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利用转座子诱变技术在大肠杆菌中定义一个rob调控子。

Defining a rob regulon in Escherichia coli by using transposon mutagenesis.

作者信息

Bennik M H, Pomposiello P J, Thorne D F, Demple B

机构信息

Department of Cancer Cell Biology, Harvard School of Public Health, Boston, Massachusetts 02115, USA.

出版信息

J Bacteriol. 2000 Jul;182(13):3794-801. doi: 10.1128/JB.182.13.3794-3801.2000.

Abstract

The Rob protein of Escherichia coli is a member of the AraC-XylS family of prokaryotic transcriptional regulators and is expressed constitutively. Deletion of the rob gene increases susceptibility to organic solvents, while overexpression of Rob increases tolerance to organic solvents and resistance to a variety of antibiotics and to the superoxide-generating compound phenazine methosulfate. To determine whether constitutive levels of Rob regulate basal gene expression, we performed a MudJ transposon screen in a rob deletion mutant containing a plasmid that allows for controlled rob gene expression. We identified eight genes and confirmed that seven are transcriptionally activated by normal expression of Rob from the chromosomal rob gene (inaA, marR, aslB, ybaO, mdlA, yfhD, and ybiS). One gene, galT, was repressed by Rob. We also demonstrated by Northern analysis that basal expression of micF is significantly higher in wild-type E. coli than in a rob deletion mutant. Rob binding to the promoter regions of most of these genes was substantiated in electrophoretic mobility shift assays. However, Mu insertions in individual Rob-regulated genes did not affect solvent sensitivity. This phenotype may depend on changes in the expression of several of these Rob-regulated genes or on other genes that were not identified. Rob clearly affects the basal expression of genes with a broad range of functions, including antibiotic resistance, acid adaptation, carbon metabolism, cell wall synthesis, central intermediary metabolism, and transport. The magnitudes of Rob's effects are modest, however, and the protein may thus play a role as a general transcription cofactor.

摘要

大肠杆菌的Rob蛋白是原核转录调节因子AraC - XylS家族的成员,其表达是组成型的。rob基因的缺失会增加对有机溶剂的敏感性,而Rob的过表达会增加对有机溶剂的耐受性以及对多种抗生素和产生超氧化物的化合物吩嗪硫酸甲酯的抗性。为了确定Rob的组成型水平是否调节基础基因表达,我们在一个rob缺失突变体中进行了MudJ转座子筛选,该突变体含有一个允许控制rob基因表达的质粒。我们鉴定出了8个基因,并证实其中7个基因在染色体rob基因正常表达Rob时被转录激活(inaA、marR、aslB、ybaO、mdlA、yfhD和ybiS)。一个基因galT被Rob抑制。我们还通过Northern分析证明,micF在野生型大肠杆菌中的基础表达明显高于rob缺失突变体。在电泳迁移率变动分析中证实了Rob与这些基因中大多数基因的启动子区域结合。然而,单个Rob调节基因中的Mu插入并不影响溶剂敏感性。这种表型可能取决于这些Rob调节基因中的几个基因的表达变化或未被鉴定的其他基因。Rob明显影响具有广泛功能的基因的基础表达,包括抗生素抗性、酸适应、碳代谢、细胞壁合成、中心中间代谢和转运。然而,Rob的影响程度较小,因此该蛋白可能作为一种一般转录辅因子发挥作用。

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