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

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 applic...

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Autores principales: Aleku, Godwin A., Prause, Christoph, Bradshaw‐Allen, Ruth T., Plasch, Katharina, Glueck, Silvia M., Bailey, Samuel S., Payne, Karl A. P., Parker, David A., Faber, Kurt, Leys, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175315/
https://www.ncbi.nlm.nih.gov/pubmed/30333895
http://dx.doi.org/10.1002/cctc.201800643
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author Aleku, Godwin A.
Prause, Christoph
Bradshaw‐Allen, Ruth T.
Plasch, Katharina
Glueck, Silvia M.
Bailey, Samuel S.
Payne, Karl A. P.
Parker, David A.
Faber, Kurt
Leys, David
author_facet Aleku, Godwin A.
Prause, Christoph
Bradshaw‐Allen, Ruth T.
Plasch, Katharina
Glueck, Silvia M.
Bailey, Samuel S.
Payne, Karl A. P.
Parker, David A.
Faber, Kurt
Leys, David
author_sort Aleku, Godwin A.
collection PubMed
description 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.
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spelling pubmed-61753152018-10-15 Terminal Alkenes from Acrylic Acid Derivatives via Non‐Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases Aleku, Godwin A. Prause, Christoph Bradshaw‐Allen, Ruth T. Plasch, Katharina Glueck, Silvia M. Bailey, Samuel S. Payne, Karl A. P. Parker, David A. Faber, Kurt Leys, David ChemCatChem Full Papers 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. John Wiley and Sons Inc. 2018-07-17 2018-09-07 /pmc/articles/PMC6175315/ /pubmed/30333895 http://dx.doi.org/10.1002/cctc.201800643 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Aleku, Godwin A.
Prause, Christoph
Bradshaw‐Allen, Ruth T.
Plasch, Katharina
Glueck, Silvia M.
Bailey, Samuel S.
Payne, Karl A. P.
Parker, David A.
Faber, Kurt
Leys, David
Terminal Alkenes from Acrylic Acid Derivatives via Non‐Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases
title Terminal Alkenes from Acrylic Acid Derivatives via Non‐Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases
title_full Terminal Alkenes from Acrylic Acid Derivatives via Non‐Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases
title_fullStr Terminal Alkenes from Acrylic Acid Derivatives via Non‐Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases
title_full_unstemmed Terminal Alkenes from Acrylic Acid Derivatives via Non‐Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases
title_short Terminal Alkenes from Acrylic Acid Derivatives via Non‐Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases
title_sort terminal alkenes from acrylic acid derivatives via non‐oxidative enzymatic decarboxylation by ferulic acid decarboxylases
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175315/
https://www.ncbi.nlm.nih.gov/pubmed/30333895
http://dx.doi.org/10.1002/cctc.201800643
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