Influence of wine-relevant metal ions on oxygen consumption kinetics and tannin-related responses in an H₂O₂-mediated accelerated model wine system.

Jiaheng Lyu, Getu Shi, Dewei Zhang, Yan Xu, Ke Tang

Journal: Food research international (Ottawa, Ont.) 2026;242(Pt 4):120128

PMID: 42637453

Abstract

This study evaluated how common wine-relevant metal ions influence oxygen consumption behavior and soluble tannin-related responses in an H₂O₂-mediated accelerated model wine system. The presence of Fe3+, Cu2+, Ca2+, Al3+, and Co2+ markedly altered oxygen consumption kinetics, which could be described using a power-function model with parameters dependent on metal ion identity and concentration. Electronic tongue measurements showed that metal ions affected instrumental astringency-related responses, while the individual contributions of metal ion properties, H₂O₂-mediated reactions, tannin-related transformations, and potential metal-tannin interactions could not be distinguished under the present experimental conditions. Chemical analyses further revealed concentration-dependent changes in the soluble tannin fraction, including variations in tannin concentration, subunit composition, and mean degree of polymerization after centrifugation. Overall, these results provide comparative empirical evidence that wine-relevant metal ions can modify oxygen consumption behavior and soluble tannin-related parameters under the defined H₂O₂-mediated accelerated model wine conditions.

Copyright © 2026 Elsevier Ltd. All rights reserved.

Address: Yantai Key Laboratory of Wine Flavour Technology, Yantai Institute of China Agricultural University, Yantai 264670, China.; Lab of Brewing Microbiology and Applied Enzymology, School of Biotechnology and Key Laboratory of Industrial Biotechnology of Ministry of Education, Jiangnan University, Wuxi 214122, PR China.; Lab of Brewing Microbiology and Applied Enzymology, School of Biotechnology and Key Laboratory of Industrial Biotechnology of Ministry of Education, Jiangnan University, Wuxi 214122, PR China. Electronic address: [email protected].

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