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恶臭假单胞菌中groESL操纵子的扩增增加了铁载体基因启动子的活性。

Amplification of the groESL operon in Pseudomonas putida increases siderophore gene promoter activity.

作者信息

Venturi V, Wolfs K, Leong J, Weisbeek P J

机构信息

Department of Molecular Cell Biology, University of Utrecht, The Netherlands.

出版信息

Mol Gen Genet. 1994 Oct 17;245(1):126-32. doi: 10.1007/BF00279758.

Abstract

Pseudobactin 358 is the yellow-green fluorescent siderophore [microbial iron(III) transport agent] produced by Pseudomonas putida WCS358 under iron-limiting conditions. The genes encoding pseudobactin 358 biosynthesis are iron-regulated at the level of transcription. In this study, the molecular characterization is reported of a cosmid clone of WCS358 DNA that can stimulate, in an iron-dependent manner, the activity of a WCS358 siderophore gene promoter in the heterologous Pseudomonas strain A225. The functional region in the clone was identified by subcloning, transposon mutagenesis and DNA sequencing as the groESL operon of strain WCS358. This increase in promoter activity was not observed when the groESL genes of strain WCS358 were integrated via a transposon vector into the genome of Pseudomonas A225, indicating that multiple copies of the operon are necessary for the increase in siderophore gene promoter activity. Amplification of the Escherichia coli and WCS358 groESL genes also increased iron-regulated promoter activity in the parent strain WCS358. The groESL operon codes for the chaperone proteins GroES and GroEL, which are responsible for mediating the folding and assembly of many proteins.

摘要

假单胞菌素358是恶臭假单胞菌WCS358在铁限制条件下产生的黄绿荧光铁载体[微生物铁(III)转运剂]。编码假单胞菌素358生物合成的基因在转录水平上受到铁的调控。在本研究中,报道了WCS358 DNA的一个黏粒克隆的分子特征,该克隆能以铁依赖的方式刺激异源假单胞菌菌株A225中WCS358铁载体基因启动子的活性。通过亚克隆、转座子诱变和DNA测序鉴定出该克隆中的功能区域为菌株WCS358的groESL操纵子。当WCS358菌株的groESL基因通过转座子载体整合到假单胞菌A225的基因组中时,未观察到启动子活性的增加,这表明该操纵子的多个拷贝对于铁载体基因启动子活性的增加是必需的。大肠杆菌和WCS358的groESL基因的扩增也增加了亲本菌株WCS358中铁调节启动子的活性。groESL操纵子编码伴侣蛋白GroES和GroEL,它们负责介导许多蛋白质的折叠和组装。

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