ExtracellularElectron Uptake Mediated by H<sub>2</sub>O<sub>2</sub>

Harvesting electricity from microbial electron transfer is believed as a promising way of renewable energy generation. However, a major challenge lies in the still-unknown mechanisms of extracellular electron transfer, especially how microbes consume electrons from the cathode to catalyze oxygen reduction. Here we report a previously undescribed yet significant extracellular electron uptake pathway mediated by inevitably produced H<sub>2</sub>O<sub>2</sub>, contributing up to 45% of the total biocurrent. This new H<sub>2</sub>O<sub>2</sub>-based bioelectrochemical respiration depends on the continuous supply of electrons from the electrode and the presence of the catalase <i>katG</i>. Selective enhancement of two-electron oxygen reduction on the cathode results in a 2.4-fold increase in biocurrent, and both autotrophic biosynthesis and energy production pathways are upregulated to sustain the H<sub>2</sub>O<sub>2</sub>-based respiration. Our results highlight the importance of two-electron oxygen reduction in bioelectron uptake at the cathode and provide a basis for the design of bioelectricity production systems.

Publication Details

Journal
Figshare
Published
2025-02-13
DOI
https://doi.org/10.1021/acs.est.4c13792.s001
Primary Topic
Microbial Fuel Cells and Bioremediation
Type
article
Field-Weighted Citation Impact
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ExtracellularElectron Uptake Mediated by H2O2

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Microbial Fuel Cells and Bioremediation
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ExtracellularElectron Uptake Mediated by H2O2

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Abstract

Harvesting electricity from microbial electron transfer is believed as a promising way of renewable energy generation. However, a major challenge lies in the still-unknown mechanisms of extracellular electron transfer, especially how microbes consume electrons from the cathode to catalyze oxygen reduction. Here we report a previously undescribed yet significant extracellular electron uptake pathway mediated by inevitably produced H<sub>2</sub>O<sub>2</sub>, contributing up to 45% of the total biocurrent. This new H<sub>2</sub>O<sub>2</sub>-based bioelectrochemical respiration depends on the continuous supply of electrons from the electrode and the presence of the catalase <i>katG</i>. Selective enhancement of two-electron oxygen reduction on the cathode results in a 2.4-fold increase in biocurrent, and both autotrophic biosynthesis and energy production pathways are upregulated to sustain the H<sub>2</sub>O<sub>2</sub>-based respiration. Our results highlight the importance of two-electron oxygen reduction in bioelectron uptake at the cathode and provide a basis for the design of bioelectricity production systems.

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Microbial Fuel Cells and Bioremediation
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