School of Biotechnology and Biomolecular Sciences , University of New South Wales , Sydney , New South Wales 2052 , Australia.
Manchester Institute of Biotechnology , University of Manchester , Manchester M1 7 DN , United Kingdom.
ACS Chem Biol. 2018 Mar 16;13(3):548-552. doi: 10.1021/acschembio.7b00846. Epub 2018 Jan 25.
Reductive dehalogenases (RDases) are key enzymes involved in the respiratory process of anaerobic organohalide respiring bacteria (ORB). Heterologous expression of respiratory RDases is desirable for structural and functional studies; however, there are few reports of successful expression of these enzymes. Dehalobacter sp. strain UNSWDHB is an ORB, whose preferred electron acceptor is chloroform. This study describes efforts to express recombinant reductive dehalogenase (TmrA), derived from UNSW DHB, using the heterologous hosts Escherichia coli and Bacillus megaterium. Here, we report the recombinant expression of soluble and functional TmrA, using B. megaterium as an expression host under a xylose-inducible promoter. Successful incorporation of iron-sulfur clusters and a corrinoid cofactor was demonstrated using UV-vis spectroscopic analyses. In vitro dehalogenation of chloroform using purified recombinant TmrA was demonstrated. This is the first known report of heterologous expression and purification of a respiratory reductive dehalogenase from an obligate organohalide respiring bacterium.
还原脱卤酶(RDases)是参与厌氧有机卤代呼吸细菌(ORB)呼吸过程的关键酶。呼吸 RDases 的异源表达对于结构和功能研究是理想的;然而,成功表达这些酶的报道很少。Dehalobacter sp. strain UNSWDHB 是一种 ORB,其首选电子受体是三氯甲烷。本研究描述了使用异源宿主大肠杆菌和巨大芽孢杆菌表达来自 UNSW DHB 的重组还原脱卤酶(TmrA)的努力。在这里,我们报告了使用巨大芽孢杆菌作为表达宿主,在木糖诱导型启动子下表达可溶性和功能性 TmrA 的情况。使用紫外可见光谱分析证明了铁硫簇和类咕啉辅因子的成功掺入。使用纯化的重组 TmrA 进行了三氯甲烷的体外脱卤反应。这是首例已知的从需有机卤代物呼吸细菌中异源表达和纯化呼吸还原脱卤酶的报道。