Electroenzymatic Cascade Enables Amino Acid Synthesis through Simultaneous Nitrite Reduction and NADH Regeneration

Abstract Amino acids are central to life and the chemical industry, yet their sustainable synthesis remains a challenge. An electroenzymatic cascade offers a promising alternative by combining the electron/proton transfer capability of electrocatalysis with the exceptional specificity of biocatalysis. Here we present a conceptually distinct electroenzymatic cascade platform that integrates electrocatalytic nitrogen oxide reduction, NADH regeneration, and enzymatic reductive amination. Using l-glutamate (l-Glu) as a model, we demonstrate that with Cu nanowires as the bifunctional electrocatalyst, the system generates NH4+ and biologically active NADH in situ, driving the production of l-Glu under mild conditions. The coupled cascade not only shifts the reaction equilibrium forward but also provides a favorable orientation and a proton-rich environment for the bioactive cofactor, boosting overall selectivity of bioactive NADH. The modular design allows straightforward adaptation to diverse substrates and electrodes, demonstrating the broad generality of this platform. This work establishes a sustainable and versatile strategy for amino acid synthesis and opens new directions for electroenzymatic production of nitrogen-containing chemicals.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-10-27
DOI
https://doi.org/10.1021/jacs.6c17043
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.00

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article

Electroenzymatic Cascade Enables Amino Acid Synthesis through Simultaneous Nitrite Reduction and NADH Regeneration

Jingshan Luo, Huimin Liu, Liyun Zhang, Hang Luo et al.
4 links
Journal of the American Chemical Society
Enzyme Catalysis and Immobilization
article

Electroenzymatic Cascade Enables Amino Acid Synthesis through Simultaneous Nitrite Reduction and NADH Regeneration

Jingshan Luo, Huimin Liu, Liyun Zhang, Hang Luo, Lu Tian
article en

Abstract

Abstract Amino acids are central to life and the chemical industry, yet their sustainable synthesis remains a challenge. An electroenzymatic cascade offers a promising alternative by combining the electron/proton transfer capability of electrocatalysis with the exceptional specificity of biocatalysis. Here we present a conceptually distinct electroenzymatic cascade platform that integrates electrocatalytic nitrogen oxide reduction, NADH regeneration, and enzymatic reductive amination. Using l-glutamate (l-Glu) as a model, we demonstrate that with Cu nanowires as the bifunctional electrocatalyst, the system generates NH4+ and biologically active NADH in situ, driving the production of l-Glu under mild conditions. The coupled cascade not only shifts the reaction equilibrium forward but also provides a favorable orientation and a proton-rich environment for the bioactive cofactor, boosting overall selectivity of bioactive NADH. The modular design allows straightforward adaptation to diverse substrates and electrodes, demonstrating the broad generality of this platform. This work establishes a sustainable and versatile strategy for amino acid synthesis and opens new directions for electroenzymatic production of nitrogen-containing chemicals.

Journal of the American Chemical Society
Nankai University (CN)
National Natural Science Foundation of China, Ministry of Education of the People's Republic of China, Tianjin Municipal Science and Technology Bureau
Openalex Percentile: Top 22%
Enzyme Catalysis and Immobilization
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