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Kotoky, R.

Publications and source records attributed to Kotoky, R..

3 recordsLinked to original sources

Extracellular RNA drives Electromethanogenesis in a Methanogenic Archaeon

Methanogenic archaea account for two-thirds of global methane emissions. Some species, including Methanosarcina barkeri, reduce CO2 by directly acquiring electrons from solid substrates. However, the mechanism of electron acquisition in M. barkeri has remained unclear because this archaeon lacks the multiheme c-type cytochromes that drive extracellular electron transfer in many other microbes. Here we show that M. barkeri releases abundant extracellular nucleic acids during early growth, primarily short RNAs (78%). These extracellular nucleic acids assemble into G-quadruplexes (G4s) and B-DNA architectures that decorate cell surfaces and link aggregates. Surface-associated G4s are folded in vivo in a conformation compatible with cofactor binding and redox chemistry. Enzymatic degradation of extracellular nucleic acids abolished electron uptake and electromethanogenesis, whereas addition of synthetic G4-RNAs doubled methane yields and lowered cell-electrode interfacial resistance. These effects were not observed when cells were grown on soluble substrates. Together, these findings identify eRNA as a previously unrecognized electron conduit in methanogens, raising the possibility that RNA-based electron transfer may predate more elaborate protein-based electron conduits, with implications for models of early earth metabolism and for the design of next-generation bioenergy systems.

microbiology↗

Cell Surface Differences within the Genus Methanosarcina Shape Interactions with the Extracellular Environment

Methanosarcina are metabolically versatile methanogenic archaea that can perform extracellular electron transfer (EET), with important ecological and biotechnological implications. These archaea are broadly classified into two types (Type I and Type II) based on their energy metabolism and are also differ in their aggregation-disaggregation behavior, cell surface properties, and electron transfer strategies. Type I Methanosarcina typically form large multicellular aggregates within a methanochondroitin extracellular matrix, thrive in organic-rich environments, play a key role in anaerobic digestion during wastewater treatment and can perform EET. However, their mechanism of EET remains unresolved. In contrast, Type II Methanosarcina rely on multiheme c-type cytochromes for EET and are better adapted to low-organic, mineral-rich environments such as deep-sea sediments and aquifers, where they contribute to methane emissions. Despite their significance, the molecular mechanisms behind EET in Methanosarcina-- particularly for Type I--remain poorly understood. This review highlights what is known and what is unknown regarding the surface biology of Methanosarcina, their EET strategies, and biogeochemical and industrial roles, emphasizing the need for further research to unlock their full potential in sustainable methane management.

microbiology↗

Adaptation of a methanogen to the constructed environment

Due to unique genomic adaptations, Methanococcus maripaludis Mic1c10 exhibits severe corrosive behavior when in direct contact with Fe0. These adaptations are linked to attachment and effective growth on constructed surfaces. One such adaptation is that of a specific [NiFe]-hydrogenase that may anchor on the cell surface via glycosyl-glycosyl interactions to receive Fe0-electrons directly. Such an evolutionary response to constructed environments requires us to rethink methane cycling in human-altered ecosystems.

microbiology↗