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首页> 外文期刊>Journal of Pure & Applied Microbiology >OmpR Regulates the Intracellular Concentration of 2,4-Diacetylphloroglucinol by Affecting the Transcriptional Activity of the Hydrolase phIG in Pseudomonas fluorescens 2P24
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OmpR Regulates the Intracellular Concentration of 2,4-Diacetylphloroglucinol by Affecting the Transcriptional Activity of the Hydrolase phIG in Pseudomonas fluorescens 2P24

机译:OmpR通过影响荧光假单胞菌2P24中水解酶phIG的转录活性来调节2,4-二乙酰基间苯三酚的细胞内浓度。

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摘要

The broad-spectrum polyketide antibiotic 2,4-diacetylphloroglucinol (2,4-DAPG) is a major determinant of the ability of the biocontrol agent Pseudomonas fluorescens 2P24 to exert its suppressive activities towards a variety of soil-borne plant pathogens. Previously, we demonstrated that dysfunction of the transcriptional regulator OmpR of the two-component regulatory system EnvZ/OmpR resulted in elevated 2,4-DAPG production in P. fluorescens 2P24. Herein, we provide evidence that OmpR might regulatethe transcriptional activity of the hydrolase phlG to influence the intracellular concentrations of 2,4-DAPG. The OmpR deletion mutant PM1102 showed increased transcriptional activity (60%) at the promoter of the phlACBD locus and elevated intracellularconcentrations (two-fold) of 2,4-DAPG. A subsequent promoter assay for phIH in PM1102 and for phIG in PM1103 [phlH] showed a negative regulatory relationship for ompR on phIH and for phIH on phlG. Additionally, we used EMSA to establish the direct binding of OmpR to the ompR promoter region and the indirect regulatory relationship of OmpR on phlACBD and phIH transcription. Based on these findings, we propose that OmpR influences the intracellular concentrations of 2,4-DAPG by regulating the transcriptional activity of the hydrolase phIG in P. fluorescens 2P24.
机译:广谱聚酮化合物抗生素2,4-二乙酰基间苯三酚(2,4-DAPG)是生物防治剂荧光假单胞菌2P24对多种土壤传播的植物病原体发挥抑制作用的能力的主要决定因素。以前,我们证明了两组分调节系统EnvZ / OmpR的转录调节子OmpR的功能障碍导致荧光假单胞菌2P24中2,4-DAPG的产生升高。在这里,我们提供的证据表明,OmpR可能调节水解酶phlG的转录活性,从而影响细胞内2,4-DAPG的浓度。 OmpR缺失突变体PM1102在phlACBD位点的启动子处显示出增加的转录活性(60%),并提高了2,4-DAPG的细胞内浓度(两倍)。随后对PM1102中的phIH和PM1103中的phIG [phlH]的启动子分析显示,phIH上的ompR和phlG上的phIH具有负调控关系。此外,我们使用EMSA建立了OmpR与ompR启动子区域的直接结合以及OmpR对phlACBD和phIH转录的间接调节关系。基于这些发现,我们建议OmpR通过调节荧光酶2P24中水解酶phIG的转录活性来影响2,4-DAPG的细胞内浓度。

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