首页> 美国卫生研究院文献>Journal of Bacteriology >Escherichia coli grpE gene codes for heat shock protein B25.3 essential for both lambda DNA replication at all temperatures and host growth at high temperature.
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Escherichia coli grpE gene codes for heat shock protein B25.3 essential for both lambda DNA replication at all temperatures and host growth at high temperature.

机译:大肠杆菌grpE基因编码热激蛋白B25.3这对于在所有温度下λDNA复制和在高温下宿主生长都是必不可少的。

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摘要

We have identified the grpE gene product as the B25.3 heat shock protein of Escherichia coli on the following evidence: (i) a protein similar in size and isoelectric point to B25.3 was induced after infection of UV-irradiated bacteria by lambda grpE+ transducing phage, (ii) mutant phage lambda grpE40, isolated by its inability to propagate on grpE280 bacteria, failed to induce the synthesis of the B25.3 protein, and (iii) lambda grpE+ revertants, derived from phage grpE40 as able to propagate on grpE280 bacteria, simultaneously recovered the ability to induce synthesis of the B25.3 protein. In addition, we show that E. coli bacteria carrying the grpE280 mutation are temperature sensitive for bacterial growth at 43.5 degrees C. Through transductional analysis and temperature reversion experiments, it was demonstrated that the grpE280 mutation is responsible for both the inability of lambda to replicate at any temperature tested and the lack of colony formation at high temperature. At the nonpermissive temperature the rates of synthesis of DNA and RNA were reduced in grpE280 bacteria.
机译:根据以下证据,我们已将grpE基因产物鉴定为大肠杆菌B25.3热休克蛋白:(i)由λgrpE +感染紫外线辐射的细菌后,诱导了大小和等电点与B25.3相似的蛋白质。转导噬菌体,(ii)因无法在grpE280细菌上繁殖而分离的突变型噬菌体λgrpE40,未能诱导B25.3蛋白的合成,以及(iii)源自噬菌体grpE40的λgrpE +回复株能够在grpE280细菌同时恢复了诱导B25.3蛋白合成的能力。此外,我们表明携带grpE280突变的大肠杆菌对43.5摄氏度的细菌生长对温度敏感。通过转导分析和温度回复实验,证明grpE280突变是造成lambda无法复制的原因在任何测试温度下,在高温下缺乏菌落形成。在非许可温度下,grpE280细菌的DNA和RNA合成速率降低。

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