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Self-immobilizing fusion enzymes for compartmentalized biocatalysis

Authors :
Christoph M. Niemeyer
Kersten S. Rabe
Marc Skoupi
Theo Peschke
Sabrina Gallus
Ishtiaq Ahmed
Teresa Burgahn
Source :
ACS catalysis, 7 (11), 7866-7872
Publication Year :
2017
Publisher :
American Chemical Society (ACS), 2017.

Abstract

The establishment of microfluidic enzyme cascades is a topical field of research and development, which is currently hampered by the lack of methodologies for mild and efficient immobilization of isolated enzymes. We here describe the use of self-immobilizing fusion enzymes for the modular configuration of microfluidic packed-bed reactors. Specifically, three different enzymes, the (R)-selective alcohol dehydrogenase LbADH, the (S)-selective methylglyoxal reductase Gre2p and the NADP(H) regeneration enzyme glucose 1-dehydrogenase GDH, were genetically fused with streptavidin binding peptide, Spy and Halo-based tags, to enable their specific and directional immobilization on magnetic microbeads coated with complementary receptors. The enzyme-modified beads were loaded in four-channel microfluidic chips to create compartments that have the capability for either (R)- or (S)-selective reduction of the prochiral CS-symmetrical substrate 5-nitrononane-2,8-dione (NDK). Analysis of the isomeric hydroxyketone and ...

Details

Language :
English
ISSN :
21555435
Database :
OpenAIRE
Journal :
ACS catalysis, 7 (11), 7866-7872
Accession number :
edsair.doi.dedup.....43fbdb9efcd1569e335ae211922baa10
Full Text :
https://doi.org/10.5445/ir/1000076605