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大肠杆菌中热休克诱导蛋白缺陷的温度敏感突变体的分离与物理图谱分析。

Isolation and physical mapping of temperature-sensitive mutants defective in heat-shock induction of proteins in Escherichia coli.

作者信息

Tobe T, Ito K, Yura T

出版信息

Mol Gen Genet. 1984;195(1-2):10-6. doi: 10.1007/BF00332716.

DOI:10.1007/BF00332716
PMID:6092838
Abstract

Mutants of Escherichia coli K12 that are partially or totally defective in induction of major heat-shock proteins and cannot grow at high temperature (42 degrees C) were isolated by localized mutagenesis. These mutants carry a single mutation in the gene htp R (formerly hin) located at min 76 on the E. coli genetic map. Some mutants exhibit delayed (partial) induction of heat-shock proteins or require a higher temperature for induction than the wild type, whereas others are not induced under any of these conditions. The maximum temperature that allows growth varies among different mutants and is correlated with the residual induction capacity. Temperature-resistant revertants obtained from each mutant are fully or partially recovered in heat-shock induction. These results indicate that the inability of htp R mutants to grow at high temperature is due to the defect in heat-shock induction. In addition, a couple of mutants was found that produce significantly higher amounts of heat-shock proteins even at 30 degrees C. The htp R gene has been cloned into plasmid pBR322 using the above mutants, and was localized to a DNA segment of 1.6 kilobase pairs. The mutants harboring certain plasmids that carry a part of htp R produce temperature-resistant recombinants at high frequency. This permits further localization of mutations within the htp R gene. Analysis of proteins encoded by each of the recombinant plasmids including the one carrying a previously isolated amber mutation (htp R165) led to the identification of a protein with an apparent molecular weight of about 36,000 daltons as the htp R gene product.

摘要

通过定位诱变分离出了大肠杆菌K12的突变体,这些突变体在主要热休克蛋白的诱导方面存在部分或完全缺陷,并且不能在高温(42℃)下生长。这些突变体在大肠杆菌遗传图谱上位于76分钟处的htp R基因(以前称为hin)中携带单个突变。一些突变体表现出热休克蛋白的延迟(部分)诱导,或者比野生型需要更高的温度来诱导,而其他突变体在任何这些条件下都不被诱导。允许生长的最高温度在不同突变体之间有所不同,并且与残余诱导能力相关。从每个突变体获得的耐温回复体在热休克诱导中完全或部分恢复。这些结果表明,htp R突变体在高温下无法生长是由于热休克诱导缺陷所致。此外,还发现了几个即使在30℃时也能产生大量热休克蛋白的突变体。利用上述突变体将htp R基因克隆到质粒pBR322中,并定位到一个1.6千碱基对的DNA片段上。携带htp R一部分的某些质粒的突变体在高频下产生耐温重组体。这允许进一步定位htp R基因内的突变。对包括携带先前分离的琥珀突变(htp R165)的重组质粒在内的每个重组质粒所编码的蛋白质进行分析,导致鉴定出一种表观分子量约为36,000道尔顿的蛋白质为htp R基因产物。

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Co-induction of DNA relaxation and synthesis of DnaK and GroEL proteins in Escherichia coli by expression of LetD (CcdB) protein, an inhibitor of DNA gyrase encoded by the F factor.F因子编码的DNA回旋酶抑制剂LetD(CcdB)蛋白的表达在大肠杆菌中共同诱导DNA松弛以及DnaK和GroEL蛋白的合成。
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