生物降解
生物转化
化学
生物修复
电化学
生物相容性材料
环境化学
纳米技术
生化工程
有机化学
电极
材料科学
污染
生态学
工程类
物理化学
生物医学工程
生物
酶
作者
Shun Che,Xun Guan,Roselyn Rodrigues,Yaochun Yu,Yongchao Xie,Chong Liu,Yujie Men
标识
DOI:10.1073/pnas.2400525121
摘要
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 6 -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.
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