Expression of functional soluble forms of human β-1,4-galactosyltransferase I, α-2,6-sialyltransferase, and α-1,3-fucosyltransferase VI in the methylotrophic yeast Pichia pastoris

被引:29
作者
Malissard, M [1 ]
Zeng, S [1 ]
Berger, EG [1 ]
机构
[1] Univ Zurich, Inst Physiol, CH-8057 Zurich, Switzerland
关键词
beta-1,4-galactosyltransferase I; alpha-2,6-sialyltransferase; alpha-1,3-fucosyltransferase VI; heterologous expression; yeast;
D O I
10.1006/bbrc.1999.1946
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cDNAs encoding soluble forms of human beta-1,4-galactosyltransferase I (EC 2.4.1.22), alpha-2,6-sialyltransferase (EC 2.4.99.1), and alpha-1,3-fucosyltransferase VI (EC 2.4.1.65), respectively, have been expressed in the methylotrophic yeast Pichia pastoris. The vector pPIC9 was used, which contains the N-terminal signal sequence of Saccharomyces cerevisiae alpha-factor to allow entry into the secretory pathway. The recombinant enzymes had similar kinetic properties as their native counterparts. Their identity was confirmed by Western blotting. Recombinant enzymes may be used for in vitro synthesis of oligosaccharides. (C) 2000 Academic Press.
引用
收藏
页码:169 / 173
页数:5
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