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多氯联苯的好氧降解

Aerobic degradation of polychlorinated biphenyls.

作者信息

Pieper Dietmar H

机构信息

Department of Environmental Microbiology, German Research Center for Biotechnology, Mascheroder Weg 1, 38124, Braunschweig, Germany.

出版信息

Appl Microbiol Biotechnol. 2005 Apr;67(2):170-91. doi: 10.1007/s00253-004-1810-4. Epub 2004 Dec 22.

DOI:10.1007/s00253-004-1810-4
PMID:15614564
Abstract

The microbial degradation of polychlorinated biphenyls (PCBs) has been extensively studied in recent years. The genetic organization of biphenyl catabolic genes has been elucidated in various groups of microorganisms, their structures have been analyzed with respect to their evolutionary relationships, and new information on mobile elements has become available. Key enzymes, specifically biphenyl 2,3-dioxygenases, have been intensively characterized, structure/sequence relationships have been determined and enzymes optimized for PCB transformation. However, due to the complex metabolic network responsible for PCB degradation, optimizing degradation by single bacterial species is necessarily limited. As PCBs are usually not mineralized by biphenyl-degrading organisms, and cometabolism can result in the formation of toxic metabolites, the degradation of chlorobenzoates has received special attention. A broad set of bacterial strategies to degrade chlorobenzoates has recently been elucidated, including new pathways for the degradation of chlorocatechols as central intermediates of various chloroaromatic catabolic pathways. To optimize PCB degradation in the environment beyond these metabolic limitations, enhancing degradation in the rhizosphere has been suggested, in addition to the application of surfactants to overcome bioavailability barriers. However, further research is necessary to understand the complex interactions between soil/sediment, pollutant, surfactant and microorganisms in different environments.

摘要

近年来,多氯联苯(PCBs)的微生物降解已得到广泛研究。在各类微生物中,联苯分解代谢基因的遗传组织已被阐明,其结构已根据进化关系进行了分析,并且关于移动元件的新信息也已获得。关键酶,特别是联苯2,3 - 双加氧酶,已得到深入表征,结构/序列关系已被确定,并且针对多氯联苯转化对酶进行了优化。然而,由于负责多氯联苯降解的代谢网络复杂,单一细菌物种降解的优化必然受到限制。由于多氯联苯通常不会被联苯降解生物矿化,并且共代谢可能导致有毒代谢物的形成,氯苯甲酸酯的降解受到了特别关注。最近已阐明了一系列广泛的细菌降解氯苯甲酸酯的策略,包括作为各种氯代芳烃分解代谢途径中心中间体的氯儿茶酚降解的新途径。为了在这些代谢限制之外优化环境中的多氯联苯降解,除了应用表面活性剂以克服生物可利用性障碍外,还建议增强根际降解。然而,有必要进一步研究以了解不同环境中土壤/沉积物、污染物、表面活性剂和微生物之间的复杂相互作用。

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