Different application dosages of a specific inactivated dry yeast ( SIDY ) : effect on the polysaccharides , phenolic and volatile contents and color of Sauvignon blanc wines

1Department of Agro-Industry and Enology, Faculty of Agronomical Sciences, University of Chile, PO Box 1004, Santa Rosa 11315, La Pintana, Santiago, Chile 2Lallemand Inc. Chile y Compañía Limitada, Rosario Norte 407, piso 6, Las Condes, Santiago, Chile 3Instituto de Ciencias Biomédicas, Facultad de Ciencias, Universidad Autónoma de Chile, Chile 4Lallemand SAS, 19 rue des Briquetiers, BP 59, 31 702 Blagnac, France


Introduction
Recently, biotechnological companies have begun to offer winemakers the new winemaking tool of yeastderived preparations.These preparations are obtained from Saccharomyces cerevisiae yeast strains and, as they can provide comparable positive effects without any potential drawbacks (Del Barrio-Galán et al., 2011), they are supplied as an alternative to the onlees wine aging technique.Due to the release of certain compounds from yeasts during autolysis, aging on lees is widely used to improve the sensory and technological quality of wines.However, it is a slow and complex process requiring several monthseven years -to be completed and it may involve some enological issues such as microbiological and organoleptic alterations (Andújar-Ortiz et al., 2013).Aging on lees also increases wine production costs, yet yeast-derived preparations can avoid or minimize the above problems because they can release major compounds of enological interest in a shorter period of time than traditional on-lees aging.Yeast-derived preparations used to shorten the aging time of wines are commonly classified as inactivated dry yeast, yeast autolysates, yeast cell walls, yeast protein extracts (Pozo-Bayón et al., 2009), and purified mannoproteins, the most widely-used being specific inactivated dry yeasts (SIDY).In the SIDY production process, the complete yeast biomass is inactivated by a specific enzymatic or thermal process to stop its metabolism and enzymatic activities with the aim of obtaining a similar product to that obtained during natural autolysis, but more rapidly and in a more controlled process (Andújar-Ortiz et al., 2013).Generally, these yeast-derived preparations are selected for their particular characteristics, such as their high polysaccharide content, mainly mannoproteins, which, due to their major influence on technological aspects and wine sensory characteristics (Doco et al., 2003), appear to be those of main enological interest.These compounds can interact with some phenolic wine compounds acting as protective colloids, preventing or limiting the oxidation of white wines (Lopez-Toledano et al., 2006;Del Barrio-Galán et al., 2016), thereby decreasing astringency and bitterness while enhancing mouthfeel (Del Barrio-Galán et al., 2012;González-Royo et al., 2017).Polysaccharides and mannoproteins can modify the volatility of some volatile compounds in the wine (Bautista et al., 2007;Chalier et al., 2007;Juega et al., 2015).In addition, some precursors present in the SIDY, such as amino acids and fatty acids, can be released into the wines, improving their flavor (Izzo and Ho, 1991 ;Mahadevan and Farmer, 2006).These compounds can also improve the protein and tartaric stability of white wines (Moine-Ledoux and Dubourdieu, 2002;Lomolino and Curioni, 2007) as well as the characteristics of sparkling wines (Núñez et al., 2006).They can also remove some mycotoxins such as ochratoxin A (Caridi et al., 2006).
Mannoproteins are synthesized and glycosylated in the yeast cytoplasm, particularly in the endoplasmic reticulum (Farkaš et al., 1976).They are then transported through a secretory route to the extracellular region where they are assembled onto the yeast cell wall (Klis, 1994) and act as a selective and protective filter to prevent chemical and βglucanase enzymatic attacks (Cid et al., 1995).When yeast cells are inactivated and then added to the wine, they can release these polysaccharides and other intracellular components (Charpentier and Freyssinet, 1989).
In general, there is a relatively wide range of recommended dosages (5-40 g hL -1 ) for applying yeast-derived preparations.It depends on the purity and solubility of the product, the type of wine, and the timing and purpose of the application.In addition, almost all of the research studies performed with these products have been undertaken using a medium-high dose (30-40 g hL -1 ) (Del Barrio-Galán et al., 2011, 2012, 2016).In these studies, it has been shown that the use of different yeast-derived preparations increased the content of polysaccharides and improved the technological and sensory characteristics of the wines with respect to a control wine.However, they have not studied the application of different dosages to improve the wine aging process.For these reasons, the objective of this work was to study the application of different SIDY dosages (low, medium and high) on a Chilean Sauvignon Blanc white wine in order to evaluate the impact on its polysaccharides, phenolic compounds, volatile compounds and color.

Materialandmethods 1.Winemakingandtreatments
The study was performed with Sauvignon Blanc grapes supplied by the Popeta winery, located in the Maipo Valley (34° 27' 3.35» S and 70° 46' 42.17» W).The alcoholic fermentation was carried out in a 300-hL stainless steel tank.The grape juice was inoculated with 20 g hL -1 of Lalvin QA23 ® Saccharomyces cerevisiae yeast strain (Lallemand-Chile).The initial parameters of the fermented wine were pH 3.62; total acidity 2.94 (g L -1 of sulphuric acid); volatile acidity 0.26 (g L -1 of acetic acid); and alcoholic degree 13.1 (% vol.).Free SO 2 was adjusted to 35 mg L -1 and then 15 L of the wine were transported in 2.5-L food-grade plastic tanks to the Department of Agro-industry and Enology (Faculty of Agronomical Sciences) of the University of Chile to apply the different treatments.The treatments lasted two months and were performed in duplicate: SIDY10 (wines with 10 g hL -1 of SIDY) ; SIDY20 (wines with 20 g hL -1 of SIDY); SIDY40 (wines with 40 g hL -1 of SIDY).Treatments were performed in a refrigerated room at a temperature of 4-6 °C.The addition of the different dosages of SIDY was as follows : the amount to be added to each treatment was weighed and resuspended in 10 times its weight in white wine.When the mixture was homogeneous, it was added to the final volume of white wine used in each treatment (2.5 L).
For a quick and optimized impact, all of the wines were stirred once a week during the first month and once every two weeks during the second.Two months after the treatment period (2MT), the wines were filtered (not clarified) through a cellulose plate filter, bottled and stored underground in a cellar for three months (3BS) at controlled temperature (14-15 °C).SIDY, named PURE-LEES LONGEVITY TM , was supplied by Lallemand-Chile.It is a specific inactivated dry yeast exhibiting a high dissolved oxygen consumption capacity, developed as a natural tool to help keep the wine in optimal conditions during storage in the cellar and aging (Sieczkowski et al., 2016).
The internal standard used for volatile compound determinations, 4-methyl-2-pentanol, was purchased from Merck (Darmstadt, Germany).Sodium chloride was obtained also from Merck.
The polydimethylsiloxane (PDMS) polymeric phase used for the extraction of volatile compounds was supplied from Gerstel (Mülheim and der Ruhr, Germany).The length of the PDMS Twisters was 10 mm and volume (thickness) was 24 mL (0.5 mm).
The polysaccharides were extracted using the methodology described by Ayestarán et al. (2004) and analyzed by HRSEC-RID.HRSEC-RID was performed using an Agilent 1260 Infinity Series liquid chromatograph (Agilent Technologies, Santa Clara, CA, USA) equipped with a G1362A refractive index detector (RID), a G1311B quaternary pump, a G1316A column oven equipped with two Shodex columns, an OHpak SB-803 HQ and a SB-804 HQ (Showa Denko, Tokyo, Japan) connected in series (300 mm × 8 mm i.d.), and a G1329A autosampler.Nine analytical standards of dextrans from Leuconostoc mesenteroides were used for column calibration.One pectin, esterified potassium salt, from citrus fruit was used as external standard for quantification.
Low molecular weight phenolic compounds (LMWPC) were extracted, concentrated and analyzed using the methodology described in Peña-Neira et al. (2007).The samples were injected in an HPLC 1100 Series system (Agilent Technologies, Santa Clara, CA, USA) consisting of a G1315B photodiode array detector (DAD), a G1311A quaternary pump, a G1379A degasser, and a G1329A autosampler.A reverse-phase Nova-Pak C18 column (4 μm, 3.9 mm i.d.× 300 mm; Waters, Milford, MA, USA) was used for HPLC-DAD analysis of LMWPC at 20 °C.Each major peak in the HPLC chromatograms of the extracts was characterized by retention time, the absorption and the spectrum form (from 210 to 360 nm).The calibration curves at 280 nm were produced by injecting the standard solutions before an extraction under the same conditions as the samples analyzed over the range of concentrations observed.
For volatile compound determination, the headspace sorptive extraction (HSSE) method described in Callejón et al. (2008) was used with slight modifications.In all cases, 7.5 mL of the sample were placed in a 20-mL vial and NaCl until saturation plus 10 µL of the internal standard were added.The headspace extraction was performed by placing a new twister in an open glass insert inside the vial and heating the sample in a water bath at 35 °C for one hour.The vial was tightly capped and, after extraction, the stir bar was removed with tweezers, rinsed with Milli-Q water, and dried with a lint-free tissue paper.Then, it was thermally desorbed in a gas chromatograph/mass spectrometer (GC/MS).
Gas chromatography analysis was carried out using a 7890B Agilent GC system coupled to a quadrupole mass spectrometer Agilent 5977 inert (Agilent Technologies, Palo Alto, CA, USA) equipped with a thermo desorption system and a cryo-focusing CIS-4 PTV injector (Gerstel).The thermal desorption was done in splitless mode with a flow rate of 70 mL min -1 .For the desorption, the temperature was held at 35 °C for 0.1 min, ramped at 60 °C min -1 to 210 °C, and then held for 5 min.The temperature of the CIS injector was held at -35 °C using liquid nitrogen for the entire desorption time and was then raised at 10 °C s -1 to 260 °C and held for 4 min.The solvent vent mode was used to transfer the sample to the analytical column.
A DB Wax capillary column with dimensions 60 m × 0.25 mm and 0.25 μm film thickness (J&W Scientific, Folsom, CA, USA) was used, and the carrier gas was helium at a flow rate of 1 mL min -1 .In the oven, the temperature was held at 35 °C for 1 min and then raised to 130 °C at 18 °C min -1 (held for 1 min).Then, the temperature was raised to 190 °C at 1 °C min -1 and subsequently to 220 °C.Electron ionization mass spectra in the full-scan mode were recorded at 70 eV with a scan range from m/z 35 to 300 amu.
Compound identification was based on mass spectra matching using the standard NIST library and the retention index (LRI) of authentic reference standards.The relative area was calculated by dividing the peak area of the target ion of each compound by the peak area of the target ion of the internal standard.

Resultsanddiscussion
Figure 1 shows the chromatographic profiles obtained for the different wines analyzed after the 2MT period.Three different polysaccharidic fractions (F1, F2 and F3) were obtained and classified according to their molecular weight.F1 had an average molecular weight (MW) of 150 kDa, F2 had an average MW of 48 kDa, and F3 had the lowest average molecular weight with MW ≥ 10 kDa.
Table 1 shows the concentrations of the different polysaccharidic fractions and the total content (sum of F1, F2 and F3 fractions) in the different treated wines.The polysaccharidic content of the wine after alcoholic fermentation was as follows : F1 73.4 mg L -1 ; F2 153 mg L -1 ; F3 43.3 mg L -1 ; and total polysaccharide content 269.2 mg L -1 .As expected, after 2MT the polysaccharide content increased as the application dosage increased, and statistically significant differences were found in the different polysaccharidic fractions among the different dosages.Compared to the SIDY10-treated wine, the total polysaccharidic content increased in the SIDY20-and SIDY40-treated wines by 15.6 % and 42.5 %, respectively.Statistically significant differences were found in the F1 fraction between the three treatments applied, thus, the application of a higher dosage of SIDY resulted in a higher concentration of this fraction.Compared to SIDY10, the SIDY20-and SIDY40-treated wines showed an increased F1 fraction content of 26 mg L -1 and .439significant differences found in F2 and F3 fractions were between SIDY10-and SIDY40-treated wines.SIDY40-treated wines showed an increase in F2 and F3 fractions content of 28 mg L -1 and 20 mg L -1 , respectively, compared to the SIDY10-treated wines.As demonstrated in other studies, this increase in polysaccharide concentration is mainly due to the release of mannoproteins from the yeast cell walls during autolysis (Charpentier et al., 2004 ;Del Barrio-Galán et al., 2011) mainly caused by wine acids which can break the yeast cells.The total polysaccharide content decreased after the 3BS analysis.This phenomenon was probably due to the filtration treatment after 2MT that was undertaken to stabilize the wines.This filtration mainly affected the higher molecular weight polysaccharides (F1) because the F2 and F3 fraction contents remained stable during bottle aging.In general, after the 3BS period the differences among the treated wines remained unaltered.Indeed, the SIDY40-treated wines had higher F1 and F3 concentrations.Finally, the SIDY20-and SIDY40-treated wines presented similar F2 fraction contents, which were significantly higher than those of the SIDY10-treated wines.
Table 2 shows the wine TP and LMWPC contents.No significant differences were found in TP after the 2MT period.After the bottle aging period the SIDY20-and SIDY40-treated wines presented higher TP contents than SIDY10 wines.These results are contrary to those obtained by González-Royo et al. (2017) in synthetic and red wines where a reduction in TP was observed when three different SIDY were added.This difference in behavior may be explained by the fact that wine matrixes are different (red vs. white wine) and that different yeast-derived preparations were studied.However, these results are in agreement with those observed by Del Barrio-Galán et al. (2012) in white wines using several yeast derivative products.They explained that a higher dosage of these products could prevent the oxidation and/or precipitation of phenolic compounds.But this fact could be due to the higher oxygen consumption carried out by this specific inactivated yeast, as proved by Sieczkowski et al. (2016).
In terms of LMWPC, the compounds with the highest content after 2MT were, in descending order, tyrosol, catechin, protocatechic acid, epicatechin and gallic acid.The different LMWPC compounds identified and quantified were grouped in hydroxybenzoic acids, hydroxycinnamic acids, hydroxycinnamic acid derivatives, flavanols, stilbenes, phenolic alcohols and flavonols to gain a better understanding of the data obtained.After the 2MT period, only some statistically significant differences were found in hydroxycinnamic acids, hydroxycinnamic acid derivatives and stilbene contents.Therefore, the SIDY40-treated wines presented a lower content of these phenolic groups than the other treatments.As mentioned in several studies, yeast cell polysaccharides can interact with the LMWPC to form polymeric structures which can either remain soluble or precipitate, thus reducing phenolic compound concentration (Razmkhab et al., 2002;Lopez-Toledano et al., 2006;Del Barrio-Galán et al., 2011, 2016).Some authors have recently shown evidence regarding the interaction (sorption) of polyphenols with yeast, inactivated yeast and yeast cell walls (Mekoue Nguela et al., 2015aNguela et al., , 2015b)).After the 3BS period, only SIDY40-treated wines presented a lower hydroxycinnamic acid derivative content.These compounds have been described as easily-oxidizable compounds (Razmkhab et al., 2002;Del Barrio-Galán et al., 2010).A reduction in these compounds can therefore imply a limitation of wine oxidation risk.On the contrary, the SIDY20and SIDY40-treated wines showed higher contents of hydroxycinnamic acids and flavanols.In the case of flavanols, it was observed that the higher the dosage, the lower the decrease in these compounds.Some authors explain that the concentrations of certain phenolic compounds depend on the balance between the oxidation and polymerization reactions that will induce a decrease in their concentration, as well as in the hydrolysis of higher oligomers that will, in turn, increase the presence of these flavanols in wines (Dallas et al., 1995).No significant differences were found in the other phenolic groups.
In this study, some statistically significant differences were found in the color of the white wines as a function of the application dosage (Table 1).After the 2MT period, no differences were found in color intensity (CI) between the different treated wines, but some differences were found in the CIELab parameters.Thus, SIDY20 and SIDY40 had lower a* values than SIDY10, but no differences were found between SIDY20 and SIDY40.As mentioned in the literature (Guzmán-Alfeo, 2010), this a* parameter is the coordinate that measures the color between red and green tones, whose usual values are lower than 1.Thus, the results obtained could indicate that SIDY20 and SIDY40 had more green notes than SIDY10, pointing out that these last wines could be getting oxidized more quickly.These results are well correlated with the lower L* values found in SIDY10 compared to SIDY20 and SIDY40.As was discussed in Guzmán-Alfeo (2010), the L* parameter is the chromatic coordinate that explains the lightness of the wines or their ability to reflect the white color, pointing out that highest values of L* are well correlated with the clarity of the wines.Thus, higher values of this parameter could indicate that wines had lower oxidative or browning notes and these results indicate that applying SIDY at 20 and 40 g hL -1 doses had the same effect.However, as was mentioned by Guzmán-Alfeo (2010), most white wines have L* values close to 100 and for this reason, since all the wines analyzed in this study have values close to 100 it is difficult to draw clear conclusions regarding this L* parameter.No differences were found in the b* coordinate at this period.
On the other hand, after the 3BS period SIDY40treated wines presented lower a* and b* value parameters than the other treatments, indicating that, in this case, the highest applied dosage of SIDY had a better effect than the other dosages for limiting or preventing wine oxidation during bottle storage.Thus, these treated wines presented better results in relation to color preservation, indicating that this specific inactivated yeast could be used as a natural tool to prevent or minimize wine oxidation during aging storage processes.The color results obtained for the SIDY40-treated wines were well-correlated with the lower values observed for some easilyoxidizable LMWPC, such as hydroxycinnamic acid derivatives.However, the content of other phenolic compounds that are also easily oxidizable, namely epicatechin, was higher in the SIDY40-treated wines.As supported by Cheynier and Ricardo da Silva (1991), flavanols are involved in chemical and enzymatic oxidative browning reactions.For these reasons, it is possible that dissolved oxygen comsumption prevented the oxidation of wine as described in the material and methods section.Total color differences (ΔEab*) were also calculated (Table 1) in order to determine whether the differences obtained in wine color using different dosages of SIDY were great enough to be distinguished by the human eye; it is worthy of note that only ΔEab* ≥ 3 are perceptible to the human eye (Martínez et al., 2001).In this study, no differences perceptible to the human eye were observed between the wines treated with the different SIDY dosages after the 2MT and 3BS periods, despite the differences in the spectrophotometric data.
Table 3 shows the volatile compounds identified in this study and the relative area of each compound.The compounds identified were grouped into esters (18), alcohols (7), volatile fatty acids (4), aldehydes (3) and ketones (2), their content depending on SIDY dosage and analysis timing.The ester group was further divided into subgroups, ethyl esters being the most abundant, followed by isoamyl, acetate and methyl esters.The ethyl octanoate was the most important ester compound (between 71.8% and 62.2% of total ester content), giving a sweet, fruity, green-apple aroma.Ethyl decanoate, isoamyl acetate, 2-phenylethyl acetate, and ethyl hexanoate also reached important levels in the wines.Other important compounds detected in the wines were 3-methyl-1-butanol, 1-hexanol, 2-phenylethanol, hexanoic acid and octanoic acid, all of which are common volatile compounds in wines.After the 2MT period the SIDY40-treated wines had a lower content of total esters, alcohols and fatty acids than the SIDY10-and SIDY20-treated wines.This was probably due the polysaccharides having an adsorption or binding effect on these volatile compounds (Comuzzo et al., 2006 ;Bautista et al., 2007).However, when the SIDY dosage is lower, this adsorption effect appears to be more intense in the case of several esters, alcohols and acids after the 3BS period.In the case of the ester group, this effect was mainly observed in ethyl, isoamyl and acetate ester subgroups and it was mainly due to the lower contents of ethyl octanoate, ethyl decanoate, ethyl hexanoate, isoamyl acetate and 2-phenylethyl acetate found.In the case of the alcohol group, we observed a similar trend to that of the esters.In general, lower SIDY dosages gave rise to wines with higher quantities of alcohols.Thus, SIDY20 and SIDY40 presented a lower content of most alcohols than SIDY10, mainly due to the lower 3-methyl-1-butanol and 1-hexanol content found.However, SIDY20 wines had a significantly higher 2-phenylethanol content than SIDY10 and SIDY40 wines.In the case of fatty acids, the SIDY20 wines presented the lowest content of isovaleric and isobutyric acids and the highest octanoic acid content.SIDY40 wines presented the lowest octanoic acid content.Some adsorption of short-and medium-chain fatty acids to SIDY was first described by Lafon-Lafourcade et al. (1984).This may have a positive effect on the sensory quality of wines because some of these compounds are responsible for certain unpleasant odors in wine (Comuzzo et al., 2006).Finally, the same tendency was observed in the aldehyde and ketone group.Therefore, the SIDY20-and SIDY40treated wines presented a lower content of total aldehydes and ketones due to the observed lower content in nonanal, furfural, acetol and acetophenone, respectively.In general, certain aldehydes and ketones are considered to be markers of wine aging because some of them are formed by the oxidation of other volatile compounds present in wine (Escudero et al., 2002) Different letters in a row indicate statistically significant differences (p < 0.05).2MT: after two months of treatment; 3BS: after three months of bottle storage.SIDY10, SIDY20 and SIDY40: wines treated with 10, 20 and 40 g hL -1 of SIDY, respectively.LRI: Linear Retention Index.these compounds could be related to better-quality white wines.ID : reliability of identification : A, mass spectrum and LRI agreed with standards ; B, mass spectrum agreed with mass spectral data base and LRI agreed with the literature data (Tao et al., 2008;Torrens et al., 2010;Gómez García-Carpintero et al., 2012); C, mass spectrum agreed with mass spectral data base.
According to the results obtained after the 2MT period, the wines treated with a higher SIDY dosage presented a lower content of most of the volatile compounds identified.This was probably due to a higher release of polysaccharides from the SIDY which could bind to the volatile compounds and reduce their content and/or volatility in the wines.This binding effect was previously described in white wines by other authors using different yeast-derived preparations and different dosages (Comuzzo et al., 2006;Bautista et al., 2007;Chalier et al., 2007;Del Barrio-Galán et al., 2010).Other authors explained that these products could have a "salting out effect", increasing the content of some volatile compounds related with other variables of wine, such as the type of macromolecules released from the yeast-derived preparations and their concentration, wine pH, alcoholic strength or other factors (Bautista et al., 2007;Comuzzo et al., 2011).This effect could have occurred to 2-phenylethanol in the case of SIDY20treated wines, which presented a significantly higher content than the other treated wines.
In general, the differences between treatments were lower after the 3BS period.No significant differences were found in total esters, except in some subgroups.In the case of total isoamyl esters, the SIDY40treated wines had a lower content compared to the other treated wines, mainly due to their effect on isoamyl acetate and isoamyl decanoate.An opposite effect was found in the total acetate ester content compared to 2MT because SIDY40-treated wines had a higher content than SIDY10-and SIDY20-treated wines, mainly due to the hexyl acetate content which remained stable in SIDY40 wines, while it decreased significantly in SIDY10 and SIDY20 wines.On the other hand, it was observed that SIDY20 and SIDY40 reduced the nerol acetate content, the latter having an important role in the floral, fruity, rose-like aroma perception (Cincotta et al., 2015).In the case of alcohols, SIDY20 and SIDY40 wines had a higher 2-phenylethanol content and a lower 1-hexanol content than SIDY10.No significant differences were found in the total acids content.However, SIDY40 wines had a significantly lower isobutyric and isovaleric acid content compared to the other treated wines.The SIDY40-treated wines had a lower nonanal and decanal content than the rest of the treated wines, reflecting a lower total aldehyde content.An opposite effect in total ketones was found after the 3BS period, observing that SIDY40 wines presented the highest content and SIDY10 the lowest, mainly due to the higher acetol content (t.i.) in SIDY40.This effect could be explained by the possible reversibility of the binding between the commercial products rich in polysaccharides and volatile compounds (Rodríguez-Bencomo et al., 2010).
Principal component analysis (PCA) selected eight principal components (PC) with an eigenvalue greater than 1, explaining 98.4% of the total variance.Figure 2 shows the distribution of the different wines on the plane defined by PC1 and PC2, which -343 -OENO One, 2018, 52, 4, 333-346 ©Université de Bordeaux (Bordeaux, France)

Table4.Principalcomponentanalysisandcomponentweightsofthemostsignificantvariables.
Weight values higher than 0.900 were selected for component 1 and weight values higher than 0.700 were selected for component 2. CI: color intensity.F1 and F2: polysaccharidic fraction 1 and 2, respectively.accounted for 70.1% of the cumulative variance and enabled significant separation of the samples.
Component 1 seems to explain the variance between the two different periods of analysis (2MT and 3BS), while component 2 seems to explain the variance between the different dosages of SIDY applied, mainly between SIDY10 and SIDY40.Table 4 shows the component weights for the variables with an absolute value higher than 0.9 and 0.7 for PC1 and PC2, respectively, which contributes most significantly to the explanatory meaning of the components.As can be seen, most of these PC1associated variables were CI and phenolic and volatile compounds, which allowed the differentiation of the wines between the two points of analysis (2MT and 3BS).In the case of PC2, the variables that contributed most significantly to the differentiation of wines by application dosages were the CIELab parameters and the F2 and F1 polysaccharide fractions.

Conclusions
In this study, an increased SIDY dosage led to an increased release of polysaccharides into the wine, principally those of high and medium molecular weight.This greater release of polysaccharides had a positive effect on the color of the wines because it prevented or reduced their degree of oxidation.This positive effect on color could have been due to the interaction of polysaccharides with certain phenolic compounds that are easily-oxidizable (hydroxycinnamic tartaric esters) and can cause browning of white wines' color.But other easilyoxidizable phenolic compounds (flavanols) did not seem to interact with polysaccharides.For this reason, the positive effect on color was mainly due to the oxygen consumption carried out by the highest dosage of SIDY.
A higher release of polysaccharides during the treatment period appears to be related to the adsorption of certain volatile compounds present in white wines, which could therefore modify their volatility, preventing their loss over time, as well as improving their persistence.However, this adsorption effect seems to be lower after bottle storage, with even the potential to be reversible, as suggested by the increase in the content of certain volatile compounds in wines with higher SIDY dosages.This effect could mean an increase and improvement of the intensity and aromatic persistence of wines over time.
Further studies should be carried out in this field to improve knowledge on how applying different dosages of SIDY affects the physical, chemical and sensory quality of Sauvignon Blanc wines and other white varieties.
Declaration of conflicting interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.