Key Laboratory of Microbiological Engineering of Agricultural Environment, Ministry of Agriculture, College of Life Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, China.
Key Laboratory of Microbiological Engineering of Agricultural Environment, Ministry of Agriculture, College of Life Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, China
Appl Environ Microbiol. 2021 Feb 26;87(6). doi: 10.1128/AEM.02652-20.
The bacterial hydrolytic dehalogenation of 4-chlorobenzoate (4CBA) is a coenzyme A (CoA)-activation-type catabolic pathway that is usually a common part of the microbial mineralization of chlorinated aromatic compounds. Previous studies have shown that the transport and dehalogenation genes for 4CBA are typically clustered as an operon and inducibly expressed in response to 4CBA. However, the associated molecular mechanism remains unknown. In this study, a gene () adjacent to the operon was predicted to encode a TetR-type transcriptional regulator in strain CD-2. The knockout strain exhibited constitutive expression of the cluster. In the host , the expression of the -fused green fluorescent protein () reporter was repressed by the introduction of the gene, and genetic studies combining various catabolic genes suggest that the ligand for FcbR may be an intermediate metabolite. Purified FcbR could bind to the DNA probe , and the metabolite 4-chlorobenzyl-CoA (4CBA-CoA) prevented FcbR binding to the P DNA probe. Isothermal titration calorimetry (ITC) measurements showed that 4CBA-CoA could bind to FcbR at a 1:1 molar ratio. DNase I footprinting showed that FcbR protected a 42-bp DNA motif (5'-GGAAATCAATAGGTCCATAGAAAATCTATTGACTAATCGAAT-3') that consists of two sequence repeats containing four pseudopalindromic sequences (5'-TCNATNGA-3'). This binding motif overlaps with the -35 box of and was proposed to prevent the binding of RNA polymerase. This study characterizes a transcriptional repressor of the operon, together with its ligand, thus identifying halogenated benzoyl-CoA as belonging to the class of ligands of transcriptional regulators. The bacterial hydrolytic dehalogenation of 4CBA is a special CoA-activation-type catabolic pathway that plays an important role in the biodegradation of polychlorinated biphenyls and some herbicides. With genetic and biochemical approaches, the present study identified the transcriptional repressor and its cognate effector of a 4CBA hydrolytic dehalogenation operon. This work extends halogenated benzoyl-CoA as a new member of CoA-derived effector compounds that mediate allosteric regulation of transcriptional regulators.
4-氯苯甲酸(4CBA)的细菌水解脱卤是一种辅酶 A(CoA)激活型分解代谢途径,通常是氯化芳香族化合物微生物矿化的常见部分。先前的研究表明,4CBA 的运输和脱卤基因通常作为一个操纵子聚类,并对 4CBA 表现出诱导表达。然而,相关的分子机制仍然未知。在这项研究中,预测菌株 CD-2 中 操纵子旁的一个基因编码一种 TetR 型转录调节因子。 基因缺失株表现出 操纵子簇的组成型表达。在宿主中,引入 基因抑制了 -融合绿色荧光蛋白()报告基因的表达,结合各种分解代谢基因的遗传研究表明,FcbR 的配体可能是一种中间代谢物。纯化的 FcbR 可以与 DNA 探针结合,而代谢物 4-氯苯甲酰辅酶 A(4CBA-CoA)可阻止 FcbR 与 P DNA 探针结合。等温滴定量热法(ITC)测量表明,4CBA-CoA 可以以 1:1 摩尔比与 FcbR 结合。DNase I 足迹实验表明,FcbR 保护一个由 42 个碱基对组成的 DNA 基序(5'-GGAAATCAATAGGTCCATAGAAAATCTATTGACTAATCGAAT-3'),该基序由两个包含四个伪回文序列(5'-TCNATNGA-3')的序列重复组成。这个结合基序与 的-35 框重叠,并被提议阻止 RNA 聚合酶的结合。本研究描述了 操纵子的转录抑制剂及其配体,从而确定卤化苯甲酰辅酶 A 属于转录调节因子配体的一类。4CBA 的细菌水解脱卤是一种特殊的 CoA 激活型分解代谢途径,在多氯联苯和一些除草剂的生物降解中起着重要作用。通过遗传和生化方法,本研究确定了 4CBA 水解脱卤操纵子的转录抑制剂及其同源效应物。这项工作将卤化苯甲酰辅酶 A 扩展为一种新的 CoA 衍生效应化合物,该化合物介导转录调节因子的变构调节。