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Real flue gas CO(2) hydrogenation to formate by an enzymatic reactor using O(2)- and CO-tolerant hydrogenase and formate dehydrogenase

It is challenging to capture carbon dioxide (CO(2)), a major greenhouse gas in the atmosphere, due to its high chemical stability. One potential practical solution to eliminate CO(2) is to convert CO(2) into formate using hydrogen (H(2)) (CO(2) hydrogenation), which can be accomplished with inexpens...

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Detalles Bibliográficos
Autores principales: Cha, Jaehyun, Lee, Jinhee, Jeon, Byoung Wook, Kim, Yong Hwan, Kwon, Inchan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579561/
https://www.ncbi.nlm.nih.gov/pubmed/37854886
http://dx.doi.org/10.3389/fbioe.2023.1265272
Descripción
Sumario:It is challenging to capture carbon dioxide (CO(2)), a major greenhouse gas in the atmosphere, due to its high chemical stability. One potential practical solution to eliminate CO(2) is to convert CO(2) into formate using hydrogen (H(2)) (CO(2) hydrogenation), which can be accomplished with inexpensive hydrogen from sustainable sources. While industrial flue gas could provide an adequate source of hydrogen, a suitable catalyst is needed that can tolerate other gas components, such as carbon monoxide (CO) and oxygen (O(2)), potential inhibitors. Our proposed CO(2) hydrogenation system uses the hydrogenase derived from Ralstonia eutropha H16 (ReSH) and formate dehydrogenase derived from Methylobacterium extorquens AM1 (MeFDH1). Both enzymes are tolerant to CO and O(2), which are typical inhibitors of metalloenzymes found in flue gas. We have successfully demonstrated that combining ReSH- and MeFDH1-immobilized resins can convert H(2) and CO(2) in real flue gas to formate via a nicotinamide adenine dinucleotide-dependent cascade reaction. We anticipated that this enzyme system would enable the utilization of diverse H(2) and CO(2) sources, including waste gases, biomass, and gasified plastics.