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BphS是假单胞菌属KKS102中参与多氯联苯/联苯降解的bph基因的关键转录调节因子。

BphS, a key transcriptional regulator of bph genes involved in polychlorinated biphenyl/biphenyl degradation in Pseudomonas sp. KKS102.

作者信息

Ohtsubo Y, Delawary M, Kimbara K, Takagi M, Ohta A, Nagata Y

机构信息

Department of Biotechnology, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.

出版信息

J Biol Chem. 2001 Sep 28;276(39):36146-54. doi: 10.1074/jbc.M100302200. Epub 2001 Jul 17.

Abstract

The bph genes in Pseudomonas sp. KKS102, which are involved in the degradation of polychlorinated biphenyl/biphenyl, are induced in the presence of biphenyl. In this study our goal was to understand the regulatory mechanisms involved in the inducible expression. The bph genes (bphEGF(orf4)A1A2A3BCD(orf1)A4R) constitute an operon, and its expression is strongly dependent on the pE promoter located upstream of the bphE gene. A bphS gene, whose deduced amino acid sequence showed homology with the GntR family transcriptional repressors, was identified at the upstream region of the bphE gene. Disruption of the bphS gene resulted in constitutive expression of bph genes, suggesting that the bphS gene product negatively regulated the pE promoter. The gel retardation and DNase footprinting analyses demonstrated specific binding of BphS to the pE promoter region and identified four BphS binding sites that were located within and immediately downstream of the -10 box of the pE promoter. The four binding sites were functional in repression because their respective elimination resulted in derepression of the pE promoter. The binding of BphS was abolished in the presence of 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid, an intermediate compound in the biphenyl degradation pathway. We concluded that the negative regulator BphS plays a central role in the regulation of bph gene expression through its action at the pE promoter.

摘要

假单胞菌属KKS102中参与多氯联苯/联苯降解的bph基因在联苯存在时被诱导表达。在本研究中,我们的目标是了解诱导表达所涉及的调控机制。bph基因(bphEGF(orf4)A1A2A3BCD(orf1)A4R)构成一个操纵子,其表达强烈依赖于位于bphE基因上游的pE启动子。在bphE基因的上游区域鉴定出一个bphS基因,其推导的氨基酸序列与GntR家族转录阻遏物具有同源性。bphS基因的破坏导致bph基因的组成型表达,这表明bphS基因产物对pE启动子起负调控作用。凝胶阻滞和DNase足迹分析证明BphS与pE启动子区域特异性结合,并鉴定出四个BphS结合位点,它们位于pE启动子-10框内及紧邻其下游。这四个结合位点在阻遏中起作用,因为它们各自的缺失导致pE启动子的去阻遏。在联苯降解途径的中间化合物2-羟基-6-氧代-6-苯基己-2,4-二烯酸存在时,BphS的结合被消除。我们得出结论,负调控因子BphS通过其在pE启动子上的作用在bph基因表达调控中起核心作用。

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