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协同的物质-微生物界面实现更深度的厌氧除氟。

Synergistic material-microbe interface toward deeper anaerobic defluorination.

机构信息

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

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

出版信息

Proc Natl Acad Sci U S A. 2024 Jul 30;121(31):e2400525121. doi: 10.1073/pnas.2400525121. Epub 2024 Jul 23.

Abstract

Per- and polyfluoroalkyl substances (PFAS), particularly the perfluorinated ones, are recalcitrant to biodegradation. By integrating an enrichment culture of reductive defluorination with biocompatible electrodes for the electrochemical process, a deeper defluorination of a C-perfluorinated unsaturated PFAS was achieved compared to the biological or electrochemical system alone. Two synergies in the bioelectrochemical system were identified: i) The in-series microbial-electrochemical defluorination and ii) the electrochemically enabled microbial defluorination of intermediates. These synergies at the material-microbe interfaces surpassed the limitation of microbial defluorination and further turned the biotransformation end products into less fluorinated products, which could be less toxic and more biodegradable in the environment. This material-microbe hybrid system brings opportunities in the bioremediation of PFAS driven by renewable electricity and warrants future research on mechanistic understanding of defluorinating and electroactive microorganisms at the material-microbe interface for system optimizations.

摘要

全氟和多氟烷基物质(PFAS),特别是全氟化物质,难以生物降解。通过将还原脱氟的富集培养与生物相容性电极集成到电化学过程中,与单独的生物或电化学系统相比,可实现 C 型全氟化不饱和 PFAS 的更深程度的脱氟。在生物电化学系统中确定了两种协同作用:i)串联微生物电化学脱氟和 ii)电激活微生物对中间体的脱氟。这些材料-微生物界面的协同作用克服了微生物脱氟的局限性,并进一步将生物转化的终产物转化为含氟量较低的产物,这些产物在环境中可能毒性更低,生物降解性更强。这种材料-微生物混合系统为可再生电力驱动的 PFAS 生物修复带来了机遇,并需要进一步研究材料-微生物界面上脱氟和电活性微生物的机制理解,以实现系统优化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7397/11295042/f2752a4948ed/pnas.2400525121fig01.jpg

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