CHANGE OF THE PHYSICO-CHEMICAL INDICES AND THE OXIDATIVE ENZYMATIC ACTIVITIES DURING THE WHITE GRAPES RIPENING

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The Annals of the University Dunarea de Jos of Galati Fascicle VI Food Technology, New Series Year III (XXXIII) Paper presented at the International Symposium Euro - aliment 29, 9 th 1 th of October 29, Galati ROMANIA CHANGE OF THE PHYSICO-CHEMICAL INDICES AND THE OXIDATIVE ENZYMATIC ACTIVITIES DURING THE WHITE GRAPES RIPENING POPESCU CARMEN Elena Doamna Food Industry College Galaţi, 169 Domnească Str., 8189, Galaţi, România, popescucarmen_18@yahoo.com POSTOLACHE ELENA Research and Development Institute in Viticulture and Vinification Bujoru, 65 G-ral E. Grigorescu Str., 852, Galaţi, România, RAPEANU GABRIELA, BULANCEA MIRCEA, HOPULELE TRAIAN Dunărea de Jos University of Galaţi, Faculty of Food Science and Engineering, 111 Domnească Str., 821, Galaţi, România, Received 17 July 29 Revised 18 September 29 The aim of this study was to follow up the evolution of both the physico-chemical indices and the dynamics of the oxidative enzymes during the maturation of white grapes, more particularly until the grapes reach technological maturity. Studying the dynamics of the physico-chemical indices during the maturation of the grapes an increase of the content of glucides, polyphenols, antiocyanins, simultaneously with the decrease of the acidity was noticed. The enzymatic activity of tyrosinase is high at the moment when the grapes are in the beginning of the ripening period and afterwards it presents a decline during the ripening of the grapes, having a relatively low level before harvesting. The enzymatic activity of the laccase increases up till the full maturity of the grapes, then it decreses a little before the harvesting of the fruit, having lower values than at the start of ripening. The enzymatic activity of the peroxidase increases up till the full maturity of the grapes, then it decreses a little before the harvesting of the fruit, having lower values than when it begins to ripen. Keywords: tyrosinase, laccase, peroxidase, mass of 1 grapes berries, sugar, acidity 1. Introduction The activity of the polyphenoloxidase in grapes was studied by many researchers due to its implications in the wine technology. Dubernet and Ribereau-Gayon P., (1973), Dubernet, (1974), highlighted two enzymes: tyrosinase, present in all grapes, and laccase, secreted by Botryotinia fuckeliana, specific to the grapes prone to mould attack. Sapis et al., (1983), diversified the substrate of the action of polyphenoloxidase on the hydroxicynamic esthers. Nakamura et al., (1983), studied some of the properties of these enzymes in Romania, the activity of the oxidative enzymes was studied by Valeria Ioniţă et al., (1994), Valeria Ioniţă, (1996), and Maria Avramescu et al.,(1996), when the dynamics of the enzymes during the grape maturation period as well as during the alcoholic fermentation was quantified. The study of the laccase activity in grapes has concerned many researchers. Cordonnier et al., (1979), studied the relationship between the degree of contamination with mould at harvest, the activity of the laccase and the ability of wine and must oxidative brownness. It was concluded that, besides the laccase, an important part is played by the nature of the substrate and its concentration. Fregoni et al., (1993), showed that the ELISA test offers variable information depending on the variety, the nature and percentage of the contamination, assessed visually on the grapes. The contamination at the lever of grapes berry is done by the presence of the extracellular enzymes secreted by Botryotinia fuckeliana. This enzyme causes the hydrolysis of the cellular membrane and the oxydation of some chemical compounds. The laccase secreted by Botryotinia fuckeliana catalyses

Change of the physico-chemical indices and the oxidative enzymatic activities during the white grapes ripening 71 the biochemical oxydations of the phenols located in the skin of the grapes and which, most often than not, lead to the oxydative brownness of the wine. The oxidative enzymes (polyphenoloyidase and the peroxydase) within the grapes are genetic characters of plants and depend on the climatic and agrotechnical factors (Sapis et al., 1983). 2. Materials and methods 2.1. Materials The research was carried out at the Research and Development Institute in Viticulture and Vinification Valea Călugărească, the Dealu Mare vineyard in 27-28. The varieties of white grapes used for the analysis were: Italian Riesling,,, and. 2.2. Sampling At the beginning of the maturation stage, the grape samples were drawn every 5 days starting with the beginning period of the ripening time specific to each variety, and as the maturation process advanced, the drawing was performed more often, every 3 days, up till the moment of the harvesting. The samples consisted of approximately 2-3 kg of grapes from each variety so as to present the average maturity of the variety. Samples were picked up from different farms of land from the Dealu Mare vineyard, which came from at least 1-2 vines from the lot situated on more than just one row. 2.3. Methods The physico-chemical analysis of the grape samples consisted in dynamics of the grape berries mass, the sugar and acidity evolution for each variety. The resulting grape berries were numbered separating the healthy grape berries from the damaged ones (crushed, mouldy). The average samples were submitted to the following determinations: - the mass of 1 grape berries (g) by picking 3 grapes berries, weighting them with the lab technical scales and ralate them to 1 grapes berries. After weighting, the grapes berries were crushed by using gauze and hand-press. The must was separated and kept in the refrigerator for 2-3 hours for clarification; - the sugar concentration (g/l) was estimated by the refractometric method; - the titrimetric determination of the total acidity (g H 2 SO 4 /L). Enzymatic activities assays. The activity of the tyrosinase and laccase was quantified using the method described by Dubernet et al., (1974). The activity of the peroxidase was assessed by using the method described by Ciopraga et al., (1978). One unit of enzymatic activity (UA) was the increase in optical density at 42 nm for tyrosinase and peroxidase and 52 nm for laccase per minute. At the same time, the polyphenoloxydase index (IPFO) and the browning index (IB) were calculated according to the method described by Leglise et al., (1969), and Mantis, (198), cited by Ioniţă et al., (1996). All the determinations were done twice and the relative standard deviations were lower than ± 1%. 3. Results and discussions At the beginning of the ripening period in the grapes, an accumulation of sugars, polyphenols and antocyanins at the same time with the decrease of the acidity, was observed. The parameters analysed during the year 28 were directly connected with the degree of grapes maturation and the climatic conditions of the vineyard. The dynamics of the physico-chemical indices during the white grapes maturation in the Dealu Mare vineyard 28 are shown in Figures 1, 2 and 3.

72 Popescu C., Postolache E., Rapeanu G., Bulancea M., Hopulele T. The weather conditions in autumn 28 led to a low contamination of grey mould favorable to high quality wines making. During the vegetation period (1.4-3.9.28) the rains fallen in the Dealu Mare vineyard caused the forced ripening of the grapes and full maturity was reached between 3. 8-9. 9. 28. In the Dealu Mare vineyard, the varieties of white wine reached full maturity at different times. The evolution of sugar content, acidity and mass index of 1 grape berries are depicted in figures 1, 2 and 3. For the white grapes Riesling Italian variety (farm 4, lot 3344) full maturity was reached on September 4th 28 with a sugar content of 271 g/l, acidity level of 5. g/l H 2 SO 4, the mass of 1 grape berries was 136 g. The full grape maturity for variety (farm 2, lot 4668) was reached on September 4 th 28 with a sugar content of 175 g/l, acidity level of 4.31 g/l H 2 SO 4, and the mass of 1 grape berries of 9 g. For variety, the full maturity of grapes was reached on September 9 th 28 with a sugar content of 16 g/l, acidity level of 4. g/l H 2 SO 4, the mass of 1 grape berries being of 16 g. The full maturity of white grapes variety was reached on September 9 th 28 with a sugar content of 186 g /l, acidity level of 4.3 g/l H 2 SO 4, the mass of 1 grape berries being of 3 g. For the grapes variety (farm 2, lot 4784) full maturity was reached on August 3 th 28 with a sugar content of 1 g/l, acidity level of 3.43 g/l H 2 SO 4, and the mass of 1 grape berries was 144 g. The grapes harvesting time was the same with the technological maturity which happened during the period September 2th September 3th 28. Table 1 shows values of the sugar, acidity and the mass of 1 grape berries at the technological maturity of grapes. Table 1. Sugar content, acidity and the mass of 1 grape berries at the technological maturity of grapes varieties studied Grapes variety Sugar, g/l Acidity, g/l H 2 SO 4 Mass of 1 grape berries, g Italian Riesling variety (farm 4, lot 3344) 234 3. 95 variety (farm 2, lot 4668) 191 3.5 138 variety (research lot) 182 3. 14 variety (farm 2, lot 4784) 191 2.6 12 Analyzing Figure 1 and 2, the presence of varieties with low sugar content (g/l) and acidity (g/l H 2 SO 4 ) () and varieties with high sugar content and acidity (Italian Riesling) were noticed. Sugar, g/l 2 1 5 8 2 8 8 3 8 4 9 9 9 9 2 9 9 3 9 Figure 1. The dynamics of the sugar content during the maturation of white grapes in Dealu Mare vineyard (28) The mass of 1 grape berries presented an increasing in evolution until the moment when the grapes were fully matured, and between the full maturity and the technological level of maturity of the grapes the mass index of the 1 grapes berries decreased gradually.

Change of the physico-chemical indices and the oxidative enzymatic activities during the white grapes ripening 73 Acidity, g/l H2SO4 9 8 7 6 5 4 3 2 1 8 2 8 8 3 8 4 9 9 9 9 2 9 9 Figure 2. The dynamics of the acidity during the maturation of white grapes in Dealu Mare vineyard (28) The mass of 1 grapes berries had low values in the case of Italian Riesling and high values for (Figure 3). 18 Mass index of 1 berries, g 16 14 12 1 8 6 4 2 8 2 8 8 3 8 4 9 9 9 9 2 9 9 Figure 3. The dynamics of the mass index of 1 grape berries during the maturation of white grapes in Dealu Mare vineyard (28) The dynamics of the tyrosinase activity during the maturation of white grapes The evolution of the tyrosinase activity according to the time to which the determination was made is presented in Figure 4 and it was noticed that they are similar for all the varieties of white grapes studied (with the exception of Italian Riesling). The evolution of tyrosinase activity depends on the climate conditions of the environment during the maturation period of white grapes, especially on the sum of rainfalls in the studied period of time (28), which determined variations in the physiologic development of the grapes. As it can be noticed in Figure 4 at the beginning of the ripening period the variety had the highest tyrosinase activity (4 UA), followed by the variety (37 UA), Fetească regală (35 UA), (3 UA) and (23 UA). The white grapes presented a tyrosinase activity which varied within limits set quite apart depending on the variety. The Italian Riesling variety was remarked during the grapes maturation (September 2 th, 28) as having a maximum activity (64 UA) and the variety with minimum activity (11.4 UA). At full maturity phase the white grapes evolve a tyrosinase activity which varied according to the variety, being remarked the variety with a maximum activity (28 UA), followed by the variety (24 UA), (2 UA), (16 UA) and with a minimum activity (12 UA). At the harvesting moment close values of the tyrosinase activity were found for the white grape varieties studied.

74 Popescu C., Postolache E., Rapeanu G., Bulancea M., Hopulele T. The activity of the tyrosinase is higher by 16.66-58.92% at full maturity than at the harvesting moment. The tyrosinase activity for each variety varies for the entire period of the grapes ripening and differs from one variety to another according to the climate conditions of the vineyard and to the year of the harvest. The tyrosinase activity was high at the beginning of the ripening process, followed by a decline during the full maturity and then the activity increased to a level which did not exceed the initial value but at the end it suddenly dropped, just before the moment of the harvesting (19-23.6 Brix). The exception was observed for the grapes Italian Riesling variety where the tyrosinase activity exceeded initially. 7 6 Tyrosinase activity, OD 42 nm/ min 5 4 3 2 1 8 2 8 8 3 8 4 9 9 9 9 Figure 4. The dynamics of the tyrosinase activity during the maturation of white grapes in Dealu Mare vineyard (28) All these factors, combined with the atmospheric conditions, growth conditions and the pattern of individual development of a specific type of grape, help to explain the variation of the activity of the tyrosinase over time. The differences between the types of grapes were: the highest tyrosinase activity was recorded for the grapes of Italian Riesling and varieties and the lowest tyrosinase activity was quantified for the grapes of variety. Therefore, it is possible to distinguish between the varieties with high tyrosinase activity (Italian Riesling, ) and varieties with low tyrosinase activity (). The activity of the tyrosinase is higher at full maturity than at the harvesting period, with 38% for the Italian Riesling, 52.5% the Fetescă regală, 16.66% the, 58.92% the and.% the. The dynamics of the laccase activity during the maturation of the white grapes The laccase activity depends on the contamination degree of the harvest with the Botryotinia fuckeliana grapes. The climate conditions of the year 28 favored a contamination of the grapes with 1% of grey mould. From the experimental data (Figure 5) the profiles of the laccase activity evolution in the white grapes was noticed to be relatively similar. At the beginning of the ripening period, the grapes with the highest laccase activity (42 UA) were from the variety, followed by (4 OD 52 nm/min), the (36 UA), the Italian Riesling (31 UA) and the with the lowest laccase activity (27 UA). At full maturity the grape variety displayed the highest laccase activity (9 UA), followed by the grapes (77 UA), the Italian Riesling grapes (7 UA), the grapes (43 UA) and the grape variety with the lowest laccase activity (41 UA). The values of laccase activity were determined at the moment of the white grapes harvesting and it presented the following levels: the grape variety with the highest laccase activity (2 UA), followed by the grapes (19 UA), the grapes (16 UA), the Fetească regală grapes ( UA) and the Italian Riesling grapes with the lowest laccase activity (13 UA). 2 9 9 3 9

Change of the physico-chemical indices and the oxidative enzymatic activities during the white grapes ripening 75 Laccase activity, OD 52 nm/ min 1 9 8 7 6 5 4 3 2 1 8 2 8 8 3 8 4 9 9 9 9 Figure 5. The dynamics of the laccase activity during the maturation of white grapes in Dealu Mare vineyard (28) 2 9 9 3 9 The activity of the laccase is higher at full maturity than during the harvesting period by 81.42% for the Italian Riesling grape variety, 63.41% variety, 62.79% variety, 74.2% variety and 78.88 % variety. Figures 4 and 5 show the activity of the laccase as being higher than the tyrosinase activity. This demonstrates that Botryotinia fuckeliana leads both to the secretion of laccase and also to the increase of the tyrosinase activity. The dynamics of the peroxydase activity during the white grapes maturation The dynamics of the peroxydase activity during the white grape ripening (Figure 6) within the studied period was similar for all varieties of white grapes studied. Starting on August th 28 the activity of the peroxydase recorded increases up until the beginning of September after when a drop in the activity of the peroxydase was noted. Peroxidase activity, OD 42 nm/min 1 9 8 7 6 5 4 3 2 1 8 2 8 8 3 8 4 9 9 9 Figure 6. The dynamics of the peroxydase activity during the maturation of white grapes in Dealu Mare vineyard (28) 9 2 9 9 3 9 Although the profiles of the enzyme activity evolution are approximately the same, the values of the peroxydase activity for the varieties of white wine differ. This can be explained by means of the climate conditions of the Dealu Mare vineyard, which caused variations on the physiological grapes evolution, but also by the different nature of the soil. During the studied period the peroxydase activity was determined at the full maturity as being different from one variety to another. In case of the white grapes there were noticed: the Muscat Ottonel grapes variety with the highest value for the peroxydase activity (9. UA), followed by the

76 Popescu C., Postolache E., Rapeanu G., Bulancea M., Hopulele T. grapes variety (8.5 UA), the (8. UA) with average activity, the Fetească regală grapes variety (5.4 UA) and the Italian Riesling grapes variety with the lowest peroxydase activity (5.2 UA). At the harvesting moment the following varieties were analyzed: the Italian Riesling with the lowest peroxydase activity (5. UA), the with an average value (5.5 UA) and the with the highest value (7. UA). The peroxydase activity is higher at full maturity than at the harvesting time with 3.84% for the Italian Riesling, 3.7% for the, 17.64% for the,.% for the and 33.88% for the. 4. Conclusions During the ripening period the evolution of phisico-chemical parameters was almost the same for all varieties of grapes studied. The sugar content increased, the acidity decreased and the mass of 1 grape berries presented an increasing till the moment when the grapes were at fully maturity, and between the full maturity and the technological level of maturity of the grapes the mass index of the 1 grape berries decreased gradually. The evolution of the oxidative enzymatic activities during the grape maturation varies depending on the variety of grapes, the harvest year and the climate conditions of the vineyard. The activity of the laccase is higher than the tyrosinase activity. This proves that Botryotinia fuckeliana leads both to the secretion of laccase and also to an increased activity of the tyrosinase. The peroxidase activity of the grapes during the maturation period is different for the varieties analysed in the present study, depending on the climate conditions of the harvest year and the physiologic state at the moment of the determination. References Avramescu, M., Varga, M. and Avramescu, A.1996. Cercetări asupra activităţii peroxidazei din struguri în centrul viticol Valea Călugărească, Analele ICVV. Valea Călugărească, vol. XV, 385-394. Ciopraga,J. şi colab.,1978. New method for the determination of peroxidase activity, Rev. Roumaine de Biochimie, (4), 9-283. Cordonnier, R., Hurtrel, J., and Binor, C. 1979. Relation entre le taux de pourriture de la vendange l'aptitude a la casse oxydasique des mouts et des vins. Groupe polyphenols, 214-219. Dubernet, M. and Ribereau- Gayon, P.1973. Présence et signification dans les mouts et dans les vins de la tyrosinase du raisin, Conn. Vigne Vin, 7, 283-32. Dubernet, M. 1974. Thèse Doctorat 3 cycle, Bordeaux. Fregoni, M., Perino, A. and Verces, A.1993. Évolution de l'infection par Botrytis cinerea des raisines et des mouts grace au test immunologique Elisa, Bull. O.I.V., 66, 169-19. Ioniţă,V.1996. Studiul activităţii lacazei din struguri atacaţi de Botrytis cinerea şi aptitudinea de casare oxidazică a mustului şi vinului, în tehnologia de producere a vinurilor albe, Analele I.C.V.V., vol. XV, 47-417. Ioniţă, V., Dumitru, P., Tudorache, A.1994. Influenţa operaţiilor de prelucrare a mustului asupra activităţii polifenoloxidazei şi a compoziţiei vinurilor albe, Analele I.C.V.V.,vol. XIV, 385-396. Nakamura, K., Amano, Y. and Kagami, M.,1983. Purification and some properties of a polyphenoloxidase from Koshu grapes, Amer. J. Enol. Vit., 34, 122-127. Sapis, J.C., Macheix, J.J. and Cordonnier, R.E. 1983. The browning capacity of grapes. I. Changes in polyphenoloxidase activities during development and maturation of the fruit, Journal of Agriculture and Food Chemistry, 31,342-345.