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Aerobic H 2 respiration enhances metabolic flexibility of methanotrophic bacteria
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Batch cultivation of Methylosinus trichosporium OB3B: IV. Production of hydrogen‐driven soluble or particulate methane monooxygenase activity
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
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Detection and localization of two hydrogenases in Methylococcus capsulatus (Bath) and their potential role in methane metabolism
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PQQ-dependent methanol dehydrogenases: rare-earth elements make a difference
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The alternative complex III: A different architecture using known building modules
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Integration of hydrogenase expression and hydrogen sensing in bacterial cell physiology
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Crystal Structure of the O 2 -Tolerant Membrane-Bound Hydrogenase 1 from Escherichia coli in Complex with Its Cognate Cytochrome b
inferredcites →https://doi.org/10.1038/356421a0openalex-snapshot
Importance of methane-oxidizing bacteria in the methane budget as revealed by the use of a specific inhibitor
inferredcites →https://doi.org/10.1038/ismej.2011.139openalex-snapshot
An improved Greengenes taxonomy with explicit ranks for ecological and evolutionary analyses of bacteria and archaea
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Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms
inferredcites →https://doi.org/10.1038/ismej.2015.153openalex-snapshot
Genomic and metagenomic surveys of hydrogenase distribution indicate H2 is a widely utilised energy source for microbial growth and survival
inferredcites →https://doi.org/10.1038/nature06411openalex-snapshot
Methane oxidation by an extremely acidophilic bacterium of the phylum Verrucomicrobia
inferredcites →https://doi.org/10.1038/nature08883openalex-snapshot
Nitrite-driven anaerobic methane oxidation by oxygenic bacteria
inferredcites →https://doi.org/10.1038/nature10504openalex-snapshot
Structural basis for a [4Fe-3S] cluster in the oxygen-tolerant membrane-bound [NiFe]-hydrogenase
inferredcites →https://doi.org/10.1038/nature12375openalex-snapshot
Anaerobic oxidation of methane coupled to nitrate reduction in a novel archaeal lineage
inferredcites →https://doi.org/10.1038/nature13192openalex-snapshot
Trace-gas metabolic versatility of the facultative methanotroph Methylocella silvestris
inferredcites →https://doi.org/10.1038/nmeth.2474openalex-snapshot
Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data
inferredcites →https://doi.org/10.1038/nmeth.2604openalex-snapshot
UPARSE: highly accurate OTU sequences from microbial amplicon reads
inferredcites →https://doi.org/10.1038/nrmicro2439openalex-snapshot
Microorganisms and climate change: terrestrial feedbacks and mitigation options
inferredcites →https://doi.org/10.1038/nrmicro2940openalex-snapshot
Structure, function and biosynthesis of O2-tolerant hydrogenases
inferredcites →https://doi.org/10.1073/pnas.0400522101openalex-snapshot
Temperature dependence of metabolic rates for microbial growth, maintenance, and survival
inferredcites →https://doi.org/10.1073/pnas.0600035103openalex-snapshot
Heterotrophic Archaea dominate sedimentary subsurface ecosystems off Peru
inferredcites →https://doi.org/10.1073/pnas.0704162105openalex-snapshot
Methane oxidation at 55°C and pH 2 by a thermoacidophilic bacterium belonging to the Verrucomicrobia phylum
inferredcites →https://doi.org/10.1073/pnas.1320586111openalex-snapshot
A soil actinobacterium scavenges atmospheric H 2 using two membrane-associated, oxygen-dependent [NiFe] hydrogenases
inferredcites →https://doi.org/10.1073/pnas.1407034111openalex-snapshot
An obligately aerobic soil bacterium activates fermentative hydrogen production to survive reductive stress during hypoxia
inferredcites →https://doi.org/10.1073/pnas.1508385112openalex-snapshot
Persistence of the dominant soil phylum Acidobacteria by trace gas scavenging
inferredcites →https://doi.org/10.1093/nar/gkr1044openalex-snapshot
IMG: the integrated microbial genomes database and comparative analysis system
inferredcites →https://doi.org/10.1093/nar/gks808openalex-snapshot
Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies
inferredcites →https://doi.org/10.1099/00207713-47-2-590openalex-snapshot
List of Bacterial Names with Standing in Nomenclature: a Folder Available on the Internet
inferredcites →https://doi.org/10.1111/1462-2920.12249openalex-snapshot
Rare earth metals are essential for methanotrophic life in volcanic mudpots
inferredcites →https://doi.org/10.1111/1462-2920.12320openalex-snapshot
Three different [ NiFe ] hydrogenases confer metabolic flexibility in the obligate aerobe M ycobacterium smegmatis
inferredcites →https://doi.org/10.1111/1462-2920.12454openalex-snapshot
Distribution and diversity of V errucomicrobia methanotrophs in geothermal and acidic environments
inferredcites →https://doi.org/10.1111/j.1462-2920.2005.00791.xopenalex-snapshot
Abundance and activity of uncultured methanotrophic bacteria involved in the consumption of atmospheric methane in two forest soils
inferredcites →https://doi.org/10.1111/j.1574-6968.2011.02315.xopenalex-snapshot
Facultative methanotrophy: false leads, true results, and suggestions for future research
inferredcites →https://doi.org/10.1111/j.1758-2229.2009.00022.xopenalex-snapshot
Environmental, genomic and taxonomic perspectives on methanotrophic Verrucomicrobia
inferredcites →https://doi.org/10.1111/j.1758-2229.2012.00370.xopenalex-snapshot
Conceptualizing functional traits and ecological characteristics of methane‐oxidizing bacteria as life strategies
inferredcites →https://doi.org/10.1126/science.1174760openalex-snapshot
Improved Attribution of Climate Forcing to Emissions
inferredcites →https://doi.org/10.1128/aem.00062-07openalex-snapshot
Naive Bayesian Classifier for Rapid Assignment of rRNA Sequences into the New Bacterial Taxonomy
inferredcites →https://doi.org/10.1128/aem.00726-11openalex-snapshot
Environmental, Biogeographic, and Biochemical Patterns of Archaea of the Family Ferroplasmaceae
inferredcites →https://doi.org/10.1128/aem.01838-14openalex-snapshot
Expanding the Verrucomicrobial Methanotrophic World: Description of Three Novel Species of Methylacidimicrobium gen. nov
inferredcites →https://doi.org/10.1128/aem.64.3.922-929.1998openalex-snapshot
Acidophilic Methanotrophic Communities from Sphagnum Peat Bogs
inferredcites →https://doi.org/10.1128/jb.00407-11openalex-snapshot
Autotrophic Methanotrophy in Verrucomicrobia: Methylacidiphilum fumariolicumSolV Uses the Calvin-Benson-Bassham Cycle for Carbon Dioxide Fixation
inferredcites →https://doi.org/10.1128/jb.173.2.697-703.1991openalex-snapshot
16S ribosomal DNA amplification for phylogenetic study
inferredcites →https://doi.org/10.1128/jb.187.13.4665-4670.2005openalex-snapshot
Methylocella Species Are Facultatively Methanotrophic
inferredcites →https://doi.org/10.1128/mmbr.59.1.48-62.1995openalex-snapshot
Energetics of bacterial growth: balance of anabolic and catabolic reactions
inferredcites →https://doi.org/10.1128/mr.53.1.68-84.1989openalex-snapshot
Physiology, biochemistry, and specific inhibitors of CH4, NH4+, and CO oxidation by methanotrophs and nitrifiers
inferredcites →https://doi.org/10.1186/1745-6150-3-26openalex-snapshot
Complete genome sequence of the extremely acidophilic methanotroph isolate V4, Methylacidiphilum infernorum, a representative of the bacterial phylum Verrucomicrobia
inferredcites →https://doi.org/10.1371/journal.pbio.0020303openalex-snapshot
Genomic Insights into Methanotrophy: The Complete Genome Sequence of Methylococcus capsulatus (Bath)
inferredcites →https://doi.org/10.3389/fmicb.2012.00266openalex-snapshot
Metabolic Regulation of “Ca. Methylacidiphilum Fumariolicum” SolV Cells Grown Under Different Nitrogen and Oxygen Limitations
inferredcites →https://doi.org/10.3389/fmicb.2012.00345openalex-snapshot
Genomic and Physiological Analysis of Carbon Storage in the Verrucomicrobial Methanotroph “Ca. Methylacidiphilum Fumariolicum” SolV
inferredcites →https://doi.org/10.3389/fmicb.2013.00067openalex-snapshot
The YNP metagenome project: environmental parameters responsible for microbial distribution in the Yellowstone geothermal ecosystem
inferredcites →https://doi.org/10.3389/fmicb.2015.00001openalex-snapshot
One Juliet and four Romeos: VeA and its methyltransferases
inferredcites →https://doi.org/10.3389/fmicb.2015.00192openalex-snapshot
Bacterial community structure across environmental gradients in permafrost thaw ponds: methanotroph-rich ecosystems
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