Reversing Electron Transfer Chain for Light-Driven Hydrogen Production in Biotic-Abiotic Hybrid Systems.
He-Xing HanLi-Jiao TianDong-Feng LiuHan-Qing YuGuo-Ping ShengYujie XiongPublished in: Journal of the American Chemical Society (2022)
The biotic-abiotic photosynthetic system integrating inorganic light absorbers with whole-cell biocatalysts innovates the way for sustainable solar-driven chemical transformation. Fundamentally, the electron transfer at the biotic-abiotic interface, which may induce biological response to photoexcited electron stimuli, plays an essential role in solar energy conversion. Herein, we selected an electro-active bacterium Shewanella oneidensis MR-1 as a model, which constitutes a hybrid photosynthetic system with a self-assembled CdS semiconductor, to demonstrate unique biotic-abiotic interfacial behavior. The photoexcited electrons from CdS nanoparticles can reverse the extracellular electron transfer (EET) chain within S. oneidensis MR-1, realizing the activation of a bacterial catalytic network with light illumination. As compared with bare S. oneidensis MR-1, a significant upregulation of hydrogen yield (711-fold), ATP, and reducing equivalent (NADH/NAD + ) was achieved in the S. oneidensis MR-1-CdS under visible light. This work sheds light on the fundamental mechanism and provides design guidelines for biotic-abiotic photosynthetic systems.
Keyphrases
- electron transfer
- visible light
- quantum dots
- genome wide identification
- contrast enhanced
- magnetic resonance
- arabidopsis thaliana
- single cell
- magnetic resonance imaging
- cell proliferation
- poor prognosis
- cell therapy
- stem cells
- mass spectrometry
- computed tomography
- room temperature
- bone marrow
- mesenchymal stem cells
- crystal structure
- high efficiency