Ang D, Chandrasekhar G N, Zylicz M, Georgopoulos C
J Bacteriol. 1986 Jul;167(1):25-9. doi: 10.1128/jb.167.1.25-29.1986.
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.
基于以下证据,我们已确定grpE基因产物为大肠杆菌的B25.3热休克蛋白:(i)用λgrpE +转导噬菌体感染紫外线照射过的细菌后,诱导出一种大小和等电点与B25.3相似的蛋白质;(ii)通过其在grpE280细菌上无法繁殖而分离出的突变噬菌体λgrpE40,未能诱导B25.3蛋白的合成;(iii)从噬菌体grpE40衍生而来、能够在grpE280细菌上繁殖的λgrpE +回复体,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突变的大肠杆菌在43.5℃下对细菌生长具有温度敏感性。通过转导分析和温度回复实验,证明grpE280突变既导致λ在任何测试温度下都无法复制,也导致在高温下无法形成菌落。在非允许温度下,grpE280细菌中DNA和RNA的合成速率降低。