and Zymomonas mobilis are two examples. -- Wayne Lee Forday, Biotechnology Department Ngee Ann Polytechnic ...
Sugar-cane-molasses fermentation by Zymomonas mobilis. Appl. Microbiol. Biotechnol., 33: 31-35.. CrossRefDirect Link ...
It can also be a product of bacterial spoilage by Zymomonas or Acetobacter. Background levels of acetaldehyde can be tasted in ...
Li, X. Z., Webb, J. S., Kjelleberg, S., & Rosche, B. (2006). Enhanced benzaldehyde tolerance in zymomonas mobilis biofilms and ...
2014) Finished Genome of Zymomonas mobilis subsp. mobilis Strain CP4, an Applied Ethanol Producer. Genome Announc 2(1). 10.1128 ...
The honey is fermented with the bacteria Zymomonas mobilis to eliminate basic sugars. The remaining long chain sugars stabilize ... To aid this microflora restoration, Mibelle Biochemistry developed Black BeeOme (INCI: Honey (and) Zymomonas Ferment Extract ( ...
Species Zymomonas mobilis [TaxId:542] [111051] (2 PDB entries). Uniprot Q9X5F2. *. Domain d1r0kc3: 1r0k C:127-264 [104731]. ... PDB Description: crystal structure of 1-deoxy-d-xylulose 5-phosphate reductoisomerase from zymomonas mobilis ... d1r0kc3 d.81.1.3 (C:127-264) 1-deoxy-D-xylulose-5-phosphate reductoisomerase {Zymomonas mobilis [TaxId: 542]} ... d1r0kc3 d.81.1.3 (C:127-264) 1-deoxy-D-xylulose-5-phosphate reductoisomerase {Zymomonas mobilis [TaxId: 542]} ...
Ingram LO, Conway T & Alterthum F. Ethanol production by Escherichia coli strains co-expressing Zymomonas PDC and ADH genes. US ...
A Golden Gate Modular Cloning Toolbox for Heterologous Gene Expression in Zymomonas mobilis. ACS Synthetic Biology 11 (11), pp ... Improvement of Acetaldehyde Production in Zymomonas mobilis by Engineering of Its Aerobic Metabolism. Frontiers in Microbiology ...
This summer Im working in Jason Peters Lab at the School of Pharmacy with a bacteria called Zymomonas mobilis and how it can ... This summer, Im working with a bacterium called Zymomonas mobilis in Michaela TerAvests lab with Magda Felczak, and I am ...
Zymomonas mobilis is a type of bacteria thats good at making alcohol. It can also be engineered to produce isoprenoids, a ... Zymomonas rapidly converts the sugars in plant cells into ethanol, and it doesnt seem to be bothered by the toxins in ... They systematically engineered strains of Zymomonas to produce more of certain enzymes, or proteins that speed up the metabolic ... Researcher Daven Khana studies the bacteria Zymomonas mobilis and its potential use in the production of biofuels and ...
Potential Production of Ethanol by Saccharomyces cerevisiae Immobilized and Coimmobilized with Zymomonas mobilis: Alternative ... by Zymomonas mobilis and Saccharomyces cerevisiae compared with free cells culture and evaluate the effect of glucose ...
... and simultaneous saccharification and fermentation with Aspergillus niger and Zymomonas mobilisisolated from... ...
Zymomonas RSV_genus975 Bacteria;Proteobacteria;Betaproteobacteria;B1-7BS;NA;NA RSV_genus976 Bacteria;Proteobacteria; ...
... were fermented to ethanol by glucose-xylose fermenting Zymomonas mobilis 8b. The best ethanol yields and rates were achieved ...
... from Zymomonas mobilis (Fig. 4A) was transferred into C. phytofermentans on the replicating pQexpE plasmid (Fig. 4B). Together ... from Zymomonas mobilis on the pQexpE plasmid (Fig. 4), which boosted substrate conversion (Fig. 5A) and restored ethanol ...
Ethanologenic organisms, such as Zymomonas mobilis, Zymobacter palmae, Acetobacter pasteurianus, or Sarcina ventriculi, and ...
  • This study analyzes the potential use of immobilized and coinmobilized systems on beads of calcium alginate for ethanol production used mango waste (Mangifera indica) by Zymomonas mobilis and Saccharomyces cerevisiae compared with free cells culture and evaluate the effect of glucose concentration on productivity in coimmobilized system using a Chemostat reactor Ommi Culture Plus. (intechopen.com)
  • Large-scale ethanol production utilizes yeast or bacteria, such as Saccharomyces cerevisiae and Zymomonas mobilis to ferment sugar syrups[ 2 ]. (biomedcentral.com)
  • Use of Carob pods for fructose syrup and ethanol production with two mutant strains Zymomonas mobilis and Saccharomyces cerevisiae were investigated. (ejpmr.com)
  • Zymomonas mobilis was chosen for this process as it is ethanol-tolerant (up to 120 grams of ethanol per litre) and productive (5-10% more ethanol than Saccharomyces). (up.ac.za)
  • Zymomonas is an unwanted waterborn bacteria in beer, creating an estery-sulfury flavor due to the production of acetaldehyde and hydrogen sulfide. (wikipedia.org)
  • Lactic acid bacteria and Zymomonas mobilis are two examples. (bio.net)
  • The honey is fermented with the bacteria Zymomonas mobilis to eliminate basic sugars. (cosmeticsandtoiletries.com)
  • Researcher Daven Khana studies the bacteria Zymomonas mobilis and its potential use in the production of biofuels and sustainable replacements for petrochemicals. (glbrc.org)
  • Zymomonas mobilis is a type of bacteria that's good at making alcohol. (glbrc.org)
  • Unlike beer, the fermenting agents present in the seed of pulque are bacteria of the species Zymomonas mobilis rather than yeast. (voodootiki.com)
  • Microbial reactions: Ethanol Production by Zymomonas mobilis. (wikipedia.org)
  • Ethanol production by Zymomonas mobilis NRRL-806 was assessed using different enzymatic hydrolysates from pretreated Eucalyptus globulus saw dust pulp. (pucv.cl)
  • The optimum growth temperature is 25 to 30 °C. Zymomonas mobilis degrades sugars to pyruvate using the Entner-Doudoroff pathway. (wikipedia.org)
  • Zymomonas rapidly converts the sugars in plant cells into ethanol, and it doesn't seem to be bothered by the toxins in solutions of broken down plant matter that can slow microbial growth. (glbrc.org)
  • The sugars in hydrolysates that were detoxified using our membrane extraction process as well as conventional ammonium hydroxide detoxification, were fermented to ethanol by glucose-xylose fermenting Zymomonas mobilis 8b. (aiche.org)
  • PSI has all associated intellectual property and patents to produce G2.0E, including process design and the proprietary Zymomonas ethanologens for efficient conversion of C5/C6 sugars made from cellulosic biomass to G2.0E. (chfca.ca)
  • Zymomonas mobilis produces near theoretical yields of ethanol and recombinant strains are candidate industrial microorganisms. (biomedcentral.com)
  • Constantin Drainas Background/Aims: This work is a study of the ability of three recombinant Zymomonas mobilis strains to release ice nucleators into their growth medium. (karger.com)
  • Improving fermentation performance of recombinant Zymomonas in acetic acid-containing media. (bvsalud.org)
  • In the fed-batch system, the rate of glucose feeding (0.5 g/h) was designed to simulate the rate of cellulolytic digestion that had been observed in a modeled SSCF process with recombinant Zymomonas . (bvsalud.org)
  • Zymomonas mobilis subsp. (rcsb.org)
  • Query: NC_006526:1202000 Zymomonas mobilis subsp. (up.ac.za)
  • Zymomonas mobilis is a bacterium that produces ethanol from glucose at up to 97% of theoretical efficiency on a carbon basis. (frontiersin.org)
  • Mamoru Yamada The respiratory chain of the ethanologenic bacterium Zymomonas mobilis was investigated, in which the pyruvate-to-ethanol pathway has been demonstrated to be mainly responsible for NADH oxidation. (karger.com)
  • The team reports the successful use of deuterated water to investigate the reversibility of glycolytic reactions on three bacterial species of industrial interest: the model bacterium Escherichia coli, the cellulolytic and ethanologenic bacterium C. thermocellum, and the ethanologenic bacterium Zymomonas mobilis , each harboring distinct versions of glycolysis. (energy.gov)
  • The methods used, included: acid hydrolysis with 2.5 M H2SO4, and simultaneous saccharification and fermentation with Aspergillus niger and Zymomonas mobilisisolated from. (academicjournals.org)
  • They systematically engineered strains of Zymomonas to produce more of certain enzymes, or proteins that speed up the metabolic process. (glbrc.org)
  • To augment ethanol production by the ET strain, an alternative ethanol production pathway comprised of pyruvate decarboxylase (Pdc) and alcohol dehydrogenase (AdhB) from Zymomonas mobilis (Fig. 4A) was transferred into C. phytofermentans on the replicating pQexpE plasmid (Fig. 4B). (researchgate.net)
  • It is the only species found in the genus Zymomonas. (wikipedia.org)
  • To aid this microflora restoration, Mibelle Biochemistry developed Black BeeOme (INCI: Honey (and) Zymomonas Ferment Extract (and) Maltodextrin (and) Water ( aqua )), an elixir that results from honey produced in isolated Swiss mountain valleys by an old, dark bee species. (cosmeticsandtoiletries.com)
  • Zymomonas have not been reported in lager breweries due to the low temperatures (8-12 °C) and stringent carbohydrate requirements (able to ferment only sucrose, glucose, and fructose). (wikipedia.org)
  • The National Renewable Energy Laboratory (NREL) is currently investigating a simultaneous saccharification and cofermentation (SSCF) process that uses a proprietary metabolically engineered strain of Zymomonas mobilis that can coferment glucose and xylose . (bvsalud.org)
  • In our previous study, we successfully engineered Zymomonas mobilis 532 (ZM532) strain by genome. (biomedcentral.com)
  • Zymomonas mobilis is traditionally used to make pulque. (wikipedia.org)
  • Improvement of Acetaldehyde Production in Zymomonas mobilis by Engineering of Its Aerobic Metabolism. (mpg.de)

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