Solar-hybrid biocatalyst for methane hydroxylation to methanol

Methane hydroxylation presents a promising approach to produce high-energy methanol from potent greenhouse gases, thereby contributing to a more sustainable future. Despite its environmental importance, current research on this process remains challenging due to the harsh operating conditions for the activation of inert C-H bond in methane. In nature, methane monooxygenase converts methane by activating the C-H bonds through its hydroxylase, under ambient conditions, receiving electrons from NADH via a reductase. Beyond the traditional biological approach, the development of NADH-independent biocatalytic systems could open new avenues for cost-effective and sustainable methane conversion. Herein, we report an NADH-free biosolar platform that activates hydroxylase for eco-friendly methanol production. The xanthene-based light harvester spontaneously associates with hydroxylase and directly transfers its photoexcited electrons to the diiron active site, eliminating the need for a cofactor or reductase. Halogenation of xanthene accelerates direct electron transfer to the active site by increasing the polarizability and spin-orbit coupling of the light harvesters. Accordingly, the direct photobiocatalytic platform achieved a methanol time yield of 7.52 mmol g<sub>cat</sub><sup>-1</sup> h<sup>-1</sup>. This work provides the design concept of solar-driven biocatalytic methane hydroxylation under ambient conditions, suggesting a promising approach for implementing methanol biomanufacturing.

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Publication Details

Journal
Nature Communications
Published
2025-10-21
DOI
https://doi.org/10.1038/s41467-025-64362-6
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
0.00

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article

Solar-hybrid biocatalyst for methane hydroxylation to methanol

Chan Beum Park, Jung-Kul Lee, Devashish Das, Rowina Lestari et al.
Nature Communications
Catalysis for Biomass Conversion
article

Solar-hybrid biocatalyst for methane hydroxylation to methanol

Chan Beum Park, Jung-Kul Lee, Devashish Das, Rowina Lestari, Jinha Jang
article en

Abstract

Methane hydroxylation presents a promising approach to produce high-energy methanol from potent greenhouse gases, thereby contributing to a more sustainable future. Despite its environmental importance, current research on this process remains challenging due to the harsh operating conditions for the activation of inert C-H bond in methane. In nature, methane monooxygenase converts methane by activating the C-H bonds through its hydroxylase, under ambient conditions, receiving electrons from NADH via a reductase. Beyond the traditional biological approach, the development of NADH-independent biocatalytic systems could open new avenues for cost-effective and sustainable methane conversion. Herein, we report an NADH-free biosolar platform that activates hydroxylase for eco-friendly methanol production. The xanthene-based light harvester spontaneously associates with hydroxylase and directly transfers its photoexcited electrons to the diiron active site, eliminating the need for a cofactor or reductase. Halogenation of xanthene accelerates direct electron transfer to the active site by increasing the polarizability and spin-orbit coupling of the light harvesters. Accordingly, the direct photobiocatalytic platform achieved a methanol time yield of 7.52 mmol g<sub>cat</sub><sup>-1</sup> h<sup>-1</sup>. This work provides the design concept of solar-driven biocatalytic methane hydroxylation under ambient conditions, suggesting a promising approach for implementing methanol biomanufacturing.

Nature CommunicationsVol. 16(1)
Korea Advanced Institute of Science and Technology (KR), Konkuk University (KR), Konkuk University Medical Center (KR)
National Research Foundation, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 71%
Catalysis for Biomass Conversion
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