Macrowine 2021
IVES 9 IVES Conference Series 9 The commercial yeast strain as a significant source of variance for tyrosol and hydroxytyrosol in white wine

The commercial yeast strain as a significant source of variance for tyrosol and hydroxytyrosol in white wine

Abstract

Tyrosol (TYR) and hydroxytyrosol (HYT) are bioactive phenols present in olive oil and wine, basic elements of the Mediterranean diet. TYR is reported in the literature for its interesting antioxidant, cardioprotective and anti-inflammatory properties. In wine, its concentration can reach values as high as about 40 mg/L [Pour Nikfardjam et al. 2007] but, more frequently, this phenol – derived from yeast metabolism of tyrosine during fermentation – is present at lower levels, generally higher in red wines compared to whites. HYT was measured for the first time by Di Tommaso et al. [1998] in Italian wines – with maximum values of 4.20 mg/L and 1.92 mg/L for red and white wines, respectively – while definitely lower concentrations have been found later in Greek samples. Concentrations of about 2-3 mg/L have been reported by Minuti et al. [2006] for red wines while Romboli et al. [2015] observed definitely higher concentrations – up to 25 mg/L – in case of slow fermentations of Sangiovese wines processed in lab-scale. Oddly, in spite of the non-negligible concentration of these compounds in wine, few data are available regarding the concentration variability of TYR and HYT due to not genetically engineered Saccharomyces cerevisiae strains available on the market and used in winery conditions. To investigate this variability, 7 yeast strains (Zymaflore VL1; Fermol Arome Plus; AWRI 796; La Claire EM2; Anchor VIN13; Zymaflore VL3; Mycoferm CRU 31) were used (15 g/hL) to ferment – on semi-industrial scale, at 18-21°C – five Pinot gris juices achieved from different vineyards. They were adequately provided with natural assimilable nitrogen (163-214 mg/L), and had been well settled (36 h, 10°C, < 100 NTU) and supplemented with 20-30 mg/L SO2. After alcoholic fermentation, wines were sulphited (80 mg/L) and maintained sur lies under argon blanketing (4°C x 90 days), with batonnage 1 time a week on average. In the transition from juice to wine, the mean concentrations of TYR and HYT increased about 60 and 20 times. In wine, TYR ranged between 4.20 and 15.51 mg/L, and HYT between 0.33 and 3.45 mg/L confirming the values in the literature. Statistically significant differences have been observed between yeast strains, both for TYR and HYT, and maximum variability between strain mean concentrations was about 35%, corresponding to a range of about 2.2 mg/L TYR and 0.55 mg/L HYT. In any case, the variability linked to the origin of the juice was higher than that linked to the Saccharomyces cerevisiae strain. Pour Nikfardjam et al. 2007]. Mitteilungen Klosterneuburg 57(3), 146-152 Di Tommaso et al. (1998). J. High Res. Chromatography 21(10), 549-553 Minuti et al. (2006). J. Chromatography A, 1114, 263-268 Romboli et al. (2015). W. J. Microbiol. Biotech. 31(7), 1137-1145.

Publication date: May 17, 2024

Issue: Macrowine 2016

Type: Poster

Authors

Tomàs Villegas*, Chiara Barnaba, Giorgio Nicolini, Luca Debiasi, Roberto Larcher, Tiziana Nardin

*fondazione E.Mach

Contact the author

Tags

IVES Conference Series | Macrowine | Macrowine 2016

Citation

Related articles…

The challenge of quality in sulphur dioxide free wines: natural polyphenol alternatives

Sulphur dioxide (SO2) seems indispensable in winemaking because of its properties. However, a current increasing concern about its allergies effects in food product has addressed the international research efforts on its replacement. This supposes a sufficient knowledge of its properties and conditions of use. Several studies compared SO2 properties against new alternatives that are supposed to overcome SO2 disadvantages. Firstly, the state of art on SO2 wine replacements is revised, and secondly, the last promising results using natural enriched polyphenol extracts are shown.

Correlations between N,S,O-heterocycle levels and age of Champagne base wines

Champagne regulation allows winegrowers to stock small amounts of still wines in order to compensate vintages’ quality shifts mainly due to climate variations. According to their technical requirements and house style some Champagne producers (commonly named “Champagne houses”) use these stored wines in the blend in order to introduce an element of complexity. These wines possess the particularity of being aged on fine lees in thermo-regulated stainless steel tanks. The Champagne house of Veuve Clicquot Ponsardin has several wines stored this way.

Ageing of sweet wines: oxygen evolution according to bung and barrel type

Barrel ageing is a crucial step in the wine process because it allows many changes to the wine as enrichment, colour stabilization, clarification and also a slow oxygenation. Effects of the oak barrel have to be known to prevent oxidation of the wine. The type of bung used during ageing is also a parameter to consider. Ageing sweet wines in barrel is a real challenge. These wines may need some oxygen at the beginning of ageing but they should be protected at the end of their maturation, to avoid oxidation.

Use of chitosan as a secondary antioxidant in juices and wines

Chitosan is a polysaccharide produced from the deacetylation of chitin extracted from crustaceous and fungi. In winemaking chitosan is mainly used in the clarification of grape juice and wine, stabilization of white wines, removal of metals and to prevent wine spoilage by undesired microorganisms. The addition of chitosan to model wine systems was able to retard browning, reduce levels of metallic ions (Fe and Cu) and to protect varietal thiols due to its antiradical activity1. The present experiment was planned in order to evaluate the use of chitosan as a secondary antioxidant at three different stages of Sauvignon blanc fermentation and winemaking. Sauvignon blanc juices from three different locations were obtained at a commercial winery in Marlborough, New Zealand. One lots of grapes was collected from a receival bin and pressed into juice with a water-bag press, and a further juice sample was collected from a commercial pressing operation. Chitosan (1 g/L, low molecular weight, 75 – 85% deacetylated) was added to the juice after pressing, after cold settling, after fermentation, or at all these stages. Controls without any chitosan additions were also prepared.

Characterization of non-Saccharomyces yeast and its interaction with Saccharomyces cerevisiae with investigation of fermentation kinetics and aromatic composition

[lwp_divi_breadcrumbs home_text="IVES" use_before_icon="on" before_icon="||divi||400" module_id="publication-ariane" _builder_version="4.20.4" _module_preset="default" module_text_align="center" module_font_size="16px" text_orientation="center"...