AI Article Synopsis

  • The reductive acetyl-CoA pathway reduces carbon dioxide to acetyl-CoA and serves as an energy conservation method, while methanogenesis is crucial for the global carbon cycle.
  • Researchers converted a methanogen into an acetogen, demonstrating that it can grow without methanogenesis by relying on carbon monoxide for energy.
  • The study suggests that methanogens have more metabolic versatility than previously thought and provides evidence that methanogenesis may have evolved from the reductive acetyl-CoA pathway.

Article 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 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764690PMC
http://dx.doi.org/10.1073/pnas.2113853119DOI Listing

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