Juárez Javier F, Liu Huixiang, Zamarro María T, McMahon Stephen, Liu Huanting, Naismith James H, Eberlein Christian, Boll Matthias, Carmona Manuel, Díaz Eduardo
From the Department of Environmental Biology, Centro de Investigaciones Biológicas-Consejo Superior de Investigaciones Científicas, Ramiro de Maeztu 9, 28040 Madrid, Spain.
the Biomedical Sciences Research Complex, University of St. Andrews, North Haugh, St. Andrews KY16 9ST, Scotland, United Kingdom, and.
J Biol Chem. 2015 May 8;290(19):12165-83. doi: 10.1074/jbc.M115.637074. Epub 2015 Mar 20.
The mbd cluster encodes the anaerobic degradation of 3-methylbenzoate in the β-proteobacterium Azoarcus sp. CIB. The specific transcriptional regulation circuit that controls the expression of the mbd genes was investigated. The PO, PB 1, and P3 R promoters responsible for the expression of the mbd genes, their cognate MbdR transcriptional repressor, as well as the MbdR operator regions (ATACN10GTAT) have been characterized. The three-dimensional structure of MbdR has been solved revealing a conformation similar to that of other TetR family transcriptional regulators. The first intermediate of the catabolic pathway, i.e. 3-methylbenzoyl-CoA, was shown to act as the inducer molecule. An additional MbdR-dependent promoter, PA, which contributes to the expression of the CoA ligase that activates 3-methylbenzoate to 3-methylbenzoyl-CoA, was shown to be necessary for an efficient induction of the mbd genes. Our results suggest that the mbd cluster recruited a regulatory system based on the MbdR regulator and its target promoters to evolve a distinct central catabolic pathway that is only expressed for the anaerobic degradation of aromatic compounds that generate 3-methylbenzoyl-CoA as the central metabolite. All these results highlight the importance of the regulatory systems in the evolution and adaptation of bacteria to the anaerobic degradation of aromatic compounds.
mbd基因簇编码β-变形菌偶氮螺菌属(Azoarcus sp.)CIB菌株中3-甲基苯甲酸的厌氧降解过程。研究了控制mbd基因表达的特定转录调控回路。已对负责mbd基因表达的PO、PB 1和P3 R启动子、它们对应的MbdR转录阻遏物以及MbdR操纵子区域(ATACN10GTAT)进行了表征。已解析出MbdR的三维结构,显示其构象与其他TetR家族转录调节因子的构象相似。分解代谢途径的第一个中间产物,即3-甲基苯甲酰辅酶A,被证明可作为诱导分子。另一个依赖MbdR的启动子PA,它有助于激活3-甲基苯甲酸生成3-甲基苯甲酰辅酶A的辅酶A连接酶的表达,被证明是有效诱导mbd基因所必需的。我们的结果表明,mbd基因簇募集了一个基于MbdR调节因子及其靶启动子的调控系统,以进化出一条独特的中心分解代谢途径,该途径仅在厌氧降解产生3-甲基苯甲酰辅酶A作为中心代谢物的芳香化合物时表达。所有这些结果都突出了调控系统在细菌进化和适应芳香化合物厌氧降解过程中的重要性。