Macrowine 2021
IVES 9 IVES Conference Series 9 Effect of supplementation with inactive yeast during alcoholic fermentation in base wine for sparkling

Effect of supplementation with inactive yeast during alcoholic fermentation in base wine for sparkling

Abstract

Foam stability of sparkling wines is significantly favored by the presence of surface active agents such as proteins and polysaccharides [1]. For that reason, the renowned sparkling wines are aged after the second fermentation in contact with the lees for several months (even years). Thereby wines are enriched in these macromolecules due to yeast autolysis. Since this practice is slow and costly, winemakers are seeking for alternative procedures to increase their concentration in base wines. In that sense, the supplementation with inactive yeast during alcoholic fermentation has been proposed [2]. The aim of this study was to determine whether this new strategy is really useful for enriching base wines in macromolecules and for improving foam properties of the base wines. MATERIAL AND METHODS: Macabeo grapes were harvested at the appropriate maturity and pressed. The grape juice was immediately sulfited and pectinolytic enzymes were added to facilitate settling. After 24 h, clean grape juices (around 70 L each) were racked into nine 100-L stainless steel tanks and were fermented under controlled temperature (16-18 ºC) with selected yeasts. Three tanks were considered as controls whereas other 6 were supplemented with 40 g/hL of 2 inactive yeasts (3 with Optiwhite and 3 with Optimumwhite; Lallemand Inc., Montreal, Canada). Once the alcoholic fermentation was finished, wines were sulfited, racked and cold stabilized. Proteins were analyzed by HRSEC-DAD [3], polysaccharides by HRSEC-RID [4] and foaming properties by the Mosalux procedure [5]. RESULTS: Both inactive yeasts increased the protein and polysaccharide concentration of the base wines in comparison with the non-supplemented control wines. Optiwhite was more effective for enriching polysaccharide concentration whereas Optimumwhite was more effective for enriching protein concentration. Regardless the foam properties, supplementation with Optiwhite originated base wines with a significant higher value of foamability (Hm) than the control. The persistence of the foam (Hs) also tended to be higher but this increase was not statistically significant. Optimumwhite also tended to increase both parameters (Hm and Hs) but none of these differences was statistically significant. CONCLUSIONS: The supplementation with inactive yeasts is a useful tool to increase protein and polysaccharide concentration of base wines and also to improve its foam properties.

REFERENCES: [1] Esteruelas M, González-Royo E, Kontoudakis N, Orte A, Cantos A, Canals JM, Zamora F (2015) J. Sci. Food Agric., 95, 2071-2080 [2] Pozo-Bayón MA, Andujar-Ortiz I, Alcalde-Hidalgo JM, Martín-Alvárez PJ, Moreno-Arribas MV (2009) J. Agric. Food Chem. 57, 10784-10792 [3] Canals JM, Arola L, Zamora F (1998) Am. J. Enol. Vitic., 49, 383-388 [4] Ayestaran B, Guadalupe Z, Leon D (2004) Anal. Chim. Acta. 513:29-39 [5] Maujean A, Poinsaut P, Dantan H, Brissonet F, Cossiez E (1990) Bull. OIV, 711-712, 405-426

Publication date: May 17, 2024

Issue: Macrowine 2016

Type: Poster

Authors

Fernando Zamora*, Elena González-Royo, Joan Miquel Canals, José María Heras, Laura Medina, Nathalie Sieczkowski

*Universitat Rovira i Virgili

Contact the author

Tags

IVES Conference Series | Macrowine | Macrowine 2016

Citation

Related articles…

Removal of Fumonisin B1 and B2 from red wine using polymeric substances

The Ability of PVPP (Polyvinylpolypyrrolidone), PVP-DEGMA-TAIC (copolimerization of N-vinyl-2-pyrrolidinone with ethylene glycol dimethacrylate and triallyl isocyanurate) and PAEGDMA
(poly(acrylamide-co-ethylene glycol dimethacrylate)) polymers was tested as removal agents for Fumonisin B1 (FB1) and Fumonisin B2 (FB2) from model solutions and red wine. The polymers removal capacity was checked at three different resident times (2, 8 and 24 hours of contact time between the polymer and the sample), showing no differences in the percentage of FB1 and FB2 removal. Then, different polymer concentrations (1, 5 and 10 mg mL-1) were tested in model solution with and without phenolics (i.e. gallic acid and 4-methylcatechol).

Impact of sulfur compounds to the antioxidant stability of white wines

The chemical mechanisms involved in oxidation/reduction potential of wine during winemaking and aging are affecting its color, aroma and taste. Chemical oxidation is one of the major causes of development of off-flavors during ageing1. Thus, the chemical changes in wine during storage should be controlled to ensure the sensory quality of the product and avoid consumer rejection that will compromise the economic value of the product. The 1-hydroxyethyl radical has been recognized as the key radical intermediate in the oxidative reactions in wine2. Based on the kinetic study of POBN-1-hydroxyethyl spin adduct formation in wines initiated via the Fenton reaction, a novel tool was recently developed in our laboratory to quantify the resistance of wines against oxidation3.

Evidence for terroir effect associated with botrytisation relatively to compounds implicated in typical aromas of noble rot sweet wines

Recent studies have demonstrated the role of certain lactones, particularly 2-nonen-4-olide, and volatile thiols (3-sulfanylhexan-1-ol) in the over ripped aromas of noble rot sweet wines (Stamatopoulos et al. 2014ab). These compounds are partly formed during the maturation and under the activity of B. cinerea on grapes. This research was carried out in the vineyard of Sauternes with aim to better understand their genesis depending on the grape over-ripening on two different soil types during 3 vintages. Thus, the study was conducted, with the Sémillon grape, during vintages 2012, 2014 & 2015, at 4 stages of over-maturation of the grapes (healthy, pourri plein, pourri roti, pourri roti + 15 days) considering two vineyard plots with different soil characteristics (calcosol & peyrosol) planted with the 315 Sémillon clone and grafted on 101-14 rootstock respectively in 1981 and 1980 and cultivated with the same vineyard management. Volatile lactones were assayed by liquid-liquid extraction followed by GC/MS analysis and the precursors of 3-sulfanylhexanol by an adaptation of the method by Capone et al. 2010 (SPE-
UPLC/FTMS).

Comprehensive two-dimensional gas chromatography coupled with Tof-MS, a powerful tool for analysis of the volatomes of grapes and wines

Comprehensive two-dimensional gas chromatography (GCxGC) has emerged as a powerful analytical technique for unraveling the volatile composition of complex matrices. This work will present three applications of GCxGC Tof-MS to the oenological field, aimed to identify novel biomarkers to be used in the quality control process of the wine industry. Comprehensive mapping of volatile compounds was conducted in a large sample of 70 sparkling wines, produced by 48 different wineries across 6 vintages and representative of the two main production areas for premium Italian sparkling wines (Franciacorta (FC) and Trentodoc (TN)), using HS-SPME followed by GCxGC-Tof-MS and multivariate analysis. Selection and identification of 196 putative biomarkers allowed clear separation of sparkling wines from FC and TN.

Effect of intra‐vineyard ripeness variation on the efficiency of commercial enzymes on berry cell wall deconstruction under winemaking conditions

Intra-vineyard variation grape berry ripening occurs within bunches, between bunches on the same vine and between vines. Although it is assumed that such variation also occurs at the grape berry cell wall level, no study to data has investigated in any depth. Here we have used a intra-vineyard panel design to investigate pooled bunches from six vines (per panel) in the context of a winemaking scenario. The dissected vineyard was harvested by separate panels, where each panel was then subjected to a standard winemaking procedure with or without the addition of three different enzyme preparations for maceration.