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热休克蛋白介导的大肠杆菌对高静水压的抗性

Heat shock protein-mediated resistance to high hydrostatic pressure in Escherichia coli.

作者信息

Aertsen Abram, Vanoirbeek Kristof, De Spiegeleer Philipp, Sermon Jan, Hauben Kristel, Farewell Anne, Nyström Thomas, Michiels Chris W

机构信息

Laboratory of Food Microbiology, Katholieke Universiteit Leuven, Leuven, Belgium.

出版信息

Appl Environ Microbiol. 2004 May;70(5):2660-6. doi: 10.1128/AEM.70.5.2660-2666.2004.

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 sigma(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.

摘要

构建了一个与无启动子绿色荧光蛋白(GFP)基因融合的大肠杆菌MG1655基因组片段的随机文库,并通过差异荧光诱导筛选暴露于亚致死性高静水压胁迫后被诱导的启动子。该筛选产生了属于热休克调节子(dnaK、lon、clpPX)的三个基因的启动子,表明热休克蛋白在抵抗和/或修复高压造成的损伤中发挥作用。一些进一步的观察结果为这一假设提供了额外支持:(i)。编码热休克特异性σ因子σ32的rpoH的表达也被高压诱导;(ii)。热休克使大肠杆菌对随后的高压失活具有显著更高的抗性,并且这种热休克诱导的耐压性与热休克基因的诱导遵循相同的时间进程;(iii)。与野生型水平相比,在三个先前分离的大肠杆菌耐压突变体中,热休克启动子的GFP基础表达水平以及通过对脉冲标记细胞提取的蛋白质进行二维十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定的几种热休克蛋白的表达增加。

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