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Monosaccharides unusual

Some yeasts are able to add other monosaccharides, like galactose (S. pombe), but with unusual bonds [70], and they also tend to phosphorylate their glycans everywhere to obtain an additional charge on proteins [71]. [Pg.45]

Fig. 4.5.4 Identification of mutations in the transferrin protein by neuraminidase treatment. Unusual patterns in the IEF of serum transferrin might lead to pitfalls in CDG diagnostics. These varying patterns are often due to mutations of charged amino acids in the protein backbone of the transferrin molecule, which might lead, for example, to an accumulation of trisialo transferrin bands (lane 3, indicated by a question mark). Further investigations are carried out by cleaving off charged sialic acid monosaccharide moieties from transferrin-linked oligosaccharides by neuraminidase treatment, followed by IEF and transferrin antibody staining. In the case of protein mutations, additional bands below (lane 4) or above (not shown) the desialylated transferrin form appear... Fig. 4.5.4 Identification of mutations in the transferrin protein by neuraminidase treatment. Unusual patterns in the IEF of serum transferrin might lead to pitfalls in CDG diagnostics. These varying patterns are often due to mutations of charged amino acids in the protein backbone of the transferrin molecule, which might lead, for example, to an accumulation of trisialo transferrin bands (lane 3, indicated by a question mark). Further investigations are carried out by cleaving off charged sialic acid monosaccharide moieties from transferrin-linked oligosaccharides by neuraminidase treatment, followed by IEF and transferrin antibody staining. In the case of protein mutations, additional bands below (lane 4) or above (not shown) the desialylated transferrin form appear...
C.-H. Lin, T. Sugai, R. L. Halcomb, Y. Ichikawa, and C. H. Wong, Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations Synthesis of both enantiomers of high-carbon monosaccharides, J. Am. Chem. Soc. 774 10138 (1992). [Pg.484]

Apart from the complexity of its monosaccharide composition and the presence of the mannose 6-phosphate derivative, this glycolipid is also unusual, in that fucose is located inside the oligosaccharide chain, which is the first time that this has been found in glycolipids. [Pg.417]

Disaccharides can have similar utility to monosaccharides in DNA delivery polymers. Trehalose, a disaccharide composed of two glucose units linked via an a-(l—>1) glycosidic bond, has been shown to have cryo- and lyo-protective properties, attributed to an unusually large hydration volume [152]. As a function of these properties, trehalose has been shown to prevent aggregation and fusion of proteins and lipids [153]. Logically, incorporation of these features into a polymer backbone could afford similar characteristics to a DNA delivery system and may prevent aggregation of polyplexes in physiological serum concentrations and ionic... [Pg.164]

N. K. Kochetkov, Unusual monosaccharides Components of O-antigenic polysaccharides of microorganisms, Russian Chem. Rev., 65 (1996) 735-768. [Pg.18]

Table I, which lists a number of mono-, oligo-, and polysaccharides and derivatives whose motional descriptions are available based on qualitative arguments, summarizes the experimental conditions and types of measurements used to obtain those descriptions. Table II deals specifically with those carbohydrates for which a quantitative treatment and dynamic modeling have been undertaken. In naming the compounds listed in Tables I and II, IUPAC rules are used for monosaccharide and less complex oligosaccharide molecules. However, empirical names are used for unusual oligosaccharides involving a complex aglycon substituent and polysaccharides. The gross motional features of a number of the compounds in Table I have been discussed in references 6-8, and will be mentioned here only if necessary for further clarification or for comparison with quantitative results. Table I, which lists a number of mono-, oligo-, and polysaccharides and derivatives whose motional descriptions are available based on qualitative arguments, summarizes the experimental conditions and types of measurements used to obtain those descriptions. Table II deals specifically with those carbohydrates for which a quantitative treatment and dynamic modeling have been undertaken. In naming the compounds listed in Tables I and II, IUPAC rules are used for monosaccharide and less complex oligosaccharide molecules. However, empirical names are used for unusual oligosaccharides involving a complex aglycon substituent and polysaccharides. The gross motional features of a number of the compounds in Table I have been discussed in references 6-8, and will be mentioned here only if necessary for further clarification or for comparison with quantitative results.
Disaccharides and even some insoluble polysaccharides are substrates, but not monosaccharides. Cellobiose oxidase is unusual among flavoproteins, as it stabilises the red anionic flavin semiquinone and forms a sulphite adduct, yet appears to produce the superoxide anion as its primary reduced oxygen product. [Pg.135]

Show the structure of D-digitoxose. What unusual features are present in this monosaccharide ... [Pg.1115]

Sucrose is unusual in that both monosaccharides are linked as acetals Because both of the potential carbonyl groups in sucrose are tied up in acetals, sucrose shows none of the typical reactions of carbonyl compounds. It will not show positive Tollens test, carmot mutarotate, etc. [Pg.56]


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See also in sourсe #XX -- [ Pg.85 ]




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