A species of gram-positive, cellulolytic bacteria in the family Clostridiaceae. It produces CELLULOSOMES which are involved in plant CELL WALL degradation.
A genus of motile or nonmotile gram-positive bacteria of the family Clostridiaceae. Many species have been identified with some being pathogenic. They occur in water, soil, and in the intestinal tract of humans and lower animals.
Extracellular structures found in a variety of microorganisms. They contain CELLULASES and play an important role in the digestion of CELLULOSE.
An endocellulase with specificity for the hydrolysis of 1,4-beta-glucosidic linkages in CELLULOSE, lichenin, and cereal beta-glucans.
A polysaccharide with glucose units linked as in CELLOBIOSE. It is the chief constituent of plant fibers, cotton being the purest natural form of the substance. As a raw material, it forms the basis for many derivatives used in chromatography, ion exchange materials, explosives manufacturing, and pharmaceutical preparations.
Polysaccharides consisting of xylose units.
An exocellulase with specificity for the hydrolysis of 1,4-beta-D-glucosidic linkages in CELLULOSE and cellotetraose. It catalyzes the hydrolysis of terminal non-reducing ends of beta-D-glucosides with release of CELLOBIOSE.
A cellulose derivative which is a beta-(1,4)-D-glucopyranose polymer. It is used as a bulk laxative and as an emulsifier and thickener in cosmetics and pharmaceuticals and as a stabilizer for reagents.
A disaccharide consisting of two glucose units in beta (1-4) glycosidic linkage. Obtained from the partial hydrolysis of cellulose.
A common inhabitant of the colon flora in human infants and sometimes in adults. It produces a toxin that causes pseudomembranous enterocolitis (ENTEROCOLITIS, PSEUDOMEMBRANOUS) in patients receiving antibiotic therapy.
Glycoside Hydrolases are a class of enzymes that catalyze the hydrolysis of glycosidic bonds, resulting in the breakdown of complex carbohydrates and oligosaccharides into simpler sugars.
Systems of enzymes which function sequentially by catalyzing consecutive reactions linked by common metabolic intermediates. They may involve simply a transfer of water molecules or hydrogen atoms and may be associated with large supramolecular structures such as MITOCHONDRIA or RIBOSOMES.
Infections with bacteria of the genus CLOSTRIDIUM.
Proteins found in any species of bacterium.
A species of anaerobic, gram-positive, rod-shaped bacteria in the family Clostridiaceae that produces proteins with characteristic neurotoxicity. It is the etiologic agent of BOTULISM in humans, wild fowl, HORSES; and CATTLE. Seven subtypes (sometimes called antigenic types, or strains) exist, each producing a different botulinum toxin (BOTULINUM TOXINS). The organism and its spores are widely distributed in nature.
Transport proteins that carry specific substances in the blood or across cell membranes.
An enzyme that catalyzes the hydrolysis of terminal, non-reducing beta-D-mannose residues in beta-D-mannosides. The enzyme plays a role in the lysosomal degradation of the N-glycosylprotein glycans. Defects in the lysosomal form of the enzyme in humans result in a buildup of mannoside intermediate metabolites and the disease BETA-MANNOSIDOSIS.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
A family of glycosidases that hydrolyse crystalline CELLULOSE into soluble sugar molecules. Within this family there are a variety of enzyme subtypes with differing substrate specificities that must work together to bring about complete cellulose hydrolysis. They are found in structures called CELLULOSOMES.
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.
Enzymes which catalyze the endohydrolysis of 1,4-beta-D-xylosidic linkages in XYLANS.
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.
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.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
A xylosidase that catalyses the random hydrolysis of 1,3-beta-D-xylosidic linkages in 1,3-beta-D-xylans.
An acute inflammation of the INTESTINAL MUCOSA that is characterized by the presence of pseudomembranes or plaques in the SMALL INTESTINE (pseudomembranous enteritis) and the LARGE INTESTINE (pseudomembranous colitis). It is commonly associated with antibiotic therapy and CLOSTRIDIUM DIFFICILE colonization.
A species of gram-positive bacteria in the family Clostridiaceae, used for the industrial production of SOLVENTS.

The interaction of carbohydrate-binding modules with insoluble non-crystalline cellulose is enthalpically driven. (1/15)

Natural cellulose exists as a composite of cellulose forms, which can be broadly characterized as crystalline or non-crystalline. The recognition of both of these forms of cellulose by the CBMs (carbohydrate-binding modules) of microbial glycoside hydrolases is important for the efficient natural and biotechnological conversion of cellulosic biomass. The category of CBM that binds insoluble non-crystalline cellulose does so with an affinity approx. 10-20-fold greater than their affinity for cello-oligosaccharides and/or soluble polysaccharides. This phenomenon has been assumed to originate from the effects of changes in configurational entropy upon binding. The loss of configurational entropy is thought to be less profound upon binding to conformationally restrained insoluble non-crystalline cellulose, resulting in larger free energies of binding. However, using isothermal titration calorimetry, it is shown that this is not the case for the high-affinity interactions of CcCBM17 (the family 17 CBM from EngF of Clostridium cellulovorans) and BspCBM28 (the family 28 CBM from Cel5A of Bacillus species 1139) with regenerated cellulose, an insoluble preparation of primarily non-crystalline cellulose. The enhanced free energy of binding of non-crystalline cellulose relative to cello-oligosaccharides is by virtue of improved enthalpy, not entropy.  (+info)

Isolation and expression of the xynB gene and its product, XynB, a consistent component of the Clostridium cellulovorans cellulosome. (2/15)

The nucleotide sequence of the Clostridium cellulovorans xynB gene, which encodes the XynB xylanase, consists of 1,821 bp and encodes a protein of 607 amino acids with a molecular weight of 65,976. XynB contains a typical N-terminal signal peptide of 29 amino acid residues, followed by a 147-amino-acid sequence that is homologous to the family 4-9 (subfamily 9 in family 4) carbohydrate-binding domain. Downstream of this domain is a family 10 catalytic domain of glycosyl hydrolase. The C terminus separated from the catalytic domain by a short linker sequence contains a dockerin domain responsible for cellulosome assembly. The XynB sequence from mass spectrometry and N-terminal amino acid sequence analyses agreed with that deduced from the nucleotide sequence. XynB was highly active toward xylan, but not active toward carboxymethyl cellulose. The enzyme was optimally active at 40 degrees C and pH 5.0. Northern hybridizations revealed that xynB is transcribed as a monocistronic 1.9-kb mRNA. RNA ligase-mediated rapid amplification of 5' cDNA ends by PCR (RLM-5'RACE PCR) analysis of C. cellulovorans RNA identified a single transcriptional start site of xynB located 47 bp upstream from the first nucleotide of the translation initiation codon. Alignment of the xynB promoter region provided evidence for highly conserved sequences that exhibited strong similarity to the sigmaA consensus promoter sequences of gram-positive bacteria. Expression of xynB mRNA increased from early to middle exponential phase and decreased during the early stationary phase when the cells were grown on cellobiose. No alternative promoter was observed by RLM-5'RACE PCR and reverse transcriptase PCR analyses during expression. The analysis of the products from xylan hydrolysis by thin-layer chromatography indicated its endoxylanase activity. The results suggest that XynB is a consistent and major cellulosomal enzyme during growth on cellulose or xylan.  (+info)

Effect of carbon source on the cellulosomal subpopulations of Clostridium cellulovorans. (3/15)

Clostridium cellulovorans produces a cellulase enzyme complex called the cellulosome. When cells were grown on different carbon substrates such as Avicel, pectin, xylan, or a mixture of all three, the subunit composition of the cellulosomal subpopulations and their enzymic activities varied significantly. Fractionation of the cellulosomes (7-11 fractions) indicated that the cellulosome population was heterogeneous, although the composition of the scaffolding protein CbpA, endoglucanase EngE and cellobiohydrolase ExgS was relatively constant. One of the cellulosomal fractions with the greatest endoglucanase activity also showed the highest or second highest cellulase activity under all growth conditions tested. The cellulosomal fractions produced from cells grown on a mixture of carbon substrates showed the greatest cellulase activity and contained CbpA, EngE/EngK, ExgS/EngH and EngL. High xylanase activity in cellulose, pectin and mixed carbon-grown cells was detected with a specific cellulosomal fraction which had relatively larger amounts of XynB, XynA and unknown proteins (35-45 kDa). These results in toto indicate that the assembly of cellulosomes occurs in a non-random fashion.  (+info)

Degradation of corn fiber by Clostridium cellulovorans cellulases and hemicellulases and contribution of scaffolding protein CbpA. (4/15)

Clostridium cellulovorans, an anaerobic bacterium, degrades native substrates efficiently by producing an extracellular enzyme complex called the cellulosome. All cellulosomal enzyme subunits contain dockerin domains that can bind to hydrophobic domains termed cohesins which are repeated nine times in CbpA, the nonenzymatic scaffolding protein of C. cellulovorans cellulosomes. In this study, the synergistic interactions of cellulases (endoglucanase E, EngE; endoglucanase L, EngL) and hemicellulases (arabinofuranosidase A, ArfA; xylanase A, XynA) were determined on the degradation of corn fiber, a natural substrate containing mainly xylan, arabinan, and cellulose. The degradation by XynA and ArfA of cellulose/arabinoxylan was greater than that of corn fiber and resulted in 2.6-fold and 1.4-fold increases in synergy, respectively. Synergistic effects were observed in increments in both simultaneous and sequential reactions with ArfA and XynA. These synergistic enzymes appear to represent potential rate-limiting enzymes for efficient hemicellulose degradation. When mini-cellulosomes were constructed from the cellulosomal enzymes (XynA and EngL) and mini-CbpA with cohesins 1 and 2 (mini-CbpA1&2) and mini-CbpA with cohesins 5 and 6 (mini-CbpA5&6), higher activity was observed than that for the corresponding enzymes alone. Based on the degradation of different types of celluloses and hemicelluloses, the interaction between cellulosomal enzymes (XynA and EngL) and mini-CbpA displayed a diversity that suggests that dockerin-cohesin interaction from C. cellulovorans may be more selective than random.  (+info)

Site-directed mutagenesis and expression of the soluble form of the family IIIa cellulose binding domain from the cellulosomal scaffolding protein of Clostridium cellulovorans. (5/15)

The planar and anchoring residues of the family IIIa cellulose binding domain (CBD) from the cellulosomal scaffolding protein of Clostridium cellulovorans were investigated by site-directed mutagenesis and cellulose binding studies. By fusion with maltose binding protein, the family IIIa recombinant wild-type and mutant CBDs from C. cellulovorans were expressed as soluble forms. Cellulose binding tests of the mutant CBDs indicated that the planar strip residues played a major role in cellulose binding and that the anchoring residues played only a minor role.  (+info)

Synthesis of Clostridium cellulovorans minicellulosomes by intercellular complementation. (6/15)

The ability of two strains of bacteria to cooperate in the synthesis of an enzyme complex (a minicellulosome) was examined. Three strains of Bacillus subtilis were constructed to express Clostridium cellulovorans genes engB, xynB, and minicbpA. MiniCbpA, EngB, and XynB were synthesized and secreted into the medium by B. subtilis. When the strains with the minicbpA and engB genes or with xynB were cocultured, minicellulosomes were synthesized, consisting in one case of miniCbpA and EngB and in the second case of miniCbpA and XynB. Both minicellulosomes showed their respective enzymatic activities. We call this phenomenon "intercellular complementation." Interesting implications concerning bacterial cooperation are suggested from these results.  (+info)

Synergistic interaction of Clostridium cellulovorans cellulosomal cellulases and HbpA. (7/15)

Clostridium cellulovorans, an anaerobic bacterium, produces a small nonenzymatic protein called HbpA, which has a surface layer homology domain and a type I cohesin domain similar to those found in the cellulosomal scaffolding protein CbpA. In this study, we demonstrated that HbpA could bind to cell wall fragments from C. cellulovorans and insoluble polysaccharides and form a complex with cellulosomal cellulases endoglucanase B (EngB) and endoglucanase L (EngL). Synergistic degradative action of the cellulosomal cellulase and HbpA complexes was demonstrated on acid-swollen cellulose, Avicel, and corn fiber. We propose that HbpA functions to bind dockerin-containing cellulosomal enzymes to the cell surface and complements the activity of cellulosomes.  (+info)

Effect of multiple copies of cohesins on cellulase and hemicellulase activities of Clostridium cellulovorans mini-cellulosomes. (8/15)

Cellulosomes in Clostridium cellulovorans are assembled by the interaction between the repeated cohesin domains of a scaffolding protein (CbpA) and the dockerin domain of enzyme components. In this study, we determined the synergistic effects on cellulosic and hemicellulosic substrates by three different recombinant mini-cellulosomes containing either endoglucanase EngB or endoxylanase XynA bound to mini-CbpA with one cohesin domain (mini-CbpA1), two cohesins (mini-CbpA12), or four cohesins (mini-CbpA1234). The assembly of EngB or XynA with mini-CbpA increased the activity against carboxymethyl cellulose, acid-swollen cellulose, Avicel, xylan, and corn fiber 1.1-1.8-fold compared with that for the corresponding enzyme alone. A most distinct improvement was shown with corn fiber, a natural substrate containing xylan, arabinan, and cellulose. However, there was little difference in activity between the three different mini-cellulosomes when the cellulosomal enzyme concentration was held constant regardless of the copy number of cohesins in the cellulosome. A synergistic effect was observed when the enzyme concentration was increased to be proportional to the number of cohesins in the mini-cellulosome. The highest degree of synergy was observed with mini-CbpA1234 (1.8-fold) and then mini-CbpA12 (1.3-fold), and the lowest synergy was observed with mini-CbpA1 (1.2-fold) when Avicel was used as the substrate. As the copy number of cohesin was increased, there was more synergy. These results indicate that the clustering effect (physical enzyme proximity) of the enzyme within the mini-cellulosome is one of the important factors for efficient degradation of plant cell walls.  (+info)

'Clostridium cellulovorans' is a species of gram-positive, rod-shaped, anaerobic bacteria that is commonly found in soil and aquatic environments. It is known for its ability to break down complex carbohydrates, such as cellulose and xylan, into simpler sugars, which it then ferments to produce various end products, including acetate, ethanol, hydrogen, and carbon dioxide.

The bacterium is of interest in the field of bioenergy, as its ability to efficiently convert plant biomass into useful chemicals has potential applications in the production of biofuels and other bioproducts. Additionally, 'C. cellulovorans' has been studied for its potential use in bioremediation, as it is capable of degrading a variety of pollutants, including polycyclic aromatic hydrocarbons (PAHs) and pesticides.

It is important to note that while 'C. cellulovorans' is generally considered to be a non-pathogenic bacterium, it can cause infections in individuals with compromised immune systems or underlying medical conditions. As with any potential pathogen, appropriate precautions should be taken when handling this organism in the laboratory setting.

'Clostridium' is a genus of gram-positive, rod-shaped bacteria that are widely distributed in nature, including in soil, water, and the gastrointestinal tracts of animals and humans. Many species of Clostridium are anaerobic, meaning they can grow and reproduce in environments with little or no oxygen. Some species of Clostridium are capable of producing toxins that can cause serious and sometimes life-threatening illnesses in humans and animals.

Some notable species of Clostridium include:

* Clostridium tetani, which causes tetanus (also known as lockjaw)
* Clostridium botulinum, which produces botulinum toxin, the most potent neurotoxin known and the cause of botulism
* Clostridium difficile, which can cause severe diarrhea and colitis, particularly in people who have recently taken antibiotics
* Clostridium perfringens, which can cause food poisoning and gas gangrene.

It is important to note that not all species of Clostridium are harmful, and some are even beneficial, such as those used in the production of certain fermented foods like sauerkraut and natto. However, due to their ability to produce toxins and cause illness, it is important to handle and dispose of materials contaminated with Clostridium species carefully, especially in healthcare settings.

Cellulosomes are large, complex enzymatic structures produced by certain anaerobic bacteria that allow them to break down and consume cellulose, a major component of plant biomass. These structures are composed of multiple enzymes that work together in a coordinated manner to degrade cellulose into simpler sugars, which the bacteria can then use as a source of energy and carbon.

The individual enzymes in a cellulosome are non-covalently associated with a central scaffoldin protein, forming a multi-enzyme complex. The scaffoldin protein contains cohesin modules that bind to dockerin modules on the enzyme subunits, creating a highly organized and stable structure.

Cellulosomes have been identified in several species of anaerobic bacteria, including members of the genera Clostridium and Ruminococcus. They are thought to play a key role in the global carbon cycle by breaking down plant material and releasing carbon dioxide back into the atmosphere.

Cellulase is a type of enzyme that breaks down cellulose, which is a complex carbohydrate and the main structural component of plant cell walls. Cellulases are produced by certain bacteria, fungi, and protozoans, and are used in various industrial applications such as biofuel production, food processing, and textile manufacturing. In the human body, there are no known physiological roles for cellulases, as humans do not produce these enzymes and cannot digest cellulose.

Cellulose is a complex carbohydrate that is the main structural component of the cell walls of green plants, many algae, and some fungi. It is a polysaccharide consisting of long chains of beta-glucose molecules linked together by beta-1,4 glycosidic bonds. Cellulose is insoluble in water and most organic solvents, and it is resistant to digestion by humans and non-ruminant animals due to the lack of cellulase enzymes in their digestive systems. However, ruminants such as cows and sheep can digest cellulose with the help of microbes in their rumen that produce cellulase.

Cellulose has many industrial applications, including the production of paper, textiles, and building materials. It is also used as a source of dietary fiber in human food and animal feed. Cellulose-based materials are being explored for use in biomedical applications such as tissue engineering and drug delivery due to their biocompatibility and mechanical properties.

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.

Cellulose 1,4-beta-Cellobiosidase is an enzyme that catalyzes the hydrolysis of cellulose, a complex carbohydrate and the main structural component of plant cell walls, into simpler sugars. Specifically, this enzyme breaks down cellulose by cleaving the 1,4-beta-glycosidic bonds between the cellobiose units that make up the cellulose polymer, releasing individual cellobiose molecules (disaccharides consisting of two glucose molecules). This enzyme is also known as cellobiohydrolase or beta-1,4-D-glucan cellobiohydrolase. It plays a crucial role in the natural breakdown of plant material and is widely used in various industrial applications, such as biofuel production and pulp and paper manufacturing.

Carboxymethylcellulose sodium is a type of cellulose derivative that is widely used in the medical and pharmaceutical fields as an excipient or a drug delivery agent. It is a white, odorless powder with good water solubility and forms a clear, viscous solution.

Chemically, carboxymethylcellulose sodium is produced by reacting cellulose, which is derived from plant sources such as wood or cotton, with sodium hydroxide and chloroacetic acid. This reaction introduces carboxymethyl groups (-CH2COO-) to the cellulose molecule, making it more soluble in water and providing negative charges that can interact with positively charged ions or drugs.

In medical applications, carboxymethylcellulose sodium is used as a thickening agent, binder, disintegrant, and suspending agent in various pharmaceutical formulations such as tablets, capsules, liquids, and semisolids. It can also be used as a lubricant in the manufacture of tablets and capsules to facilitate their ejection from molds or dies.

Carboxymethylcellulose sodium has been shown to have good biocompatibility and low toxicity, making it a safe and effective excipient for use in medical and pharmaceutical applications. However, like any other excipient, it should be used with caution and in appropriate amounts to avoid any adverse effects or interactions with the active ingredients of the drug product.

Cellobiose is a disaccharide made up of two molecules of glucose joined by a β-1,4-glycosidic bond. It is formed when cellulose or beta-glucans are hydrolyzed, and it can be further broken down into its component glucose molecules by the action of the enzyme beta-glucosidase. Cellobiose has a sweet taste, but it is not as sweet as sucrose (table sugar). It is used in some industrial processes and may have potential applications in the food industry.

'Clostridium difficile' (also known as 'C. difficile' or 'C. diff') is a type of Gram-positive, spore-forming bacterium that can be found in the environment, including in soil, water, and human and animal feces. It is a common cause of healthcare-associated infections, particularly in individuals who have recently received antibiotics or have other underlying health conditions that weaken their immune system.

C. difficile produces toxins that can cause a range of symptoms, from mild diarrhea to severe colitis (inflammation of the colon) and potentially life-threatening complications such as sepsis and toxic megacolon. The most common toxins produced by C. difficile are called TcdA and TcdB, which damage the lining of the intestine and cause inflammation.

C. difficile infections (CDIs) can be difficult to treat, particularly in severe cases or in patients who have recurrent infections. Treatment typically involves discontinuing any unnecessary antibiotics, if possible, and administering specific antibiotics that are effective against C. difficile, such as metronidazole, vancomycin, or fidaxomicin. In some cases, fecal microbiota transplantation (FMT) may be recommended as a last resort for patients with recurrent or severe CDIs who have not responded to other treatments.

Preventing the spread of C. difficile is critical in healthcare settings, and includes measures such as hand hygiene, contact precautions, environmental cleaning, and antibiotic stewardship programs that promote the appropriate use of antibiotics.

Glycoside hydrolases are a class of enzymes that catalyze the hydrolysis of glycosidic bonds found in various substrates such as polysaccharides, oligosaccharides, and glycoproteins. These enzymes break down complex carbohydrates into simpler sugars by cleaving the glycosidic linkages that connect monosaccharide units.

Glycoside hydrolases are classified based on their mechanism of action and the type of glycosidic bond they hydrolyze. The classification system is maintained by the International Union of Biochemistry and Molecular Biology (IUBMB). Each enzyme in this class is assigned a unique Enzyme Commission (EC) number, which reflects its specificity towards the substrate and the type of reaction it catalyzes.

These enzymes have various applications in different industries, including food processing, biofuel production, pulp and paper manufacturing, and biomedical research. In medicine, glycoside hydrolases are used to diagnose and monitor certain medical conditions, such as carbohydrate-deficient glycoprotein syndrome, a rare inherited disorder affecting the structure of glycoproteins.

Multienzyme complexes are specialized protein structures that consist of multiple enzymes closely associated or bound together, often with other cofactors and regulatory subunits. These complexes facilitate the sequential transfer of substrates along a series of enzymatic reactions, also known as a metabolic pathway. By keeping the enzymes in close proximity, multienzyme complexes enhance reaction efficiency, improve substrate specificity, and maintain proper stoichiometry between different enzymes involved in the pathway. Examples of multienzyme complexes include the pyruvate dehydrogenase complex, the citrate synthase complex, and the fatty acid synthetase complex.

Clostridium infections are caused by bacteria of the genus Clostridium, which are gram-positive, rod-shaped, spore-forming, and often anaerobic organisms. These bacteria can be found in various environments, including soil, water, and the human gastrointestinal tract. Some Clostridium species can cause severe and potentially life-threatening infections in humans. Here are some of the most common Clostridium infections with their medical definitions:

1. Clostridioides difficile infection (CDI): An infection caused by the bacterium Clostridioides difficile, previously known as Clostridium difficile. It typically occurs after antibiotic use disrupts the normal gut microbiota, allowing C. difficile to overgrow and produce toxins that cause diarrhea, colitis, and other gastrointestinal symptoms. Severe cases can lead to sepsis, toxic megacolon, or even death.
2. Clostridium tetani infection: Also known as tetanus, this infection is caused by the bacterium Clostridium tetani. The spores of this bacterium are commonly found in soil and animal feces. They can enter the body through wounds, cuts, or punctures, germinate, and produce a potent exotoxin called tetanospasmin. This toxin causes muscle stiffness and spasms, particularly in the neck and jaw (lockjaw), which can lead to difficulty swallowing, breathing, and potentially fatal complications.
3. Clostridium botulinum infection: This infection is caused by the bacterium Clostridium botulinum and results in botulism, a rare but severe paralytic illness. The bacteria produce neurotoxins (botulinum toxins) that affect the nervous system, causing symptoms such as double vision, drooping eyelids, slurred speech, difficulty swallowing, dry mouth, and muscle weakness. In severe cases, botulism can lead to respiratory failure and death.
4. Gas gangrene (Clostridium perfringens infection): A rapidly progressing soft tissue infection caused by Clostridium perfringens or other clostridial species. The bacteria produce potent exotoxins that cause tissue destruction, gas production, and widespread necrosis. Gas gangrene is characterized by severe pain, swelling, discoloration, and a foul-smelling discharge. If left untreated, it can lead to sepsis, multi-organ failure, and death.
5. Clostridioides difficile infection (C. difficile infection): Although not caused by a typical clostridial species, C. difficile is a gram-positive, spore-forming bacterium that can cause severe diarrhea and colitis, particularly in hospitalized patients or those who have recently taken antibiotics. The bacteria produce toxins A and B, which damage the intestinal lining and contribute to inflammation and diarrhea. C. difficile infection can range from mild to life-threatening, with complications such as sepsis, toxic megacolon, and bowel perforation.

Bacterial proteins are a type of protein that are produced by bacteria as part of their structural or functional components. These proteins can be involved in various cellular processes, such as metabolism, DNA replication, transcription, and translation. They can also play a role in bacterial pathogenesis, helping the bacteria to evade the host's immune system, acquire nutrients, and multiply within the host.

Bacterial proteins can be classified into different categories based on their function, such as:

1. Enzymes: Proteins that catalyze chemical reactions in the bacterial cell.
2. Structural proteins: Proteins that provide structural support and maintain the shape of the bacterial cell.
3. Signaling proteins: Proteins that help bacteria to communicate with each other and coordinate their behavior.
4. Transport proteins: Proteins that facilitate the movement of molecules across the bacterial cell membrane.
5. Toxins: Proteins that are produced by pathogenic bacteria to damage host cells and promote infection.
6. Surface proteins: Proteins that are located on the surface of the bacterial cell and interact with the environment or host cells.

Understanding the structure and function of bacterial proteins is important for developing new antibiotics, vaccines, and other therapeutic strategies to combat bacterial infections.

'Clostridium botulinum' is a gram-positive, rod-shaped, anaerobic bacteria that produces one or more neurotoxins known as botulinum toxins. These toxins are among the most potent naturally occurring biological poisons and can cause a severe form of food poisoning called botulism in humans and animals. Botulism is characterized by symmetrical descending flaccid paralysis, which can lead to respiratory and cardiovascular failure, and ultimately death if not treated promptly.

The bacteria are widely distributed in nature, particularly in soil, sediments, and the intestinal tracts of some animals. They can form spores that are highly resistant to heat, chemicals, and other environmental stresses, allowing them to survive for long periods in adverse conditions. The spores can germinate and produce vegetative cells and toxins when they encounter favorable conditions, such as anaerobic environments with appropriate nutrients.

Human botulism can occur through three main routes of exposure: foodborne, wound, and infant botulism. Foodborne botulism results from consuming contaminated food containing preformed toxins, while wound botulism occurs when the bacteria infect a wound and produce toxins in situ. Infant botulism is caused by the ingestion of spores that colonize the intestines and produce toxins, mainly affecting infants under one year of age.

Prevention measures include proper food handling, storage, and preparation practices, such as cooking and canning foods at appropriate temperatures and for sufficient durations. Wound care and prompt medical attention are crucial in preventing wound botulism. Vaccines and antitoxins are available for prophylaxis and treatment of botulism in high-risk individuals or in cases of confirmed exposure.

Carrier proteins, also known as transport proteins, are a type of protein that facilitates the movement of molecules across cell membranes. They are responsible for the selective and active transport of ions, sugars, amino acids, and other molecules from one side of the membrane to the other, against their concentration gradient. This process requires energy, usually in the form of ATP (adenosine triphosphate).

Carrier proteins have a specific binding site for the molecule they transport, and undergo conformational changes upon binding, which allows them to move the molecule across the membrane. Once the molecule has been transported, the carrier protein returns to its original conformation, ready to bind and transport another molecule.

Carrier proteins play a crucial role in maintaining the balance of ions and other molecules inside and outside of cells, and are essential for many physiological processes, including nerve impulse transmission, muscle contraction, and nutrient uptake.

Beta-Mannosidase is an enzyme that breaks down complex carbohydrates known as glycoproteins. It does this by catalyzing the hydrolysis of beta-mannosidic linkages, which are specific types of chemical bonds that connect mannose sugars within glycoproteins.

This enzyme plays an important role in the normal functioning of the body, particularly in the breakdown and recycling of glycoproteins. A deficiency in beta-mannosidase activity can lead to a rare genetic disorder known as beta-Mannosidosis, which is characterized by the accumulation of mannose-rich oligosaccharides in various tissues and organs, leading to progressive neurological deterioration and other symptoms.

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.

Cellulases are a group of enzymes that break down cellulose, which is a complex carbohydrate and the main structural component of plant cell walls. These enzymes are produced by various organisms, including bacteria, fungi, and protozoa. They play an important role in the natural decomposition process and have various industrial applications, such as in the production of biofuels, paper, and textiles.

Cellulases work by hydrolyzing the beta-1,4 glycosidic bonds between the glucose molecules that make up cellulose, breaking it down into simpler sugars like glucose. This process is known as saccharification. The specific type of cellulase enzyme determines where on the cellulose molecule it will cleave the bond.

There are three main types of cellulases: endoglucanases, exoglucanases, and beta-glucosidases. Endoglucanases randomly attack internal bonds in the amorphous regions of cellulose, creating new chain ends for exoglucanases to act on. Exoglucanases (also known as cellobiohydrolases) cleave cellobiose units from the ends of the cellulose chains, releasing cellobiose or glucose. Beta-glucosidases convert cellobiose into two molecules of glucose, which can then be further metabolized by the organism.

In summary, cellulases are a group of enzymes that break down cellulose into simpler sugars through hydrolysis. They have various industrial applications and play an essential role in natural decomposition processes.

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.

Endo-1,4-beta Xylanases are a type of enzyme that catalyze the endohydrolysis of 1,4-beta-D-xylosidic linkages in xylans, which are complex polysaccharides made up of beta-1,4-linked xylose residues. Xylan is a major hemicellulose component found in the cell walls of plants, and endo-1,4-beta Xylanases play an important role in the breakdown and digestion of plant material by various organisms, including bacteria, fungi, and animals. These enzymes are widely used in industrial applications, such as biofuel production, food processing, and pulp and paper manufacturing, to break down xylans and improve the efficiency of various processes.

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.

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.

A base sequence in the context of molecular biology refers to the specific order of nucleotides in a DNA or RNA molecule. In DNA, these nucleotides are adenine (A), guanine (G), cytosine (C), and thymine (T). In RNA, uracil (U) takes the place of thymine. The base sequence contains genetic information that is transcribed into RNA and ultimately translated into proteins. It is the exact order of these bases that determines the genetic code and thus the function of the DNA or RNA molecule.

Xylan Endo-1,3-beta-Xylosidase is an enzyme that breaks down xylan, which is a major component of hemicellulose in plant cell walls. This enzyme specifically catalyzes the hydrolysis of 1,3-beta-D-xylosidic linkages in xylans, resulting in the release of xylose units from the xylan backbone. It is involved in the process of breaking down plant material for various industrial applications and in the natural decomposition of plants by microorganisms.

Pseudomembranous enterocolitis is a medical condition characterized by inflammation of the inner lining of the small intestine (enteritis) and large intestine (colitis), resulting in the formation of pseudomembranes – raised, yellowish-white plaques composed of fibrin, mucus, and inflammatory cells. The condition is most commonly caused by a toxin produced by the bacterium Clostridioides difficile (C. difficile), which can overgrow in the gut following disruption of the normal gut microbiota, often after antibiotic use. Symptoms may include diarrhea, abdominal cramps, fever, nausea, and dehydration. Severe cases can lead to complications such as sepsis, toxic megacolon, or even death if left untreated. Treatment typically involves discontinuing the offending antibiotic, administering oral metronidazole or vancomycin to eliminate C. difficile, and managing symptoms with supportive care. In some cases, fecal microbiota transplantation (FMT) may be considered as a treatment option.

'Clostridium acetobutylicum' is a gram-positive, spore-forming, rod-shaped bacterium that is commonly found in soil and aquatic environments. It is a species of the genus Clostridium, which includes many bacteria capable of producing industrial chemicals through fermentation.

'Clostridium acetobutylicum' is particularly known for its ability to produce acetic acid and butyric acid, as well as solvents such as acetone and butanol, during the process of anaerobic respiration. This makes it a potential candidate for biotechnological applications in the production of biofuels and other industrial chemicals.

However, like many Clostridium species, 'Clostridium acetobutylicum' can also produce toxins and cause infections in humans and animals under certain circumstances. Therefore, it is important to handle this organism with care and follow appropriate safety protocols when working with it in a laboratory setting.

"Clostridium cellulovorans" at the Encyclopedia of Life LPSN Type strain of Clostridium cellulovorans at BacDive - the Bacterial ... Clostridium cellulovorans is an anaerobic, mesophilic, spore-forming cellulolytic bacterium. Its cells are gram-positive and ... Koukiekolo R, Cho HY, Kosugi A, Inui M, Yukawa H, Doi RH (July 2005). "Degradation of corn fiber by Clostridium cellulovorans ... Doi RH, Tamaru Y (2001). "The Clostridium cellulovorans cellulosome: an enzyme complex with plant cell wall degrading activity ...
Tamaru Y, Doi RH (March 2001). "Pectate lyase A, an enzymatic subunit of the Clostridium cellulovorans cellulosome". ...
January 2011). "Structural and functional analysis of three β-glucosidases from bacterium Clostridium cellulovorans, fungus ...
Clostridium acetobutylicum Clostridium cellulolyticum Clostridium cellulovorans Clostridium clariflavum Clostridium josui ... The scaffoldin of some cellulosomes, an example being that of Clostridium thermocellum, contains a carbohydrate-binding module ... Dockerin Organelle Bayer, EA; Kenig, R; Lamed, R (1983). "Adherence of Clostridium thermocellum to cellulose". J. Bacteriol. ... Clostridium papyrosolvens Clostridium thermocellum (treated as model organism in cellulose utilization and also anaerobic ...
"Clostridium cellulofermentans" Clostridium cellulosi Clostridium cellulovorans Clostridium chartatabidum Clostridium chauvoei ... Clostridium baratii Clostridium beihaiense Clostridium beijerinckii Clostridium diolis Clostridium bornimense Clostridium ... Clostridium aceticum Clostridium acetireducens Clostridium acetobutylicum Clostridium acidisoli Clostridium aciditolerans ... Clostridium aestuarii Clostridium akagii Clostridium algidicarnis Clostridium algifaecis Clostridium algoriphilum Clostridium ...
Clostridium cellulolyticum MeSH B03.300.390.400.200.205 - Clostridium cellulovorans MeSH B03.300.390.400.200.215 - Clostridium ... Clostridium cellulolyticum MeSH B03.510.415.400.200.205 - Clostridium cellulovorans MeSH B03.510.415.400.200.215 - Clostridium ... Clostridium symbiosum MeSH B03.300.390.400.200.722 - Clostridium tertium MeSH B03.300.390.400.200.725 - Clostridium tetani MeSH ... Clostridium symbiosum MeSH B03.510.415.400.200.722 - Clostridium tertium MeSH B03.510.415.400.200.725 - Clostridium tetani MeSH ...
"Clostridium cellulovorans" at the Encyclopedia of Life LPSN Type strain of Clostridium cellulovorans at BacDive - the Bacterial ... Clostridium cellulovorans is an anaerobic, mesophilic, spore-forming cellulolytic bacterium. Its cells are gram-positive and ... Koukiekolo R, Cho HY, Kosugi A, Inui M, Yukawa H, Doi RH (July 2005). "Degradation of corn fiber by Clostridium cellulovorans ... Doi RH, Tamaru Y (2001). "The Clostridium cellulovorans cellulosome: an enzyme complex with plant cell wall degrading activity ...
... www.metabiom.org/microbiota/1722/clostridium-cellulovorans. Keywords: Microbiome, Dysbiosis, Microbiota, Organism, Bacteria ...
... from Clostridium cellulovorans. Together they form a unique fingerprint. ...
Clostridium carboxidivorans and Clostridium cellulovorans *Laura Feliu-Paradeda ... Design and validation of a multiplex PCR method for the simultaneous quantification of Clostridium acetobutylicum, ...
Clostridium cellulovorans Proteomic Responses to Butanol Stress. Costa P, Usai G, Re A, Manfredi M, Mannino G, Bertea CM, ...
Celluloseabbaukinetik; Vollsynthetisches Medium; Clostridium cellulovorans; Clostridium cellulolyticum. Übersetzte Stichworte: ... Cellulose hydrolysis kinetics; Artificial medium; Clostridium cellulovorans; Clostridium cellulolyticum. TU-Systematik:. CIT ...
Exoproteome analysis of Clostridium cellulovorans in natural soft-biomass degradation Clostridium cellulovorans is an anaerobic ... Clostridium cellulovorans is an anaerobic, cellulolytic bacterium, capable of effectively degrading and metabolizing various ... Elucidation of the recognition mechanisms for hemicellulose and pectin in Clostridium cellulovorans using intracellular ...
Journal Article] Exoproteome profiles of Clostridium cellulovorans on various carbon sources2013. *. Author(s). K. Mtsui, J. ... Elucidation of the recognition mechanisms in Clostridium cellulovoransPrincipal Investigator. *. Principal Investigator. Ueda ... Presentation] Intracellular and extracellular time-course proteome analyses of Clostridium cellulovorans grown on xylan2015. * ... Journal Article] Display of Clostridium cellulovorans xylose isomerase on the cell surface of S, cerevisiae and its direct ...
8 Bacteria Clostridium cellulovorans BAV13080.1 ncbi GH31_8 Bacteria Clostridium cellulovorans 743B ADL50832.1 ncbi GH31_8 ...
dash; Clostridium cellulosi *‐ Clostridium cellulovorans *‐ Clostridium citroniae *‐ Clostridium clostridioforme ... https://www.metabiom.org/microbiota/591/clostridium-methylpentosum. Keywords: Microbiome, Dysbiosis, Microbiota, Organism, ... ClostridiumClostridium methylpentosum {10000688}. Record Keys. Parent:. Clostridium. Definition:. Clostridium methylpentosum ...
dash; Clostridium cellulosi *‐ Clostridium cellulovorans *‐ Clostridium citroniae *‐ Clostridium clostridioforme ... https://www.metabiom.org/microbiota/1890/clostridium-sartagoforme. Keywords: Microbiome, Dysbiosis, Microbiota, Organism, ...
dash; Clostridium cellulosi *‐ Clostridium cellulovorans *‐ Clostridium citroniae *‐ Clostridium clostridioforme ... https://www.metabiom.org/microbiota/719/clostridium-beijerinckii. Keywords: Microbiome, Dysbiosis, Microbiota, Organism, ...
1992). Primary sequence analysis of Clostridium cellulovorans cellulose binding protein A. Proc Natl Acad Sci U S A. 1992;89(8 ... 2005). Cellulase, clostridia, and ethanol. Microbiol Mol Biol Rev. 2005;69(1):124-54. DOI:10.1128/MMBR.69.1.124-154.2005 , ... Bayer EA, Kenig R, and Lamed R. (1983). Adherence of Clostridium thermocellum to cellulose. J Bacteriol. 1983;156(2):818-27. ... Discovery of the cellulosome in Clostridium thermocellum [23, 24]. *Demonstration of true cellulase activity by the cellulosome ...
Clostridium cellulovorans 31% * Thermotoga maritima 31% * cellodextrin 31% * streptopain 31% * Lentinula 30% ...
Clostridium cellulovorans 743B chromosome, complete genome. putative sulfonate/nitrate transport system substrate-binding ... Clostridium kluyveri DSM 555 chromosome, complete genome. transporter. 9e-07. 54.7. NC_016627:1807866:1827562. 1827562. 1828554 ... Clostridium acetobutylicum DSM 1731 chromosome, complete genome. sulfate ABC transporter periplasmic-binding protein. 5e-09. 62 ... Clostridium acetobutylicum ATCC 824, complete genome. ABC-type probable sulfate transporter, periplasmic binding protein. 5e-09 ...
Clostridium cellulovorans 743B chromosome, complete genome. DNA mismatch repair protein MutS domain-containing protein. 2e-06. ... Host Lineage: Clostridium botulinum; Clostridium; Clostridiaceae; Clostridiales; Firmicutes; Bacteria. General Information: ... Clostridium perfringens SM101, complete genome. MutS2 family protein. 0. 848. NC_003366:2143173:2157777. 2157777. 2160137. 2361 ... Clostridium cellulolyticum H10, complete genome. MutS2 family protein. 0. 642. NC_016627:2870900:2885510. 2885510. 2887891. ...
Clostridium cellulovorans metabolism of cellulose as studied by comparative proteomic approach. 2020 Usai, G.; Cirrincione, S ... Clostridium cellulovorans metabolism of cellulose as studied by comparative proteomic approach / Usai, G.; Cirrincione, S.; Re ...
Endoglucanase B (engB) from Clostridium cellulovorans. *Xylanases Y (XynY) and Z (xynZ) from Clostridium thermocellum. ... Endo-β-1,3-1,4 glucanase (licB) from Clostridium thermocellum. *Cellulose integrating protein (cipA) from Clostridium ... Gram-positive, thermophilic anaerobes such as Clostridium thermocellum or Clostridium cellulolyticum secretes a highly active ... Cellulose degradation by Clostridium thermocellum: from manure to molecular biology.. Source. FEMS Microbiol. Lett. 79:523-528( ...
Clostridium thermocellum [18], and Clostridium cellulovorans [24]. Comparably, there is no report of using Saccharomyces ... The family 11 carbohydrate-binding module of Clostridium thermocellum Lic26A-Cel5E accommodates beta-1,4- and beta-1,3-1,4- ... cellulases by fusion with cellulose-binding domain of noncellulosomal cellulase engd from Clostridium cellulovorans. Proteins. ... Biochemical characterization and structural analysis of a bifunctional cellulase/xylanase from Clostridium thermocellum. J Biol ...
Endoglucanase D OS=Clostridium cellulovorans (strain ATCC 35296 / DSM 3052 / OCM 3 / 743B) GN=engD PE=1 SV=2. 128. 302. 6.0E-08 ... Endoglucanase B OS=Clostridium cellulovorans (strain ATCC 35296 / DSM 3052 / OCM 3 / 743B) GN=engB PE=3 SV=1. 136. 302. 3.0E-06 ... Endoglucanase A OS=Clostridium cellulolyticum (strain ATCC 35319 / DSM 5812 / JCM 6584 / H10) GN=celCCA PE=1 SV=1. 117. 302. ... Endoglucanase C307 OS=Clostridium sp. (strain F1) GN=celC307 PE=1 SV=1. 136. 269. 2.0E-06. ...
Structural and functional analysis of three β-glucosidases from bacterium Clostridium cellulovorans, fungus Trichoderma reesei ...
Hyeon JE, Yu KO, Suh DJ, Suh YW, Lee SE, Lee J, Han SO: Production of minicellulosomes from Clostridium cellulovorans for the ... Cho HY, Yukawa H, Inui M, Doi RH, Wong SL: Production of minicellulosomes from Clostridium cellulovorans in Bacillus subtilis ... Zverlov VV, Klupp M, Krauss J, Schwarz WH: Mutations in the scaffoldin gene, cipA, of Clostridium thermocellum with impaired ... Lu Y, Zhang YH, Lynd LR: Enzyme-microbe synergy during cellulose hydrolysis by Clostridium thermocellum. Proc Natl Acad Sci U S ...
Clostridium cavendishii DSM 21758 (UP000184310) Clostridium celatum DSM 1785 (UP000010420) Clostridium cellulovorans (strain ... F0Z4B7_9CLOT Clostridium sp. DL-VIII (UP000005106) G7M539_9CLOT G7MCB9_9CLOT Clostridium sp. DMHC 10 (UP000037118) Clostridium ... N3C (UP000184869) Clostridium sp. SM-530-WT-3G (UP000545014) Clostridium sp. USBA 49 (UP000190748) A0A1T4XDV7_9CLOT Clostridium ... CAG:302 (UP000018278) Clostridium sp. CAG:306 (UP000018008) Clostridium sp. CAG:307 (UP000018128) R7GCS1_9CLOT Clostridium sp. ...
... biomass for generation of cellulose-hemicellulose fractions amenable towards Clostridium cellulovorans during fermentation ... cellulovorans through CBP method. The strain yielded maximum 78.45 mL of cumulative hydrogen with hydrogen production rate of ...
Clostridium cavendishii DSM 21758 (UP000184310) Clostridium celatum DSM 1785 (UP000010420) Clostridium cellulovorans (strain ... Clostridium niameyense (UP000473885) Clostridium novyi (strain NT) (UP000008220) Clostridium oryzae (UP000190080) Clostridium ... Clostridium indicum (UP000260680) Clostridium intestinale URNW (UP000016721) Clostridium isatidis (UP000264883) Clostridium ... Clostridium Clostridium aceticum (UP000035704) Clostridium acetireducens DSM 10703 (UP000175744) Clostridium acetobutylicum ( ...
Clostridium cellulovorans), ScaB (AAT79550.1 Bacteroides cellulosolvens), CipA (Q06851, Clostridium thermocellum), CipC ( ... AAC28899.2, Clostridium cellulolyticum H10), ScaB (CAC34385.1, Ruminococcus flavefaciens 17), CipA (BAA32429.1, Clostridium ... The analysis also identified 675 putative scaffoldin proteins, of which 55 were homologs of C. cellulovorans CbpA, 304 of B. ... josui), CipA (AAK78886.1, Clostridium acetobutylicum ATCC 824), ScaA (AAG01230.2, Pseudobacteroides cellulosolvens). The ...
... the cellulase EngD from Clostridium cellulovorans, and some other GH5s. In contrast, the positive glucose-binding subsites of ...
... derived from the cellulose-binding Protein A of Clostridium cellulovorans. The bifunctional fusion protein was expressed in ... derived from the cellulose-binding Protein A of Clostridium cellulovorans. The bifunctional fusion protein was expressed in ... derived from the cellulose-binding Protein A of Clostridium cellulovorans. The bifunctional fusion protein was expressed in ... derived from the cellulose-binding Protein A of Clostridium cellulovorans. The bifunctional fusion protein was expressed in ...
  • Structural analyses of ZgEngA(GH5_4) reveal that all the amino acid residues involved in the catalytic triad and in the negative glucose-binding subsites are conserved, when compared with the closest relative, the cellulase EngD from Clostridium cellulovorans, and some other GH5s. (unl.edu)
  • Much of our understanding of its catalytic components, architecture, and mechanisms of attachment to the bacterial cell and to cellulose, has been derived from the study of Clostridium thermocellum [ 1 , 2 , 3 , 4 ]. (cazypedia.org)
  • Xylanases Y (XynY) and Z (xynZ) from Clostridium thermocellum. (expasy.org)
  • Endo-β-1,3-1,4 glucanase (licB) from Clostridium thermocellum. (expasy.org)
  • Cellulose integrating protein (cipA) from Clostridium thermocellum. (expasy.org)
  • Cellulose degradation by Clostridium thermocellum: from manure to molecular biology. (expasy.org)
  • Calcium-binding affinity and calcium-enhanced activity of Clostridium thermocellum endoglucanase D. (expasy.org)
  • Sequencing of a Clostridium thermocellum gene (cipA) encoding the cellulosomal SL-protein reveals an unusual degree of internal homology. (expasy.org)
  • Two saccharolytic bacteria of interest for development of CBP-enabling microbes are Clostridium thermocellum and Thermoanaerobacterium saccharolyticum , both Gram-positive, thermophilic anaerobes. (biomedcentral.com)
  • Endoglucanases A (celCCA), C (celCCC), D (celCCD), F (celCCF) and G (celCCG) from Clostridium cellulolyticum. (expasy.org)
  • Clostridium perfringens" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (ucdenver.edu)
  • This graph shows the total number of publications written about "Clostridium perfringens" by people in this website by year, and whether "Clostridium perfringens" was a major or minor topic of these publications. (ucdenver.edu)
  • Below are the most recent publications written about "Clostridium perfringens" by people in Profiles. (ucdenver.edu)
  • Immunization with recombinant bivalent chimera r-Cpae confers protection against alpha toxin and enterotoxin of Clostridium perfringens type A in murine model. (ucdenver.edu)
  • Heterologous protection against alpha toxins of Clostridium perfringens and Staphylococcus aureus induced by binding domain recombinant chimeric protein. (ucdenver.edu)
  • In silico, in vitro and in vivo analysis of binding affinity between N and C-domains of Clostridium perfringens alpha toxin. (ucdenver.edu)
  • Taguchi optimization of duplex PCR for simultaneous identification of Staphylococcus aureus and Clostridium perfringens alpha toxins. (ucdenver.edu)
  • General Information: Clostridium botulinum A ATCC 19397 (NCTC 4587, NCTC 7272) is a stock, type A toxin-producing, laboratory strain of known toxicity. (up.ac.za)
  • Clostridium cellulovorans is an anaerobic, mesophilic, spore-forming cellulolytic bacterium. (wikipedia.org)
  • Isolation and Characterization of an Anaerobic, Cellulolytic Bacterium, Clostridium cellulovorans sp. (wikipedia.org)
  • Immobilization is required for most of these applications, Here we describe a genetic-engineering approach to immobilizing ProtA on cellulose, by fusing it to cellulose-binding domain (CBD) derived from the cellulose-binding Protein A of Clostridium cellulovorans. (huji.ac.il)
  • Query: NC_009697:3291500:3294924 Clostridium botulinum A str. (up.ac.za)
  • Clostridium botulinum A str. (up.ac.za)
  • Clostridium botulinum A2 str. (up.ac.za)
  • Clostridium botulinum B1 str. (up.ac.za)
  • Clostridium botulinum Ba4 str. (up.ac.za)
  • Dorn-In S, Schwaiger K, Springer C, Barta L, Ulrich S, Gareis M. Development of a multiplex qPCR for the species identification of Clostridium estertheticum , C. frigoriphilum , C. bowmanii and C. tagluense -like from blown pack spoilage (BPS) meats and from wild boars. (dsmz.de)
  • The Thl enzyme was engineered by introducing homologous mutations previously identified in Clostridium acetobutylicum . (biomedcentral.com)
  • However, a recent study combining metabolic engineering and process engineering demonstrated the potential of commercial-level production of n -butanol by Clostridium acetobutylicum [ 12 ]. (biomedcentral.com)
  • One major problem of ABE (acetone, butanol and ethanol) fermentation is high oxygen sensitivity of Clostridium acetobutylicum . (biomedcentral.com)
  • The endospore forming, gram-positive Clostridium acetobutylicum is a classic example of fermentative obligate anaerobes. (biomedcentral.com)
  • Clostridium cellulovorans is an anaerobic, mesophilic, spore-forming cellulolytic bacterium. (wikipedia.org)
  • Isolation and Characterization of an Anaerobic, Cellulolytic Bacterium, Clostridium cellulovorans sp. (wikipedia.org)
  • Spring S, Merkhoffer B, Weiss N, Kroppenstedt RM, Hippe H, Stackebrandt E. Characterization of novel psychrophilic clostridia from an Antarctic microbial mat: description of Clostridium frigoris sp. (dsmz.de)
  • During fermentation process, the high ratio of Clostridium and low ratio of Bacillus composition indicated that this symbiotic system was an effective and easily controlled cultivation model for ABE fermentation under microaerobic conditions. (biomedcentral.com)
  • Especie tipo del género CLOSTRIDIUM, bacteria grampositiva de la familia Clostridiaceae. (bvsalud.org)