" Candidatus Thermonerobacter thiotrophicus," A Non-phototrophic Member of the Bacteroidetes/Chlorobi With Dissimilatory Sulfur Metabolism in Hot Spring Mat Communities
In this study we present evidence for a novel, thermophilic bacterium with dissimilatory sulfur metabolism, tentatively named " Thermonerobacter thiotrophicus," which is affiliated with the and which we predict to be a sulfate reducer. Dissimilatory sulfate reduction (DSR) is an important...
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Veröffentlicht in: | Frontiers in microbiology 2019-01, Vol.9, p.3159-3159 |
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Sprache: | eng |
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Zusammenfassung: | In this study we present evidence for a novel, thermophilic bacterium with dissimilatory sulfur metabolism, tentatively named "
Thermonerobacter thiotrophicus," which is affiliated with the
and which we predict to be a sulfate reducer. Dissimilatory sulfate reduction (DSR) is an important and ancient metabolic process for energy conservation with global importance for geochemical sulfur and carbon cycling. Characterized sulfate-reducing microorganisms (SRM) are found in a limited number of bacterial and archaeal phyla. However, based on highly diverse environmental
sequences, a variety of uncultivated and unidentified SRM must exist. The recent development of high-throughput sequencing methods allows the phylogenetic identification of some of these uncultured SRM. In this study, we identified a novel putative SRM inhabiting hot spring microbial mats that is a member of the OPB56 clade ("
. Kapabacteria") within the
superphylum. Partial genomes for this new organism were retrieved from metagenomes from three different hot springs in Yellowstone National Park, United States, and Japan. Supporting the prediction of a sulfate-reducing metabolism for this organism during period of anoxia, diel metatranscriptomic analyses indicate highest relative transcript levels
for all DSR-related genes at night. The presence of terminal oxidases, which are transcribed during the day, further suggests that these organisms might also perform aerobic respiration. The relative phylogenetic proximity to the sulfur-oxidizing, chlorophototrophic
further raises new questions about the evolution of dissimilatory sulfur metabolism. |
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ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2018.03159 |