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J. Biol. Chem., Vol. 255, Issue 21, 10232-10238, Nov, 1980
RB Trimble, F Maley and AL Tarentino
Conditions are described for optimizing the synthesis of large
oligosaccharide-lipids in microsomal preparations from Saccharomyces
cerevisiae. On incubating microsomes, with GDP-[14C]Man, the major product
obtained was Man9GlcNAc2-P-P-dolichol, but when both GDP- [14C]Man and
UDP-[3H]Glc were present in the incubation mixture about half of the
Man9GlcNAc2 was elongated to Glc3Man9GlcNAc2-P-P-dolichol. Unlike
particulate fractions from mammalian systems, little glucosylation of the
yeast microsomal oligosaccharide-lipid was obtained when the concentration
of UDP-Glc was less than 10 microM, but the synthesis of this product could
be maximized by raising the concentration of UDP-Glc to 50 microM. Analysis
of the yeast Man9GlcNAc2 species confirmed that 8 of the 9 mannose residues
could be released with alpha-mannosidase, while the remaining mannosyl
residue was in the core trisaccharide, Manbeta 1 leads to 4GlcNAc beta 1
leads to 4GlcNAc. Treatment of Glc3Man9GlcNAc2 with alpha-mannosidase
released 5 of 9 mannose residues and yielded Glc3Man4GlcNAc2. This product
appeared to be identical with that obtained in parallel experiments with
double labeled oligosaccharide-lipid synthesized in oviduct microsomes.
Streptomyces plicatus endo-beta-N- acetylglucosaminidase H (Endo-H)
treatment of yeast microsomal glycoproteins that were labeled with sugar
nucleotides established that 15% of the label was associated with N-linked
oligosaccharides. The remaining labeled sugars were released with alkali,
indicating that they were linked to serine or threonine. Based on the size
and distribution of [3H]glucose and [14C]mannose in the Endo-H-released
oligosaccharides, it was concluded that Glc3Man9GlcNAc2 was the primary
species transferred to proteins in the yeast system.
Characterization of large oligosaccharide-lipids synthesized in vitro by microsomes from Saccharomyces cerevisiae
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