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The Role of Acyl-Glucose in Anthocyanin Modifications

Higher plants can produce a wide variety of anthocyanin molecules through modification of the six common anthocyanin aglycons that they present. Thus, hydrophilic anthocyanin molecules can be formed and stabilized by glycosylation and acylation. Two types of glycosyltransferase (GT) and acyltransfer...

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Autores principales: Sasaki, Nobuhiro, Nishizaki, Yuzo, Ozeki, Yoshihiro, Miyahara, Taira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271837/
https://www.ncbi.nlm.nih.gov/pubmed/25405291
http://dx.doi.org/10.3390/molecules191118747
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author Sasaki, Nobuhiro
Nishizaki, Yuzo
Ozeki, Yoshihiro
Miyahara, Taira
author_facet Sasaki, Nobuhiro
Nishizaki, Yuzo
Ozeki, Yoshihiro
Miyahara, Taira
author_sort Sasaki, Nobuhiro
collection PubMed
description Higher plants can produce a wide variety of anthocyanin molecules through modification of the six common anthocyanin aglycons that they present. Thus, hydrophilic anthocyanin molecules can be formed and stabilized by glycosylation and acylation. Two types of glycosyltransferase (GT) and acyltransferase (AT) have been identified, namely cytoplasmic GT and AT and vacuolar GT and AT. Cytoplasmic GT and AT utilize UDP-sugar and acyl-CoA as donor molecules, respectively, whereas both vacuolar GT and AT use acyl-glucoses as donor molecules. In carnation plants, vacuolar GT uses aromatic acyl-glucoses as the glucose donor in vivo; independently, vacuolar AT uses malylglucose, an aliphatic acyl-glucose, as the acyl-donor. In delphinium and Arabidopsis, p-hydroxybenzoylglucose and sinapoylglucose are used in vivo as bi-functional donor molecules by vacuolar GT and AT, respectively. The evolution of these enzymes has allowed delphinium and Arabidopsis to utilize unique donor molecules for production of highly modified anthocyanins.
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spelling pubmed-62718372019-01-07 The Role of Acyl-Glucose in Anthocyanin Modifications Sasaki, Nobuhiro Nishizaki, Yuzo Ozeki, Yoshihiro Miyahara, Taira Molecules Review Higher plants can produce a wide variety of anthocyanin molecules through modification of the six common anthocyanin aglycons that they present. Thus, hydrophilic anthocyanin molecules can be formed and stabilized by glycosylation and acylation. Two types of glycosyltransferase (GT) and acyltransferase (AT) have been identified, namely cytoplasmic GT and AT and vacuolar GT and AT. Cytoplasmic GT and AT utilize UDP-sugar and acyl-CoA as donor molecules, respectively, whereas both vacuolar GT and AT use acyl-glucoses as donor molecules. In carnation plants, vacuolar GT uses aromatic acyl-glucoses as the glucose donor in vivo; independently, vacuolar AT uses malylglucose, an aliphatic acyl-glucose, as the acyl-donor. In delphinium and Arabidopsis, p-hydroxybenzoylglucose and sinapoylglucose are used in vivo as bi-functional donor molecules by vacuolar GT and AT, respectively. The evolution of these enzymes has allowed delphinium and Arabidopsis to utilize unique donor molecules for production of highly modified anthocyanins. MDPI 2014-11-14 /pmc/articles/PMC6271837/ /pubmed/25405291 http://dx.doi.org/10.3390/molecules191118747 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sasaki, Nobuhiro
Nishizaki, Yuzo
Ozeki, Yoshihiro
Miyahara, Taira
The Role of Acyl-Glucose in Anthocyanin Modifications
title The Role of Acyl-Glucose in Anthocyanin Modifications
title_full The Role of Acyl-Glucose in Anthocyanin Modifications
title_fullStr The Role of Acyl-Glucose in Anthocyanin Modifications
title_full_unstemmed The Role of Acyl-Glucose in Anthocyanin Modifications
title_short The Role of Acyl-Glucose in Anthocyanin Modifications
title_sort role of acyl-glucose in anthocyanin modifications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271837/
https://www.ncbi.nlm.nih.gov/pubmed/25405291
http://dx.doi.org/10.3390/molecules191118747
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