Burkholderia xenovorans LB400联苯双加氧酶及突变体对DDTs的降解

The degradation of DDTs by Burkholderia xenovorans LB400 biphenyl dioxygenase and mutants

摘要:

DDTs（dichlorodiphenyltrichloroethane，1，1，1-三氯-2，2-双氯苯基乙烷）是一种典型的持久性有机污染物，曾在疟疾防治和农业除虫方面被广泛应用。虽然包括我国在内的很多国家已经禁止使用DDTs，但目前对环境中DDTs的检测发现它仍然广泛存在且具有新的输入源。DDTs的持续存在对近海生态系统和人类健康具有一定危害，因此它所造成的环境污染问题仍然值得关注。由于Rieske型芳香羟化双加氧酶能够起始多种持久性污染物的降解，过去的几十年里一直是芳香化合物降解领域的焦点。[目的] 为探讨联苯双加氧酶对DDTs的降解特性及机制，本研究选取了食异生素伯克霍尔德氏菌LB400（Burkholderia xenovorans）联苯双加氧酶及突变体对p，p'-DDT和o，p'-DDT的降解过程进行研究。[方法] 以BphAE_LB400为亲本，通过两步定点突变将283位的丝氨酸突变为蛋氨酸，获得突变体BphAE_S283M。通过比较亲本酶与突变体对DDTs的催化性能，模拟突变蛋白结构和分子对接等方法，探究其降解特性及机制。[结果] BphAE_LB400和突变体BphAE_S283M都无法降解对位的p，p'-DDT，但突变体BphAE_S283M可以代谢o，p'-DDT并产生2个立体异构体。对接p，p'-DDT的BphAE_LB400和BphAE_S283M的结构分析表明，BphAE_LB400和BphAE_S283M中p，p'-DDT的反应环均不与原晶体结构中的联苯反应环重合。而对接o，p'-DDT的BphAE_S283M的结构分析表明o，p'-DDT的反应环与晶体结构中的联苯反应环距离很近，且2、3位的碳原子与单核铁原子催化中心的距离在0.5 nm以内，此外，BphAE_S283M的催化腔表面积和体积比BphAE_LB400更大，这很可能有助于BphAE_S283M与o，p'-DDT的结合。[结论] 283位氨基酸是影响BphAE_LB400对DDTs的催化代谢能力的关键氨基酸残基，它可以通过调节反应碳原子与催化中心的距离以及催化腔的大小来影响底物特异性。本次研究进一步阐明了283位氨基酸残基的影响机理，为更有效修复DDTs污染提供理论依据和技术支持。

关键词:DDTs;联苯双加氧酶;Burkholderia xenovorans LB400;底物特异性

Abstract:

Dicholodiphenyltrichloroethanes (DDTs) is probably the best known and typical persistent organic pollutant in the world, which has been widely used in malaria control and agricultural deworming. They are still detected in various environmental matrices and has new input sources although their usage in agriculture has been banned in China and others. Numerous concerns have arisen over the past decades about the adverse environmental impacts(including harm to offshore ecosystem and human health) of DDTs. There has been a considerable interest over the last decades for the Rieske-type arylhydroxylating dioxygenases (RHDs) as they are seen as potentially capable of initiating their degradation. [Objective] In order to explore the degradation characteristics and mechanism of biphenyl dioxygenase(BPDO) on DDTs, we selected Burkholderia xenovorans LB400 biphenyl dioxygenase and its mutants to explore the degradation process of p,p'-DDT and o,p'-DDT. [Methods] Using BphAE_LB400 as parent, the mutant BphAE_S283M was obtained by two-step site-directed mutagenesis from Ser to Met. The degradation characteristics and mechanism of wild type and mutant were explored by comparing the catalytic performance of wild type and mutant to DDTs, simulating the structure of mutant protein and molecular docking. [Results] The data showed that BphAE_LB400 and BphAE_S283Mcould not be degraded p,p'-DDT, but BphAE_S283M metabolized o,p'-DDT and produced two stereoisomers. The structural analysis of BphAE_LB400 and BphAE_S283M showed that the reaction ring of p,p'-DDT did not coincide with the biphenyl reaction ring in the original crystal structure. In the o,p'-DDT-BphAE_S283M conformation, the proximal ring did not fit the biphenyl reactive ring as well, but its orientation toward the catalytic Fe²⁺ places two vicinal atoms at a distance(within 0.5 nm) that would allow a catalytic reaction. In addition, the surface area and volume of the catalytic cavity of BphAE_S283M is larger than that of BphAE_LB400, which is likely to contribute to the combination of BphAE_S283M and o,p'-DDT. [Conclusion] 283 is the key amino acid residue that affects the catalytic metabolism of BPDO to DDTs. It can affect the substrate specificity by adjusting the distance between the reaction carbon atom and the catalytic center and the size of the catalytic cavity. This will provide better insights about the bases for BPDO broad substrate range and about the mechanisms by which the enzyme evolves to change or expand its substrate range and its stereo- and regiospecificity.

Key words:DDTs;BPDO;Burkholderia xenovorans LB400;substrate specificity