Macrowine 2021
IVES 9 IVES Conference Series 9 Identification of caffeic acid as a major component of Moscatel wine protein sediment

Identification of caffeic acid as a major component of Moscatel wine protein sediment

Abstract

Proteins play a significant role in the colloidal stability and clarity of white wines [1]. However, under conditions of high temperatures during storage or transportation, the proteins themselves can self-aggregate into light-dispersing particles causing the so-called protein haze [2]. Formation of these unattractive precipitates in bottled wine is a common defect of commercial wines, making them unacceptable for sale [3]. Previous studies identified the presence of phenolic compounds in the natural precipitate of white wine [4], contributing to the hypothesis that these compounds could be involved in the mechanism of protein haze formation. The objective of this study was to isolate and identify the compounds contained in induced wine protein haze precipitate after alkaline hydrolysis. The heat-induced protein precipitate from five liters of white Moscatel of Alexandria wine was subjected to alkaline hydrolysis in 2 M NaOH, 10 mM EDTA and 1% (w/v) L-ascorbic acid following a protocol described elsewhere [5] with some modifications. The alkaline hydrolyzed sample was subjected to liquid-liquid extraction with ethyl acetate and evaporated to dryness. The extract was further fractionated using reversed phase-high performance liquid chromatography-diode array detector (RP-HPLC-DAD). The major compound present was found to be caffeic acid amongst other minor, unidentified compounds. Caffeic acid was identified by UV-vis spectra and the structure validated by 1H nuclear magnetic resonance (NMR). This work corroborates the observation that phenolic compounds, and caffeic acid in particular, may participate in wine protein haze formation since it is the major compound nonprotein compound present in Moscatel wine protein sediment.

References: [1] F.X. Sauvage, B. Bach, M. Moutounet, and A. Vernhet, Food Chemistry, 2010, 118, 26-34. [2] E.J. Waters, W. Wallace, and P.J. Williams, Journal of Agricultural and Food Chemistry, 1992, 40, 1514-1519. [3] G. Tabilo-Munizaga, T.A. Gordon, R. Villalobos-Carvajal, L. Moreno-Osorio, F.N. Salazar, M. Perez-Won, and S. Acuna, Food Chemistry , 2014, 155, 214-220. [4] M. Esteruelas, N. Kontoudakis, M. Gil, M.F. Fort, J.M. Canals, and F. Zamora, Food Research International, 2011, 44, 77-83. [5] Nardini, M., E. Cirillo, F. Natella, and C. Scaccini, Journal of Agricultural and Food Chemistry, 2002, 50, 5735-5741.

Publication date: May 17, 2024

Issue: Macrowine 2016

Type: Poster

Authors

Ricardo Chagas*, Ana Lourenço, Luísa Carvalho, Ricardo Ferreira, Sara Monteiro

*FCT/UNL

Contact the author

Tags

IVES Conference Series | Macrowine | Macrowine 2016

Citation

Related articles…

Effect of concentration and competition between different fungicide residues on the adsorption efficiency of activated vegetal fibres for treatment of wine

Vineyards are strongly exposed to fungal diseases, attacks from insects and competition with weeds. Most treatments used on grape vines contain synthetic active substances, which may be transferred to the wine. Such pesticides have a negative image because many active substances are potential health hazards. A specific oenological treatment allowing the reduction of pesticide residues in wine based on activated vegetable fibres (AVF) is under examination by the International Organisation for Vine and Wine. This technique works efficiently and alters the wine only little (Lempereur et al. 2014).

A multivariate approach using attenuated total reflectance mid-infrared spectroscopy to measure the surface mannoproteins and β-glucans of yeast cell walls during wine fermentations

Yeast cells possess a cell wall comprising primarily glycoproteins, mannans, and glucan polymers. Several yeast phenotypes relevant for fermentation, wine processing, and wine quality are correlated with cell wall properties. To investigate the effect of wine fermentation on cell wall composition, a study was performed using mid-infrared (MIR) spectroscopy coupled with multivariate methods (i.e., PCA and OPLS-DA). A total of 40 yeast strains were evaluated, including Saccharomyces strains (laboratory and industrial) and non-Saccharomyces species. Cells were fermented in both synthetic MS300 and Chardonnay grape must to stationery phase, processed, and scanned in the MIR spectrum.

Proteomic and activity characterization of exocellular laccases from three Botrytis cinerea strains

Botrytis cinerea is a fungus that causes common infection in grapes and other fruits. In winemaking, its presence can be both considered desirable in the case of noble rot infection or undesirable when grey rot is developed. This fungus produces an extracellular enzyme known as laccase which is able to cause oxidation of phenolic compounds present in must and wine, causing most of the times a decrease in its quality and problems during the winemaking process [1]. Material and methods: Three B. cinerea strains (B0510, VA612 and RM344) were selected and grown in a liquid medium adapted from one previously described [2]. The enzyme was isolated by tangential ultrafiltration of the culture medium using a QuixStand system equipped with a 30 KDa filtration membrane.

Modulating role of SO2 in white wine protein haze formation

Despite the extensive research performed during the last decades, the multifactorial mechanism responsible for the white wine protein haze formation is not fully characterized. Herein, a new model is proposed, which is based on the experimental identification of sulfur dioxide as a major modulating factor inducing wine protein haze upon heating. As opposed to other reducing agents, such as 2-mercaptoethanol, dithiothreitol and tris(2-carboxyethyl)phosphine hydrochloride (TCEP), the addition of SO2 to must/wine upon heating cleaves intraprotein disulfide bonds, hinders thiol-disulfide exchange during protein interactions and can lead to the formation of novel inter/intraprotein disulfide bonds. Those are eventually responsible for wine protein aggregation which follows a nucleation-growth kinetic model as shown by dynamic light scattering [1].

Comparison of fortified, sfursat and passito winemaking techniques for the enhancement of the oenological potential of the black grape cultivar Moscato nero d’Acqui (Vitis vinifera L.)

One of the key factors of the economical development of viticulture and wine industry in specific limited areas is the exploitation of ancient, local grape varieties. Therefore, in recent years the growing interest to rediscover minor varieties, previously cultivated, has promoted many studies. With this regard, the focus of this study was the Vitis vinifera L. cultivar Moscato nero d’Acqui, nowadays found only in old vineyards in the Acqui zone (North-West Italy). In particular, the aims of this work were: i) to investigate secondary metabolites profile of the grapes, and ii) to evaluate the attitude to the production of special wines.