Sato T, Ohki M, Yura T, Ito K
J Bacteriol. 1979 May;138(2):305-13. doi: 10.1128/jb.138.2.305-313.1979.
The mutant divE42(Ts) of Escherichia coli K-12, defective in the synthesis of membrane proteins and in the transcription of the lac operon at high temperature, has been further characterized. It was found that a mutation (divE42) located at about min 22 on the E. coli chromosome map is responsible for the Lac- phenotype and temperature-sensitive growth. The mutation could be contransduced with serC, pyrD, or pyrC by phage P1 at a frequency of 4, 16, or 0.5%, respectively, the gene order being serC-pyrD-ompA-sulA-divE-pyrC. Examination of temperature-independent revertants and Pyr+ transductants revealed that all the mutant phenotypes examined (deficiencies in the increase of activities of some membrane enzymes, expression of the lac operon, and synthesis of several other proteins) are due to a single mutation (divE42) which is recessive to the wild-type (divE+) allele. Protein synthesis in the mutant was also analyzed by dodecyl sulfate-polyacrylamide gel electrophoresis. Synthesis of a number of proteins, including membrane proteins, was found to decrease significantly, whereas that of an elongation factor, EF-Tu, increased upon transfer of a log-phase culture to high temperature (42 degrees C). These effects of temperature shift-up on protein synthesis were evident within 5 min under the conditions used.
对大肠杆菌K-12的突变体divE42(Ts)进行了进一步表征,该突变体在高温下膜蛋白合成以及乳糖操纵子转录方面存在缺陷。研究发现,位于大肠杆菌染色体图谱约22分钟处的一个突变(divE42)导致了Lac-表型和温度敏感型生长。该突变可分别以4%、16%或0.5%的频率被噬菌体P1与serC、pyrD或pyrC共转导,基因顺序为serC-pyrD-ompA-sulA-divE-pyrC。对温度不依赖型回复突变体和Pyr+转导子的检测表明,所检测的所有突变表型(一些膜酶活性增加缺陷、乳糖操纵子表达以及其他几种蛋白质的合成)均归因于单个突变(divE42),该突变相对于野生型(divE+)等位基因是隐性的。还通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析了突变体中的蛋白质合成。发现包括膜蛋白在内的多种蛋白质的合成显著减少,而在对数期培养物转移至高温(42℃)时,延伸因子EF-Tu的合成增加。在所使用的条件下,温度升高对蛋白质合成的这些影响在5分钟内就很明显。