Sumbel Yaqoob, Chen Wu, Chao Li, Jose Manuel Diaz Antunes and Mengyan Li*,
{"title":"Anaerobic Biotransformation and Biodefluorination of 6:2 Fluorotelomer Carboxylic Acid by Biosolids under the Nitrate-Reducing Condition","authors":"Sumbel Yaqoob, Chen Wu, Chao Li, Jose Manuel Diaz Antunes and Mengyan Li*, ","doi":"10.1021/acsestwater.5c0000910.1021/acsestwater.5c00009","DOIUrl":null,"url":null,"abstract":"<p >The prevalence of per- and polyfluoroalkyl substances and their precursors, specifically 6:2 fluorotelomer carboxylic acid (6:2 FTCA), in the environment attests to their importance as contaminants of regulatory concern. This study compared three redox conditions (i.e., nitrate reduction, sulfate reduction, and methanogenesis) on biotransformation and biodefluorination of 6:2 FTCA using biosolids mixed from three wastewater treatment plants. Expected redox conditions were achieved in nitrate-reducing and methanogenic microcosms, but not in sulfate-amended treatments. Over 5 months of incubation, significant 6:2 FTCA removal (0.265 μM/day) was depleted under the nitrate-reducing condition, while minimal or no biotransformation was observed under the sulfate-amended or methanogenic conditions. This observed decline in 6:2 FTCA was accompanied by a decrease in nitrate (∼28 mM) and an increase in inorganic fluoride (∼28 μM), correlating to a loss of ∼0.70 fluoride per removed 6:2 FTCA molecule. Less fluorinated compounds 5:3 fluorotelomer carboxylic acid (5:3 FTCA) and perfluorohexanoic acid (PFHxA) were also detected under the nitrate-reducing condition. Microbial community analysis revealed the increase of <i>Anaerolineae</i>, which could be accountable for 6:2 FTCA biotransformation under nitrate-reducing conditions. Results indicate anaerobic biotransformation is dependent on the availability of specific election acceptors, informing future strategies to enhance the biotransformation rate and biodefluorination extent.</p>","PeriodicalId":93847,"journal":{"name":"ACS ES&T water","volume":"5 5","pages":"2412–2420 2412–2420"},"PeriodicalIF":4.8000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS ES&T water","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsestwater.5c00009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The prevalence of per- and polyfluoroalkyl substances and their precursors, specifically 6:2 fluorotelomer carboxylic acid (6:2 FTCA), in the environment attests to their importance as contaminants of regulatory concern. This study compared three redox conditions (i.e., nitrate reduction, sulfate reduction, and methanogenesis) on biotransformation and biodefluorination of 6:2 FTCA using biosolids mixed from three wastewater treatment plants. Expected redox conditions were achieved in nitrate-reducing and methanogenic microcosms, but not in sulfate-amended treatments. Over 5 months of incubation, significant 6:2 FTCA removal (0.265 μM/day) was depleted under the nitrate-reducing condition, while minimal or no biotransformation was observed under the sulfate-amended or methanogenic conditions. This observed decline in 6:2 FTCA was accompanied by a decrease in nitrate (∼28 mM) and an increase in inorganic fluoride (∼28 μM), correlating to a loss of ∼0.70 fluoride per removed 6:2 FTCA molecule. Less fluorinated compounds 5:3 fluorotelomer carboxylic acid (5:3 FTCA) and perfluorohexanoic acid (PFHxA) were also detected under the nitrate-reducing condition. Microbial community analysis revealed the increase of Anaerolineae, which could be accountable for 6:2 FTCA biotransformation under nitrate-reducing conditions. Results indicate anaerobic biotransformation is dependent on the availability of specific election acceptors, informing future strategies to enhance the biotransformation rate and biodefluorination extent.