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Simultaneous aerobic and anaerobic respiration in hot spring chemolithotrophic bacteria
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Simultaneous aerobic and anaerobic respiration in hot spring chemolithotrophic bacteria
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Simultaneous aerobic and anaerobic respiration in hot spring chemolithotrophic bacteria
Simultaneous aerobic and anaerobic respiration in hot spring chemolithotrophic bacteria
Journal Article

Simultaneous aerobic and anaerobic respiration in hot spring chemolithotrophic bacteria

2025
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Overview
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 2 ). 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 2 ), elemental sulfur (S 0 ), and O 2 . 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 2 measured via gas chromatography and detection of transcripts for proteins involved in S 0 and O 2 reduction in H 2 /S 0 /O 2 -grown cultures confirmed co-occurring aerobic and anaerobic metabolism. This aerobic, S 0 -reducing metabolism is suggested to provide a competitive advantage in environments where O 2 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 2 -dependent abiotic oxidation of produced sulfide. These observations challenge existing paradigms of strict delineations between aerobic and anaerobic metabolism. Anaerobic and aerobic metabolisms are considered to be spatially or temporally segregated. Here, the authors provide evidence for co-occurring aerobic and anaerobic respiration in a chemolithotrophic bacterium isolated from a hot spring in Yellowstone, challenging the existing paradigm.