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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-6175315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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