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Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines

[Image: see text] Oxidative coupling of hydroxycinnamoylagmatines in barley (Hordeum vulgare) and related Hordeum species is part of the plant defense mechanism. Three linkage types have been reported for hydroxycinnamoylagmatine dimers, but knowledge on oxidative coupling reactions underlying their...

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Autores principales: van Zadelhoff, Annemiek, Meijvogel, Lieke, Seelen, Anna-Marie, de Bruijn, Wouter J.C., Vincken, Jean-Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9801423/
https://www.ncbi.nlm.nih.gov/pubmed/36516832
http://dx.doi.org/10.1021/acs.jafc.2c07457
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author van Zadelhoff, Annemiek
Meijvogel, Lieke
Seelen, Anna-Marie
de Bruijn, Wouter J.C.
Vincken, Jean-Paul
author_facet van Zadelhoff, Annemiek
Meijvogel, Lieke
Seelen, Anna-Marie
de Bruijn, Wouter J.C.
Vincken, Jean-Paul
author_sort van Zadelhoff, Annemiek
collection PubMed
description [Image: see text] Oxidative coupling of hydroxycinnamoylagmatines in barley (Hordeum vulgare) and related Hordeum species is part of the plant defense mechanism. Three linkage types have been reported for hydroxycinnamoylagmatine dimers, but knowledge on oxidative coupling reactions underlying their formation is limited. In this study, the monomers coumaroylagmatine, feruloylagmatine, and sinapoylagmatine were each incubated with horseradish peroxidase. Their coupling reactivity was in line with the order of peak potentials measured: sinapoylagmatine (245 mV) > feruloylagmatine (341 mV) > coumaroylagmatine (506 mV). Structure elucidation of fourteen in vitro coupling products by NMR and MS revealed that the three main linkage types were identical to those naturally present in Hordeum species, namely, 4-O-7′/3-8′, 2-7′/8-8′, and 8-8′/9-N-7′. Furthermore, we identified two linkage types that were not previously reported for hydroxycinnamoylagmatine dimers, namely, 8-8′ and 4-O-8′. We conclude that oxidative coupling by horseradish peroxidase can be used for biomimetic formation of natural antifungal hydroxycinnamoylagmatine dimers from barley.
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spelling pubmed-98014232022-12-31 Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines van Zadelhoff, Annemiek Meijvogel, Lieke Seelen, Anna-Marie de Bruijn, Wouter J.C. Vincken, Jean-Paul J Agric Food Chem [Image: see text] Oxidative coupling of hydroxycinnamoylagmatines in barley (Hordeum vulgare) and related Hordeum species is part of the plant defense mechanism. Three linkage types have been reported for hydroxycinnamoylagmatine dimers, but knowledge on oxidative coupling reactions underlying their formation is limited. In this study, the monomers coumaroylagmatine, feruloylagmatine, and sinapoylagmatine were each incubated with horseradish peroxidase. Their coupling reactivity was in line with the order of peak potentials measured: sinapoylagmatine (245 mV) > feruloylagmatine (341 mV) > coumaroylagmatine (506 mV). Structure elucidation of fourteen in vitro coupling products by NMR and MS revealed that the three main linkage types were identical to those naturally present in Hordeum species, namely, 4-O-7′/3-8′, 2-7′/8-8′, and 8-8′/9-N-7′. Furthermore, we identified two linkage types that were not previously reported for hydroxycinnamoylagmatine dimers, namely, 8-8′ and 4-O-8′. We conclude that oxidative coupling by horseradish peroxidase can be used for biomimetic formation of natural antifungal hydroxycinnamoylagmatine dimers from barley. American Chemical Society 2022-12-14 2022-12-28 /pmc/articles/PMC9801423/ /pubmed/36516832 http://dx.doi.org/10.1021/acs.jafc.2c07457 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle van Zadelhoff, Annemiek
Meijvogel, Lieke
Seelen, Anna-Marie
de Bruijn, Wouter J.C.
Vincken, Jean-Paul
Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines
title Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines
title_full Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines
title_fullStr Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines
title_full_unstemmed Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines
title_short Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines
title_sort biomimetic enzymatic oxidative coupling of barley phenolamides: hydroxycinnamoylagmatines
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9801423/
https://www.ncbi.nlm.nih.gov/pubmed/36516832
http://dx.doi.org/10.1021/acs.jafc.2c07457
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