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荧光假单胞菌M114中假铁载体M114对铁摄取基因的调控:pbrA σ因子基因不介导铁载体调控反应。

Regulation of the iron uptake genes in Pseudomonas fluorescens M114 by pseudobactin M114: the pbrA sigma factor gene does not mediate the siderophore regulatory response.

作者信息

Callanan M, Sexton R, Dowling D N, O'Gara F

机构信息

Department of Microbiology, University College Cork, Ireland.

出版信息

FEMS Microbiol Lett. 1996 Oct 15;144(1):61-6. doi: 10.1111/j.1574-6968.1996.tb08509.x.

Abstract

The iron-regulated PbrA sigma factor dictates the production of the siderophore, pseudobactin M114, and its cognate outer membrane receptor, PbuA, in Pseudomonas fluorescens M114. However, the siderophore molecule also has a role in regulating the expression of the siderophore biosynthetic and siderophore receptor genes in P. fluorescens M114. This is based on the fact that beta-galactosidase levels from lacZ fusions of M114 siderophore promoters (biosynthetic and receptor) were reduced in M114 siderophore biosynthetic mutants compared to wild-type M114. Expression of both promoters was increased by the addition of pseudobactin M114 to the growth medium. This effect was widespread and applicable to all but one of the siderophore negative strains of M114 tested. Furthermore, it was demonstrated that transcription of the pbr A sigma factor gene was not reduced in the siderophore biosynthetic mutants. This excludes the possibility that reduced expression of the siderophore biosynthetic and receptor promoters in the siderophore biosynthetic mutants is mediated at the level of expression of the pbr A gene itself. In addition, it was noted that the siderophore regulated response was applicable to promoters with and without the DNA sequence motif, (G/C)CTAAATCCC, which is required for iron-regulated expression of some pseudomonad promoters.

摘要

铁调节的PbrAσ因子决定了荧光假单胞菌M114中铁载体假单胞菌素M114及其同源外膜受体PbuA的产生。然而,该铁载体分子在调节荧光假单胞菌M114中铁载体生物合成基因和铁载体受体基因的表达方面也发挥作用。这是基于以下事实:与野生型M114相比,M114铁载体生物合成突变体中M114铁载体启动子(生物合成和受体)的lacZ融合体的β-半乳糖苷酶水平降低。向生长培养基中添加假单胞菌素M114可增加两个启动子的表达。这种效应具有普遍性,适用于除一个测试的M114铁载体阴性菌株外的所有菌株。此外,还证明了在铁载体生物合成突变体中pbr Aσ因子基因的转录并未减少。这排除了铁载体生物合成突变体中铁载体生物合成启动子和受体启动子表达降低是由pbr A基因本身表达水平介导的可能性。此外,还注意到铁载体调节反应适用于具有和不具有DNA序列基序(G/C)CTAAATCCC的启动子,该基序是一些假单胞菌启动子铁调节表达所必需的。

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