Formate‐Mediated Electroenzymatic Synthesis via Biological Cofactor NADH

Author:

Wang Chuanjun12,Dong Wenjin2,Zhang Pengye2,Ma Yaya2,Han Zhiwei2,Zou Yutai23,Wang Wenshuo2,Li Hao1ORCID,Hollmann Frank4,Liu Jian23ORCID

Affiliation:

1. School of Material Science and Engineering Shandong University of Science and Technology Qingdao 266590 China

2. Key Laboratory of Photoelectric Conversion and Utilization of Solar Energy Qingdao New Energy Shandong Laboratory Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao 266101 China

3. College of Materials Science and Engineering Qingdao University of Science and Technology Qingdao 266042 China

4. Department of Biotechnology Delft University of Technology Delft, The Netherlands

Abstract

AbstractSynthetic biohybrid systems by coupling artificial system with nature's machinery may offer a disruptive solution to address the global energy crisis. We developed a versatile electroenzymatic pathway for the continuous synthesis of valuable chemicals, facilitated by formate‐driven NADH regeneration. Utilizing a bismuth electrocatalyst, we achieved stable CO2 reduction to formate with approximately 90 % Faraday efficiency at a current density of 150 mA cm−2. The generated formate acts as a mediator to regenerate NADH, which is then coupled with immobilized redox enzymes—alcohol dehydrogenase (ADH), L‐lactate dehydrogenase (LDH), and L‐glutamate dehydrogenase (GDH)—to produce targeted chemicals at significant rates and exceptionally high turnover numbers (1.8×106 to 3.1×106). These achievements not only underscore the efficiency of the system but also its practical applicability in industrial settings. By leveraging in situ generated formate, this innovative approach demonstrates the potential of integrating electrocatalysis with enzymatic reactions for sustainable and efficient chemical production on a practical scale.

Publisher

Wiley

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