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首页> 外文期刊>Microbiological Research >Differential control of the PcoI/PcoR quorum-sensing system in Pseudomonas fluorescens 2P24 by sigma factor RpoS and the GacS/GacA two-component regulatory system
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Differential control of the PcoI/PcoR quorum-sensing system in Pseudomonas fluorescens 2P24 by sigma factor RpoS and the GacS/GacA two-component regulatory system

机译:σ因子RpoS和GacS / GacA两组分调节系统对荧光假单胞菌2P24中PcoI / PcoR群体感应系统的差异控制

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摘要

A quorum-sensing (QS) locus PcoI/PcoR had been identified previously in the biological control bacterium Pseudomonas fluorescens 2P24. In this paper, we investigated the upstream regulators that influence the transcription of the N-acyl homoserine lactone (AHL) biosynthase gene pcoI using a chromosomal pcoI approximately equal to lacZ fusion reporter strain. Stationary sigma factor RpoS was identified as a negative regulator of QS system using a random mini-Tn5 mutant procedure. Furthermore, deletion mutagenesis and complementation experiments demonstrated that the two-component system GacS/GacA positively regulated the QS system by upregulating pcoI transcription. However, compared with the gacA or gacS mutant, introduction of a second mutation of rpoS in the gacA super(-) or gacS super(-) background did not lead to further change in the transcriptional expression of the pcoI gene or the synthesis of AHL. Our results suggest that in strain 2P24, RpoS could only play its negative regulatory role on the pcoI gene under a functional GacS/GacA system background.
机译:先前已在生物控制细菌荧光假单胞菌2P24中确定了群体感应(QS)基因座PcoI / PcoR。在本文中,我们使用大约等于lacZ融合报告基因株的染色体pcoI,研究了影响N-酰基高丝氨酸内酯(AHL)生物合成酶基因pcoI转录的上游调控因子。使用随机mini-Tn5突变程序将固定的Sigma因子RpoS鉴定为QS系统的负调节剂。此外,缺失诱变和互补实验表明,两组分系统GacS / GacA通过上调pcoI转录而积极调节QS系统。但是,与gacA或gacS突变体相比,在gacA super(-)或gacS super(-)背景中引入rpoS的第二个突变不会导致pcoI基因的转录表达或AHL合成的进一步改变。我们的结果表明,在功能性GacS / GacA系统背景下,RpoS在2P24菌株中只能对pcoI基因发挥负调控作用。

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