4.6 Article

Shedding Light on Microbial Dark Matter: Insights Into Novel Cloacimonadota and Omnitrophota From an Antarctic Lake

期刊

FRONTIERS IN MICROBIOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.741077

关键词

Cloacimonadota; Omnitrophota; cellulosome; autotrophy; metagenome; Antarctic bacteria

资金

  1. Australian Research Council [DP150100244]
  2. Australian Antarctic Science program [4031]

向作者/读者索取更多资源

Through genomic analysis, novel metabolic traits of Candidatus bacterial phyla Cloacimonadota and Omnitrophota have been identified, including carbon fixation using reverse tricarboxylic acid cycle, and strong biosynthetic capacity for organic compounds. Both taxa are inferred to form metabolic interactions with hydrogen-consuming partners in Ace Lake, occupying specific niches.
The potential metabolism and ecological roles of many microbial taxa remain unknown because insufficient genomic data are available to assess their functional potential. Two such microbial dark matter taxa are the Candidatus bacterial phyla Cloacimonadota and Omnitrophota, both of which have been identified in global anoxic environments, including (but not limited to) organic-carbon-rich lakes. Using 24 metagenome-assembled genomes (MAGs) obtained from an Antarctic lake (Ace Lake, Vestfold Hills), novel lineages and novel metabolic traits were identified for both phyla. The Cloacimonadota MAGs exhibited a capacity for carbon fixation using the reverse tricarboxylic acid cycle driven by oxidation of hydrogen and sulfur. Certain Cloacimonadota MAGs encoded proteins that possess dockerin and cohesin domains, which is consistent with the assembly of extracellular cellulosome-like structures that are used for degradation of polypeptides and polysaccharides. The Omnitrophota MAGs represented phylogenetically diverse taxa that were predicted to possess a strong biosynthetic capacity for amino acids, nucleosides, fatty acids, and essential cofactors. All of the Omnitrophota were inferred to be obligate fermentative heterotrophs that utilize a relatively narrow range of organic compounds, have an incomplete tricarboxylic acid cycle, and possess a single hydrogenase gene important for achieving redox balance in the cell. We reason that both Cloacimonadota and Omnitrophota form metabolic interactions with hydrogen-consuming partners (methanogens and Desulfobacterota, respectively) and, therefore, occupy specific niches in Ace Lake.

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