Abstract
Oxidation reactions involving phenolics might change the chemical and sensory profile of wines. While oxidation is a long-standing problem in winemaking, a definitive understanding of its chemical mechanisms is lacking, and such an understanding could allow us to better predict and control wine aging. We briefly summarize and discuss the current knowledge on the chemistry of wine phenolic oxidation and propose, along with other researchers, a new, comprehensive scheme in which the Fenton reaction and hydroxyl radicals have an essential role. This hypothesis suggests that catalytic iron converts wine’s hydrogen peroxide into hydroxyl radical. This leads to a much stronger and less selective oxidant that could react with almost all wine components, in proportion to their concentration and with little selectivity for antioxidant properties. This reaction could produce many electrophilic oxidation products, mainly aldehydes and ketones, that could further modify the chemical composition and sensory perception of wine. While the brevity of this report precludes a full review of oxidation, our aim is to stimulate more study and debate on the mechanisms in wine oxidation chemistry.
Footnotes
Acknowledgments: The authors thank the following organizations for their financial support: American Vineyard Foundation, Fulbright, Laspau, Wine Spectator, Rhone Rangers, and Jastro Shields.
This article was originally presented at the ASEV 56th Annual Meeting Phenolics Symposium, 20–21 June 2005, Seattle, WA. All phenolics symposium articles were peer reviewed by two fellow presenters, and James Harbertson, Mark Downey, and Sara Spayd served as technical editors of the articles.
From the ASEV 2005 Phenolics Symposium
- Copyright © 2006 by the American Society for Enology and Viticulture