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E. coli Nickel‐Iron Hydrogenase 1 Catalyses Non‐native Reduction of Flavins: Demonstration for Alkene Hydrogenation by Old Yellow Enzyme Ene‐reductases

A new activity for the [NiFe] uptake hydrogenase 1 of Escherichia coli (Hyd1) is presented. Direct reduction of biological flavin cofactors FMN and FAD is achieved using H(2) as a simple, completely atom‐economical reductant. The robust nature of Hyd1 is exploited for flavin reduction across a broad...

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Detalles Bibliográficos
Autores principales: Joseph Srinivasan, Shiny, Cleary, Sarah E., Ramirez, Miguel A., Reeve, Holly A., Paul, Caroline E., Vincent, Kylie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252551/
https://www.ncbi.nlm.nih.gov/pubmed/33721401
http://dx.doi.org/10.1002/anie.202101186
Descripción
Sumario:A new activity for the [NiFe] uptake hydrogenase 1 of Escherichia coli (Hyd1) is presented. Direct reduction of biological flavin cofactors FMN and FAD is achieved using H(2) as a simple, completely atom‐economical reductant. The robust nature of Hyd1 is exploited for flavin reduction across a broad range of temperatures (25–70 °C) and extended reaction times. The utility of this system as a simple, easy to implement FMNH(2) or FADH(2) regenerating system is then demonstrated by supplying reduced flavin to Old Yellow Enzyme “ene‐reductases” to support asymmetric alkene reductions with up to 100 % conversion. Hyd1 turnover frequencies up to 20.4 min(−1) and total turnover numbers up to 20 200 were recorded during flavin recycling.