Metagenomic analysis of a high carbon dioxide subsurface microbial community populated by chemolithoautotrophs and bacteria and archaea from candidate phyla
Summary Research on geologic carbon sequestration raises questions about potential impacts of subsurface microbiota on carbon cycling and biogeochemistry. Subsurface, high‐CO2 systems are poorly biologically characterized, partly because of difficulty accessing high‐volume, uncontaminated samples. C...
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Published in | Environmental microbiology Vol. 18; no. 6; pp. 1686 - 1703 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.06.2016
Wiley Subscription Services, Inc Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | Summary
Research on geologic carbon sequestration raises questions about potential impacts of subsurface microbiota on carbon cycling and biogeochemistry. Subsurface, high‐CO2 systems are poorly biologically characterized, partly because of difficulty accessing high‐volume, uncontaminated samples. CO2‐driven Crystal Geyser (CG, Utah, USA), an established geologic carbon sequestration analogue, provides high volumes of deep (∼ 200–500 m) subsurface fluids. We explored microbial diversity and metabolic potential in this high‐CO2 environment by assembly and analysis of metagenomes recovered from geyser water filtrate. The system is dominated by neutrophilic, iron‐oxidizing bacteria, including ‘marine’ Mariprofundus (Zetaproteobacteria) and ‘freshwater’ Gallionellales, sulfur‐oxidizing Thiomicrospira crunogena and Thiobacillus‐like Hydrogenophilales. Near‐complete genomes were reconstructed for these bacteria. CG is notably populated by a wide diversity of bacteria and archaea from phyla lacking isolated representatives (candidate phyla) and from as‐yet undefined lineages. Many bacteria affiliate with OD1, OP3, OP9, PER, ACD58, WWE3, BD1‐5, OP11, TM7 and ZB2. The recovery of nearly 100 genes encoding ribulose‐1,5 bisphosphate carboxylase‐oxygenase subunit proteins of the Calvin cycle and AMP salvage pathways suggests a strong biological role in high‐CO2 subsurface carbon cycling. Overall, we predict microbial impacts on subsurface biogeochemistry via iron, sulfur, and complex carbon oxidation, carbon and nitrogen fixation, fermentation, hydrogen metabolism, and aerobic and anaerobic respiration. |
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Bibliography: | ark:/67375/WNG-KBWR8MWL-H Department of Energy (DOE) - No. DE-AC02-05CH11231 Fig. S1. Zetaproteobacteria 16S rRNA gene phylogeny. Table S1. CG2_0.2A 16S rRNA gene phylogenetic predictions. Table S2. Comparison of scaffolds and coverage in CG2_3.0 and CG2_0.2B. Table S3. CG2_0.2B and CG2_3.0 OTU counts. Table S4. Solution chemistry. Table S5. CG2_0.2A single-copy gene inventory by bin. Appendix S1. Supplementary online material. ArticleID:EMI12817 istex:9DC68A6401E8892FA66A2BAE64C1D10B52096A5F ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 AC02-05CH11231 USDOE Office of Science (SC), Basic Energy Sciences (BES) |
ISSN: | 1462-2912 1462-2920 |
DOI: | 10.1111/1462-2920.12817 |