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  2. Glycosidic bond - Wikipedia

    en.wikipedia.org/wiki/Glycosidic_bond

    A glycosidic bond or glycosidic linkage is a type of ether bond that joins a ... The best condition for use of CP was found to be in the presence of IL AMMOENG 101 ...

  3. Glycoside - Wikipedia

    en.wikipedia.org/wiki/Glycoside

    There are also numerous enzymes that can form and break glycosidic bonds. The most important cleavage enzymes are the glycoside hydrolases, and the most important synthetic enzymes in nature are glycosyltransferases. Genetically altered enzymes termed glycosynthases have been developed that can form glycosidic bonds in excellent yield ...

  4. Glycoside hydrolase - Wikipedia

    en.wikipedia.org/wiki/Glycoside_hydrolase

    Glycoside hydrolases are found in essentially all domains of life. In prokaryotes , they are found both as intracellular and extracellular enzymes that are largely involved in nutrient acquisition. One of the important occurrences of glycoside hydrolases in bacteria is the enzyme beta-galactosidase (LacZ), which is involved in regulation of ...

  5. Polysaccharide - Wikipedia

    en.wikipedia.org/wiki/Polysaccharide

    Glycogen is a polymer of α(1→4) glycosidic bonds linked with α(1→6)-linked branches. Glycogen is found in the form of granules in the cytosol/cytoplasm in many cell types and plays an important role in the glucose cycle.

  6. Disaccharide - Wikipedia

    en.wikipedia.org/wiki/Disaccharide

    The glycosidic bond can be formed between any hydroxy group on the component monosaccharide. So, even if both component sugars are the same (e.g., glucose), different bond combinations (regiochemistry) and stereochemistry (alpha-or beta-) result in disaccharides that are diastereoisomers with different chemical and physical properties ...

  7. Sucrose - Wikipedia

    en.wikipedia.org/wiki/Sucrose

    Likewise, gastric acidity converts sucrose to glucose and fructose during digestion, the bond between them being an acetal bond which can be broken by an acid. Given (higher) heats of combustion of 1349.6 kcal/mol for sucrose, 673.0 for glucose, and 675.6 for fructose, [ 13 ] hydrolysis releases about 1.0 kcal (4.2 kJ) per mole of sucrose, or ...

  8. Trehalose - Wikipedia

    en.wikipedia.org/wiki/Trehalose

    Trehalose is a disaccharide formed by a 1,1-glycosidic bond between two α-glucose units. It is found in nature as a disaccharide and also as a monomer in some polymers. [7] Two other stereoisomers exist: α,β-trehalose, also called neotrehalose, and β,β-trehalose, also called isotrehalose. Neither of these alternate isomers has been ...

  9. Alpha glucan - Wikipedia

    en.wikipedia.org/wiki/Alpha_glucan

    Alpha-glucan is also commonly found in bacteria, yeasts, plants, and insects. Whereas the main pathway of α-glucan synthesis is via glycosidic bonds of glucose monomers, α-glucan can be comparably synthesized via the maltosyl transferase GlgE and branching enzyme GlgB. [2] This alternative pathway is common in many bacteria, which use GlgB ...