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Terminal Alkenes from Acrylic Acid Derivatives via Non-Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases

Authors :
Godwin A. Aleku
Silvia M. Glueck
Karl A. P. Payne
Ruth T. Bradshaw-Allen
David A. Parker
Katharina Plasch
Samuel S. Bailey
Kurt Faber
Christoph Prause
David Leys
Source :
ChemCatChem, Chemcatchem, Aleku, G A, Prause, C, Bradshaw-Allen, R T, Plasch, K, Glueck, S M, Bailey, S S, Payne, K A P, Parker, D A, Faber, K & Leys, D 2018, ' Terminal Alkenes from Acrylic Acid Derivatives via Non-Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases ', ChemCatChem, vol. 10, no. 17, pp. 3736-3745 . https://doi.org/10.1002/cctc.201800643
Publication Year :
2018

Abstract

Fungal ferulic acid decarboxylases (FDCs) belong to the UbiD-family of enzymes and catalyse the reversible (de)carboxylation of cinnamic acid derivatives through the use of a prenylated flavin cofactor. The latter is synthesised by the flavin prenyltransferase UbiX. Herein, we demonstrate the applicability of FDC/UbiX expressing cells for both isolated enzyme and whole-cell biocatalysis. FDCs exhibit high activity with total turnover numbers (TTN) of up to 55000 and turnover frequency (TOF) of up to 370 min−1. Co-solvent compatibility studies revealed FDC's tolerance to some organic solvents up 20 % v/v. Using the in-vitro (de)carboxylase activity of holo-FDC as well as whole-cell biocatalysts, we performed a substrate profiling study of three FDCs, providing insights into structural determinants of activity. FDCs display broad substrate tolerance towards a wide range of acrylic acid derivatives bearing (hetero)cyclic or olefinic substituents at C3 affording conversions of up to >99 %. The synthetic utility of FDCs was demonstrated by a preparative-scale decarboxylation.

Details

ISSN :
18673880
Volume :
10
Issue :
17
Database :
OpenAIRE
Journal :
ChemCatChem
Accession number :
edsair.doi.dedup.....d47da3d88bac37e5b51a070c1718f0cb
Full Text :
https://doi.org/10.1002/cctc.201800643