bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.01.08.698499

Acetogenic methane-carbon monoxide comproportionation: an exergonic but unobserved microbial metabolism

Abstract

Microbial metabolism relies on redox reactions that exploit chemical disequilibria. While aerobic carbon oxidation, carbon fixation, and fermentation are well studied, the broader space of anaerobic carbon redox reactions remains underexplored. In this study, carbon comproportionation, or reverse fermentation, reactions are identified as a previously unrecognized and potentially favorable class of microbial carbon redox transformations. Particular attention is given to the reaction between methane (CH4) and carbon monoxide (CO) to form acetate, a reaction that has not previously been evaluated despite the widespread occurrence of CH4 and CO in anoxic systems. Gibbs energies ({Delta}Gr) for this reaction were calculated across broad ranges of temperature, pH, and dissolved CH4 and CO concentrations using measured physicochemical data from a wide variety of environmental systems. We show that acetogenic CH4-CO comproportionation is exergonic in all environments where both substrates were detected. The most favorable energetic conditions occur at high pH, low temperature, and high reactant concentrations, consistent with cool serpentinizing systems. In several settings, the calculated Gibbs energy yields and energy densities overlap or exceed known anaerobic metabolisms involving CH4, CO, and acetate. These results demonstrate that acetogenic CH4-CO comproportionation can support microbial energy conservation in a variety of settings. To determine if this metabolism could have operated on early Earth or Mars, modeled fluid compositions show that this reaction is also exergonic under plausible physicochemical regimes. This work broadens the suite of possible microbial energy metabolisms and provides testable criteria for evaluating carbon-based catabolic reactions on Earth and on other planetary bodies. Plain Language SummaryMicroorganisms obtain energy by catalyzing chemical reactions in their environment. The energy available from a reaction can be quantified using Gibbs energies of reaction ({Delta}Gr). When {Delta}Gr < 0, energy is released that microorganisms can use to build biomass and carry out other activities. In this study, we predicted a new energy-yielding reaction that could potentially support microbial life. In this reaction, methane (CH4) is oxidized using carbon monoxide (CO) to produce acetate. Using thermodynamic calculations and measured geochemical data from natural environments, we show that this reaction can release usable energy under a wide range of conditions, including continental serpentinizing systems, the deep continental and marine subsurface, and geothermal springs. We also predict that this reaction could support life under plausible early Earth conditions and in modeled Martian fluids. Together, these observations identify the reaction of CH4 and CO to form acetate as a potentially viable microbial energy source in anoxic environments on Earth and other planetary bodies.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Aronson, H. S., Leavitt, W. D., LaRowe, D. E.. 2026-01-08. Acetogenic methane-carbon monoxide comproportionation: an exergonic but unobserved microbial metabolism. https://doi.org/10.64898/2026.01.08.698499

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Matrix-controlled emergence of biofilm architecture shapes antimicrobial survival

Biofilms are structured microbial communities whose extracellular matrix is widely regarded as a basis of their protection against antimicrobial compounds. Yet how matrix production by individual bacteria gives rise to collective architecture and antimicrobial protection remains poorly understood. Here, we systematically varied expression of the master biofilm regulator csgD in Salmonella enterica and found that increasing matrix production reorganizes biofilms from dense, isotropic packings into sparse, nematically aligned communities by altering cell-cell interactions. By combining experimentally measured biofilm architectures with reaction-diffusion modeling, we show that these structural changes produce distinct patterns of antimicrobial killing, ranging from preferential killing near the liquid-biofilm interface to more uniform killing throughout the community. Consequently, increasing matrix production unexpectedly reduces antimicrobial survival by shifting the biofilm into different transport regimes, while strain-specific physiological differences further modulate antimicrobial depletion. Rather than acting as a passive barrier, EPS therefore shapes antimicrobial susceptibility by reorganizing biofilm architecture and its transport properties. EPS thus provides a physical link between molecular regulation, collective architecture and antimicrobial survival, providing a quantitative framework for understanding how cellular matrix production generates emergent biofilm function.

microbiology↗

Mapping virulence-associated protein interaction networks reveals regulators of thermotolerance in Cryptococcus neoformans

Protein-protein interactions (PPIs) influence critical biological processes in pathogenic microorganisms, such as the human fungal pathogen, Cryptococcus neoformans. Fungal thermotolerance and stress response pathways are key virulence determinants that directly impact pathogen adaptation and survival and the infection process. To establish a comprehensive baseline of PPIs in C. neoformans and explore these interactions to infer functional roles for uncharacterized proteins, we applied size exclusion chromatography coupled with mass spectrometry to the secreted and cellular proteomes of the fungi. As a result, 216 and 1699 unique proteins were identified across 24 secretome and proteome fractions, respectively. The predicted secretome networks included expected proteins associated with vesicles and virulence, indicating a role in extracellular defense. Whereas the cryptococcal proteome highlighted interactions among proteins with defined roles in fungal virulence for protein stability and thermotolerance, including two previously uncharacterized proteins, CNAG_00287 and CNAG_05199, putatively involved in complex formation with heat-shock proteins (HSP). Based on sequence and structure homology, we propose that CNAG_00287 is a tetratricopeptide repeat-containing co-chaperone that modulates Hsp 70 activity and CNAG_05199 functions as a Hsp70. We validated the thermotolerance role of CNAG_00287 in heat-related stress, as its absence significantly impaired fungal growth in nutrient-limited media at 37 {degrees}C. Together, this work resolves virulence-associated PPIs within C. neoformans and reveals new molecular regulators of thermotolerance that underpin fungal pathogenicity.

microbiology↗

Environmental filtering and host identity collectively shape root-associated microbiomes of Ericaceae and ectomycorrhizal plants in fumarole fields

Background Symbiosis with microbes is a key strategy that has enabled plants to colonize extreme environments. Since the benefits conferred by root-associated microbes depend on both environmental conditions and host-microbe combinations, plant adaptation to harsh environments is closely linked to the assembly of root microbial communities. Understanding how environmental and host filtering jointly shape these communities is therefore fundamental to elucidating the mechanisms underlying plant adaptation to extreme environments. Results In this study, we investigated the differentiation of root-associated prokaryotic and fungal communities and individual operational taxonomic units (OTUs) across two contrasting habitats surrounding fumaroles, solfatara-field and forest-edge habitats, and six dominant Ericaceae and ectomycorrhizal plant taxa. Prokaryotic and fungal OTUs rarely exhibited strong preferences for both habitat and host identity. Instead, many of prokaryotic and fungal OTUs specialized to one of these niches, collectively generating root microbial communities differentiated by both factors. Nonetheless, striking specializations in habitat and host niches were observed in the fungal family Hyaloscyphaceae (Helotiales). To gain insight into the evolutionary basis of microbial specialization, we examined phylogenetic signals in preference phenotypes. The resulting weak phylogenetic signals in these preference phenotypes further suggest that this fungal clade has undergone substantial ecological divergence. Conclusion Overall, our findings indicate that root-associated microbial communities in extreme environments are assembled through the accumulation of microbial taxa specialized to either habitat or host, and that strong ecological specialization in fungi can arise with little phylogenetic constraint.

microbiology↗