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Egas, R. A.

Publications and source records attributed to Egas, R. A..

3 recordsLinked to original sources

Adaptation of the freshwater anaerobic methanotroph 'Ca. Methanoperedens vercellensis' to low pH levels reveals membrane lipid remodelling

Anaerobic methanotrophic archaea are key members of the biological methane filter, thereby preventing emissions of this strong greenhouse gas into the atmosphere. Previous studies on freshwater anaerobic methanotrophs targeted the activity of these microorganisms at circumneutral pH whereas molecular ecology studies identified this phylotype also in acidic environments such as peatlands; it is currently unknown whether they can adapt to low pH and remain effective in the biological methane filter in low pH environments. Here we show that a granular enrichment culture of the freshwater methanotroph Ca. M. vercellensis loses activity when experiencing pH stress but remains metabolically active down to pH 5.65 with appropriate adaptation time, indicating that adaptive changes are necessary to accommodate anaerobic methane oxidation at lower pH. Analyses of archaeal lipids revealed an increase in zwitterionic intact polar lipids over anionic lipids as an adaptation. This coincided with a change in granule structure while methane oxidation rate and enrichment state of Ca. M. vercellensis remained stable. We show that Ca. M. vercellensis remains metabolically active at lower pH values, despite increased maintenance energy demands and the need for cytoplasmic pH homeostasis. Our study demonstrates that adaptations to stress by slow-growing microorganisms may require long-term observation and is thereby instrumental for a better understanding of methane cycling in acidic ecosystems.

microbiology↗

Proton stress adaptation in acidophilic sulfate-reducing bacteria: insights from Acididesulfobacillus acetoxydans for acid mine drainage bioremediation

Acid mine drainage (AMD) waters are a global environmental threat due to their extremely low pH (<3) and high metal loads. Acidophilic sulfate-reducing bacteria (aSRB) can mitigate AMD by reducing sulfate to sulfide, a proton-consuming process that also precipitates metals as metal sulfides. Although sulfate reduction has been observed in AMD waters, most characterized aSRB are only moderately acidophilic and originate from protected microniches. Here, we examined the pH tolerance and proton stress adaptation of the complete organic acid-oxidizing aSRB Acididesulfobacillus acetoxydans. Continuous chemostat cultivations were operated across a pH gradient, achieving steady states from pH 5.0 (optimum) down to 2.9, with microcosms showing metabolic activity even at pH 2.5 which is typical AMD-acidity. Transcriptomic profiles remained remarkably stable across conditions, except for upregulation of the K+-transporting ATPase (kdpABC) at lower pH, suggesting an increased reliance on the chemiosmotic gradient to impede proton influx. Lipid analysis revealed increased core lipid saturation, mid-chain methylation and a shift in priming precursors from leucine to valine at low pH, indicating reduced membrane permeability and more energy-efficient biosynthetic pathways. These adaptations impede proton entry demonstrating adaptation of aSRB to AMD-like acidity and removes the critical pH bottleneck for AMD bioremediation and metal recovery. SynopsisThis study shows acidophilic sulfate-reducing bacteria can adapt to AMD-like acidity while retaining metabolic activity, underscoring their potential for AMD bioremediation and biotechnology.

microbiology↗

Carbon monoxide metabolism in freshwater anaerobic methanotrophic archaea

Anaerobic methanotrophic archaea mitigate methane emissions in anoxic environments as key members of the biological methane filter. Despite their ecological significance, physiology of anaerobic methanotrophs remains poorly understood. Here, we demonstrate that the freshwater methanotroph Candidatus Methanoperedens BLZ2 prefers carbon monoxide (CO) over methane as an electron donor. In the absence of respiratory nitrate, CO oxidation led to acetogenesis and methanogenesis with rates comparable to methane oxidation. The circularized genome of Ca. M. BLZ2 encodes six Ni-dependent carbon monoxide dehydrogenases (CODHs), three of which were highly expressed. Furthermore, we identified a 156-kbp mobile genetic element carrying central metabolic gene clusters, including two additional, highly expressed CODHs. CODH genes were widespread in Methanoperedenaceae and showed diverse evolutionary affiliations, including Methanocomedenaceae anaerobic methanotrophs and bacterial lineages. These findings highlight a novel metabolism and genome plasticity in anaerobic methanotrophs challenging their classification as obligate methanotrophs and their ecological role in anoxic carbon cycling.

microbiology↗