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A biochemical framework for anaerobic oxidation of methane driven by Fe(III)-dependent respiration

Consumption of methane by aerobic and anaerobic microbes governs the atmospheric level of this powerful greenhouse gas. Whereas a biochemical understanding of aerobic methanotrophy is well developed, a mechanistic understanding of anaerobic methanotrophy has been prevented by the unavailability of p...

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Autores principales: Yan, Zhen, Joshi, Prachi, Gorski, Christopher A., Ferry, James G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915437/
https://www.ncbi.nlm.nih.gov/pubmed/29691409
http://dx.doi.org/10.1038/s41467-018-04097-9
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author Yan, Zhen
Joshi, Prachi
Gorski, Christopher A.
Ferry, James G.
author_facet Yan, Zhen
Joshi, Prachi
Gorski, Christopher A.
Ferry, James G.
author_sort Yan, Zhen
collection PubMed
description Consumption of methane by aerobic and anaerobic microbes governs the atmospheric level of this powerful greenhouse gas. Whereas a biochemical understanding of aerobic methanotrophy is well developed, a mechanistic understanding of anaerobic methanotrophy has been prevented by the unavailability of pure cultures. Here we report a biochemical investigation of Methanosarcina acetivorans, a methane-producing species capable of anaerobic methanotrophic growth dependent on reduction of Fe(III). Our findings support a pathway anchored by Fe(III)-dependent mechanisms for energy conservation driving endergonic reactions that are key to methanotrophic growth. The pathway is remarkably similar to pathways hypothesized for uncultured anaerobic methanotrophic archaea. The results contribute to an improved understanding of the methane cycle that is paramount to understanding human interventions influencing Earth’s climate. Finally, the pathway enables advanced development and optimization of biotechnologies converting methane to value-added products through metabolic engineering of M. acetivorans.
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spelling pubmed-59154372018-04-27 A biochemical framework for anaerobic oxidation of methane driven by Fe(III)-dependent respiration Yan, Zhen Joshi, Prachi Gorski, Christopher A. Ferry, James G. Nat Commun Article Consumption of methane by aerobic and anaerobic microbes governs the atmospheric level of this powerful greenhouse gas. Whereas a biochemical understanding of aerobic methanotrophy is well developed, a mechanistic understanding of anaerobic methanotrophy has been prevented by the unavailability of pure cultures. Here we report a biochemical investigation of Methanosarcina acetivorans, a methane-producing species capable of anaerobic methanotrophic growth dependent on reduction of Fe(III). Our findings support a pathway anchored by Fe(III)-dependent mechanisms for energy conservation driving endergonic reactions that are key to methanotrophic growth. The pathway is remarkably similar to pathways hypothesized for uncultured anaerobic methanotrophic archaea. The results contribute to an improved understanding of the methane cycle that is paramount to understanding human interventions influencing Earth’s climate. Finally, the pathway enables advanced development and optimization of biotechnologies converting methane to value-added products through metabolic engineering of M. acetivorans. Nature Publishing Group UK 2018-04-24 /pmc/articles/PMC5915437/ /pubmed/29691409 http://dx.doi.org/10.1038/s41467-018-04097-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yan, Zhen
Joshi, Prachi
Gorski, Christopher A.
Ferry, James G.
A biochemical framework for anaerobic oxidation of methane driven by Fe(III)-dependent respiration
title A biochemical framework for anaerobic oxidation of methane driven by Fe(III)-dependent respiration
title_full A biochemical framework for anaerobic oxidation of methane driven by Fe(III)-dependent respiration
title_fullStr A biochemical framework for anaerobic oxidation of methane driven by Fe(III)-dependent respiration
title_full_unstemmed A biochemical framework for anaerobic oxidation of methane driven by Fe(III)-dependent respiration
title_short A biochemical framework for anaerobic oxidation of methane driven by Fe(III)-dependent respiration
title_sort biochemical framework for anaerobic oxidation of methane driven by fe(iii)-dependent respiration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915437/
https://www.ncbi.nlm.nih.gov/pubmed/29691409
http://dx.doi.org/10.1038/s41467-018-04097-9
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