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JBC, Vol. 254, Issue 11, 4554-4559, Jun, 1979
T. Liu, B. Stetson, S. J. Turco, S. C. Hubbard and P. W. Robbins
The lipid-linked oligosaccharide synthesized in vitro, in the presence of
1.0 microM UDP-[3H]Glc, GDP-[14C]Man, and UDP-GlcNAc has been isolated and
the structure of the oligosaccharide has been analyzed. The oligosaccharide
contains 2 N-acetylglucosamine, 9 mannose, and 3 glucose residues. The
N-acetylglucosamine residues are located at the reducing terminus. The 3
glucose residues are arranged in a linear order at one of the nonreducing
termini in the sequence Glc 1,2--Glc 1,3--Glc--(Man)9 (GlcNAc)2. The
structural analysis was made possible largely by the availability of
glucosidase preparations of fungal anad microsomal origin which remove
glucose residues from the oligosaccharide without releasing mannose
residues.
Arrangement of glucose residues in the lipid-linked oligosaccharide precursor of asparaginyl oligosaccharides
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