Macrowine 2021
IVES 9 IVES Conference Series 9 Update knowledge about the presence of condensed tannins in grapes and their contributions to astringency perception

Update knowledge about the presence of condensed tannins in grapes and their contributions to astringency perception

Abstract

Condensed tannin is a principle group of polyphenol compounds derived from grape, greatly contributing to the bioactivity and the sensory perception of wine. Condensed tannins present as a heterogeneous mixture in nature involving various degrees of both polymerization and galloylation. Even though multiple attempts focusing on fractionation of grape condensed tannins by solid-phase have been conducted over the past decades, few individual tannins have been purified and identified. Hence, our knowledge on grape and wine condensed tannin moleculars has to be limited at the several known monomeric, dimeric and trimeric proanthocyanidins. In the present study, a rapid and effective approach was developed to isolate the galloylated proanthocyanidin from the non-galloylated forms in grape seed tannins and fractionate the non-galloylated proanthocyanidin according to their degree of polymerization by the technique of Centrifugal partition chromatography (CPC). The application of CPC on grape tannins fractionation is efficient, less-time consuming, less expensive and with higher recovery. More importantly, it could effectively isolate galloylated tannins at the beginning and eliminate its interference in the other fractions. After fractionation performed by the technique of CPC, the repurification was achieved by either preparative hydrophilic interaction chromatography or reversed phase high-performance liquid chromatography (HPLC). Eventually, a series of individual condensed tannins with certain degree of polymerization and galloylation from grape were isolated successively. Analyte identity and purity were examined by reversed-phase UPLC-DAD-ESI-Q-TOF and normal-phase HPLC-UV-Fluo-MS, respectively. The astringency perception contributions of the purified individual tannins were examined by the approach of salivary binding ability test. The results were observed by HPLC-Fluo and quantified by the difference of the amount of proanthocyanidins between before and after interaction.

Publication date: May 17, 2024

Issue: Macrowine 2016

Type: Poster

Authors

Wen Ma*, Hua Li, Michael Jourdes, Pierre Waffo-Téguo, Pierre-Louis Teissedre

*ISVV

Contact the author

Tags

IVES Conference Series | Macrowine | Macrowine 2016

Citation

Related articles…

Chemical markers in wine related to low levels of yeast available nitrogen in the grape

Nitrogen is an important nutrient of yeast and its low content in grape must is a major cause for sluggish fermentations. To prevent problems during fermentation, a supplementation of the must with ammonium salts or more complex nitrogen mixtures is practiced in the cellar. However this correction seems to improve only partially the quality of wine [1]. In fact, yeast is using nitrogen in many of its metabolic pathways and depending of the sort of the nitrogen source (ammonium or amino acids) it produces different flavor active compounds. A limitation in amino acids can lead to a change in the metabolic pathways of yeast and consequently alter wine quality.

Extraction of pathogenesis-related proteins and phenolics in Sauvignon Blanc as affected by different

The composition of wine is largely determined by the composition of pre-fermentation juice, which is influenced by extraction of grape components. Different grape harvesting and processing conditions could affect the extraction of grape components into juice. Among these grape components, pathogenesis-related (PR) proteins are of great concern for white wine maker as they are the main cause of haze formation in finished white wine. If not removed before bottling, these PR proteins may progress into haze through the formation of complex with phenolics under certain conditions. Thaumatin-like proteins (TLPs) and chitinases are the main constituents of PR proteins found in protein haze.

New biological tools to control and secure malolactic fermentation in high pH wines

Originally, the role of the malolactic fermentation (MLF) was simply to improve the microbial stability of wine via biological deacidification. However, there is an accumulation of evidence to support the fact that lactic acid bacteria (LAB) also contribute positively to the taste and aroma of wine. Many different LAB enter into grape juice and wine from the surface of grape berries, cluster stems, vine leaves, soil and winery equipment. Due to the highly selective environment of juices and wine, only a few types of LAB are able to grow.

Innovations in the use of bentonite in enology: interactions with grape and wine proteins, colloids, polyphenols and aroma compounds.

The use of bentonite in oenology rounds around the limpidity and the stability that determine consumer acceptability. As a matter of fact, the haze formation in wine reduces its commercial value and makes it unacceptable for sale. Stabilization treatments are, therefore, essential to ensure a long-time limpidity and to forecast the formation of deposits in the bottle. Bentonite that is normally used in oenology for clarifying-fining purpose, shows a natural clay-based mineral structure allowing it to swell and to jelly in water and hence in must and wine.

Interactions of wine polyphenols with dead or living Saccharomyces cerevisiae Yeast Cells and Cell Walls: polyphenol location by microscopy

Tannin, anthocyanins and their reaction products play a major role in the quality of red wines. They contribute to their sensory characteristics, particularly colour and astringency. Grape tannins and anthocyanins are extracted during red wine fermentation. However, their concentration and composition change over time, due to their strong chemical reactivity1. It is also well known that yeasts influence the wine phenolic content, either through the release of metabolites involved in the formation of derived pigments1, or through polyphenol adsorption2,3.