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Direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with CO(2)-reducing methanogenesis

Electric syntrophy between fatty acid oxidizers and methanogens through direct interspecies electron transfer (DIET) is essential for balancing acidogenesis and methanogenesis in anaerobic digestion. Promoting DIET using electrically conductive additives proved effective in enhancing methanogenesis;...

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Detalles Bibliográficos
Autores principales: Jung, Heejung, Yu, Hyeonjung, Lee, Changsoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448109/
https://www.ncbi.nlm.nih.gov/pubmed/37636045
http://dx.doi.org/10.1016/j.isci.2023.107504
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author Jung, Heejung
Yu, Hyeonjung
Lee, Changsoo
author_facet Jung, Heejung
Yu, Hyeonjung
Lee, Changsoo
author_sort Jung, Heejung
collection PubMed
description Electric syntrophy between fatty acid oxidizers and methanogens through direct interspecies electron transfer (DIET) is essential for balancing acidogenesis and methanogenesis in anaerobic digestion. Promoting DIET using electrically conductive additives proved effective in enhancing methanogenesis; however, its possibility to affect other microbial redox reactions in methanogenic systems has been little studied. This study provides the first confirmation of the electro-syntrophic coupling of sulfide oxidation to S(0) with CO(2)-reducing methanogenesis in sulfur-rich methanogenic cultures supplemented with conductive magnetite (100–700-nm particle size). The H(2)S content in biogas, initially exceeding 5000 ppmv, decreased to below 1 ppmv along with an accumulation of extracellular S(0) (60–70 mg/L; initially <1 mg/L) at a magnetite dose of 20 mM Fe, while there were no significant changes in methane yield. A comprehensive polyphasic approach demonstrated that the S(0) formation occurs through electro-syntrophic oxidation of sulfide coupled with CO(2)-reducing methanogenesis, involving Methanothrix as the dominant methanogen.
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spelling pubmed-104481092023-08-25 Direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with CO(2)-reducing methanogenesis Jung, Heejung Yu, Hyeonjung Lee, Changsoo iScience Article Electric syntrophy between fatty acid oxidizers and methanogens through direct interspecies electron transfer (DIET) is essential for balancing acidogenesis and methanogenesis in anaerobic digestion. Promoting DIET using electrically conductive additives proved effective in enhancing methanogenesis; however, its possibility to affect other microbial redox reactions in methanogenic systems has been little studied. This study provides the first confirmation of the electro-syntrophic coupling of sulfide oxidation to S(0) with CO(2)-reducing methanogenesis in sulfur-rich methanogenic cultures supplemented with conductive magnetite (100–700-nm particle size). The H(2)S content in biogas, initially exceeding 5000 ppmv, decreased to below 1 ppmv along with an accumulation of extracellular S(0) (60–70 mg/L; initially <1 mg/L) at a magnetite dose of 20 mM Fe, while there were no significant changes in methane yield. A comprehensive polyphasic approach demonstrated that the S(0) formation occurs through electro-syntrophic oxidation of sulfide coupled with CO(2)-reducing methanogenesis, involving Methanothrix as the dominant methanogen. Elsevier 2023-08-01 /pmc/articles/PMC10448109/ /pubmed/37636045 http://dx.doi.org/10.1016/j.isci.2023.107504 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Jung, Heejung
Yu, Hyeonjung
Lee, Changsoo
Direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with CO(2)-reducing methanogenesis
title Direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with CO(2)-reducing methanogenesis
title_full Direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with CO(2)-reducing methanogenesis
title_fullStr Direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with CO(2)-reducing methanogenesis
title_full_unstemmed Direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with CO(2)-reducing methanogenesis
title_short Direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with CO(2)-reducing methanogenesis
title_sort direct interspecies electron transfer enables anaerobic oxidation of sulfide to elemental sulfur coupled with co(2)-reducing methanogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448109/
https://www.ncbi.nlm.nih.gov/pubmed/37636045
http://dx.doi.org/10.1016/j.isci.2023.107504
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