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四氯化碳的微生物降解:生物修复的机制和展望。

Microbial degradation of tetrachloromethane: mechanisms and perspectives for bioremediation.

机构信息

Département Micro-organismes, Génomes, Environnement, Université de Strasbourg, UMR 7156 CNRS, Strasbourg, France.

出版信息

FEMS Microbiol Ecol. 2010 Nov;74(2):257-75. doi: 10.1111/j.1574-6941.2010.00935.x. Epub 2010 Aug 2.

DOI:10.1111/j.1574-6941.2010.00935.x
PMID:20695893
Abstract

Toxic man-made compounds released into the environment represent potential nutrients for bacteria, and microorganisms growing with such compounds as carbon and energy sources can be used to clean up polluted sites. However, in some instances, microorganisms contribute to contaminant degradation without any apparent benefit for themselves. Such cometabolism plays an important part in bioremediation, but is often difficult to control. Microbial degradation of tetrachloromethane (carbon tetrachloride, CCl(4)), a toxic ozone-depleting organic solvent mainly of anthropogenic origin, is only known to occur by cometabolic reduction under anoxic conditions. Yet no microbial system capable of using CCl(4) as the sole carbon source has been described. Microbial growth based on CCl(4) as a terminal electron acceptor has not been reported, although corresponding degradation pathways would yield sufficient energy. Known modes for the biodegradation of CCl(4) involve several microbial metabolites, mainly metal-bound coenzymes and siderophores, which are produced by facultative or strictly anaerobic bacteria and methanogenic Archaea. Recent reports have demonstrated that CCl(4) dechlorination rates are enhanced by redox-active organic compounds such as humic acids and quinones, which act as shuttles between electron-providing microorganisms and CCl(4) as a strong electron acceptor. The key factors underlying dechlorination of CCl(4), the practical aspects and specific requirements for microorganism-associated degradation of CCl(4) at contaminated sites and perspectives for future developments are discussed.

摘要

有毒的人造化合物释放到环境中代表了细菌潜在的营养物质,而以这些化合物为碳和能源来源生长的微生物可以用来清理污染场地。然而,在某些情况下,微生物在没有明显自身受益的情况下促进污染物的降解。这种共代谢在生物修复中起着重要作用,但往往难以控制。微生物对四氯化碳(四氯化碳,CCl(4))的降解,一种主要源自人为的有毒消耗臭氧有机溶剂,仅在缺氧条件下通过共代谢还原才被认为是可能的。然而,还没有描述过能够将 CCl(4) 用作唯一碳源的微生物系统。虽然相应的降解途径会产生足够的能量,但尚未报道基于 CCl(4) 作为末端电子受体的微生物生长。已知的 CCl(4) 生物降解途径涉及几种微生物代谢物,主要是金属结合辅酶和铁载体,这些代谢物由兼性或严格厌氧细菌和产甲烷古菌产生。最近的报告表明,氧化还原活性有机化合物如腐殖酸和醌可以增强 CCl(4) 的脱氯速率,它们作为电子供体微生物和 CCl(4 之间的穿梭物质,CCl(4 是一种强电子受体。讨论了 CCl(4)脱氯的关键因素、微生物相关的 CCl(4)在污染场地降解的实际方面和具体要求,以及未来发展的前景。

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