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Updated: Apr 7, 2026

Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1
Published on: April 16, 2018
Cyclic adenosine monophosphate (cAMP) signaling reprograms extracellular electron transfer of Shewanella oneidensis
Lang Zhou1, Xiaozhen Xu2, Caiyi Li2
1Guangxi Microorganism and Enzyme Research Center of Engineering Technology, College of Life Science and Technology, Guangxi University, Nanning, Guangxi 530004, China; Guangxi Academy of Sciences, Nanning, Guangxi 530007, China.
Abstract:
Limited extracellular electron transfer (EET) efficiency constrains the electrocatalytic performance of Shewanella oneidensis MR-1. Although the c-type cytochrome (c-Cyts) network is essential for EET, its regulatory mechanisms remain incompletely understood. This study systematically compared the effects of overexpressing c-Cyts components versus cAMP receptor protein (CRP) modulation on EET efficiency in microbial fuel cells (MFCs). Overexpression of individual c-Cyts failed to enhance EET. In contrast, coexpression of CymA, CctA, and MtrCBA (strain CC-Mtr) increased the maximum power density to 0.29 W/m2, 29.5% higher than MR-1. This indicates that efficient EET requires synergistic activity of a transmembrane electron transfer chain. However, strain CC-Mtr exhibited impaired growth. By comparison, cAMP-CRP global regulation markedly upregulated genes involved in c-Cyts biosynthesis, cytochrome maturation, and anaerobic carbon metabolism. This strategy improved both the electron transfer chain and cellular growth. In the cyaC strain, where intracellular cAMP levels were 2.8-fold higher than in MR-1, the MFC current density reached 0.94 A/m², a 32.1% increase over the wild-type and 11.7% higher than strain CC-Mtr. These findings demonstrate that EET can be effectively enhanced by upregulating the full electron transport chain and cAMP-CRP mediated global regulation, offering a promising strategy for optimizing electron transfer in microbial electrosynthesis systems.
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