Simultaneous aerobic and anaerobic respiration in hot spring chemolithotrophic bacteria

Aerobic and anaerobic organisms and their functions are spatially or temporally decoupled at scales ranging from individual cells to ecosystems and from minutes to hours. This is due to competition for energy substrates and/or biochemical incompatibility with oxygen (O<sub>2</sub>). Here we report a chemolithotrophic Aquificales bacterium, Hydrogenobacter, isolated from a circumneutral hot spring in Yellowstone National Park (YNP) capable of simultaneous aerobic and anaerobic respiration when provided with hydrogen (H<sub>2</sub>), elemental sulfur (S<sup>0</sup>), and O<sub>2</sub>. Cultivation experiments demonstrated that simultaneous aerobic and anaerobic respiration enhanced growth rates and final cell concentrations when compared to those grown aerobically or anaerobically. Consumption of O<sub>2</sub> measured via gas chromatography and detection of transcripts for proteins involved in S<sup>0</sup> and O<sub>2</sub> reduction in H<sub>2</sub>/S<sup>0</sup>/O<sub>2</sub>-grown cultures confirmed co-occurring aerobic and anaerobic metabolism. This aerobic, S<sup>0</sup>-reducing metabolism is suggested to provide a competitive advantage in environments where O<sub>2</sub> availability is low and variable. Genomic data indicating the prevalence of proteins allowing for this hybrid form of energy metabolism among bacteria and archaea suggest it to be widespread but previously overlooked due to rapid, O<sub>2</sub>-dependent abiotic oxidation of produced sulfide. These observations challenge existing paradigms of strict delineations between aerobic and anaerobic metabolism.

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Publication Details

Journal
Nature Communications
Published
2025-01-27
DOI
https://doi.org/10.1038/s41467-025-56418-4
Citations
4
Primary Topic
Microbial Community Ecology and Physiology
Type
article
Field-Weighted Citation Impact
6.87

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article

Simultaneous aerobic and anaerobic respiration in hot spring chemolithotrophic bacteria

Daniel R. Colman, Lisa M. Keller, Eric S. Boyd
4 citations
Nature Communications
Microbial Community Ecology and Physiology
6.87
article

Simultaneous aerobic and anaerobic respiration in hot spring chemolithotrophic bacteria

Daniel R. Colman, Lisa M. Keller, Eric S. Boyd
article en
4 citations

Abstract

Aerobic and anaerobic organisms and their functions are spatially or temporally decoupled at scales ranging from individual cells to ecosystems and from minutes to hours. This is due to competition for energy substrates and/or biochemical incompatibility with oxygen (O<sub>2</sub>). Here we report a chemolithotrophic Aquificales bacterium, Hydrogenobacter, isolated from a circumneutral hot spring in Yellowstone National Park (YNP) capable of simultaneous aerobic and anaerobic respiration when provided with hydrogen (H<sub>2</sub>), elemental sulfur (S<sup>0</sup>), and O<sub>2</sub>. Cultivation experiments demonstrated that simultaneous aerobic and anaerobic respiration enhanced growth rates and final cell concentrations when compared to those grown aerobically or anaerobically. Consumption of O<sub>2</sub> measured via gas chromatography and detection of transcripts for proteins involved in S<sup>0</sup> and O<sub>2</sub> reduction in H<sub>2</sub>/S<sup>0</sup>/O<sub>2</sub>-grown cultures confirmed co-occurring aerobic and anaerobic metabolism. This aerobic, S<sup>0</sup>-reducing metabolism is suggested to provide a competitive advantage in environments where O<sub>2</sub> availability is low and variable. Genomic data indicating the prevalence of proteins allowing for this hybrid form of energy metabolism among bacteria and archaea suggest it to be widespread but previously overlooked due to rapid, O<sub>2</sub>-dependent abiotic oxidation of produced sulfide. These observations challenge existing paradigms of strict delineations between aerobic and anaerobic metabolism.

Nature CommunicationsVol. 16(1)
Montana State University (US)
National Aeronautics and Space Administration, W. M. Keck Foundation, Nuclear Safety and Security Commission, National Park Service
Openalex Percentile: Top 4%
Microbial Community Ecology and Physiology
6.87
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