Quinones as Strecker degradation reagents in wine oxidation processes

Copyright © 2017 Elsevier Ltd. All rights reserved..

The Strecker aldehydes formed during the reaction between α-amino acids (phenylalanine or methionine) and either gallic acid, caffeic acid or (+)-catechin ortho-quinones were evaluated in wine-model systems. It was demonstrated that phenylacetaldehyde was formed by quinone intermediates at wine pH. The highest amounts of phenylacetaldehyde during the 10days of experiment (69±5µg/L/day; 7x>Control) were obtained from (+) catechin, followed by gallic acid (61±4µg/L/day; 6x>Control) and caffeic acid (41±4µg/L/day; 4x>Control). The intermediate structures delivered from the reaction of ortho-quinones with α-amino acids were demonstrated by MSn.

Medienart:

E-Artikel

Erscheinungsjahr:

2017

Erschienen:

2017

Enthalten in:

Zur Gesamtaufnahme - volume:228

Enthalten in:

Food chemistry - 228(2017) vom: 01. Aug., Seite 618-624

Sprache:

Englisch

Beteiligte Personen:

Oliveira, Carla Maria [VerfasserIn]
Santos, Sónia A O [VerfasserIn]
Silvestre, Armando J D [VerfasserIn]
Barros, António S [VerfasserIn]
Ferreira, António César Silva [VerfasserIn]
Silva, Artur M S [VerfasserIn]

Links:

Volltext

Themen:

(+)-Catechin (PubChem CID: 9064)
Amino Acids
Amino acids
Caffeic acid (PubChem CID: 689043)
Gallic acid (PubChem CID: 370)
Indicators and Reagents
Journal Article
Oxidation
Oxygen
Phenolics
Quinones
Strecker aldehydes
Wine

Anmerkungen:

Date Completed 01.05.2017

Date Revised 02.12.2018

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.foodchem.2017.02.034

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM270074783