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NanoFe(3)O(4) as Solid Electron Shuttles to Accelerate Acetotrophic Methanogenesis by Methanosarcina barkeri

Magnetite nanoparticles (nanoFe(3)O(4)) have been reported to facilitate direct interspecies electron transfer (DIET) between syntrophic bacteria and methanogens thereby improving syntrophic methanogenesis. However, whether or how nanoFe(3)O(4) affects acetotrophic methanogenesis remain unknown. Her...

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Autores principales: Fu, Li, Zhou, Ting, Wang, Jingyuan, You, Lexing, Lu, Yahai, Yu, Linpeng, Zhou, Shungui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411705/
https://www.ncbi.nlm.nih.gov/pubmed/30891017
http://dx.doi.org/10.3389/fmicb.2019.00388
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author Fu, Li
Zhou, Ting
Wang, Jingyuan
You, Lexing
Lu, Yahai
Yu, Linpeng
Zhou, Shungui
author_facet Fu, Li
Zhou, Ting
Wang, Jingyuan
You, Lexing
Lu, Yahai
Yu, Linpeng
Zhou, Shungui
author_sort Fu, Li
collection PubMed
description Magnetite nanoparticles (nanoFe(3)O(4)) have been reported to facilitate direct interspecies electron transfer (DIET) between syntrophic bacteria and methanogens thereby improving syntrophic methanogenesis. However, whether or how nanoFe(3)O(4) affects acetotrophic methanogenesis remain unknown. Herein, we demonstrate the unique role of nanoFe(3)O(4) in accelerating methane production from direct acetotrophic methanogenesis in Methanosarcina-enriched cultures, which was further confirmed by pure cultures of Methanosarcina barkeri. Compared with other nanomaterials of higher electrical conductivity such as carbon nanotubes and graphite, nanoFe(3)O(4) with mixed valence Fe(II) and Fe(III) had the most significant stimulatory effect on methane production, suggesting its redox activity rather than electrical conductivity led to enhanced methanogenesis by M. barkeri. Cell morphology and spectroscopy analysis revealed that nanoFe(3)O(4) penetrated into the cell membrane and cytoplasm of M. barkeri. These results provide the unprecedented possibility that nanoFe(3)O(4) in the cell membrane of methanogens serve as electron shuttles to facilitate intracellular electron transfer and thus enhance methane production. This work has important implications not only for understanding the mechanisms of mineral-methanogen interaction but also for optimizing engineered methanogenic processes.
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spelling pubmed-64117052019-03-19 NanoFe(3)O(4) as Solid Electron Shuttles to Accelerate Acetotrophic Methanogenesis by Methanosarcina barkeri Fu, Li Zhou, Ting Wang, Jingyuan You, Lexing Lu, Yahai Yu, Linpeng Zhou, Shungui Front Microbiol Microbiology Magnetite nanoparticles (nanoFe(3)O(4)) have been reported to facilitate direct interspecies electron transfer (DIET) between syntrophic bacteria and methanogens thereby improving syntrophic methanogenesis. However, whether or how nanoFe(3)O(4) affects acetotrophic methanogenesis remain unknown. Herein, we demonstrate the unique role of nanoFe(3)O(4) in accelerating methane production from direct acetotrophic methanogenesis in Methanosarcina-enriched cultures, which was further confirmed by pure cultures of Methanosarcina barkeri. Compared with other nanomaterials of higher electrical conductivity such as carbon nanotubes and graphite, nanoFe(3)O(4) with mixed valence Fe(II) and Fe(III) had the most significant stimulatory effect on methane production, suggesting its redox activity rather than electrical conductivity led to enhanced methanogenesis by M. barkeri. Cell morphology and spectroscopy analysis revealed that nanoFe(3)O(4) penetrated into the cell membrane and cytoplasm of M. barkeri. These results provide the unprecedented possibility that nanoFe(3)O(4) in the cell membrane of methanogens serve as electron shuttles to facilitate intracellular electron transfer and thus enhance methane production. This work has important implications not only for understanding the mechanisms of mineral-methanogen interaction but also for optimizing engineered methanogenic processes. Frontiers Media S.A. 2019-03-05 /pmc/articles/PMC6411705/ /pubmed/30891017 http://dx.doi.org/10.3389/fmicb.2019.00388 Text en Copyright © 2019 Fu, Zhou, Wang, You, Lu, Yu and Zhou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Fu, Li
Zhou, Ting
Wang, Jingyuan
You, Lexing
Lu, Yahai
Yu, Linpeng
Zhou, Shungui
NanoFe(3)O(4) as Solid Electron Shuttles to Accelerate Acetotrophic Methanogenesis by Methanosarcina barkeri
title NanoFe(3)O(4) as Solid Electron Shuttles to Accelerate Acetotrophic Methanogenesis by Methanosarcina barkeri
title_full NanoFe(3)O(4) as Solid Electron Shuttles to Accelerate Acetotrophic Methanogenesis by Methanosarcina barkeri
title_fullStr NanoFe(3)O(4) as Solid Electron Shuttles to Accelerate Acetotrophic Methanogenesis by Methanosarcina barkeri
title_full_unstemmed NanoFe(3)O(4) as Solid Electron Shuttles to Accelerate Acetotrophic Methanogenesis by Methanosarcina barkeri
title_short NanoFe(3)O(4) as Solid Electron Shuttles to Accelerate Acetotrophic Methanogenesis by Methanosarcina barkeri
title_sort nanofe(3)o(4) as solid electron shuttles to accelerate acetotrophic methanogenesis by methanosarcina barkeri
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411705/
https://www.ncbi.nlm.nih.gov/pubmed/30891017
http://dx.doi.org/10.3389/fmicb.2019.00388
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