ArticlePloS one2013
Methyl fluoride affects methanogenesis rather than community composition of methanogenic archaea in a rice field soil.
Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 17 citations in OpenAlex.
- Seasonal Dynamics of Abundance, Structure, and Diversity of Methanogens and Methanotrophs in Lake Sediments.Microbial ecology · 2021Article
- Hydrogenotrophic Methanogenesis Under Alkaline Conditions.Frontiers in microbiology · 2020Article
- Article
- Carbon Isotope Fractionation during Catabolism and Anabolism in Acetogenic Bacteria Growing on Different Substrates.Applied and environmental microbiology · 2016Article
- Potential for direct interspecies electron transfer in an electric-anaerobic system to increase methane production from sludge digestion.Scientific reports · 2015Article
- Metabolic and trophic interactions modulate methane production by Arctic peat microbiota in response to warming.Proceedings of the National Academy of Sciences of the United States of America · 2015Article
- Effective Suppression of Methane Emission by 2-Bromoethanesulfonate during Rice Cultivation.PloS one · 2015Article
- Methane production potentials, pathways, and communities of methanogens in vertical sediment profiles of river Sitka.Frontiers in microbiology · 2015Article
- High concentrations of methyl fluoride affect the bacterial community in a thermophilic methanogenic sludge.PloS one · 2014Article
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The metabolic pathways of methane formation vary with environmental conditions, but whether this can also be linked to changes in the active archaeal community structure remains uncertain. Here, we show that the suppression of aceticlastic methanogenesis by methyl fluoride (CH(3)F) caused surprisingly little differences in community composition of active methanogenic archaea from a rice field soil. By measuring the natural abundances of carbon isotopes we found that the effective dose for a 90% inhibition of aceticlastic methanogenesis in anoxic paddy soil incubations was <0.75% CH(3)F (v/v). The construction of clone libraries as well as t-RFLP analysis revealed that the active community, as indicated by mcrA transcripts (encoding the α subunit of methyl-coenzyme M reductase, a key enzyme for methanogenesis), remained stable over a wide range of CH(3)F concentrations and represented only a subset of the methanogenic community. More precisely, Methanocellaceae were of minor importance, but Methanosarcinaceae dominated the active population, even when CH(3)F inhibition only allowed for aceticlastic methanogenesis. In addition, we detected mcrA gene fragments of a so far unrecognised phylogenetic cluster. Transcription of this phylotype at methyl fluoride concentrations suppressing aceticlastic methanogenesis suggests that the respective organisms perform hydrogenotrophic methanogenesis. Hence, the application of CH(3)F combined with transcript analysis is not only a useful tool to measure and assign in situ acetate usage, but also to explore substrate usage by as yet uncultivated methanogens.
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