Proceedings of the National Academy of Sciences · 2017 · 119 citations · 64 references
Life SciencesEcologyMicrobiologyMetabolismMicrobial EcologyMicrobial MetabolismDeep-sea MicrobiologyMicrobial BioenergeticsMicrobial BiogeochemistryMicrobial GrowthMicrobial MetabolomicsSediment MicrobiologyHydrocarbon-degrading MicrobesMetabolic Activity AssaysMicrobial Biomass MeasurementMicrobial Metabolism In The Deep SubsurfaceSecondary Ion Mass SpectrometryStable Isotope ProbingStable Isotope RatiosSubsurface Sediment Microbiology
N-labeled methanol, methylamine, and ammonium added at low (micromolar) concentrations to investigate methylotrophy in the deep subseafloor biosphere. Although the cell densities were low (50-2,000 cells per cubic centimeter), bulk geochemical measurements and single-cell-targeted nanometer-scale secondary ion mass spectrometry demonstrated active metabolism of methylated substrates by the thermally adapted microbial assemblage, with differing substrate utilization profiles between coal and shale incubations. The conversion of labeled methylamine and methanol was predominantly through heterotrophic processes, with only minor stimulation of methanogenesis. These findings were consistent with in situ and incubation 16S rRNA gene surveys. Microbial growth estimates in the incubations ranged from several months to over 100 y, representing some of the slowest direct measurements of environmental microbial biosynthesis rates. Collectively, these data highlight a small, but viable, deep coal bed biosphere characterized by extremely slow-growing heterotrophs that can utilize a diverse range of carbon and nitrogen substrates.
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R: A Language and Environment for Statistical Computing
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