Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1784861494253453312 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9801423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT vanzadelhoffannemiek biomimeticenzymaticoxidativecouplingofbarleyphenolamideshydroxycinnamoylagmatines AT meijvogellieke biomimeticenzymaticoxidativecouplingofbarleyphenolamideshydroxycinnamoylagmatines AT seelenannamarie biomimeticenzymaticoxidativecouplingofbarleyphenolamideshydroxycinnamoylagmatines AT debruijnwouterjc biomimeticenzymaticoxidativecouplingofbarleyphenolamideshydroxycinnamoylagmatines AT vinckenjeanpaul biomimeticenzymaticoxidativecouplingofbarleyphenolamideshydroxycinnamoylagmatines |