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由MetJ介导的鼠伤寒沙门氏菌metE和metR基因的调控是通过一个共同的操纵子区域实现的。

MetJ-mediated regulation of the Salmonella typhimurium metE and metR genes occurs through a common operator region.

作者信息

Wu W F, Urbanowski M L, Stauffer G V

机构信息

Department of Microbiology, University of Iowa, Iowa City 52242.

出版信息

FEMS Microbiol Lett. 1993 Apr 1;108(2):145-50. doi: 10.1111/j.1574-6968.1993.tb06090.x.

Abstract

In Salmonella typhimurium the metE and metR promoters overlap and are divergently transcribed. Three tandem repeats of an 8 bp sequence defined previously as the metE operator site for MetJ-mediated repression also overlap the -35 region of the metR promoter. Starting with a metE-lacZ.metR-galK double gene fusion, site-directed mutagenesis was used to change nucleotides in each of the repeat units from the consensus sequence. Each mutation, along with the wild-type metE-lacZ.metR-galK gene fusion, was cloned into phage lambda gt2. Regulation of the metE and metR genes was examined by measuring beta-galactosidase and galactokinase levels in Escherichia coli strains lysogenized with phage carrying the wild-type and mutant fusions. Mutations in each of the 8 bp repeat units disrupt MetJ-mediated repression for both the metE-lacZ and metR-galK gene fusions, suggesting that the metE and metR genes share a common operator site for the MetJ repressor.

摘要

在鼠伤寒沙门氏菌中,metE和metR启动子相互重叠且转录方向相反。先前被定义为MetJ介导的阻遏作用的metE操纵位点的一个8 bp序列的三个串联重复序列也与metR启动子的 -35区域重叠。从metE-lacZ.metR-galK双基因融合体开始,使用定点诱变将每个重复单元中的核苷酸从共有序列进行改变。每个突变连同野生型metE-lacZ.metR-galK基因融合体一起被克隆到噬菌体λgt2中。通过测量用携带野生型和突变融合体的噬菌体溶源化的大肠杆菌菌株中的β-半乳糖苷酶和半乳糖激酶水平,来检测metE和metR基因的调控。8 bp重复单元中的每个突变都会破坏MetJ对metE-lacZ和metR-galK基因融合体的介导的阻遏作用,这表明metE和metR基因共享MetJ阻遏物的一个共同操纵位点。

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