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Interface-engineered iron single-atom biohybrids for efficient CO2-to-bioplastic conversion
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DOI：10.1038/s41467-026-76902-9.png)
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Abstract
En 中文
A hybrid system combining water electrolysis and H2 autotrophic microorganism enables sustainable CO2 valorization, but is hindered by low H2 bioavailability and sluggish hydrogenase kinetics. Here, we report an interface-engineered inorganic–biological biohybrid, constructed by covalently anchoring iron single-atom catalysts (ISA) onto Cupriavidus necator (C.N@ISA) via click chemistry. The ISA anchored interface generates a localized H2-rich microenvironment, accelerates H2 dissociation, while the synergy between ISA and polyethylene glycol-phenylboronate linker stabilizes the inorganic-biological hybrid interface and promotes electron/proton transfer across microbial membrane. These coupled effects boost reduced form of nicotinamide adenine dinucleotide (NADH) regeneration and adenosine triphosphate (ATP) synthesis. In addition, ISA exhibits nanozyme-like activity, scavenging reactive oxygen species to protect cell viability. As a result, C.N@ISA achieves CO2-to-bioplastic poly-β-hydroxybutyrate production of 1058.8 mg L−1 with a Faradaic efficiency of 42.0%. Integrating theoretical calculations, electrochemical analysis, and transcriptomics confirms that ISA simultaneously enriches and activates H2 while reinforcing intracellular metabolism, offering a generalizable strategy for carbon-negative biomanufacturing. The integration of inorganic–microbial systems offers promise for CO2-to-chemical conversion but faces efficiency bottlenecks. Here, the authors report an engineering strategy of anchoring iron single-atom catalysts onto bacterial membranes to achieve enhanced bioplastic production.
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15.7
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9.2W
Citations:
91.2W