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在酿酒酵母中生产与人类兼容的高甘露糖型(Man5GlcNAc2)糖链。

Production of human compatible high mannose-type (Man5GlcNAc2) sugar chains in Saccharomyces cerevisiae.

作者信息

Chiba Y, Suzuki M, Yoshida S, Yoshida A, Ikenaga H, Takeuchi M, Jigami Y, Ichishima E

机构信息

Central Laboratories for Key Technology, KIRIN Brewery Co., Ltd., Yokohama, Kanagawa 236-0004, Japan.

出版信息

J Biol Chem. 1998 Oct 9;273(41):26298-304. doi: 10.1074/jbc.273.41.26298.

Abstract

A yeast mutant capable of producing Man5GlcNAc2 human compatible sugar chains on glycoproteins was constructed. An expression vector for alpha-1,2-mannosidase with the "HDEL" endoplasmic reticulum retention/retrieval tag was designed and expressed in Saccharomyces cerevisiae. An in vitro alpha-1,2-mannosidase assay and Western blot analysis showed that it was successfully localized in the endoplasmic reticulum. A triple mutant yeast lacking three glycosyltransferase activities was then transformed with an alpha-1, 2-mannosidase expression vector. The oligosaccharide structures of carboxypeptidase Y as well as cell surface glycoproteins were analyzed, and the recombinant yeast was shown to produce a series of high mannose-type sugar chains including Man5GlcNAc2. This is the first report of a recombinant S. cerevisiae able to produce Man5GlcNAc2-oligosaccharides, the intermediate for hybrid-type and complex-type sugar chains.

摘要

构建了一种能够在糖蛋白上产生Man5GlcNAc2人源兼容糖链的酵母突变体。设计了带有“HDEL”内质网保留/回收标签的α-1,2-甘露糖苷酶表达载体,并在酿酒酵母中表达。体外α-1,2-甘露糖苷酶测定和蛋白质印迹分析表明它成功定位于内质网中。然后用α-1,2-甘露糖苷酶表达载体转化缺乏三种糖基转移酶活性的三重突变酵母。分析了羧肽酶Y以及细胞表面糖蛋白的寡糖结构,结果表明重组酵母能产生包括Man5GlcNAc2在内的一系列高甘露糖型糖链。这是关于能够产生Man5GlcNAc2-寡糖(杂合型和复合型糖链的中间体)的重组酿酒酵母的首次报道。

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