<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Che S</submitter><funding>HHS | NIH | National Institute of Environmental Health Sciences</funding><funding>DOD | Strategic Environmental Research and Development Program</funding><funding>NIEHS NIH HHS</funding><funding>DOD | Strategic Environmental Research and Development Program (SERDP)</funding><funding>HHS | NIH | National Institute of Environmental Health Sciences (NIEHS)</funding><pagination>e2400525121</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11295042</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>121(31)</volume><pubmed_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&lt;sub>6&lt;/sub>-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 b</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pubmed_title>Synergistic material-microbe interface toward deeper anaerobic defluorination.</pubmed_title><pmcid>PMC11295042</pmcid><funding_grant_id>ER20-1541</funding_grant_id><funding_grant_id>R01 ES032668</funding_grant_id><funding_grant_id>R01ES032668</funding_grant_id><pubmed_authors>Rodrigues R</pubmed_authors><pubmed_authors>Che S</pubmed_authors><pubmed_authors>Men Y</pubmed_authors><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Guan X</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synergistic material-microbe interface toward deeper anaerobic defluorination.</name><description>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&lt;sub>6&lt;/sub>-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 b</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-03T23:36:43.421Z</modification><creation>2025-04-03T23:36:43.421Z</creation></dates><accession>S-EPMC11295042</accession><cross_references><pubmed>39042683</pubmed><doi>10.1073/pnas.2400525121</doi></cross_references></HashMap>