Better than Nature: Nicotinamide Biomimetics That Outperform Natural Coenzymes

Open Access
Authors
  • T. Knaus
  • C.E. Paul
  • C.W. Levy
  • S. de Vries
Publication date 2016
Journal Journal of the American Chemical Society
Volume | Issue number 138 | 3
Pages (from-to) 1033-1039
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
Abstract
The search for affordable, green biocatalytic processes is a challenge for chemicals manufacture. Redox biotransformations are potentially attractive, but they rely on unstable and expensive nicotinamide coenzymes that have prevented their widespread exploitation. Stoichiometric use of natural coenzymes is not viable economically, and the instability of these molecules hinders catalytic processes that employ coenzyme recycling. Here, we investigate the efficiency of man-made synthetic biomimetics of the natural coenzymes NAD(P)H in redox biocatalysis. Extensive studies with a range of oxidoreductases belonging to the ene reductase family show that these biomimetics are excellent analogues of the natural coenzymes, revealed also in crystal structures of the ene reductase XenA with selected biomimetics. In selected cases, these biomimetics outperform the natural coenzymes. Better-than-Nature biomimetics should find widespread application in fine and specialty chemicals production by harnessing the power of high stereo-, regio-, and chemoselective redox biocatalysts and enabling reactions under mild conditions at low cost.
Document type Article
Note With supporting information
Language English
Related dataset 5CPL : The crystal structure of Xenobiotic reductase A (XenA) from Pseudomonas putida in complex with a nicotinamide mimic (mNH2) 5CPM : XenA from Pseudomonas putida in complex with NADPH4. 5CPN : Crystal structure of XenA from Pseudomonas putida in complex with an NADH mimic (mAc)
Published at https://doi.org/10.1021/jacs.5b12252
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