Affiliation:
1. Laboratory of Food Microbiology, Katholieke Universiteit Leuven, Leuven, Belgium
2. Department of Cell and Molecular Biology-Microbiology, Göteborg University, Göteborg, Sweden
Abstract
ABSTRACT
A random library of
Escherichia coli
MG1655 genomic fragments fused to a promoterless green fluorescent protein (GFP) gene was constructed and screened by differential fluorescence induction for promoters that are induced after exposure to a sublethal high hydrostatic pressure stress. This screening yielded three promoters of genes belonging to the heat shock regulon (
dnaK
,
lon
,
clpPX
), suggesting a role for heat shock proteins in protection against, and/or repair of, damage caused by high pressure. Several further observations provide additional support for this hypothesis: (i) the expression of
rpoH
, encoding the heat shock-specific sigma factor σ
32
, was also induced by high pressure; (ii) heat shock rendered
E. coli
significantly more resistant to subsequent high-pressure inactivation, and this heat shock-induced pressure resistance followed the same time course as the induction of heat shock genes; (iii) basal expression levels of GFP from heat shock promoters, and expression of several heat shock proteins as determined by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis of proteins extracted from pulse-labeled cells, was increased in three previously isolated pressure-resistant mutants of
E. coli
compared to wild-type levels.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
125 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献