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首页> 外文期刊>Biotechnology & Biotechnological Equipment >Molecular Modelling and Functional Studies of the Non-Stereospecific ???±-Haloalkanoic Acid Dehalogenase (DehE) from Rhizobium SP. RC1 and its Association with 3-Chloropropionic Acid (???2-Chlorinated Aliphatic Acid)
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Molecular Modelling and Functional Studies of the Non-Stereospecific ???±-Haloalkanoic Acid Dehalogenase (DehE) from Rhizobium SP. RC1 and its Association with 3-Chloropropionic Acid (???2-Chlorinated Aliphatic Acid)

机译:根瘤菌属SP的非立体特异性α-卤代链烷酸脱卤酶(DehE)的分子模型和功能研究。 RC1及其与3-氯代丙酸(2-氯代脂族酸)的缔合

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摘要

Many environmental pollutions are caused by the abundance of xenobiotic compounds in nature. For instance, halogenated compounds released from chemical industries were proven to be toxic and recalcitrant in the environment. However, haloalkanoic acid dehalogenases can catalyse the removal of halides from organic haloacids and thus have gained interest for bioremediation and synthesis of industrial chemicals. This study presents the first structural model and the key residues of the non-stereospecific haloalkanoic acid dehalogenase, DehE, from Rhizobium sp. RC1. The enzyme was built using a homology modelling technique; the structure of DehI from Pseudomonas putida PP3 was used as a template, because of its homology to DehE. The structure of DehE consists of only ???±-helices. Twelve conserved residues that line the active site were identified: Trp34, Ala36, Phe37, Asn114, Tyr117 Ala187, Ser188, Asp189, Tyr265, Phe268, Ile269, and Ile272. These residues are consistent with the residues found in the active site of DehI and D, L-DEX 113 from Pseudomonas sp. 113. Asp189 activates the water molecule as a nucleophile to attack the substrate chiral centre, which would result in an inversion of configuration of either D- or L-substrates. Both D- and L-substrates bind to and interact with the enzyme by hydrogen bonding with three residues, Trp34, Phe37, and Ser188. In addition, a putative tunnel was also identified that would provide a channel for the substrate to access the binding site. Based on computational analysis, DehE was proven to have the substrate affinity towards 3-chloropropionic acid (3CP)/???2-chlorinated aliphatic acid, however, its dehalogenation process is far from clear. This DehE structural information will allow for rational design of non-stereospecific haloalkanoic acid dehalogenases in the future.
机译:自然界中大量异种生物化合物造成许多环境污染。例如,从化学工业中释放出来的卤代化合物被证明在环境中是有毒的和难降解的。但是,卤代链烷酸脱卤酶可以催化从有机卤代酸中除去卤化物,因此引起了对生物修复和工业化学品合成的兴趣。这项研究介绍了根瘤菌的非立体特异性卤代链烷酸脱卤酶DehE的第一个结构模型和关键残基。 RC1。使用同源建模技术构建了酶;由于恶臭假单胞菌PP3的DehI与DehE具有同源性,因此将其结构用作模板。 DehE的结构仅由+/-螺旋组成。确定了排列在活性位点上的十二个保守残基:Trp34,Ala36,Phe37,Asn114,Tyr117 Ala187,Ser188,Asp189,Tyr265,Phe268,Ile269和Ile272。这些残基与在假单胞菌属种的DehI和D,L-DEX 113的活性位点中发现的残基一致。 113. Asp189将水分子作为亲核试剂激活,攻击底物手性中心,这将导致D或L底物的构型反转。 D底物和L底物都通过氢键与三个残基Trp34,Phe37和Ser188结合并与酶相互作用。另外,还鉴定了推定的通道,该通道将为底物提供通道以进入结合位点。根据计算分析,证明DehE对3-氯丙酸(3CP)/β2-氯代脂肪酸具有底物亲和力,但是,其脱卤过程还很不清楚。该DehE结构信息将允许将来合理设计非立体特异性卤代链烷酸脱卤素酶。

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