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Bootstrapped Biocatalysis: Biofilm‐Derived Materials as Reversibly Functionalizable Multienzyme Surfaces

Cell‐free biocatalysis systems offer many benefits for chemical manufacturing, but their widespread applicability is hindered by high costs associated with enzyme purification, modification, and immobilization on solid substrates, in addition to the cost of the material substrates themselves. Herein...

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Bibliographic Details
Published in:ChemCatChem 2017-12, Vol.9 (23), p.4328-4333
Main Authors: Nussbaumer, Martin G., Nguyen, Peter Q., Tay, Pei K. R., Naydich, Alexander, Hysi, Erisa, Botyanszki, Zsofia, Joshi, Neel S.
Format: Article
Language:English
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Summary:Cell‐free biocatalysis systems offer many benefits for chemical manufacturing, but their widespread applicability is hindered by high costs associated with enzyme purification, modification, and immobilization on solid substrates, in addition to the cost of the material substrates themselves. Herein, we report a “bootstrapped” biocatalysis substrate material that is produced directly in bacterial culture and is derived from biofilm matrix proteins, which self‐assemble into a nanofibrous mesh. We demonstrate that this material can simultaneously purify and immobilize multiple enzymes site specifically and directly from crude cell lysates by using a panel of genetically programmed, mutually orthogonal conjugation domains. We further demonstrate the utility of the technique in a bienzymatic stereoselective reduction coupled with a cofactor recycling scheme. The domains allow for several cycles of selective removal and replacement of enzymes under mild conditions to regenerate the catalyst system. Double take: We show that a “bootstrapped” biocatalysis substrate material can both purify and immobilize multiple enzymes site specifically and directly from crude cell lysates. We demonstrate the utility of the technique in a bienzymatic stereoselective reduction coupled with a cofactor recycling scheme. The domains allow for several cycles of selective removal and replacement of enzymes under mild conditions to regenerate the catalyst system.
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201701221