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  2. Carbohydrate - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate

    Lactose is a disaccharide found in animal milk. It consists of a molecule of D-galactose and a molecule of D-glucose bonded by beta-1-4 glycosidic linkage.. A carbohydrate (/ ˌ k ɑːr b oʊ ˈ h aɪ d r eɪ t /) is a biomolecule consisting of carbon (C), hydrogen (H) and oxygen (O) atoms, usually with a hydrogen–oxygen atom ratio of 2:1 (as in water) and thus with the empirical formula C m ...

  3. Carbohydrate conformation - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_conformation

    The chair conformation of six-membered rings have a dihedral angle of 60° between adjacent substituents thus usually making it the most stable conformer. Since there are two possible chair conformation steric and stereoelectronic effects such as the anomeric effect, 1,3-diaxial interactions, dipoles and intramolecular hydrogen bonding must be taken into consideration when looking at relative ...

  4. Glycobiology - Wikipedia

    en.wikipedia.org/wiki/Glycobiology

    Since the structure of a glycan may depend on the expression, activity and accessibility of the different biosynthetic enzymes, it is not possible to use recombinant DNA technology in order to produce large quantities of glycans for structural and functional studies as it is for proteins.

  5. Polysaccharide - Wikipedia

    en.wikipedia.org/wiki/Polysaccharide

    They are long-chain polymeric carbohydrates composed of monosaccharide units bound together by glycosidic linkages. This carbohydrate can react with water using amylase enzymes as catalyst, which produces constituent sugars (monosaccharides or oligosaccharides). They range in structure from linear to highly branched.

  6. Oligosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Oligosaccharide_nomenclature

    An oligosaccharide has both a reducing and a non-reducing end. The reducing end of an oligosaccharide is the monosaccharide residue with hemiacetal functionality, thereby capable of reducing the Tollens’ reagent, while the non-reducing end is the monosaccharide residue in acetal form, thus incapable of reducing the Tollens’ reagent. [2]

  7. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    Fructose is soluble in water, alcohol, and ether. [9] The two enantiomers of each pair generally have vastly different biological properties. 2-Ketohexoses are stable over a wide pH range, and with a primary p K a of 10.28, will only deprotonate at high pH, so are marginally less stable than aldohexoses in solution.

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  9. Hemicellulose - Wikipedia

    en.wikipedia.org/wiki/Hemicellulose

    [9] [10] Several forms of glucan synthase from CSLF and CSLH have been identified. [9] [10] All of them are responsible for addition of glucose to the backbone and all are capable of producing both β1-3 and β1-4 linkages, however, it is unknown how much each specific enzyme contributes to the distribution of β1-3 and β1-4 linkages. [9] [10]