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从伯氏疏螺旋体中分离dnaJ、dnaK和grpE同源物并对大肠杆菌突变体进行互补作用

Isolation of dnaJ, dnaK, and grpE homologues from Borrelia burgdorferi and complementation of Escherichia coli mutants.

作者信息

Tilly K, Hauser R, Campbell J, Ostheimer G J

机构信息

Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana 59840.

出版信息

Mol Microbiol. 1993 Feb;7(3):359-69. doi: 10.1111/j.1365-2958.1993.tb01128.x.

Abstract

The heat-shock proteins DnaJ, DnaK, and GrpE are involved in the replication of various species of DNA in Escherichia coli, in addition to their roles in other processes, including protein disaggregation and export. We have cloned the Borrelia burgdorferi homologues of these genes. DNA sequence analysis revealed an open reading frame encoding a protein that is 62% identical to the E. coli DnaK protein. Genes homologous to the E. coli grpE and dnaJ genes, encoding products 28% and 39% identical to their homologues, are located up- and downstream, respectively, of the B. burgdorferi dnaK gene. No obvious promoters were detected in the sequenced DNA, although a potential transcription terminator was found downstream of the dnaJ gene, so these three genes may form an operon, perhaps with a fourth gene located upstream of the grpE gene. The grpE homologue complemented an E. coli grpE mutant and the dnaJ homologue complemented an E. coli dnaJ mutant, whereas the B. burgdorferi dnaK gene did not complement dnaK mutants.

摘要

热休克蛋白DnaJ、DnaK和GrpE除了在包括蛋白质解聚和输出等其他过程中发挥作用外,还参与大肠杆菌中各种DNA的复制。我们已经克隆了这些基因的伯氏疏螺旋体同源物。DNA序列分析揭示了一个编码与大肠杆菌DnaK蛋白有62%同一性的蛋白质的开放阅读框。与大肠杆菌grpE和dnaJ基因同源的基因,其编码产物与其同源物分别有28%和39%的同一性,它们分别位于伯氏疏螺旋体dnaK基因的上游和下游。在测序的DNA中未检测到明显的启动子,尽管在dnaJ基因下游发现了一个潜在的转录终止子,因此这三个基因可能形成一个操纵子,也许还有一个位于grpE基因上游的第四个基因。grpE同源物补充了大肠杆菌grpE突变体,dnaJ同源物补充了大肠杆菌dnaJ突变体,而伯氏疏螺旋体dnaK基因不能补充dnaK突变体。

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