Deconstructing Methanosarcina acetivorans into an acetogenic archaeon

  • Christian Schone
  • , Anja Poehlein
  • , Nico Jehmlich
  • , Norman Adlung
  • , Rolf Daniel
  • , Martin von Bergen
  • , Silvan Scheller
  • , Michael Rother*
  • *Corresponding author for this work

    Research output: Contribution to journalArticleScientificpeer-review

    Abstract

    The reductive acetyl-coenzyme A (acetyl-CoA) pathway, whereby carbon dioxide is sequentially reduced to acetyl-CoA via coenzyme-bound C1 intermediates, is the only autotrophic pathway that can at the same time be the means for energy conservation. A conceptually similar metabolism and a key process in the global carbon cycle is methanogenesis, the biogenic formation of methane. All known methanogenic archaea depend on methanogenesis to sustain growth and use the reductive acetyl-CoA pathway for autotrophic carbon fixation. Here, we converted a methanogen into an acetogen and show that Methanosarcina acetivorans can dispense with methanogenesis for energy conservation completely. By targeted disruption of the methanogenic pathway, followed by adaptive evolution, a strain was created that sustained growth via carbon monoxide–dependent acetogenesis. A minute flux (less than 0.2% of the carbon monoxide consumed) through the methane-liberating reaction remained essential, indicating that currently living methanogens utilize metabolites of this reaction also for anabolic purposes. These results suggest that the metabolic flexibility of methanogenic archaea might be much greater than currently known. Also, our ability to deconstruct a methanogen into an acetogen by merely removing cellular functions provides experimental support for the notion that methanogenesis could have evolved from the reductive acetyl-coenzyme A pathway.

    Original languageEnglish
    Article numbere2113853119
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume119
    Issue number2
    DOIs
    Publication statusPublished - 11 Jan 2022
    MoE publication typeA1 Journal article-refereed

    Funding

    M.V. and N.J. acknowledge support from the Helmholtz Centre for Environmental Research for the ProMetheus platform for proteomics and metabolomics. This work was supported by grants from the Graduate Academy of the Technische Universität Dresden to C.S., Novo Nordisk Foundation Grant NNF19OC0055464 to N.A., and Academy of Finland Grant 326020 to S.S.

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 7 - Affordable and Clean Energy
      SDG 7 Affordable and Clean Energy

    Keywords

    • Acetogenic
    • Acetyl-CoA pathway
    • Methanogenic
    • Methanosarcina
    • Carbon Monoxide/metabolism
    • Methanomicrobiaceae
    • Acetyl Coenzyme A/metabolism
    • Proteome
    • Methanosarcina/genetics
    • Carbon Dioxide/metabolism
    • Methane/metabolism
    • Archaea/genetics
    • Genome

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