The plasmid F OmpP protease, a homologue of OmpT, as a potential obstacle to E-coli-based protein production

被引:16
作者
Matsuo, E
Sampei, G
Mizobuchi, K
Ito, K [1 ]
机构
[1] Kyoto Univ, Inst Virus Res, Kyoto 6068507, Japan
[2] Univ Electrocommun, Dept Appl Phys & Chem, Tokyo 1828585, Japan
基金
日本学术振兴会;
关键词
OmpT; SecY; OmpP; F plasmid; recombinant protein; Escherichia coli;
D O I
10.1016/S0014-5793(99)01418-0
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
OmpT, an outer membrane-localized protease of Escherichia coli, cleaves a number of exogenous and endogenous proteins during their purification. SecY, an endogenous membrane protein, is a target of this artificial proteolysis in vitro. Were we report that SecY cleavage occurs even in cell extracts from omp T-disrupted cells, if they carry an F plasmid derivative, A gene, ompP, On the F plasmid was shown to be responsible for this proteolysis. These results indicate that the absence of an F-like plasmid should be checked when choosing a host strain for E. coli-based protein production. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:6 / 8
页数:3
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