Unexpected metabolic rewiring of CO<sub>2</sub> fixation in H<sub>2</sub>-mediated materials-biology hybrids.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37816063.
- Also identified by DOI 10.1073/pnas.2308373120 and PMC identifier 10589654.
- Licence recorded as CC BY-NC-ND.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
A hybrid approach combining water-splitting electrochemistry and H<sub>2</sub>-oxidizing, CO<sub>2</sub>-fixing microorganisms offers a viable solution for producing value-added chemicals from sunlight, water, and air. The classic wisdom without thorough examination to date assumes that the electrochemistry in such a H<sub>2</sub>-mediated process is innocent of altering microbial behavior. Here, we report unexpected metabolic rewiring induced by water-splitting electrochemistry in H<sub>2</sub>-oxidizing acetogenic bacterium <i>Sporomusa ovata</i> that challenges such a classic view. We found that the planktonic <i>S. ovata</i> is more efficient in utilizing reducing equivalent for ATP generation in the materials-biology hybrids than cells grown with H<sub>2</sub> supply, supported by our metabolomic and proteomic studies. The efficiency of utilizing reducing equivalents and fixing CO<sub>2</sub> into acetate has increased from less than 80% of chemoautotrophy to more than 95% under electroautotrophic conditions. These observations unravel previously underappreciated materials' impact on microbial metabolism in seemingly simply H<sub>2</sub>-mediated charge transfer between biotic and abiotic components. Such a deeper understanding of the materials-biology interface will foster advanced design of hybrid systems for sustainable chemical transformation.
Medical subject headings
- Carbon Dioxide
- Proteomics