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电动力学强化修复三氯乙烯污染低渗透土壤:土著微生物群落时空变化及生物脱卤活性的机理见解。

Electrokinetic-Enhanced Bioremediation of Trichloroethylene-Contaminated Low-Permeability Soils: Mechanistic Insight from Spatio-Temporal Variations of Indigenous Microbial Community and Biodehalogenation Activity.

机构信息

State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, No. 68 Jincheng Street, East Lake High-Tech Development Zone, Wuhan 430078, P. R. China.

Hubei Key Laboratory of Yangtze Catchment Environmental Aquatic Science, School of Environmental Studies, China University of Geosciences, No. 68 Jincheng Street, East Lake High-Tech Development Zone, Wuhan 430078, P. R. China.

出版信息

Environ Sci Technol. 2023 Mar 28;57(12):5046-5055. doi: 10.1021/acs.est.3c00278. Epub 2023 Mar 16.

Abstract

Electrokinetic-enhanced bioremediation (EK-Bio), particularly bioaugmentation with injection of biodehalogenation functional microbes such as , has been documented to be effective in treating a low-permeability subsurface matrix contaminated with chlorinated ethenes. However, the spatio-temporal variations of indigenous microbial community and biodehalogenation activity of the background matrix, a fundamental aspect for understanding EK-Bio, remain unclear. To fill this gap, we investigated the variation of trichloroethylene (TCE) biodehalogenation activity in response to indigenous microbial community succession in EK-Bio by both column and batch experiments. For a 195 day EK-Bio column (∼1 V/cm, electrolyte circulation, lactate addition), biodehalogenation activity occurred first near the cathode (<60 days) and then spread to the anode (>90 days), which was controlled by electron acceptor (i.e., Fe(III)) competition and microbe succession. Amplicon sequencing and metagenome analysis revealed that iron-reducing bacteria (, , ) were enriched within initial 60 d and were gradually replaced by organohalide-respiring bacteria (versatile and obligate ) afterward. Iron-reducing bacteria required an initial long time to consume the competitive electron acceptors so that an appropriate reductive condition could be developed for the enrichment of organohalide-respiring bacteria and the enhancement of TCE biodehalogenation activity.

摘要

电动力学增强生物修复(EK-Bio),特别是通过注射生物脱卤化功能微生物(如 )进行生物增强,已被证明可有效处理受氯化碳氢化合物污染的低渗透性地下基质。然而,背景基质中土著微生物群落和生物脱卤化活性的时空变化,这是理解 EK-Bio 的一个基本方面,仍然不清楚。为了填补这一空白,我们通过柱实验和批量实验研究了 EK-Bio 中土著微生物群落演替对三氯乙烯(TCE)生物脱卤化活性的影响。在一个 195 天的 EK-Bio 柱(约 1 V/cm,电解质循环,添加乳酸盐)中,生物脱卤化活性首先在阴极附近发生(<60 天),然后扩散到阳极(>90 天),这由电子受体(即 Fe(III))竞争和微生物演替控制。扩增子测序和宏基因组分析表明,铁还原菌(、、)在最初的 60 天内得到了富集,随后被有机卤化物呼吸菌(多功能 和专性 )所取代。铁还原菌需要初始的长时间来消耗竞争电子受体,以便为有机卤化物呼吸菌的富集和 TCE 生物脱卤化活性的增强创造适当的还原条件。

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