Photo-enzyme-membrane for ethylene glycol synthesis

The light-driven enzyme catalytic system composed of NAD(P)H regeneration and NAD(P)H-dependent enzymatic process emerges as a biomanufacturing platform for the synthesis of value-added chemicals, where the photo-responsive materials absorb solar energy to drive mass conversion. Herein, we report a photo-enzyme-membrane (PEM) catalytic system coupled with multi-enzyme cascade for ethylene glycol (EG) synthesis, in which membrane mediates energy transfer and mass conversion. Covalent organic polymer membrane as photo-membrane (PM) affords efficient NADH supply through synergistic intensification of electron transfer and proton transfer, where the bipyridine moiety mediates fast electron transfer from the generation site, and the sulfonic acid moiety facilitates proton transfer by enriching protons. Meanwhile, NADH-dependent enzyme is absorbed on PM followed by coating with a silica layer to form PEM, where the enzyme-bearing silica layer is defined as enzyme-membrane (EM). The enzymatic process is intensified by mitigating the adverse effects of PM on enzyme activity through precise regulation of EM thickness. Further, a dual-channel reactor is constructed for sustainable synthesis of EG with an initial synthesis rate of 2.43 mmol g<sub>PEM</sub><sup>-1</sup> h<sup>-1</sup> by continuous supply of methanol. Our study offers an efficient and durable light-driven enzyme catalytic system for the synthesis of C<sub>2+</sub> from C<sub>1</sub> chemicals.

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Publication Details

Journal
Nature Communications
Published
2026-02-16
DOI
https://doi.org/10.1038/s41467-026-69637-0
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.00

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article

Photo-enzyme-membrane for ethylene glycol synthesis

Yi Yang, Shiyi Zhu, Yu Chen, Zhongyi Jiang et al.
Nature Communications
Enzyme Catalysis and Immobilization
article

Photo-enzyme-membrane for ethylene glycol synthesis

Yi Yang, Shiyi Zhu, Yu Chen, Zhongyi Jiang, Shusong Liu, Yang Yang, J K Shi, Mengshi Jia, Xinyu Mao, Wenping Li, Chen Tao, Yiying Sun, Shihao Li
article en

Abstract

The light-driven enzyme catalytic system composed of NAD(P)H regeneration and NAD(P)H-dependent enzymatic process emerges as a biomanufacturing platform for the synthesis of value-added chemicals, where the photo-responsive materials absorb solar energy to drive mass conversion. Herein, we report a photo-enzyme-membrane (PEM) catalytic system coupled with multi-enzyme cascade for ethylene glycol (EG) synthesis, in which membrane mediates energy transfer and mass conversion. Covalent organic polymer membrane as photo-membrane (PM) affords efficient NADH supply through synergistic intensification of electron transfer and proton transfer, where the bipyridine moiety mediates fast electron transfer from the generation site, and the sulfonic acid moiety facilitates proton transfer by enriching protons. Meanwhile, NADH-dependent enzyme is absorbed on PM followed by coating with a silica layer to form PEM, where the enzyme-bearing silica layer is defined as enzyme-membrane (EM). The enzymatic process is intensified by mitigating the adverse effects of PM on enzyme activity through precise regulation of EM thickness. Further, a dual-channel reactor is constructed for sustainable synthesis of EG with an initial synthesis rate of 2.43 mmol g<sub>PEM</sub><sup>-1</sup> h<sup>-1</sup> by continuous supply of methanol. Our study offers an efficient and durable light-driven enzyme catalytic system for the synthesis of C<sub>2+</sub> from C<sub>1</sub> chemicals.

Nature CommunicationsVol. 17(1)
Nanjing Tech University (CN), Radboud University Nijmegen (NL), Tianjin University (CN), Hainan University (CN), Radboud University Medical Center (NL), Tianjin Synthetic Material Research Institute (China) (CN), Radboud Institute for Molecular Life Sciences (NL), Institute of Process Engineering (CN)
State Key Laboratory of Biochemical Engineering, National Key Research and Development Program of China
Responsible consumption and production
Openalex Percentile: Top 54%
Enzyme Catalysis and Immobilization
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