| Literature DB >> 30380178 |
Theo Peschke1, Patrick Bitterwolf1, Sabrina Gallus1, Yong Hu1, Claude Oelschlaeger2, Norbert Willenbacher2, Kersten S Rabe1, Christof M Niemeyer1.
Abstract
Continuous flow biocatalysis is an emerging field of industrial biotechnology that uses enzymes immobilized in flow channels for the production of value-added chemicals. We describe the construction of self-assembling all-enzyme hydrogels that are comprised of two tetrameric enzymes. The stereoselective dehydrogenase LbADH and the cofactor-regenerating glucose 1-dehydrogenase GDH were genetically fused with a SpyTag or SpyCatcher domain, respectively, to generate two complementary homo-tetrameric building blocks that polymerize under physiological conditions into porous hydrogels. Mounted in microfluidic reactors, the gels show excellent stereoselectivity with near quantitative conversion in the reduction of prochiral ketones along with high robustness under process and storage conditions. The gels function as compartment that retains intermediates thus enabling high total turnover numbers of the expensive cofactor NADP(H).Entities:
Keywords: enzymes; flow biocatalysis; immobilization; microreactors; stereoselective reactions
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Year: 2018 PMID: 30380178 DOI: 10.1002/anie.201810331
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336