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  Bioelectrocatalytic CO2 reduction by Mo-dependent formylmethanofuran dehydrogenase

Sahin, S., Lemaire, O. N., Belhamri, M., Kurth, J. M., Welte, C. U., Wagner, T., & Milton, R. D. (2023). Bioelectrocatalytic CO2 reduction by Mo-dependent formylmethanofuran dehydrogenase. Angewandte Chemie International Edition,. doi:10.1002/anie.202311981.

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-000D-B413-2 版のパーマリンク: https://hdl.handle.net/21.11116/0000-000E-427A-F
資料種別: 学術論文
その他のタイトル : Angewandte Chemie International Edition

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 作成者:
Sahin, Selmihan1, 著者
Lemaire, Olivier N.1, 著者
Belhamri, Mélissa1, 著者
Kurth, Julia M.2, 著者
Welte, Cornelia U.1, 著者
Wagner, Tristan1, 著者
Milton, Ross D1, 著者
所属:
1external, ou_persistent22              
2Microcosm Earth Center, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, Hans-Meerwein-Str. 4, 35032 Marburg, Germany, ou_3511059              

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キーワード: bioelectrocatalysis, CO2-sequestration, Formylmethanofuran dehydrogenase, Molybdopterin cofactor, Direct electron transfer
 要旨: Massive efforts are invested in developing innovative CO2-sequestration strategies to counter climate change and transform CO2 into higher-value products. CO2-capture by reduction is a chemical challenge, and attention is turned toward biological systems that selectively and efficiently catalyse this reaction under mild conditions and in aqueous solvents. While few reports have evaluated the effectiveness of isolated bacterial formate dehydrogenases as catalysts for the reversible electrochemical reduction of CO2, it is imperative to explore other enzymes among the natural reservoir of potential models that might exhibit higher turnover rates or preferential directionality for the reductive reaction. Here, we present electroenzymatic catalysis of formylmethanofuran dehydrogenase, a CO2-reducing-and-fixing biomachinery isolated from a thermophilic methanogen, which was deposited on a graphite rod electrode to enable direct electron transfer for electroenzymatic CO2 reduction. The gas is reduced with a high Faradaic efficiency (109 ± 1%), where a low affinity for formate prevents its electrochemical reoxidation and favours formate accumulation. These properties make the enzyme an excellent tool for electroenzymatic CO2-fixation and inspiration for protein engineering that would be beneficial for biotechnological purposes to convert the greenhouse gas into stable formate that can subsequently be safely stored, transported, and used for power generation without energy loss.

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 日付: 2023-09
 出版の状態: 出版
 ページ: -
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 識別子(DOI, ISBNなど): URI: https://doi.org/10.1002/anie.202311981
DOI: 10.1002/anie.202311981
 学位: -

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出版物 1

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出版物名: Angewandte Chemie International Edition
  省略形 : Angew. Chem., Int. Ed.
種別: 学術雑誌
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所属:
出版社, 出版地: Weinheim : Wiley-VCH
ページ: e202311981 巻号: - 通巻号: e202311981 開始・終了ページ: - 識別子(ISBN, ISSN, DOIなど): ISSN: 1433-7851
CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851