Key Laboratory of Agricultural Environmental Microbiology, Ministry of Agriculture, College of Life Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, China.
School of Life Science and Technology, Nanyang Normal University, Nanyang, Henan, China.
Appl Environ Microbiol. 2018 Aug 17;84(17). doi: 10.1128/AEM.00623-18. Print 2018 Sep 1.
The herbicide dicamba is initially demethylated to 3,6-dichlorosalicylate (3,6-DCSA) in Ndbn-20 and is subsequently 5-hydroxylated to 3,6-dichlorogentisate (3,6-DCGA). In the present study, two glutathione-dependent 3,6-DCGA dehalogenases, DsmH1 and DsmH2, were identified in strain Ndbn-20. DsmH2 shared a low identity (only 31%) with the tetrachlorohydroquinone (TCHQ) dehalogenase PcpC from ATCC 39723, while DsmH1 shared a high identity (79%) with PcpC. In the phylogenetic tree of related glutathione -transferases (GSTs), DsmH1 and DsmH2, together with PcpC and the 2,5-dichlorohydroquinone dehalogenase LinD, formed a separate clade. DsmH1 and DsmH2 were synthesized in BL21 and purified as His-tagged enzymes. Both enzymes required glutathione (GSH) as a cofactor and could 6-dechlorinate 3,6-DCGA to 3-chlorogentisate DsmH2 had a significantly higher catalytic efficiency toward 3,6-DCGA than DsmH1. Transcription and disruption analysis revealed that DsmH2 but not DsmH1 was responsible for the 6-dechlorination of 3,6-DCGA in strain Ndbn-20 Furthermore, we propose a novel eta class of GSTs to accommodate the four bacterial dehalogenases PcpC, LinD, DsmH1, and DsmH2. Dicamba is an important herbicide, and its use and leakage into the environment have dramatically increased since the large-scale planting of genetically modified (GM) dicamba-resistant crops in 2015. However, the complete catabolic pathway of dicamba has remained unknown, which limits ecotoxicological studies of this herbicide. Our previous study revealed that 3,6-DCGA was an intermediate of dicamba degradation in strain Ndbn-20. In this study, we identified two glutathione-dependent 3,6-DCGA dehalogenases, DsmH1 and DsmH2, and demonstrated that DsmH2 is physiologically responsible for the 6-dechlorination of 3,6-DCGA in strain Ndbn-20. GSTs play an important role in the detoxification and degradation of a variety of endogenous and exogenous toxic compounds. On the basis of their sequence identities, phylogenetic status, and functions, the four bacterial GSH-dependent dehalogenases (PcpC, LinD, DsmH1, and DsmH2) were reclassified as a new eta class of GSTs. This study helps us to elucidate the microbial catabolism of dicamba and enhances our understanding of the diversity and functions of GSTs.
该除草剂二甲苯草胺最初在 Ndbn-20 中被去甲基化为 3,6-二氯邻苯二甲酸(3,6-DCSA),随后被 5-羟化为 3,6-二氯龙胆酸盐(3,6-DCGA)。在本研究中,在菌株 Ndbn-20 中鉴定出两种谷胱甘肽依赖的 3,6-DCGA 脱卤酶 DsmH1 和 DsmH2。DsmH2 与 ATCC 39723 中的四氯对苯二酚(TCHQ)脱卤酶 PcpC 的同源性仅为 31%(仅 31%),而 DsmH1 与 PcpC 的同源性高达 79%。在相关谷胱甘肽转移酶(GSTs)的系统发育树中,DsmH1 和 DsmH2 与 PcpC 和 2,5-二氯对苯二酚脱卤酶 LinD 一起形成一个单独的分支。DsmH1 和 DsmH2 在 BL21 中合成并作为 His 标记的酶进行纯化。两种酶都需要谷胱甘肽(GSH)作为辅因子,并且可以将 3,6-DCGA 6-去氯化为 3-氯龙胆酸盐。DsmH2 对 3,6-DCGA 的催化效率明显高于 DsmH1。转录和破坏分析表明,DsmH2 而不是 DsmH1 负责菌株 Ndbn-20 中 3,6-DCGA 的 6-去氯化。此外,我们提出了一种新的 eta 类 GSTs,以适应四种细菌脱卤酶 PcpC、LinD、DsmH1 和 DsmH2。二甲苯草胺是一种重要的除草剂,自 2015 年大规模种植抗二甲苯草胺的转基因(GM)作物以来,其使用和泄漏到环境中的情况急剧增加。然而,二甲苯草胺的完全代谢途径仍然未知,这限制了对该除草剂的生态毒理学研究。我们之前的研究表明,3,6-DCGA 是菌株 Ndbn-20 中二甲苯草胺降解的中间产物。在本研究中,我们鉴定了两种谷胱甘肽依赖的 3,6-DCGA 脱卤酶 DsmH1 和 DsmH2,并证明 DsmH2 在生理上负责菌株 Ndbn-20 中 3,6-DCGA 的 6-去氯化。GSTs 在各种内源性和外源性有毒化合物的解毒和降解中发挥着重要作用。基于它们的序列同一性、系统发育地位和功能,四种细菌 GSH 依赖性脱卤酶(PcpC、LinD、DsmH1 和 DsmH2)被重新分类为新的 eta 类 GSTs。本研究有助于阐明二甲苯草胺的微生物代谢,并增强我们对 GSTs 的多样性和功能的理解。