Unexpected metabolic rewiring of CO fixation in H-mediated materials-biology hybrids.

A hybrid approach combining water-splitting electrochemistry and H-oxidizing, CO-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-mediated process is innocent of altering microbial behavior. Here, we report unexpected metabolic rewiring induced by water-splitting electrochemistry in H-oxidizing acetogenic bacterium that challenges such a classic view. We found that the planktonic is more efficient in utilizing reducing equivalent for ATP generation in the materials-biology hybrids than cells grown with H supply, supported by our metabolomic and proteomic studies. The efficiency of utilizing reducing equivalents and fixing CO 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-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.