Authors
Ying Yang, Xin Wang, Tao Zhou, Zipeng Zhu, Yuanyuan Wang, Xiang Gao, Yiliang Lin
Published in
Science advances. Volume 12. Issue 40. Pages eaef4504. Oct 02, 2026. Epub Oct 02, 2026.
Abstract
Integrating light-harvesting materials with non-photosynthetic microbes offers a promising route to convert sunlight into chemicals. However, many existing biohybrid systems lack a clear architectural basis linking external light capture to intracellular redox processes. Inspired by the modular architecture of anoxygenic photosynthesis, we report a dual biohybrid system for light-enhanced chemical production in Escherichia coli. The system combines extracellular conjugated polymer nanoparticles as light-harvesting antenna with intracellularly biomineralized CdS nanoparticles as reaction-center-like charge-separation modules. This architecture supports light-enhanced malate production, yielding nearly a 30-fold enhancement relative to unmodified cells. Illumination-dependent studies reveal that activity is governed by light absorption, photon flux, and the intracellular redox environment. Fluorescence lifetime imaging microscopy further indicates photophysical coupling between the polymer and CdS components, consistent with energy transfer across the bio-synthetic interface and enhanced intracellular redox activity. Together, these results show how modular organization at the bio-synthetic interface can couple light harvesting with intracellular redox chemistry in living systems.
PMID:
42826201
Bibliographic data and abstract were imported from PubMed on 03 Oct 2026.
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