7.7) and from oak.
FIGURE 2.12 Formation of sotolon in wines.
Sotolon (4,5‐dimethyl‐3‐hydroxy‐2‐furanone), a highly aromatic compound (Figure 2.12), is also formed during wine aging by the non‐enzymatically catalyzed condensation of α‐ketobutyric acid and acetaldehyde (Section 8.7). It is thus found in Vin Jaune from the Jura region, where it is responsible for the walnut aroma so typical of this wine (Martin et al., 1992), but also in dry and sweet white wines that have gone through oxidative phenomena (Section 8.7).
Lastly, oak releases lactones into wine during barrel aging (Section 13.7.4). The cis and trans isomers of β‐methyl‐γ‐octalactone (Figure 2.13) are known as oak lactones or whisky lactones. The pure compounds have a coconut odor, and when diluted, they are reminiscent of oaky wines. Concentrations in wine are on the order of a few tens of milligrams per liter, considerably higher than the perception threshold (a few tens of micrograms per liter).
FIGURE 2.13 β ‐Methyl‐γ‐octalactone.
References
1 Arctander S. (1969) Perfume and Flavor Chemicals. Selbstverlag, Montclair, NJ.
2 Bertrand A. (1983) Volatiles from grape must fermentation. In Flavor of Distilled Beverages, Origin and Development (Ed J.R. Piggot). Ellis Horwood Ltd.
3 Cameleyre M., Lytra G., Tempere S. and Barbe J.C. (2015) J. Agric. Food Chem., 63, 9777–9788.
4 Cameleyre M., Lytra G., Tempere S. and Barbe J.C. (2017) Food Chem., 237, 364–371.
5 Diaz‐Maroto M.C., Schneider R. and Baumes R. (2005) J. Agric. Food Chem., 53, 9, 3503–3509.
6 Dubois P. (1993) Rev. Fr. Œnol., 144, 63.
7 Falcao L., Lytra G., Darriet P. and Barbe J.‐C. (2012) Food Chem., 132, 230–236.
8 Gammacurta M., Marchand S., Lytra G., Barbe J.‐C., Moine V. and de Revel G. (2015) OENO, Bordeaux.
9 Garofolo A. and Piracci A. (1994) Bull. OIV, 67, 757–758, 225.
10 Guth H. (1997) J. Agric. Food Chem., 45(8), 3027–3032.
11 Jackson R.S. (1994) Wine Sciences. Principles and Applications. Academic Press, San Diego.
12 Lytra G., Tempere S., de Revel G. and Barbe J.‐C. (2012) J. Agric. Food Chem., 60, 1503–1509.
13 Lytra G., Tempere S., Le Floch A., de Revel G. and Barbe J.‐C. (2013) J. Agric. Food Chem., 61, 8504–8513.
14 Lytra G., Tempere S., de Revel G. and Barbe J.‐C. (2014) J. Agric. Food Chem., 62, 5005–5010.
15 Lytra G., Cameleyre M., Tempere S. and Barbe J.C. (2015) J. Agric. Food Chem., 63, 10484–10491.
16 Lytra G., Franc C., Cameleyre M. and Barbe J.‐C. (2017) J. Agric. Food Chem., 65, 5018–5025.
17 Martin B., Etievant P., Le Quere J.‐L. and Schlich P. (1992) J. Agric. Food Chem., 40, 475.
18 Martin G. and Brun S. (1987) Bull. OIV, 671–672, 131.
19 Pineau B., Barbe J.C., Van Leeuwen C. and Dubourdieu D. (2009) J. Agric. Food Chem., 57, 3702–3708.
20 Ribéreau‐Gayon J., Peynaud E., Ribéreau‐Gayon P. and Sudraud P. (1982) Analyse et Contrôle des Vins, 2nd edition. Sciences et Techniques du Vin, Vol. I. Dunod, Paris.
21 Skrzydlewska E. (2003) Toxicol. Mech. Methods, 13, 277.
Конец ознакомительного фрагмента.
Текст предоставлен ООО «ЛитРес».
Прочитайте эту книгу целиком, купив полную легальную версию на ЛитРес.
Безопасно оплатить книгу можно банковской картой Visa, MasterCard, Maestro, со счета мобильного телефона, с платежного терминала, в салоне МТС или Связной, через PayPal, WebMoney, Яндекс.Деньги, QIWI Кошелек, бонусными картами или другим удобным Вам способом.