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氯化二噁英的微生物降解

Microbial degradation of chlorinated dioxins.

作者信息

Field Jim A, Sierra-Alvarez Reyes

机构信息

Department of Chemical and Environmental Engineering, University of Arizona, Tucson, AZ 85721, USA.

出版信息

Chemosphere. 2008 Apr;71(6):1005-18. doi: 10.1016/j.chemosphere.2007.10.039. Epub 2008 Feb 20.

Abstract

Polychlorinated dibenzo-p-dioxins (PCDD) and polychlorinated dibenzofurans (PCDF) were introduced into the biosphere on a large scale as by-products from the manufacture of chlorinated phenols and the incineration of wastes. Due to their high toxicity they have been the subject of great public and scientific scrutiny. The evidence in the literature suggests that PCDD/F compounds are subject to biodegradation in the environment as part of the natural chlorine cycle. Lower chlorinated dioxins can be degraded by aerobic bacteria from the genera of Sphingomonas, Pseudomonas and Burkholderia. Most studies have evaluated the cometabolism of monochlorinated dioxins with unsubstituted dioxin as the primary substrate. The degradation is usually initiated by unique angular dioxygenases that attack the ring adjacent to the ether oxygen. Chlorinated dioxins can also be attacked cometabolically under aerobic conditions by white-rot fungi that utilize extracellular lignin degrading peroxidases. Recently, bacteria that can grow on monochlorinated dibenzo-p-dioxins as a sole source of carbon and energy have also been characterized (Pseudomonas veronii). Higher chlorinated dioxins are known to be reductively dechlorinated in anaerobic sediments. Similar to PCB and chlorinated benzenes, halorespiring bacteria from the genus Dehalococcoides are implicated in the dechlorination reactions. Anaerobic sediments have been shown to convert tetrachloro- to octachlorodibenzo-p-dioxins to lower chlorinated dioxins including monochlorinated congeners. Taken as a whole, these findings indicate that biodegradation is likely to contribute to the natural attenuation processes affecting PCDD/F compounds.

摘要

多氯代二苯并 - 对 - 二噁英(PCDD)和多氯代二苯并呋喃(PCDF)作为制造氯酚和废物焚烧的副产品被大规模引入生物圈。由于它们的高毒性,一直受到公众和科学界的密切关注。文献中的证据表明,PCDD/F化合物作为自然氯循环的一部分在环境中会发生生物降解。低氯代二噁英可被鞘氨醇单胞菌属、假单胞菌属和伯克霍尔德菌属的需氧细菌降解。大多数研究评估了以未取代二噁英为主要底物时一氯代二噁英的共代谢情况。降解通常由攻击与醚氧相邻环的独特角双加氧酶引发。在需氧条件下,氯代二噁英也可被利用细胞外木质素降解过氧化物酶的白腐真菌共代谢攻击。最近,还鉴定出了能以一氯代二苯并 - 对 - 二噁英作为唯一碳源和能源生长的细菌(维罗纳假单胞菌)。已知高氯代二噁英在厌氧沉积物中会发生还原脱氯。与多氯联苯和氯苯类似,脱卤球菌属的卤呼吸细菌参与脱氯反应。厌氧沉积物已被证明能将四氯至八氯代二苯并 - 对 - 二噁英转化为包括一氯代同系物在内的低氯代二噁英。总体而言,这些发现表明生物降解可能有助于影响PCDD/F化合物的自然衰减过程。

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