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…

A combination of biotechnology tools and coopers elements for an alternative the addition of SO2 at the end of the malolactic fermentation in red wines or at the “mutage” for the “liquoreux” wines

In red wines the post-MLF SO2 addition is an essential event. It is also the case for the “mutage” during the elaboration of the “liquoreux”. At these moments SO2 plays an antimicrobial action and an antioxidant effect. But at current pH of wines, ensuring a powerful molecular SO2 has become very difficult. Recent work on Brettanomyces strains have also shown that some strains are resistant up to 1.2 mg / L of molecular SO2. It’s also the case of the some Saccharomuces or Zygosaccharomyces strains suitable to re-ferment “liquoreux” wines after the “mutage”.

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 free and glycosidically bound simple phenols in hybrid grape varieties using liquid chromatography coupled to high resolution mass (q-orbitrap)

Vitis vinifera is one of the most diffused grapevines over the word and it is the raw material for high quality wines production. The availability of more resistant interspecific hybrid vine varieties, developed from crosses between Vitis vinifera and other Vitis species, has generating much interest, also due to the low environmental effect of production. However, hybrid grape wine composition and varietal differences between interspecific hybrids are not well defined. Different studies revealed that wine consumption has health effects due to its high content of antioxidants, as phenolic compounds. In particular, simple phenols are appreciated not only for their physiological health benefits, including antioxidant, anti-inflammatory and cardioprotective effects, but also because they affect wines organoleptic profile and have a significant role in defining their nutritional characteristics.

What about oxygen transfer during wine aging in barrels?

During wine aging, several complex phenomena of gas transfer take place in barrels due to the wine/oak contact. The efficiency of this gas transfer varies according to oak wood’s intrinsic physical properties. This research aims to better understand oxygen transfer phenomena through dry oak staves and especially through stave gaps, in order to reevaluate the importance of barrel-making on a barrel’s supply of oxygen. Experimentation was based on the development of an innovative permeameter of laboratory scale, for which the principal operating conditions concerning applied pressure, the choice of liquid phase/gas phase, and the grain type of oak are taken into account and investigated. With a specially developed tightening system, the existing pressure at stave gaps in a barrel could be reproduced on a laboratory scale in order to estimate its influence on oxygen transfer efficiency.

Supramolecular approaches to the study of the astringency elicited by wine phenolic compounds

The objective of this study is to review the scientific evidences and to advance into the knowledge of the molecular mechanisms of astringency. Astringency has been described as the drying, roughing and puckering sensation perceived when some food and beverages are tasted (1). The main, but possibly not the only, mechanism for the astringency is the precipitation of salivary proteins (2,3). Between phenolic compounds found in red wines, flavan-3-ols are the group usually related to the development of this sensation. Other compounds, phenolic or not, like anthocyanins, polysaccharides and mannoproteins could act modifying or modulating astringency perception by hindering the interaction between flavanols and salivary proteins either because of their interaction with the flavanols or because of their interaction with the salivary proteins.