H<sub>2</sub>-Independent Growth of the Hydrogenotrophic Methanogen <named-content content-type="genus-species">Methanococcus maripaludis</named-content>

ABSTRACT Hydrogenotrophic methanogenic Archaea require reduced ferredoxin as an anaplerotic source of electrons for methanogenesis. H2 oxidation by the hydrogenase Eha provides these electrons, consistent with an H2 requirement for growth. Here we report the identification of alternative pathways of...

Full description

Bibliographic Details
Main Authors: Kyle C. Costa, Thomas J. Lie, Michael A. Jacobs, John A. Leigh
Format: Article
Language:English
Published: American Society for Microbiology 2013-05-01
Series:mBio
Online Access:https://journals.asm.org/doi/10.1128/mBio.00062-13
_version_ 1818431746562064384
author Kyle C. Costa
Thomas J. Lie
Michael A. Jacobs
John A. Leigh
author_facet Kyle C. Costa
Thomas J. Lie
Michael A. Jacobs
John A. Leigh
author_sort Kyle C. Costa
collection DOAJ
description ABSTRACT Hydrogenotrophic methanogenic Archaea require reduced ferredoxin as an anaplerotic source of electrons for methanogenesis. H2 oxidation by the hydrogenase Eha provides these electrons, consistent with an H2 requirement for growth. Here we report the identification of alternative pathways of ferredoxin reduction in Methanococcus maripaludis that operate independently of Eha to stimulate methanogenesis. A suppressor mutation that increased expression of the glycolytic enzyme glyceraldehyde-3-phosphate:ferredoxin oxidoreductase resulted in a strain capable of H2-independent ferredoxin reduction and growth with formate as the sole electron donor. In this background, it was possible to eliminate all seven hydrogenases of M. maripaludis. Alternatively, carbon monoxide oxidation by carbon monoxide dehydrogenase could also generate reduced ferredoxin that feeds into methanogenesis. In either case, the reduced ferredoxin generated was inefficient at stimulating methanogenesis, resulting in a slow growth phenotype. As methanogenesis is limited by the availability of reduced ferredoxin under these conditions, other electron donors, such as reduced coenzyme F420, should be abundant. Indeed, when F420-reducing hydrogenase was reintroduced into the hydrogenase-free mutant, the equilibrium of H2 production via an F420-dependent formate:H2 lyase activity shifted markedly toward H2 compared to the wild type. IMPORTANCE Hydrogenotrophic methanogens are thought to require H2 as a substrate for growth and methanogenesis. Here we show alternative pathways in methanogenic metabolism that alleviate this H2 requirement and demonstrate, for the first time, a hydrogenotrophic methanogen that is capable of growth in the complete absence of H2. The demonstration of alternative pathways in methanogenic metabolism suggests that this important group of organisms is metabolically more versatile than previously thought.
first_indexed 2024-12-14T15:54:12Z
format Article
id doaj.art-8c1756233a9b4953acf48bd5038ec03e
institution Directory Open Access Journal
issn 2150-7511
language English
last_indexed 2024-12-14T15:54:12Z
publishDate 2013-05-01
publisher American Society for Microbiology
record_format Article
series mBio
spelling doaj.art-8c1756233a9b4953acf48bd5038ec03e2022-12-21T22:55:18ZengAmerican Society for MicrobiologymBio2150-75112013-05-014210.1128/mBio.00062-13H<sub>2</sub>-Independent Growth of the Hydrogenotrophic Methanogen <named-content content-type="genus-species">Methanococcus maripaludis</named-content>Kyle C. Costa0Thomas J. Lie1Michael A. Jacobs2John A. Leigh3Department of Microbiology, University of Washington, Seattle, Washington, USADepartment of Microbiology, University of Washington, Seattle, Washington, USADepartment of Microbiology, University of Washington, Seattle, Washington, USADepartment of Microbiology, University of Washington, Seattle, Washington, USAABSTRACT Hydrogenotrophic methanogenic Archaea require reduced ferredoxin as an anaplerotic source of electrons for methanogenesis. H2 oxidation by the hydrogenase Eha provides these electrons, consistent with an H2 requirement for growth. Here we report the identification of alternative pathways of ferredoxin reduction in Methanococcus maripaludis that operate independently of Eha to stimulate methanogenesis. A suppressor mutation that increased expression of the glycolytic enzyme glyceraldehyde-3-phosphate:ferredoxin oxidoreductase resulted in a strain capable of H2-independent ferredoxin reduction and growth with formate as the sole electron donor. In this background, it was possible to eliminate all seven hydrogenases of M. maripaludis. Alternatively, carbon monoxide oxidation by carbon monoxide dehydrogenase could also generate reduced ferredoxin that feeds into methanogenesis. In either case, the reduced ferredoxin generated was inefficient at stimulating methanogenesis, resulting in a slow growth phenotype. As methanogenesis is limited by the availability of reduced ferredoxin under these conditions, other electron donors, such as reduced coenzyme F420, should be abundant. Indeed, when F420-reducing hydrogenase was reintroduced into the hydrogenase-free mutant, the equilibrium of H2 production via an F420-dependent formate:H2 lyase activity shifted markedly toward H2 compared to the wild type. IMPORTANCE Hydrogenotrophic methanogens are thought to require H2 as a substrate for growth and methanogenesis. Here we show alternative pathways in methanogenic metabolism that alleviate this H2 requirement and demonstrate, for the first time, a hydrogenotrophic methanogen that is capable of growth in the complete absence of H2. The demonstration of alternative pathways in methanogenic metabolism suggests that this important group of organisms is metabolically more versatile than previously thought.https://journals.asm.org/doi/10.1128/mBio.00062-13
spellingShingle Kyle C. Costa
Thomas J. Lie
Michael A. Jacobs
John A. Leigh
H<sub>2</sub>-Independent Growth of the Hydrogenotrophic Methanogen <named-content content-type="genus-species">Methanococcus maripaludis</named-content>
mBio
title H<sub>2</sub>-Independent Growth of the Hydrogenotrophic Methanogen <named-content content-type="genus-species">Methanococcus maripaludis</named-content>
title_full H<sub>2</sub>-Independent Growth of the Hydrogenotrophic Methanogen <named-content content-type="genus-species">Methanococcus maripaludis</named-content>
title_fullStr H<sub>2</sub>-Independent Growth of the Hydrogenotrophic Methanogen <named-content content-type="genus-species">Methanococcus maripaludis</named-content>
title_full_unstemmed H<sub>2</sub>-Independent Growth of the Hydrogenotrophic Methanogen <named-content content-type="genus-species">Methanococcus maripaludis</named-content>
title_short H<sub>2</sub>-Independent Growth of the Hydrogenotrophic Methanogen <named-content content-type="genus-species">Methanococcus maripaludis</named-content>
title_sort h sub 2 sub independent growth of the hydrogenotrophic methanogen named content content type genus species methanococcus maripaludis named content
url https://journals.asm.org/doi/10.1128/mBio.00062-13
work_keys_str_mv AT kyleccosta hsub2subindependentgrowthofthehydrogenotrophicmethanogennamedcontentcontenttypegenusspeciesmethanococcusmaripaludisnamedcontent
AT thomasjlie hsub2subindependentgrowthofthehydrogenotrophicmethanogennamedcontentcontenttypegenusspeciesmethanococcusmaripaludisnamedcontent
AT michaelajacobs hsub2subindependentgrowthofthehydrogenotrophicmethanogennamedcontentcontenttypegenusspeciesmethanococcusmaripaludisnamedcontent
AT johnaleigh hsub2subindependentgrowthofthehydrogenotrophicmethanogennamedcontentcontenttypegenusspeciesmethanococcusmaripaludisnamedcontent