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Authors Williams

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Williams, Kenneth H.


Publications
5

CitationNamesAbstract
Complete 4.55-Megabase-Pair Genome of “ Candidatus Fluviicola riflensis,” Curated from Short-Read Metagenomic Sequences Banfield et al. (2017). Genome Announcements 5 (47) Ca. Fluviicola riflensis
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Unusual respiratory capacity and nitrogen metabolism in a Parcubacterium (OD1) of the Candidate Phyla Radiation Castelle et al. (2017). Scientific Reports 7 (1) “Parcunitrobacterota” Ca. Parcunitrobacter nitroensis
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Thousands of microbial genomes shed light on interconnected biogeochemical processes in an aquifer system Anantharaman et al. (2016). Nature Communications 7 (1) 24 Names
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Unusual biology across a group comprising more than 15% of domain Bacteria Brown et al. (2015). Nature 523 (7559) 12 Names
Extraordinary phylogenetic diversity and metabolic versatility in aquifer sediment Castelle et al. (2013). Nature Communications 4 (1) “Zixiibacteriota” “Woykeibacteriota”

Complete 4.55-Megabase-Pair Genome of “ Candidatus Fluviicola riflensis,” Curated from Short-Read Metagenomic Sequences
ABSTRACT We report the 4.55-Mbp genome of “ Candidatus Fluviicola riflensis” ( Bacteroidetes ) that was manually curated to completion from Illumina data. “ Ca . Fluviicola riflensis” is a facultative anaerobe. Its ability to grow over a range of O 2 levels may favor its proliferation in an aquifer adjacent to the Colorado River in the United States.
Unusual respiratory capacity and nitrogen metabolism in a Parcubacterium (OD1) of the Candidate Phyla Radiation
AbstractThe Candidate Phyla Radiation (CPR) is a large group of bacteria, the scale of which approaches that of all other bacteria. CPR organisms are inferred to depend on other community members for many basic cellular building blocks and all appear to be obligate anaerobes. To date, there has been no evidence for any significant respiratory capacity in an organism from this radiation. Here we report a curated draft genome for ‘Candidatus Parcunitrobacter nitroensis’ a member of the Parcubacteria (OD1) superphylum of the CPR. The genome encodes versatile energy pathways, including fermentative and respiratory capacities, nitrogen and fatty acid metabolism, as well as the first complete electron transport chain described for a member of the CPR. The sequences of all of these enzymes are highly divergent from sequences found in other organisms, suggesting that these capacities were not recently acquired from non-CPR organisms. Although the wide respiration-based repertoire points to a different lifestyle compared to other CPR bacteria, we predict similar obligate dependence on other organisms or the microbial community. The results substantially expand the known metabolic potential of CPR bacteria, although sequence comparisons indicate that these capacities are very rare in members of this radiation.
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Thousands of microbial genomes shed light on interconnected biogeochemical processes in an aquifer system
AbstractThe subterranean world hosts up to one-fifth of all biomass, including microbial communities that drive transformations central to Earth’s biogeochemical cycles. However, little is known about how complex microbial communities in such environments are structured, and how inter-organism interactions shape ecosystem function. Here we apply terabase-scale cultivation-independent metagenomics to aquifer sediments and groundwater, and reconstruct 2,540 draft-quality, near-complete and complete strain-resolved genomes that represent the majority of known bacterial phyla as well as 47 newly discovered phylum-level lineages. Metabolic analyses spanning this vast phylogenetic diversity and representing up to 36% of organisms detected in the system are used to document the distribution of pathways in coexisting organisms. Consistent with prior findings indicating metabolic handoffs in simple consortia, we find that few organisms within the community can conduct multiple sequential redox transformations. As environmental conditions change, different assemblages of organisms are selected for, altering linkages among the major biogeochemical cycles.
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