Mutation of the homologue of GDP-mannose pyrophosphorylase alters cell wall structure, protein glycosylation and secretion in Hansenula polymorpha

被引:30
作者
Agaphonov, MO
Packeiser, AN
Chechenova, MB
Choi, ES
Ter-Avanesyan, MD
机构
[1] Cardiol Res Ctr, Inst Expt Cardiol, Moscow 121552, Russia
[2] Korea Res Inst Biosci & Biotechnol, Div Life Sci, Taejon 305600, South Korea
关键词
cell wall; Hansenula polymorpha; protein glycosylation; protein secretion; urinary type plasminogen activator; yeast;
D O I
10.1002/yea.678
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
A Hansenula polymorpha mutant with enhanced ability to secrete a heterologous protein has been isolated. The mutation defines a gene, designated OPU24, which encodes a protein highly homologous to GDP-mannose pyrophosphorylase Psa1p/Srb1p/Vig9p of Saccharomyces cerevisiae and CaSrb1p of Candida albicans. The opu24 mutant manifests phenotypes similar to those of S, cerevisiae mutants depleted for GDP-mannose, such as cell wall fragility and defects in N- and O-glycosylation of secreted proteins. The influence of the opu24 mutation on endoplasmic reticulum-associated protein degradation is discussed. The GenBank Accession No. for the OPU24 sequence is AF234177, Copy-right (C) 2001 John Wiley & Sons, Ltd.
引用
收藏
页码:391 / 402
页数:12
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