• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用 PAA 包覆的水铁矿作为电子受体增强 Acidimicrobium sp. Strain A6 的 Feammox 活性并降解全氟辛酸 (PFOA)。

Enhanced Feammox activity and perfluorooctanoic acid (PFOA) degradation by Acidimicrobium sp. Strain A6 using PAA-coated ferrihydrite as an electron acceptor.

机构信息

Department of Civil and Environmental Engineering, Princeton University, Princeton, NJ 08544, USA.

Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA.

出版信息

J Hazard Mater. 2023 Oct 5;459:132039. doi: 10.1016/j.jhazmat.2023.132039. Epub 2023 Jul 12.

DOI:10.1016/j.jhazmat.2023.132039
PMID:37480613
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10529297/
Abstract

Acidimicrobium sp. Strain A6 (A6) can degrade perfluoroalkyl acids (PFAAs) by oxidizing NH while reducing Fe(Ⅲ). However, supplying and distributing Fe(III) phases in sediments is challenging since surface charges of Fe(III)-phases are typically positive while those of sediments are negative. Therefore, ferrihydrite particles were coated with polyacrylic acid (PAA) with four different molecular weights, resulting in a negative zeta potential on their surface. Zeta potential was determined as a function of pH and PAA loading, with the lowest value observed when the PAA/ferrihydrite ratio was > 1/5 (w/w) at a pH of 5.5. Several 50-day incubations with an A6-enrichment culture were conducted to determine the effect of PAA-coated ferrihydrite as the electron acceptor of A6 on the Feammox activity and PFOA degradation. NH oxidation, PFOA degradation, production of shorter-chain PFAS, and F were observed in all PAA-coated samples. The 6 K and 450 K treatments exhibited significant reductions in PFOA concentration and substantial F production compared to incubations with bare ferrihydrite. Electrochemical impedance spectroscopy showed lowered charge transfer resistance in the presence of PAA-coated ferrihydrite, indicating that PAAs facilitated electron transfer to ferrihydrite. This study highlights the potential of PAA-coated ferrihydrite in accelerating PFAS defluorination, providing novel insights for A6-based bioremediation strategies.

摘要

嗜酸微生物菌株 A6(A6)可以通过氧化 NH 同时还原 Fe(Ⅲ)来降解全氟烷基酸(PFAAs)。然而,在沉积物中供应和分布 Fe(Ⅲ)相具有挑战性,因为 Fe(Ⅲ)相的表面电荷通常为正,而沉积物的表面电荷为负。因此,用四种不同分子量的聚丙烯酸(PAA)对水铁矿颗粒进行了包覆,使其表面带负电荷。通过测定 pH 值和 PAA 负载量之间的关系来确定 ζ 电位,当 PAA/水铁矿的比例(w/w)在 pH 值为 5.5 时大于 1/5 时,观察到 ζ 电位最低。进行了多次为期 50 天的 A6 富集培养实验,以确定作为 A6 电子受体的 PAA 包覆水铁矿对 Feammox 活性和 PFOA 降解的影响。在所有 PAA 包覆的样品中均观察到 NH 氧化、PFOA 降解、较短链 PFAS 和 F 的生成。与 bare ferrihydrite 相比,6K 和 450K 处理显著降低了 PFOA 浓度并产生了大量的 F。电化学阻抗谱表明,在 PAA 包覆水铁矿存在的情况下,电荷转移电阻降低,表明 PAAs 促进了电子向水铁矿的转移。本研究强调了 PAA 包覆水铁矿在加速 PFAS 脱氟方面的潜力,为基于 A6 的生物修复策略提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/78ad901ad6b5/nihms-1919929-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/96f9fea84876/nihms-1919929-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/64083079fd31/nihms-1919929-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/ce99891ce915/nihms-1919929-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/91f9f76d53e5/nihms-1919929-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/3ddf5a9ed506/nihms-1919929-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/78ad901ad6b5/nihms-1919929-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/96f9fea84876/nihms-1919929-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/64083079fd31/nihms-1919929-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/ce99891ce915/nihms-1919929-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/91f9f76d53e5/nihms-1919929-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/3ddf5a9ed506/nihms-1919929-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e5/10529297/78ad901ad6b5/nihms-1919929-f0007.jpg

相似文献

1
Enhanced Feammox activity and perfluorooctanoic acid (PFOA) degradation by Acidimicrobium sp. Strain A6 using PAA-coated ferrihydrite as an electron acceptor.利用 PAA 包覆的水铁矿作为电子受体增强 Acidimicrobium sp. Strain A6 的 Feammox 活性并降解全氟辛酸 (PFOA)。
J Hazard Mater. 2023 Oct 5;459:132039. doi: 10.1016/j.jhazmat.2023.132039. Epub 2023 Jul 12.
2
Anaerobic degradation of perfluorooctanoic acid (PFOA) in biosolids by Acidimicrobium sp. strain A6.嗜酸菌 A6 对生物固体中全氟辛酸(PFOA)的厌氧降解作用。
J Hazard Mater. 2022 Feb 15;424(Pt D):127699. doi: 10.1016/j.jhazmat.2021.127699. Epub 2021 Nov 6.
3
Defluorination of PFAS by Acidimicrobium sp. strain A6 and potential applications for remediation.嗜酸菌 A6 对全氟辛烷磺酸的脱氟作用及其在修复中的潜在应用。
Methods Enzymol. 2024;696:287-320. doi: 10.1016/bs.mie.2024.01.013. Epub 2024 Feb 15.
4
Modeling the kinetics of perfluorooctanoic and perfluorooctane sulfonic acid biodegradation by Acidimicrobium sp. Strain A6 during the feammox process.铁氨氧化过程中嗜酸微菌属菌株A6对全氟辛酸和全氟辛烷磺酸生物降解动力学的建模。
J Hazard Mater. 2023 Apr 15;448:130903. doi: 10.1016/j.jhazmat.2023.130903. Epub 2023 Jan 28.
5
Stimulating Acidimicrobium sp. Strain A6 in iron-rich, acidic sediments from AFFF-impacted sites for PFAS defluorination.在受 AFFF 影响的富含铁、酸性沉积物中刺激嗜酸微生物菌株 A6 进行 PFAS 脱氟。
Sci Total Environ. 2024 Dec 10;955:176801. doi: 10.1016/j.scitotenv.2024.176801. Epub 2024 Oct 9.
6
Defluorination of Perfluorooctanoic Acid (PFOA) and Perfluorooctane Sulfonate (PFOS) by sp. Strain A6.sp. 菌株 A6 对全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)的脱氟作用。
Environ Sci Technol. 2019 Oct 1;53(19):11410-11419. doi: 10.1021/acs.est.9b04047. Epub 2019 Sep 18.
7
Biodegradation of PFOA in microbial electrolysis cells by Acidimicrobiaceae sp. strain A6.嗜酸菌属 A6 菌株在微生物电解池内对全氟辛酸的生物降解作用。
Chemosphere. 2022 Apr;292:133506. doi: 10.1016/j.chemosphere.2021.133506. Epub 2022 Jan 4.
8
Electrode Colonization by the Feammox Bacterium sp. Strain A6.电极为 Feammox 菌 A6 菌株定植。
Appl Environ Microbiol. 2018 Nov 30;84(24). doi: 10.1128/AEM.02029-18. Print 2018 Dec 15.
9
Isolation and characterization of an ammonium-oxidizing iron reducer: Acidimicrobiaceae sp. A6.一株氨氧化亚铁还原菌的分离鉴定及其特性研究: Acidimicrobiaceae 菌 A6.
PLoS One. 2018 Apr 11;13(4):e0194007. doi: 10.1371/journal.pone.0194007. eCollection 2018.
10
Anaerobic ammonium oxidation coupled to iron reduction in constructed wetland mesocosms.人工湿地中厌氧氨氧化耦合铁还原的研究。
Sci Total Environ. 2019 Jan 15;648:984-992. doi: 10.1016/j.scitotenv.2018.08.189. Epub 2018 Aug 17.

引用本文的文献

1
Perfluoroalkane Sulfonamides and Derivatives, a Different Class of PFAS: Sorption and Microbial Biotransformation Insights.全氟烷烃磺酰胺及其衍生物,一类不同的全氟和多氟烷基物质:吸附及微生物生物转化研究见解
Environ Sci Technol. 2025 Jun 10;59(22):10734-10749. doi: 10.1021/acs.est.5c00906. Epub 2025 May 25.
2
Thermochemical Recycling and Degradation Strategies of Halogenated Polymers (F-, Cl-, Br-): A Holistic Review Coupled with Mechanistic Insights.卤代聚合物(F-、Cl-、Br-)的热化学回收与降解策略:结合机理见解的全面综述
Chem Rec. 2025 Jun;25(6):e202500022. doi: 10.1002/tcr.202500022. Epub 2025 Apr 7.
3
Rapid degradation of perfluorooctane sulfonic acid (PFOS) and perfluorononanoic acid (PFNA) through bimetallic catalyst of FeO/MnO and unravelling the effect of support SiO.

本文引用的文献

1
Microbial Defluorination of Unsaturated Per- and Polyfluorinated Carboxylic Acids under Anaerobic and Aerobic Conditions: A Structure Specificity Study.微生物脱除不饱和全氟及多氟羧酸在厌氧和好氧条件下:结构特异性研究。
Environ Sci Technol. 2022 Apr 19;56(8):4894-4904. doi: 10.1021/acs.est.1c05509. Epub 2022 Apr 4.
2
Polyacrylic Acid Nanoplatforms: Antimicrobial, Tissue Engineering, and Cancer Theranostic Applications.聚丙烯酸纳米平台:抗菌、组织工程及癌症诊疗应用
Polymers (Basel). 2022 Mar 21;14(6):1259. doi: 10.3390/polym14061259.
3
Biodegradation of PFOA in microbial electrolysis cells by Acidimicrobiaceae sp. strain A6.
通过FeO/MnO双金属催化剂实现全氟辛烷磺酸(PFOS)和全氟壬酸(PFNA)的快速降解并揭示载体SiO的作用
Heliyon. 2024 Jul 5;10(14):e34199. doi: 10.1016/j.heliyon.2024.e34199. eCollection 2024 Jul 30.
4
Defluorination of PFAS by Acidimicrobium sp. strain A6 and potential applications for remediation.嗜酸菌 A6 对全氟辛烷磺酸的脱氟作用及其在修复中的潜在应用。
Methods Enzymol. 2024;696:287-320. doi: 10.1016/bs.mie.2024.01.013. Epub 2024 Feb 15.
嗜酸菌属 A6 菌株在微生物电解池内对全氟辛酸的生物降解作用。
Chemosphere. 2022 Apr;292:133506. doi: 10.1016/j.chemosphere.2021.133506. Epub 2022 Jan 4.
4
Anaerobic degradation of perfluorooctanoic acid (PFOA) in biosolids by Acidimicrobium sp. strain A6.嗜酸菌 A6 对生物固体中全氟辛酸(PFOA)的厌氧降解作用。
J Hazard Mater. 2022 Feb 15;424(Pt D):127699. doi: 10.1016/j.jhazmat.2021.127699. Epub 2021 Nov 6.
5
PFAS and Dissolved Organic Carbon Enrichment in Surface Water Foams on a Northern U.S. Freshwater Lake.全氟和多氟烷基物质(PFAS)以及溶解有机碳在美国北部淡水湖表面泡沫水中的富集会导致环境和人类健康问题。
Environ Sci Technol. 2020 Nov 17;54(22):14455-14464. doi: 10.1021/acs.est.0c05697. Epub 2020 Nov 8.
6
Microbial Cleavage of C-F Bonds in Two C Per- and Polyfluorinated Compounds via Reductive Defluorination.通过还原脱氟作用微生物裂解两种全氟和多氟化合物中的 C-F 键。
Environ Sci Technol. 2020 Nov 17;54(22):14393-14402. doi: 10.1021/acs.est.0c04483. Epub 2020 Oct 29.
7
Fluorochemicals biodegradation as a potential source of trifluoroacetic acid (TFA) to the environment.氟化学品的生物降解可能是三氟乙酸(TFA)向环境释放的一个潜在来源。
Chemosphere. 2020 Sep;254:126894. doi: 10.1016/j.chemosphere.2020.126894. Epub 2020 Apr 24.
8
PFAS concentrations in soils: Background levels versus contaminated sites.土壤中的全氟烷基物质(PFAS)浓度:背景水平与污染场地。
Sci Total Environ. 2020 Oct 20;740:140017. doi: 10.1016/j.scitotenv.2020.140017. Epub 2020 Jun 6.
9
Defluorination of Perfluorooctanoic Acid (PFOA) and Perfluorooctane Sulfonate (PFOS) by sp. Strain A6.sp. 菌株 A6 对全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)的脱氟作用。
Environ Sci Technol. 2019 Oct 1;53(19):11410-11419. doi: 10.1021/acs.est.9b04047. Epub 2019 Sep 18.
10
Maternal exposure to perfluorooctanoic acid (PFOA) causes liver toxicity through PPAR-α pathway and lowered histone acetylation in female offspring mice.母体暴露于全氟辛酸(PFOA)可通过 PPAR-α 途径和降低雌性后代小鼠组蛋白乙酰化引起肝毒性。
Environ Sci Pollut Res Int. 2019 Jun;26(18):18866-18875. doi: 10.1007/s11356-019-05258-z. Epub 2019 May 7.