Comparative genomics reveals electron transfer and syntrophic mechanisms differentiating methanotrophic and methanogenic archaea

Grayson L. Chadwick(California Institute of Technology), Connor T. Skennerton(California Institute of Technology), Rafael Laso-Pérez(University of Bremen), Andy O Leu(The University of Queensland), Daan R. Speth(California Institute of Technology), Hang Yu(California Institute of Technology), Connor Morgan‐Lang(University of British Columbia), Roland Hatzenpichler(California Institute of Technology), Danielle Goudeau(Joint Genome Institute), Rex R. Malmstrom(Joint Genome Institute), William J. Brazelton(University of Utah), Tanja Woyke(Joint Genome Institute), Steven Hallam(University of British Columbia), Gene W. Tyson(The University of Queensland), Gunter Wegener(University of Bremen), Antje Boëtius(Alfred-Wegener-Institut Helmholtz-Zentrum für Polar- und Meeresforschung), Victoria J. Orphan(California Institute of Technology)
PLoS Biology
January 5, 2022
Cited by 151Open Access
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Abstract

The anaerobic oxidation of methane coupled to sulfate reduction is a microbially mediated process requiring a syntrophic partnership between anaerobic methanotrophic (ANME) archaea and sulfate-reducing bacteria (SRB). Based on genome taxonomy, ANME lineages are polyphyletic within the phylum Halobacterota, none of which have been isolated in pure culture. Here, we reconstruct 28 ANME genomes from environmental metagenomes and flow sorted syntrophic consortia. Together with a reanalysis of previously published datasets, these genomes enable a comparative analysis of all marine ANME clades. We review the genomic features that separate ANME from their methanogenic relatives and identify what differentiates ANME clades. Large multiheme cytochromes and bioenergetic complexes predicted to be involved in novel electron bifurcation reactions are well distributed and conserved in the ANME archaea, while significant variations in the anabolic C1 pathways exists between clades. Our analysis raises the possibility that methylotrophic methanogenesis may have evolved from a methanotrophic ancestor.


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