Experimental and theoretical studies on the acetaldehyde reaction with (+)-catechin.


Journal

Food chemistry
ISSN: 1873-7072
Titre abrégé: Food Chem
Pays: England
ID NLM: 7702639

Informations de publication

Date de publication:
15 Nov 2023
Historique:
received: 15 01 2023
revised: 28 05 2023
accepted: 04 06 2023
medline: 19 7 2023
pubmed: 22 6 2023
entrez: 21 6 2023
Statut: ppublish

Résumé

Acetaldehyde plays a key role in determining some wine properties. Interesting is the reaction of acetaldehyde with flavonoids, as the ensuing products can alter wine color, astringency, colloidal stability. Many studies reported on the formation of ethylidene-bridged flavan-3-ols as products of the reaction between acetaldehyde and either (+)-catechin or (-)-epicatechin. In white wines after one year of incubation with acetaldehyde only vinyl-(+)-catechin and vinyl-(-)-epicatechin were observed, while no ethylidene linked oligomers were detected. This observation prompted us to study the reaction of (+)-catechin with acetaldehyde in wine model solution through an experimental and theoretical approach, with the purpose of exploring the nature of the species involved along with the mechanisms leading to them. The products of the reaction were observed over 38 days. The results showed that ethylidene-bridged catechins are the first products to be formed but over time the dissociation of these dimers causes vinyl-catechins to accumulate.

Identifiants

pubmed: 37343411
pii: S0308-8146(23)01174-3
doi: 10.1016/j.foodchem.2023.136556
pii:
doi:

Substances chimiques

Catechin 8R1V1STN48
Acetaldehyde GO1N1ZPR3B
Flavonoids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

136556

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Raffaele Cucciniello (R)

Department of Chemistry and Biology 'Adolfo Zambelli', University of Salerno, Via Giovanni Paolo II, 132, Fisciano, Province of Salerno 84084, Italy.

Michele Tomasini (M)

Department of Chemistry and Biology 'Adolfo Zambelli', University of Salerno, Via Giovanni Paolo II, 132, Fisciano, Province of Salerno 84084, Italy; Institut de Química Computacional i Catàlisi and Departament de Química, Universitat de Girona, c/Maria Aurèlia Capmany 69, Girona, Catalonia 17003, Spain.

Anna Russo (A)

Department of Chemistry and Biology 'Adolfo Zambelli', University of Salerno, Via Giovanni Paolo II, 132, Fisciano, Province of Salerno 84084, Italy.

Laura Falivene (L)

Department of Chemistry and Biology 'Adolfo Zambelli', University of Salerno, Via Giovanni Paolo II, 132, Fisciano, Province of Salerno 84084, Italy. Electronic address: lafalivene@unisa.it.

Angelita Gambuti (A)

Department of Agricultural Sciences, Section of Vine and Wine Sciences, University of Napoli 'Federico II', Viale Italia, Avellino 83100, Italy.

Martino Forino (M)

Department of Agricultural Sciences, Section of Vine and Wine Sciences, University of Napoli 'Federico II', Viale Italia, Avellino 83100, Italy.

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Classifications MeSH