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Fe/S Redox-Coupled Mercury Transformation Mediated by Acidithiobacillus ferrooxidans ATCC 23270 under Aerobic and/or Anaerobic Conditions

Bioleaching processes or microbially mediated iron/sulfur redox processes in acid mine drainage (AMD) result in mineral dissolution and transformation, the release of mercury and other heavy metal ions, and changes in the occurrence forms and concentration of mercury. However, pertinent studies on t...

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Autores principales: Liu, Yue, Gu, Chenyun, Liu, Hongchang, Zhou, Yuhang, Nie, Zhenyuan, Wang, Yirong, Chen, Lu, Xia, Jinlan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141921/
https://www.ncbi.nlm.nih.gov/pubmed/37110452
http://dx.doi.org/10.3390/microorganisms11041028
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author Liu, Yue
Gu, Chenyun
Liu, Hongchang
Zhou, Yuhang
Nie, Zhenyuan
Wang, Yirong
Chen, Lu
Xia, Jinlan
author_facet Liu, Yue
Gu, Chenyun
Liu, Hongchang
Zhou, Yuhang
Nie, Zhenyuan
Wang, Yirong
Chen, Lu
Xia, Jinlan
author_sort Liu, Yue
collection PubMed
description Bioleaching processes or microbially mediated iron/sulfur redox processes in acid mine drainage (AMD) result in mineral dissolution and transformation, the release of mercury and other heavy metal ions, and changes in the occurrence forms and concentration of mercury. However, pertinent studies on these processes are scarce. Therefore, in this work, the Fe/S redox-coupled mercury transformation mediated by Acidithiobacillus ferrooxidans ATCC 23270 under aerobic and/or anaerobic conditions was studied by combining analyses of solution behavior (pH, redox potential, and Fe/S/Hg ion concentrations), the surface morphology and elemental composition of the solid substrate residue, the Fe/S/Hg speciation transformation, and bacterial transcriptomics. It was found that: (1) the presence of Hg(2+) significantly inhibited the apparent iron/sulfur redox process; (2) the addition of Hg(2+) caused a significant change in the composition of bacterial surface compounds and elements such as C, N, S, and Fe; (3) Hg mainly occurred in the form of Hg(0), HgS, and HgSO(4) in the solid substrate residues; and (4) the expression of mercury-resistant genes was higher in earlier stages of growth than in the later stages of growth. The results indicate that the addition of Hg(2+) significantly affected the iron/sulfur redox process mediated by A. ferrooxidans ATCC 23270 under aerobic, anaerobic, and coupled aerobic–anaerobic conditions, which further promoted Hg transformation. This work is of great significance for the treatment and remediation of mercury pollution in heavy metal-polluted areas.
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spelling pubmed-101419212023-04-29 Fe/S Redox-Coupled Mercury Transformation Mediated by Acidithiobacillus ferrooxidans ATCC 23270 under Aerobic and/or Anaerobic Conditions Liu, Yue Gu, Chenyun Liu, Hongchang Zhou, Yuhang Nie, Zhenyuan Wang, Yirong Chen, Lu Xia, Jinlan Microorganisms Article Bioleaching processes or microbially mediated iron/sulfur redox processes in acid mine drainage (AMD) result in mineral dissolution and transformation, the release of mercury and other heavy metal ions, and changes in the occurrence forms and concentration of mercury. However, pertinent studies on these processes are scarce. Therefore, in this work, the Fe/S redox-coupled mercury transformation mediated by Acidithiobacillus ferrooxidans ATCC 23270 under aerobic and/or anaerobic conditions was studied by combining analyses of solution behavior (pH, redox potential, and Fe/S/Hg ion concentrations), the surface morphology and elemental composition of the solid substrate residue, the Fe/S/Hg speciation transformation, and bacterial transcriptomics. It was found that: (1) the presence of Hg(2+) significantly inhibited the apparent iron/sulfur redox process; (2) the addition of Hg(2+) caused a significant change in the composition of bacterial surface compounds and elements such as C, N, S, and Fe; (3) Hg mainly occurred in the form of Hg(0), HgS, and HgSO(4) in the solid substrate residues; and (4) the expression of mercury-resistant genes was higher in earlier stages of growth than in the later stages of growth. The results indicate that the addition of Hg(2+) significantly affected the iron/sulfur redox process mediated by A. ferrooxidans ATCC 23270 under aerobic, anaerobic, and coupled aerobic–anaerobic conditions, which further promoted Hg transformation. This work is of great significance for the treatment and remediation of mercury pollution in heavy metal-polluted areas. MDPI 2023-04-14 /pmc/articles/PMC10141921/ /pubmed/37110452 http://dx.doi.org/10.3390/microorganisms11041028 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Yue
Gu, Chenyun
Liu, Hongchang
Zhou, Yuhang
Nie, Zhenyuan
Wang, Yirong
Chen, Lu
Xia, Jinlan
Fe/S Redox-Coupled Mercury Transformation Mediated by Acidithiobacillus ferrooxidans ATCC 23270 under Aerobic and/or Anaerobic Conditions
title Fe/S Redox-Coupled Mercury Transformation Mediated by Acidithiobacillus ferrooxidans ATCC 23270 under Aerobic and/or Anaerobic Conditions
title_full Fe/S Redox-Coupled Mercury Transformation Mediated by Acidithiobacillus ferrooxidans ATCC 23270 under Aerobic and/or Anaerobic Conditions
title_fullStr Fe/S Redox-Coupled Mercury Transformation Mediated by Acidithiobacillus ferrooxidans ATCC 23270 under Aerobic and/or Anaerobic Conditions
title_full_unstemmed Fe/S Redox-Coupled Mercury Transformation Mediated by Acidithiobacillus ferrooxidans ATCC 23270 under Aerobic and/or Anaerobic Conditions
title_short Fe/S Redox-Coupled Mercury Transformation Mediated by Acidithiobacillus ferrooxidans ATCC 23270 under Aerobic and/or Anaerobic Conditions
title_sort fe/s redox-coupled mercury transformation mediated by acidithiobacillus ferrooxidans atcc 23270 under aerobic and/or anaerobic conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141921/
https://www.ncbi.nlm.nih.gov/pubmed/37110452
http://dx.doi.org/10.3390/microorganisms11041028
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