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  2. Cellobiose - Wikipedia

    en.wikipedia.org/wiki/Cellobiose

    The chemical structure of cellobiose is derived from the condensation of a pair of β-glucose molecules forming a β(1→4) bond. It can be hydrolyzed to glucose enzymatically or with acid. Cellobiose has eight free alcohol (OH) groups, one acetal linkage, and one hemiacetal linkage, which give rise to strong inter- and intramolecular hydrogen ...

  3. C12H22O11 - Wikipedia

    en.wikipedia.org/wiki/C12H22O11

    The molecular form C 12 H 22 O 11 (molar mass: 342.29 g/mol, exact mass : 342.116212) may refer to: . Disaccharides. Allolactose; Cellobiose; Galactose-alpha-1,3-galactose; Gentiobiose (amygdalose)

  4. Cellulose 1,4-β-cellobiosidase (non-reducing end) - Wikipedia

    en.wikipedia.org/wiki/Cellulose_1,4-β...

    CBH1 Structure, generated using pymol CBH1 zoomed in on the active site where cellulose is cleaved into cellobiose, generated using pymol. After above step, the process for creating ethanol is as follows: [9] 3. Separation of sugars from other plant material. 4. Microbial fermentation of the sugar solution to create alcohol. 5. Distillation to ...

  5. What is sugar alcohol and is it bad for you? Here's the ...

    www.aol.com/sugar-alcohol-reduced-calorie...

    What is sugar alcohol? According to Beaumont Health, sugar alcohol is a reduced-calorie sweetener. It is a carbohydrate with a chemical makeup similar to sugar — meaning it can activate ...

  6. Sugar alcohol - Wikipedia

    en.wikipedia.org/wiki/Sugar_alcohol

    Sugar alcohols can be, and often are, produced from renewable resources.Particular feedstocks are starch, cellulose and hemicellulose; the main conversion technologies use H 2 as the reagent: hydrogenolysis, i.e. the cleavage of C−O single bonds, converting polymers to smaller molecules, and hydrogenation of C=O double bonds, converting sugars to sugar alcohols.

  7. Glycosidic bond - Wikipedia

    en.wikipedia.org/wiki/Glycosidic_bond

    The reaction often favors formation of the α-glycosidic bond as shown due to the anomeric effect. A glycosidic bond is formed between the hemiacetal or hemiketal group of a saccharide (or a molecule derived from a saccharide) and the hydroxyl group of some compound such as an alcohol. A substance containing a glycosidic bond is a glycoside.

  8. β-Glucosidase - Wikipedia

    en.wikipedia.org/wiki/Β-Glucosidase

    In the case of β-glucosidase, two carboxylate residues of glucosides, cellobiose, cellotriose, cellotetraose are involved at the active site. The purpose of the reaction is to remove the residues from disaccharide cellobiose to produce glucose during the hydrolysis of biomass. [ 7 ]

  9. Reducing sugar - Wikipedia

    en.wikipedia.org/wiki/Reducing_sugar

    A reducing sugar is one that reduces another compound and is itself oxidized; that is, the carbonyl carbon of the sugar is oxidized to a carboxyl group. [2] A sugar is classified as a reducing sugar only if it has an open-chain form with an aldehyde group or a free hemiacetal group. [3]