首页> 外文期刊>Applied Microbiology >The Operon Encoding Hydrolytic Dehalogenation of 4-Chlorobenzoate Is Transcriptionally Regulated by the TetR-Type Repressor FcbR and Its Ligand 4-Chlorobenzoyl Coenzyme A
【24h】

The Operon Encoding Hydrolytic Dehalogenation of 4-Chlorobenzoate Is Transcriptionally Regulated by the TetR-Type Repressor FcbR and Its Ligand 4-Chlorobenzoyl Coenzyme A

机译:编码4-氯苯甲酸盐的水解脱卤素的操纵子通过TETR型抑制剂FCBR及其配体4-氯苯酰基辅酶A转录调节

获取原文
           

摘要

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 fcbBAT1T2T3C operon and inducibly expressed in response to 4CBA. However, the associated molecular mechanism remains unknown. In this study, a gene ( fcbR ) adjacent to the fcb operon was predicted to encode a TetR-type transcriptional regulator in Comamonas sediminis strain CD-2. The fcbR knockout strain exhibited constitutive expression of the fcb cluster. In the host Escherichia coli , the expression of the P_(fcb) -fused green fluorescent protein ( gfp ) reporter was repressed by the introduction of the fcbR 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 P_(fcb) DNA probe in vitro , and the metabolite 4-chlorobenzyl-CoA (4CBA-CoA) prevented FcbR binding to the P _(fcb) 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 P_(fcb) and was proposed to prevent the binding of RNA polymerase. This study characterizes a transcriptional repressor of the fcb operon, together with its ligand, thus identifying halogenated benzoyl-CoA as belonging to the class of ligands of transcriptional regulators.IMPORTANCE 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.
机译:4-氯苯甲酸盐(4CBA)的细菌水解脱卤是一种辅酶A(COA) - 术 - 型分解代谢途径,其通常是氯化芳族化合物的微生物矿化的常见部分。先前的研究表明,4CBA的传输和脱卤素通常以FCBBAT1T2T3C操纵子聚集,并响应于4CBA诱导表达。然而,相关的分子机制仍然未知。在该研究中,预计与FCB操纵子相邻的基因(FCBR)在Comamonas Sediminis菌株CD-2中编码四型转录调节剂。 FCBR敲除应变表现出FCB簇的组成型表达。在宿主大肠杆菌中,通过引入FCBR基因来抑制P_(FCB)的绿色荧光蛋白(GFP)记者的表达,并结合各种分解代谢基因的遗传研究表明FCBR的配体可能是中间体代谢物。纯化的FCBR可以在体外结合P_(FCB)DNA探针,并且代谢物4-氯苄基-COA(4CBA-COA)防止FCBR与P _(FCB)DNA探针结合。等温滴定热量法(ITC)测量表明,4CBA-CoA可以以1:1摩尔比结合FCBR。 DNase I脚印显示FCBR保护42-BP DNA基序(5'- GGAAATCAATAGGTCCATAGAAAATCTATTADAATCGAAT -3'),其由含有四个假盲常青序列(5'-TCNATGA-3')的两种序列重复组成。该绑定基序与α35盒P_(FCB)重叠,并提出了防止RNA聚合酶的结合。该研究表征了FCB操纵子的转录压缩机,以及其配体,从而鉴定卤代苯甲酰-CoA,如属转录调节剂的配体类别。重量分析4CBA的细菌水解除去是一种特殊的CoA活化型分解代谢途径这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水解除去型术的转录阻遏物及其同源效应。该工作将卤代苯甲酰基-CoA延伸为CoA衍生的效应化合物的新成员,其介导转录调节剂的变构调节。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号