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Ryu, Jungki
Bioinspired Functional Materials Lab.
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Fortification of FeS Clusters Reshapes Anaerobic CO Dehydrogenase into an Air-Viable Enzyme Through Multilayered Sealing of O2 Tunnels

Author(s)
Kim, Suk MinKong, So YeonKang, JinguJi, Jeong SeokKang, Sung HeuckYoon, Hye-JinKim, HyunwooRyu, JungkiLee, Hyung HoKim, Yong Hwan
Issued Date
2025-08
DOI
10.1002/anie.202508565
URI
https://scholarworks.unist.ac.kr/handle/201301/87204
Citation
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.64, no.33, pp.e202508565
Abstract
The inherent O2 sensitivity of Ni─Fe carbon monoxide dehydrogenases (CODHs), crucial for rapid CO to CO2 interconversion, presents substantial challenges for industrial application. Transforming CO/CO2, a prevalent anthropogenic air pollutant, into valuable carbon chemicals either directly or through intermediate steps via biocatalytic methods offers a promising pathway to achieve net-zero emissions across industries and the environment. However, completely eliminating oxygen from industrial biotransformations, especially under ambient conditions, is exceedingly onerous. Here, we engineered variants of the CODH2 from Carboxydothermus hydrogenoformans (ChCODH2) with dual blocking at both the O2 entrance and near the active site, effectively sealing the tunnel against atmospheric O2 levels (20%). The O2-tunnel engineered A559W/V610H variant demonstrated a marked improvement in air stability, with a half-life of 24.6 h compared to the wild type's 2.4 h. Crystallographic snapshots of this air-viable variant after 24 h of exposure revealed the robust integrity of the fortified FeS and NiFeS clusters. Additionally, electro-enzymatic reactions corroborated its CO/CO2 conversion capability even in ubiquitous air. These findings, which address the O2 sensitivity of anaerobic enzymes caused by O2-induced metal cluster collapse, enhance their potential for biological CO/CO2 transformations in O2-rich environments, thereby broadening their industrial viability and applicability.
Publisher
John Wiley & Sons Ltd.
ISSN
1433-7851
Keyword (Author)
CO dehydrogenaseEnzyme engineering
Keyword
CARBON-MONOXIDE DEHYDROGENASE

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