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通过还原脱氟作用微生物裂解两种全氟和多氟化合物中的 C-F 键。

Microbial Cleavage of C-F Bonds in Two C Per- and Polyfluorinated Compounds via Reductive Defluorination.

机构信息

Department of Chemical and Environmental Engineering, University of California, Riverside, California 92521, United States.

Department of Civil and Environmental Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.

出版信息

Environ Sci Technol. 2020 Nov 17;54(22):14393-14402. doi: 10.1021/acs.est.0c04483. Epub 2020 Oct 29.

Abstract

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 C 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, , were not responsible for the defluorination as no growth of or active expression of 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.

摘要

C-F 键是自然界中最强的单键之一。尽管微生物还原脱卤作用在其他有机卤化物中广为人知,但除了一项关于三氟乙酸盐的不可重复的单一研究外,没有关于全氟化化合物的微生物还原脱氟作用的记录。在这里,我们通过有机卤化物呼吸微生物群落的还原脱氟作用,报告了两种 C 型全氟化和多氟化化合物中 C-F 键的断裂。当乳酸盐作为电子供体时,通过释放 F 和形成相应的产物证明了还原脱氟作用,并且氟化合物是唯一的电子受体。在种子培养物中,主要的脱氯物种 , 没有参与脱氟作用,因为没有观察到 或还原脱卤酶的活性表达。这表明群落中的少数系统发育群体可能负责还原脱氟作用。这些发现扩展了我们对微生物还原脱卤作用的基本知识,并需要进一步研究负责微生物和酶的富集、鉴定和分离。鉴于含氟有机物(例如全氟和多氟烷基物质)的广泛使用和新出现的关注,特别是全氟化物质,在常见的厌氧条件下发现微生物脱氟作用可能为这些臭名昭著的污染物的环境命运和潜在的生物修复策略提供有价值的见解。

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