Abstract
Fermentations using different yeast strains can result in varying concentrations of volatile thiols and substantial sensory effects in young Sauvignon blanc wines. These yeast-derived aroma differences are generally thought to be short lived; therefore, Sauvignon blanc wines made using different yeast strains in two separate studies were investigated after three years of cellar storage. Differences were observed in the volatile composition and sensory profiles of the three-year-old wines that, when compared with the six-month data, demonstrated the continued influence of yeast strains. This observation provides further evidence that choice of yeast strain is important to wine flavor.
Until recently there was limited data to support the proposition that differences in production of volatile compounds due to the effect of yeast strain may be great enough to affect wine sensory properties. Recent work has now clearly demonstrated that inoculation with commercial Saccharomyces wine yeast strains can result in a wide range of sensory profiles (King et al. 2008, 2010, Swiegers et al. 2009) that can be sufficiently large to affect consumer preference (King et al. 2010). These studies also confirmed that the strains differed in their production of volatile thiols and esters, important volatile compounds to Sauvignon blanc wine aroma, and that these differences were related to the observed sensory properties. In the wine industry and among the research community, it is a common assumption that, if evident in young wines soon after bottling, any yeast-derived aroma and flavor differences are likely to be short lived.
Most of the reported studies investigating yeast strain effects over time have involved extended yeast lees contact postfermentation. Yeast autolysis using different strains has been shown to affect the chemical composition and sensory profiles of Champagne wines over three years (Leroy et al. 1990), the color and aging potential of one-year-old Sherry wines (Lopez-Toledano et al. 2006), the chemical composition of nine-month-old Macabeo wines (Loscos et al. 2009), and the sensory properties of Vin Santo wines after 18 months of barrel aging (Domizio et al. 2007). To our knowledge, there are no reports investigating continued differences in flavor caused by yeast strains during fermentation.
The aim of the study was to determine whether yeast strain-derived flavor differences in young Sauvignon blanc wines were retained after prolonged bottle aging. Two sample sets made with different yeast strains reported to have significant volatile composition and sensory differences at six months postbottling (King et al. 2008, Swiegers et al. 2009) were examined after three years of cellar storage.
Materials and Methods
Wines.
Small-scale (20 L) fermentations of homogenized and unfiltered Sauvignon blanc grape juice from the same vineyard in the Adelaide Hills (Australia) were conducted using different yeast strains over two consecutive vintages (2005 and 2006). In 2005, seven commercial Saccharomyces yeast strains in single-strain fermentations were investigated: Vin7, Vin13, NT116 (Anchor Yeast, Cape Town, South Africa), QA23, L2056 (Lalvin, Lallemand, Montreal, Canada), and X5, VL3 (Laffort Oenologie, Bordeaux, France). In 2006, seven treatments were conducted: three single-strain fermentations, Vin7, QA23, and Vin13; two coinoculated fermentations containing equal proportions of Vin7 and QA23 (Vin7/QA23) and Vin7 and Vin13 (Vin7/Vin13); and two equal blends of the single-strain wines after fermentation, Vin7 and QA23 (Vin7+QA23) and Vin7 and Vin13 (Vin7+Vin13).
The winemaking procedures are detailed in previous publications (King et al. 2008, Swiegers et al. 2009). Prior to bottling, a sulfur dioxide addition in the form of potassium metabisulfite was made to all wines to obtain a final free sulfur dioxide concentration of 25 to 30 mg/L. The wines were bottled in 750 mL (2005) and 375 mL (2006) clear glass bottles under inert gas, and sealed with roll-on tamper-evident screwcaps. The wines were stored upright, away from light at approximately 15°C (range 14 to 17°C), until analysis.
The methodology and results of the analysis conducted six months after bottling are detailed elsewhere for the 2005 (Swiegers et al. 2009) and 2006 (King et al. 2008) wines. Three fermentation replicates of all treatments were produced for both vintages; however, only one fermentation replicate of each treatment was tested after three years of bottle storage; the six-month analyses indicated that there were negligible differences among fermentation replicates (King et al. 2008, Swiegers et al. 2009).
Chemical analyses.
All treatments were analyzed for standard chemical composition after three years in bottle, as detailed in Iland et al. (2004). Fifteen fermentation-derived volatile compounds (six acetate esters, five fatty acid ethyl esters, four higher alcohols) were measured in duplicate for all treatments three years after bottling, using a published method (Siebert et al. 2005), modified for the 2006 wines using high-volume headspace instead of solid-phase microextraction. For the 2005 wines, eight additional volatile compounds (one higher alcohol, seven volatile acids) were measured.
The volatile thiol compounds 4-mercapto-4-methylpentan-2-one (4MMP), 3-mercaptohexanol (3MH), and 3-mercaptohexyl acetate (3MHA) were measured in all treatments for both vintages, using a published method (Tominaga et al. 1998). The concentrations of the volatile compounds for the three-year-old wines are previously reported (King 2010).
Sensory analyses.
Descriptive analyses were conducted on all treatments from both vintages three years after bottling, using a consensus training method previously described (King et al. 2008). Differences in the procedure were as follows. For the 2005 wines, 10 assessors (seven females), all experienced descriptive analysis panelists, rated 11 aroma attributes. Three training sessions were conducted prior to formally rating the wines: two 120-min discussion sessions and one practice rating session. The samples were assessed under sodium lighting in isolated, temperature controlled (22 to 24°C), ventilated tasting booths. Each sample was presented at a constant volume (30 mL) in ISO coded, covered tasting glasses in a random and balanced order across the judges. In a separate study, the 2006 wines were assessed by 10 experienced descriptive analysis panelists (six female) who rated one appearance, 13 aroma, and 10 palate attributes. Training and rating sessions were conducted as outlined for the 2005 analysis. FIZZ software (version 2.1, Biosystèmes, Couternon, France) was used for the collection of all sensory data. The seven yeast treatments in the 2005 wines were assessed in triplicate, while the 2006 wines were assessed in quadruplicate. Sensory attributes were agreed upon by the panelists for the analyses of both vintages and the composition of the reference standards and synonyms are provided in Table 1.
Sensory attributes and their reference standard compositions and synonyms for the descriptive sensory analyses of three-year-old Sauvignon blanc wines made in 2005 and 2006.
Data analysis.
The sensory data were analyzed using analysis of variance (ANOVA) for each attribute, testing for the effects of treatment, presentation replicate and judge, treating judge as a random effect (JMP 5.1, SAS Institute, Cary, NC). One-way ANOVA was used to analyze the chemical data and compounds from technical duplicates showing no yeast treatment difference were eliminated from further analysis. Odor activity values were calculated for each volatile compound using aroma detection thresholds taken from King et al. (2008). Principal component analyses (PCA) were performed on the correlation matrix of the mean attribute ratings across the panelists and replicates and the mean volatile compound concentrations, for those that were significantly different among the yeast treatments.
Results and Discussion
Of the 11 aroma attributes rated in the 2005 wines after three years of bottle aging, three attributes were significantly different among treatments at p < 0.05: aroma intensity, canned lychee, and fresh green. The sweaty attribute (p < 0.10) was also included in the analysis. For the chemical composition of the 2005 wines at three years, there were differences among the treatments for most of the volatile compounds measured. The principal component analysis (PCA) biplot (Figure 1A) shows the different aroma attributes and explains 92% of the variance. The different volatile compounds are also shown (Figure 1B), with 59% of variance explained.
Principal component analysis (PCA) biplots of the different aroma attributes (A) and volatile compounds (B) for three-year-old wines made in 2005 using seven different yeast treatments (closed circles). Volatile compounds in italic font indicate an odor activity value greater than 1.0.
The yeast treatment Vin7, situated on the far right side of the biplots, was rated highest in the attributes aroma intensity, canned lychee, and sweaty (Figure 1A) and had relatively high concentrations of the volatile thiols 4MMP, 3MH, and 3MHA and the fruity compounds 3-methylbutyl acetate, 2-methylpropyl acetate, ethyl butanoate, and ethyl-2-methylpropanoate, as well as most of the higher alcohols and volatile acids measured (Figure 1B). These results are similar to the Vin7 wines at six months, where the wines had high concentrations of all volatile thiol compounds and high ratings for the sweaty sensory attribute (Swiegers et al. 2009). The canned lychee attribute was closely associated with the Vin7 yeast treatment, which had the highest volatile thiol concentrations; therefore, we can speculate that the canned lychee attribute is related to the presence of volatile thiols in aged white wines, although it has not previously been described.
The X5 yeast treatment was rated highest in the fresh green attribute (Figure 1A). All other yeast treatments had similar sensory profiles, except the VL3 yeast treatment had significantly lower ratings for the attribute aroma intensity than the Vin13 treatment. There were significant differences in the chemical compositions of the yeast treatments, illustrated by their vertical spread along PC2 (Figure 1B). The Vin13 and NT116 yeast treatments were highest in ethyl propanoate, ethyl lactate, and butanol, whereas the QA23, L2056, and X5 treatments were high in propanoic acid, and VL3 yeast treatment was high in 2-methylbutyl acetate and hexanol.
From an ANOVA of the sensory descriptive data for the 2006 wines assessed three years postbottling, the attributes yellow (color), overall fruit flavor, prickly, yeasty/cheesy, sweetness, and bitter were significantly different among the wines at p < 0.05. Two other attributes were included in further analysis: cat urine/sweaty and solvent (p < 0.10). The sensory and chemical data for the 2006 wines at three years are shown. The PCA biplot of the aroma attributes explains 76% of the total variance (Figure 2A), while the PCA biplot of the volatile compounds explains 78% of the variance (Figure 2B).
Principal component analysis (PCA) biplots of the different aroma attributes (A) and volatile compounds (B) for three-year-old wines made in 2006 using seven different treatments (closed circles). Italicized volatile compounds have an odor activity value greater than 1.0. Yeast treatments with a slash (/) represent coinoculations and and those with a plus (+) represent blended wines of Vin7 and QA23, and Vin7 and Vin13 yeast strains.
The Vin7 yeast treatment and two blended wines Vin7+QA23 and Vin7+Vin13 were rated highly in the attributes solvent and overall fruit flavor (Figure 2A). The Vin7 yeast treatment and the blended wines had high concentrations of volatile acidity and ethyl acetate, as well as 4MMP, 2-methylpropyl acetate, 2-methylbutyl acetate, 2-methylpropanol, and 3-methylbutanol (Figure 2B). The aroma profiles of these wines reflect the high concentrations of volatile acidity and high ratings of white vinegar observed in the young wines (King et al. 2008). These treatments also retained relatively high concentrations of the volatile thiol 4MMP (King et al. 2008), the sensory contribution of which may be masked by the solvent attribute.
The Vin13 yeast treatment and the two coinoculated wines Vin7/Vin13 and Vin7/QA23 were situated in the left side of the biplot (Figure 2A), rated high in the cat urine/sweaty and prickly aromas. Vin13 was rated highly in the yeasty/cheesy attribute, along with QA23 yeast treatment, situated at the bottom of the biplot. Vin13 and Vin7/Vin13 yeast treatments had high concentrations of the volatile thiol 3MH, as well as 3-methylbutyl acetate, phenylethyl acetate, ethyl-2-methylpropanoate, ethyl-3-methylbutanoate, and butanol (Figure 2B). Vin7/QA23 coinoculation also had relatively high concentrations of 3MH and high concentrations of hexyl acetate, ethyl propanoate and hexanol, similar to QA23, hence its position near the bottom of the biplot (Figure 2B).
The wine aroma profiles of the coinoculated wines at three years were similar to those measured at six months, with high concentrations of volatile thiols and highest ratings for the volatile thiol-related sensory attributes box hedge and passionfruit (King et al. 2008). The cat urine/sweaty attribute in the three-year-old wines is synonymous with box hedge (King et al. 2011), which was used as a reference standard for this attribute (Table 1).
The wines in both sets of samples studied had large differences in sensory properties after three years of bottle storage, which could be characterized using sensory descriptive analysis methodology, rather than requiring more sensitive sensory tests, such as discrimination tests (Stone and Sidel 2004). As expected, the three-year-old Sauvignon blanc wines no longer exhibited most of the fresh, fruity aromas that distinguished the treatments at six months, such as estery, confectionary, and floral (King et al. 2008, Swiegers et al. 2009). This result was common to all treatments for both vintages and was associated with a decrease in most of the fruity acetate esters, as reported elsewhere (Rapp 1998). There was, nonetheless, a substantial degree of commonality evident among the sensory properties measured at six months and those perceived at three years for both vintages, partly because young wines with high initial concentrations of volatile thiols remain relatively high in these compounds after three years of bottle aging and continue to display volatile thiol-related sensory attributes. A similar theory was suggested whereby yeast strains that produce high concentrations of ester compounds, and thus, higher initial fruity aroma ratings soon after bottling, can result in a longer shelf life of the wine (Lilly et al. 2000).
There was some treatment variation in free and total sulfur dioxide concentrations. All treatments had relatively low free sulfur dioxide levels, ranging from 8 to 13 mg/L (data not shown), with the lowest concentrations in the wines made with the strains Vin13, Vin7, and NT116 in the 2005 wines, and all the treatments in the 2006 wines, except the coinoculated wines. There was no significant relationship between free sulfur dioxide levels and ratings for any of the sensory attributes in the two sample sets, indicating that the slight variation in sulfur dioxide was not the cause of the sensory differences observed.
Conclusion
Results strongly indicate that yeast strains can continue to have an effect on the sensory and chemical profiles of wine, even after an extended period of bottle age. While most modern Sauvignon blanc wines will be consumed well before the three-year aging point studied here, the study shows clearly that wines that are drunk during the usual commercial shelf life of this wine type will be very likely to show similar differences to those that were evident in the wine soon after fermentation. Thus, yeast strain selection by wine producers, at least for Sauvignon blanc wines made with no oak influence and designed for freshness and fruity flavors, can have a lasting and important effect on wine style and quality.
Acknowledgments
Acknowledgments: The Australian Wine Research Institute (AWRI), a member of the Wine Innovation Cluster, is supported by Australian grapegrowers and winemakers and the Australian Government through funding by the Grape and Wine Research and Development Corporation (GWRDC). The project was cofunded by scholarships from the Australian Government, GWRDC, and the University of Adelaide.
The authors gratefully acknowledge the efforts of Brooke Travis and the sensory panelists and thank the following for their help with volatile analyses: Tracey Siebert and Dimitra Capone (AWRI), Meagan Mercurio (Metabolomics Aust.), Laura Nicolau (University of Auckland, NZ), and SARCO Laboratoire (Floriac, France).
Footnotes
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↵3 (present address) Christian Hansen A/S, Bøge Allé 10-12, DK-2970 Hørsholm, Denmark.
- Received July 1, 2010.
- Revision received November 1, 2010.
- Accepted February 1, 2011.
- Published online December 1969
- © 2011 by the American Society for Enology and Viticulture