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荧光假单胞菌2P24中sigma因子RpoS和GacS/GacA双组分调控系统对PcoI/PcoR群体感应系统的差异调控

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.

作者信息

Yan Qing, Wu Xiao-Gang, Wei Hai-Lei, Wang Hui-Min, Zhang Li-Qun

机构信息

Department of Plant Pathology, China Agricultural University, Beijing 100094, China.

出版信息

Microbiol Res. 2009;164(1):18-26. doi: 10.1016/j.micres.2008.02.001. Epub 2008 Apr 18.

Abstract

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 pcoIColon, two colonslacZ 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(-) or gacS(-) 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.

摘要

群体感应(QS)位点PcoI/PcoR先前已在生防细菌荧光假单胞菌2P24中被鉴定出来。在本文中,我们使用染色体pcoI::lacZ融合报告菌株,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。利用随机mini-Tn5突变程序,静止期σ因子RpoS被鉴定为QS系统的负调控因子。此外,缺失诱变和互补实验表明,双组分系统GacS/GacA通过上调pcoI转录正向调控QS系统。然而,与gacA或gacS突变体相比,在gacA(-)或gacS(-)背景中引入rpoS的第二个突变并没有导致pcoI基因转录表达或AHL合成的进一步变化。我们的结果表明,在2P24菌株中,RpoS只能在功能性GacS/GacA系统背景下对pcoI基因发挥其负调控作用。

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