Interaction between nitrate and trichloroethene bioreduction in mixed anaerobic cultures.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-01-15 eCollection Date: 2024-01-01 DOI:10.3389/fmicb.2024.1504235
Dong-Mei Yang, Fen-Li Min, Ying Li, Jia-Lu Ling, Hui-Xian Zhong, Yu-Chun Xia, Ying Feng, Li-Ya Zhao, Zhao-Hua Li, Li-Lian Wen
{"title":"Interaction between nitrate and trichloroethene bioreduction in mixed anaerobic cultures.","authors":"Dong-Mei Yang, Fen-Li Min, Ying Li, Jia-Lu Ling, Hui-Xian Zhong, Yu-Chun Xia, Ying Feng, Li-Ya Zhao, Zhao-Hua Li, Li-Lian Wen","doi":"10.3389/fmicb.2024.1504235","DOIUrl":null,"url":null,"abstract":"<p><p>Bioremediation of trichloroethene (TCE)-contaminated sites often leads to groundwater acidification, while nitrate-polluted sites tend to generate alkalization. TCE and nitrate often coexist at contaminated sites; however, the pH variation caused by nitrate self-alkalization and TCE self-acidification and how these processes affect nitrate reduction and reductive dichlorination, have not been studied. This study investigated the interaction between nitrate and TCE, two common groundwater co-contaminants, during bioreduction in serum bottles containing synthetic mineral salt media and microbial consortia. Our results showed that TCE concentrations up to 0.3 mM stimulated nitrate reduction, while the effect of nitrate on TCE reductive dechlorination was more complex. Nitrate primarily inhibited the reduction of TCE to dichloroethene (DCE) but enhanced the reduction of vinyl chloride (VC) to ethene. Mechanistic analysis suggested that this inhibition was due to the thermodynamic favorability of nitrate reduction over TCE reduction, while the promotion of VC reduction was linked to pH stabilization via self-alkalization. As the initial nitrate concentration increased from 0 to 3 mM, the relative abundance of putatively denitrifying genera, such as <i>Petrimonas</i> and <i>Trichlorobacter</i>, increased. However, the abundance of fermentative <i>Clostridium</i> sharply declined from 31.11 to 1.51%, indicating strong nitrate inhibition. Additionally, the relative abundance of <i>Dehalococcoides</i>, a genus capable of reducing TCE to ethene, slightly increased from 23.91 to 24.26% at nitrate concentrations up to 0.3 mM but decreased to 18.65% as the nitrate concentration increased to 3 mM, suggesting that <i>Dehalococcoides</i> exhibits a degree of tolerance to high nitrate concentrations under specific conditions. Overall, our findings highlight the potential for simultaneous reduction of TCE and nitrate, even at elevated concentrations, facilitated by self-regulating pH control in anaerobic mixed dechlorinating consortia. This study provides novel insights into bioremediation strategies for addressing co-contaminated sites.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":"15 ","pages":"1504235"},"PeriodicalIF":4.0000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11778175/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmicb.2024.1504235","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Bioremediation of trichloroethene (TCE)-contaminated sites often leads to groundwater acidification, while nitrate-polluted sites tend to generate alkalization. TCE and nitrate often coexist at contaminated sites; however, the pH variation caused by nitrate self-alkalization and TCE self-acidification and how these processes affect nitrate reduction and reductive dichlorination, have not been studied. This study investigated the interaction between nitrate and TCE, two common groundwater co-contaminants, during bioreduction in serum bottles containing synthetic mineral salt media and microbial consortia. Our results showed that TCE concentrations up to 0.3 mM stimulated nitrate reduction, while the effect of nitrate on TCE reductive dechlorination was more complex. Nitrate primarily inhibited the reduction of TCE to dichloroethene (DCE) but enhanced the reduction of vinyl chloride (VC) to ethene. Mechanistic analysis suggested that this inhibition was due to the thermodynamic favorability of nitrate reduction over TCE reduction, while the promotion of VC reduction was linked to pH stabilization via self-alkalization. As the initial nitrate concentration increased from 0 to 3 mM, the relative abundance of putatively denitrifying genera, such as Petrimonas and Trichlorobacter, increased. However, the abundance of fermentative Clostridium sharply declined from 31.11 to 1.51%, indicating strong nitrate inhibition. Additionally, the relative abundance of Dehalococcoides, a genus capable of reducing TCE to ethene, slightly increased from 23.91 to 24.26% at nitrate concentrations up to 0.3 mM but decreased to 18.65% as the nitrate concentration increased to 3 mM, suggesting that Dehalococcoides exhibits a degree of tolerance to high nitrate concentrations under specific conditions. Overall, our findings highlight the potential for simultaneous reduction of TCE and nitrate, even at elevated concentrations, facilitated by self-regulating pH control in anaerobic mixed dechlorinating consortia. This study provides novel insights into bioremediation strategies for addressing co-contaminated sites.

求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信