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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Environmental microbiology 2016-06, Vol.18 (6), p.1686-1703
Hauptverfasser: Emerson, Joanne B., Thomas, Brian C., Alvarez, Walter, Banfield, Jillian F.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung: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.
ISSN:1462-2912
1462-2920
DOI:10.1111/1462-2920.12817