脱卤球绦虫
脱氯作用
卤化
化学
还原消去
生物修复
电子受体
还原胺化
富集培养
组合化学
立体化学
药物化学
有机化学
污染
细菌
催化作用
生物降解
生物
生态学
聚合物
遗传学
共聚物
氯乙烯
作者
Yaochun Yu,Kunyang Zhang,Zhong Li,Changxu Ren,Jin Y. Chen,Ying‐Hsuan Lin,Jinyong Liu,Yujie Men
标识
DOI:10.1021/acs.est.0c04483
摘要
The C–F bond is one of the strongest single bonds in nature. Although microbial reductive dehalogenation is well known for the other organohalides, no microbial reductive defluorination has been documented for perfluorinated compounds except for a single, nonreproducible study on trifluoroacetate. Here, we report on C–F bond cleavage in two C6 per- and polyfluorinated compounds via reductive defluorination by an organohalide-respiring microbial community. The reductive defluorination was demonstrated by the release of F– and the formation of the corresponding product when lactate was the electron donor, and the fluorinated compound was the sole electron acceptor. The major dechlorinating species in the seed culture, Dehalococcoides, were not responsible for the defluorination as no growth of Dehalococcoides or active expression of Dehalococcoides-reductive dehalogenases was observed. It suggests that minor phylogenetic groups in the community might be responsible for the reductive defluorination. These findings expand our fundamental knowledge of microbial reductive dehalogenation and warrant further studies on the enrichment, identification, and isolation of responsible microorganisms and enzymes. Given the wide use and emerging concerns of fluorinated organics (e.g., per- and polyfluoroalkyl substances), particularly the perfluorinated ones, the discovery of microbial defluorination under common anaerobic conditions may provide valuable insights into the environmental fate and potential bioremediation strategies of these notorious contaminants.
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