References: Loyola R, Herrera D, Mas A, Wong DCJ, Höll J, Cavallini E et al., The photomorphogenic factors UV‐B RECEPTOR 1, ELONGATED HYPOCOTYL 5, and HY5 HOMOLOGUE are part of the UV‐B signalling pathway in grapevine and mediate flavonol accumulation in response to the environment. J Exp Bot 67:5429–5445 (2016).
Makris DP, Kallithraka S and Kefalas P, Flavonols in grapes, grape products, and wines: burden, profile, and influential parameters. J Food Compos Anal 19:396–404 (2006).
Castillo‐Muñoz N, Gómez‐Alonso S, García‐Romero E and Hermosín‐Gutiérrez I, Flavonol profiles of Vitis vinifera red grapes and their single‐cultivar wines. J Agric Food Chem 55:992–1002 (2007).
Waterhouse AL, Sacks GL and Jeffery DW, Understanding Wine Chemistry. Wiley, Hoboken, NJ (2016).
Jeffery DW, Parker M and Smith PA, Flavonol composition of Australian red and white wines determined by high‐performance liquid chromatography. Aust J Grape Wine Res 14:153–161 (2008).
Vouillamoz JOSÈ, Monaco A, Costantini L, Stefanini M, Scienza A and Grando MS, The parentage of ‘Sangiovese’, the most important Italian wine grape. Vitis 46:19–22 (2007).
Compendium Vol1_EN.pdf (oiv.int).
Lanati D, Cascio P, Pollon M, Corona O and Marchi D, Solubility of quercetin in wines. South African J Enol Vitic 43:146–156 (2022).
Klitou P, Rosbottom I and Simone E, Synthonic modeling of quercetin and its hydrates: explaining crystallization behavior in terms of molecular conformation and crystal packing. Cryst Growth Des 19:4774–4783 (2019).
McGinty J, Yazdanpanah N, Price C, ter Horst JH and Sefcik J, Nucleation and crystal growth in continuous crystallization, in The Handbook of Continuous Crystallization. Royal Society of Chemistry, Cambridge, UK, pp. 1–50 (2020).
Boulton RB, Singleton VL, Bisson LF and Kunkee RE, Principles and Practices of Winemaking. Springer, New York, NY, pp. 320–335 (1999).
Forino M, Cassiano C, Gambuti A, Picariello L, Aversano R, Villano C et al., Aging behavior of two red wines from the PIWI pathogen‐resistant grapevines ‘Cabernet Eidos’ and ‘Merlot Khorus’. ACS Food Sci Technol 2:638–646 (2022).
OIV, Compendium of International Methods of Wine and Must Analysis. Office International de la Vigne et du Vin, Paris, France (2017).
Yang P, Li H, Wang H, Han F, Jing S, Yuan C et al., Dispersive liquid–liquid microextraction method for HPLC determination of phenolic compounds in wine. Food Anal Methods 10:2383–2397 (2017).
Abraham MH and Acree WE Jr, On the solubility of quercetin. J Mol Liq 197:157–159 (2014).
Gambuti A, Picariello L, Rinaldi A, Forino M, Blaiotta G, Moine V et al., New insights into the formation of precipitates of quercetin in Sangiovese wines. J Food Sci Technol 57:2602–2611 (2020).
Trouillas P, Sancho‐García JC, De Freitas V, Gierschner J, Otyepka M and Dangles O, Stabilizing and modulating color by copigmentation: insight from theory and experiment. Chem Rev 116:4937–4982 (2016).
Gordillo B, Rodríguez‐Pulido FJ, González‐Miret ML, Quijada‐Morín N, Rivas‐Gonzalo JC, García‐Estévez I et al., Application of differential colorimetry to evaluate anthocyanin–flavonol–flavanol ternary copigmentation interactions in model solutions. J Agric Food Chem 63:7645–7653 (2015).
Fulcrand H, Cameira dos Santos PJ, Sarni‐Manchado P, Cheynier V and Bonvin JF, Structure of new anthocyanin‐derived wine pigments. J Chem Soc Perkin Trans 1:735–739 (1996).
Murota K, Shimizu S, Chujo H, Moon JH and Terao J, Efficiency of absorption and metabolic conversion of quercetin and its glucosides in human intestinal cell line Caco‐2 arch. Biochem Biophys 384:391–397 (2000).
Rothwell JA, Day AJ and Morgan MR, Experimental determination of octanol–water partition coefficients of quercetin and related flavonoids. J Agric Food Chem 53:4355–4360 (2005).
Calias P, Galanopoulos T, Maxwell M, Khayat A, Graves D, Antoniades HN et al., Synthesis of inositol 2‐phosphate‐quercetin conjugates. Carbohydr Res 292:83–90 (1996).
Chen S, Xing X‐H, Huang J‐J and Xu MS, Enzyme‐assisted extraction of flavonoids from Ginkgo biloba leaves: improvement effect of flavonol transglycosylation catalyzed by Penicillium decumbens cellulase enzyme microb. Dent Tech 48:100–105 (2011).
Plaza M, Pozzo T, Liu J, Gulshan Ara KZ, Turner C and Nordberg Karlsson E, Substituent effects on in vitro antioxidizing properties, stability, and solubility in flavonoids. J Agric Food Chem 62:3321–3333 (2014).
Boulton R, The copigmentation of anthocyanins and its role in the color of red wine: a critical review. Am J Enol Vitic 52:67–87 (2001).
Picariello L, Rinaldi A, Moio L, Moine V and Gambuti A, Fining strategies for quercetin deposit prevention in Sangiovese wines. LWT 185:115218 (2023).
Boulton RB, Singleton VL, Bisson LF and Kunkee RE, Principles and Practices of Winemaking. Springer Science & Business Media, New York (1996).
Dunsford P and Boulton R, The kinetics of potassium bitartrate crystallization from table wines. I. Effect of particle size, particle surface area and agitation. Am J Enol Vitic 32:100–105 (1981).
Somers TC and Ziemelis G, Flavonol haze in white wines. Vitis 24:43–50 (1985).
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