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Regulation of the PcoI/PcoR quorum-sensing system in Pseudomonas fluorescens 2P24 by the PhoP/PhoQ two-component system

机译:通过PHOP / PHOQ双组分系统对荧光荧光荧光荧光笔2P24中的PCoI / PCOR频率传感系统的调节

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A quorum-sensing locus, pcoI/pcoR, which is involved in the regulation of root colonization and plant disease-suppressive ability, was previously identified in Pseudomonas fluorescens 2P24. In this study, we performed random mutagenesis using mini-Tn5 in order to screen the upstream transcriptional regulators of pcoI, a biosynthase gene responsible for the synthesis of N-acylhomoserine lactone signal molecules. Two mutants, PM400 and PM410, with elevated pcoI gene promoter activity, were identified from ~10?000 insertion clones. The amino acid sequences of the interrupted genes in these two mutants were highly similar to PhoQ, a sensor protein of the two-component regulatory system PhoP/PhoQ, which responds to environmental Mg2+ starvation and regulates virulence in Salmonella typhimurium and antimicrobial peptide resistance in Pseudomonas aeruginosa. The promoter activity of pcoI was also induced under low-Mg2+ conditions in the 2P24 strain of P. fluorescens. Deletion mutagenesis and complementation experiments demonstrated that the transcription of pcoI was negatively regulated by the sensor PhoQ but positively regulated by the response regulator PhoP. Genetic evidence also indicated that transcription of the outer-membrane protein gene oprH was induced by Mg2+ starvation through regulation of the wild-type PhoP/PhoQ system. Additionally, PhoQ was involved in biofilm formation by 2P24 under low-Mg2+ conditions through a PhoP-independent pathway.
机译:在假单胞菌2p24中鉴定了批量传感基因座,涉及根部定植和植物抑制能力的调节和植物抑制能力的基因座。在这项研究中,我们使用Mini-TN5进行随机诱变,以筛选PCOI的上游转录调节剂,该研究负责合成N-酰基骨内酯内酯的内酯分子的生物合成酶基因。从〜10 000个插入克隆鉴定出具有升高的PCOI基因启动子活性的两个突变体PM400和PM410。这两个突变体中断基因的氨基酸序列与phoq,双组分调节系统phop / phopq的传感器蛋白质高度相似,这对环境Mg2 +饥饿并调节了沙门氏菌的血硫脲和抗微生物肽抗性的毒力铜绿假单胞菌。在P.荧光的2P24菌株的低Mg2 +条件下也诱导了PCOI的启动子活性。缺失诱变和互补实验表明,PCOI的转录被传感器Phoq对响应调节率阳性调节负调节。遗传证据还表明,通过调节野生型PHOP系统,通过Mg2 +饥饿诱导外膜蛋白基因OPRH的转录。另外,通过与不同的途径途径,在低Mg2 +条件下通过2p24参与Biofilm形成。

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