{"@context":"https://schema.org","@type":"ScholarlyArticle","headline":"Genus-specific remodeling of carbon and energy metabolism facilitates acetoclastic methanogenesis in\n Methanosarcina\n spp. and\n Methanothrix\n spp.","author":[{"@type":"Person","name":"Blake E Downing"},{"@type":"Person","name":"Dinesh Gupta"},{"@type":"Person","name":"Katie E Shalvarjian"},{"@type":"Person","name":"Dipti D Nayak"}],"datePublished":"2026","isPartOf":{"@type":"Periodical","name":"Journal of bacteriology"},"identifier":"https://doi.org/10.1128/jb.00448-25","description":"ABSTRACT\n \n \n \n Methanogenic archaea (methanogens) are microorganisms that obligately produce methane as a byproduct of their energy metabolism. While most methanogens grow on CO\n 2\n +H\n 2\n , isolates of the genera\n Methanosarcina\n and\n Methanothrix\n can use acetate as the sole substrate for methanogenesis. Methanogenic growth on acetate, i.e., acetoclastic methanogenesis, is hypothesized to require two distinct genetic modules: one for the activation of acetate to acetyl-CoA and another for producing a chemiosmotic gradient using electrons derived from ferredoxin. In\n Methanosarcina\n spp., the activation of acetate to acetyl-CoA is mediated by acetate kinase (Ack) and phosphotransacetylase (Pta), whereas\n Methanothrix\n spp. encode AMP-forming acetyl-CoA synthetases (Acs). The\n Rhodobacter\n nitrogen fixation complex (Rnf) or energy-converting hydrogenase (Ech) is critical for energy conservation in\n Methanosarcina\n spp. during growth on acetate, and a F\n 420\n :methanophenazine oxidoreductase-like complex (Fpo′) likely plays an analogous role in\n Methanothrix\n spp. Here, we tested the proposed modularity of these pathways to facilitate acetoclastic methanogenesis. First, we surveyed over 100 genomes within the class\n Methanosarcinia\n to show that the genomic potential for acetoclastic methanogenesis is widespread. We then used the genetically tractable strain,\n Methanosarcina acetivorans,\n to build all modular combinations that might support acetoclastic methanogenesis. Our results indicate that Acs, while functional, cannot replace Ack+Pta to rescue acetate growth in\n M. acetivorans\n . Similarly, the Fpo′ bioenergetic complex cannot replace Rnf. As such, our work suggests that, in addition to horizontal gene transfer of core catabolic modules, acetoclastic metabolism in methanogens requires changes to core energy metabolism too.\n \n \n \n IMPORTANCE\n \n A large fraction of biogenic methane is derived from acetate, yet acetoclastic methanogens, i.e., methanogens that grow on acetate, remain poorly characterized due to their slow growth. Two groups of methanogens,\n Methanosarcina\n spp. and\n Methanothrix\n spp., perform acetoclastic methanogenesis using distinct sets of genes for acetate activation and energy conservation. It is widely hypothesized that these genetic modules from\n Methanosarcina\n spp. and\n Methanothrix\n spp. are functionally analogous and would thus be interchangeable. To test this hypothesis, we engineered different combinations of modules for acetoclastic growth in\n Methanosarcina acetivorans\n . Our results challenge this hypothesized paradigm of modularity, and we posit that other changes to the carbon and electron transfer pathways are crucial for the emergence of acetoclastic methanogenesis.\n \n ","url":"https://innscience.ca/en/community/literature/doi_10_1128_jb_00448_25"}