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Deazaflavins as photocatalysts for the direct reductive regeneration of flavoenzymes

Authors :
van Schie, M.M.C.H. (author)
Younes, S.H.H. (author)
Rauch, M.C.R. (author)
Pesic, M. (author)
Paul, C.E. (author)
Arends, I.W.C.E. (author)
Hollmann, F. (author)
van Schie, M.M.C.H. (author)
Younes, S.H.H. (author)
Rauch, M.C.R. (author)
Pesic, M. (author)
Paul, C.E. (author)
Arends, I.W.C.E. (author)
Hollmann, F. (author)
Publication Year :
2018

Abstract

Deazaflavins are potentially useful redox mediators for the direct, nicotinamide-independent regeneration of oxidoreductases. Especially the O2-stability of their reduced forms have attracted significant interest for the regeneration of monooxygenases. In this contribution we further investigate the photochemical properties of deazaflavins and investigate the scope and limitations of deazaflavin-based photoenzymatic reaction systems.<br />Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.<br />BT/Biocatalysis<br />BT/Biotechnology

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1085128961
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.mcat.2018.04.015