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寡糖脂的生物合成。α-1,2-甘露糖基-甘露糖键的形成。

The biosynthesis of oligosaccharide-lipids. Formation of an alpha-1,2-mannosyl-mannose linkage.

作者信息

Schutzbach J S, Springfield J D, Jensen J W

出版信息

J Biol Chem. 1980 May 10;255(9):4170-5.

PMID:6154707
Abstract

An enzyme present in rabbit liver microsomes has been found to catalyze mannosyltransfer from GDP-mannose to exogenously added oligosaccharide-lipid acceptor resulting in the formation of an alpha-1,2-mannosyl-mannose linkage. Several lines of evidence suggest that the product is a heptasaccharide containing a single 1,6-linked branched glycosyl unit with 65% of the newly added mannosyl units in a terminal nonreducing position. The enzyme has been solubilized with non-ionic detergents and was partially purified on DEAE-cellulose and hydroxylapatite. The partially purified enzyme no longer catalyzed the formation of dolichol-P-mannose indicating a direct transfer from GDP-mannose to oligosaccharide-lipid acceptor.

摘要

已发现兔肝微粒体中存在的一种酶可催化将GDP-甘露糖中的甘露糖基转移至外源添加的寡糖脂受体上,从而形成α-1,2-甘露糖基-甘露糖键。多条证据表明,产物是一种七糖,含有一个单一的1,6-连接的分支糖基单元,新添加的甘露糖基单元中有65%位于末端非还原位置。该酶已用非离子型去污剂溶解,并在DEAE-纤维素和羟基磷灰石上进行了部分纯化。部分纯化的酶不再催化多萜醇-P-甘露糖的形成,这表明是从GDP-甘露糖直接转移至寡糖脂受体。

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