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控制pVI150上源自假单胞菌的(甲基)苯酚dmp操纵子的σ54依赖性Po启动子的生长阶段依赖性转录。

Growth phase-dependent transcription of the sigma(54)-dependent Po promoter controlling the Pseudomonas-derived (methyl)phenol dmp operon of pVI150.

作者信息

Sze C C, Moore T, Shingler V

机构信息

Department of Cell and Molecular Biology, Umeå University, Sweden.

出版信息

J Bacteriol. 1996 Jul;178(13):3727-35. doi: 10.1128/jb.178.13.3727-3735.1996.

DOI:10.1128/jb.178.13.3727-3735.1996
PMID:8682773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC232629/
Abstract

Transcription from Pseudomonas-derived -24, -12 Po promoter of the pVI150-encoded dmp operon is mediated by the sigma 54-dependent DmpR activator in response to the presence of aromatic pathway substrates in the medium. However, global regulatory mechanisms are superimposed on this regulatory system so that the specific response to aromatic effectors is absent in cultures until the stationary phase is reached. Here we genetically dissect the system to show that the growth phase response is faithfully mimicked by a minimal system composed of the dmpR regulatory gene and the Po promoter regulatory region and can be reproduced in heterologous Escherichia coli. Using this system, we show that the growth phase-dependent DmpR-mediated response to aromatic compounds is limited to fast-growing cultures. Thus, during exponential growth of cultures in minimal media containing different carbon sources, the response to aromatics is immediate, while the response is suppressed in cultures grown on rich media until the exponential-to-stationary phase transition. Elements known to be involved in the DmpR-mediated transcription from Po were analyzed for the ability to influence the growth phase response. Most dramatically, overexpression of DmpR was shown to completely abolish the growth phase response, suggesting that a negatively acting factor may mediate this level of regulation. The possible mechanism of action and integration (of the specific regulation of the dmp operon-encoded catabolic enzymes with the physiological status of the bacteria are discussed.

摘要

假单胞菌来源的pVI150编码的dmp操纵子的-24、-12 Po启动子的转录由依赖σ54的DmpR激活剂介导,以响应培养基中芳香族途径底物的存在。然而,全局调控机制叠加在这个调控系统上,以至于在达到稳定期之前,培养物中对芳香族效应物的特异性反应不存在。在这里,我们通过基因分析该系统,以表明由dmpR调控基因和Po启动子调控区域组成的最小系统能如实地模拟生长阶段反应,并且可以在异源大肠杆菌中重现。使用这个系统,我们表明生长阶段依赖的DmpR介导的对芳香族化合物的反应仅限于快速生长的培养物。因此,在含有不同碳源的基本培养基中培养物指数生长期间,对芳香族化合物的反应是即时的,而在丰富培养基上生长的培养物中,该反应在指数期到稳定期转变之前被抑制。分析了已知参与Po的DmpR介导转录的元件影响生长阶段反应的能力。最显著的是,DmpR的过表达被证明完全消除了生长阶段反应,这表明一个负向作用因子可能介导了这种调控水平。讨论了dmp操纵子编码的分解代谢酶的特异性调控与细菌生理状态的可能作用机制和整合。

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