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MOF‐Hosted Enzymes for Continuous Flow Catalysis in Aqueous and Organic Solvents

Fully exploiting the potential of enzymes in cell‐free biocatalysis requires stabilization of the catalytically active proteins and their integration into efficient reactor systems. Although in recent years initial steps towards the immobilization of such biomolecules in metal–organic frameworks (MO...

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Detalles Bibliográficos
Autores principales: Greifenstein, Raphael, Ballweg, Tim, Hashem, Tawheed, Gottwald, Eric, Achauer, David, Kirschhöfer, Frank, Nusser, Michael, Brenner‐Weiß, Gerald, Sedghamiz, Elaheh, Wenzel, Wolfgang, Mittmann, Esther, Rabe, Kersten S., Niemeyer, Christof M., Franzreb, Matthias, Wöll, Christof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314721/
https://www.ncbi.nlm.nih.gov/pubmed/35133704
http://dx.doi.org/10.1002/anie.202117144
Descripción
Sumario:Fully exploiting the potential of enzymes in cell‐free biocatalysis requires stabilization of the catalytically active proteins and their integration into efficient reactor systems. Although in recent years initial steps towards the immobilization of such biomolecules in metal–organic frameworks (MOFs) have been taken, these demonstrations have been limited to batch experiments and to aqueous conditions. Here we demonstrate a MOF‐based continuous flow enzyme reactor system, with high productivity and stability, which is also suitable for organic solvents. Under aqueous conditions, the stability of the enzyme was increased 30‐fold, and the space–time yield exceeded that obtained with other enzyme immobilization strategies by an order of magnitude. Importantly, the infiltration of the proteins into the MOF did not require additional functionalization, thus allowing for time‐ and cost‐efficient fabrication of the biocatalysts using label‐free enzymes.