Glycoconjugates galactose

Takami S., Getchell M. and Getchell T. (1995). Resolution of sensory and mucoid glycoconjugates with terminal O-galactose residues in the mucomicrovillar complex of the vomeronasal sensory epithelium by dual confocal laser-scanning microscopy. Cell Tiss Res 280, 211-216. 

Bayer, E.A., Ben-Hur, H., and Wilchek, M. (1988) Biocytin hydrazide—a selective label for sialic acids, galactose, and other sugars in glycoconjugates using avidin-biotin technology. Anal. Biochem. 170, 271-281. 

In the literature, there are several examples of partial hydrolysis of polysaccharides or glycoconjugates containing 2-amino-2-deoxyhex-ose residues. One example is the hydrolysis of carboxyl-reduced, N deacetylated chondroitin, with the formation of 4-0-(2-amino-2-deoxy-/3-D-galactopyranosyl)-D-glucose.51 Another is the isolation of 6-0-(2-amino-2-deoxy-/8-D-galactopyranosyl)-D-galactose after N-de-acetylation and partial hydrolysis of the pentasaccharide (19) obtained... 

Glycoprotein Galactosyltransferase Assays. In order to further investigate the effects of TPA and RA on glycoconjugate metabolism, UDP-galactose DSG-fetuin galactosyltransferase activity was assayed. Table II shows the results of this study. The effects of TPA and RA on... 

Sialidase or NA is the second glycoprotein on the virion surface. One of the most important functions of sialidase is associated with the release of virus progeny from infected host cells to repeat the cycle of infection [6, 50], The enzyme catalyzes the hydrolysis of sialic acid residues from glycoconjugates on the cell surface with either Neu5Ac(a2 3)Gal or Neu5Ac(a2 6)Gal linkages (Gal=galactose) [60, 61]. 

Prieels et al. (1976) studied the binding of glycoconjugates with galactosyltransferase in both the presence and absence of a-lactalbumin. They concluded that, in contrast to its ability to inhibit AT-acetyllactos-amine production, a-lactalbumin does not inhibit the transfer of d-galactose to oligomers of A -acetylglucosamine or to glycopeptides. 

Figure 2 Examples of glycosyl donors. Nucleotide donors are represented by UDP-galactose (UDP-Gal), GDP-fucose (GDP-Fuc), GMP-N-acetyIneuraminic acid (CMP-sialic acid, CMP-Neu5Ac), GDP-galactose (GDP-Gal), dTDP-rhamnose (dTDP-Rha), and dTDP-daunosamine lipid phosphate donors are represented by Lipid II and dolichol-phosphate-glucose (Dol-P-GIc) sugar phosphate donors are represented by glucose-1-phosphate. The saccharides are transferred from these donors by GTs to form oligo/polysaccharides and glycoconjugate products.

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