Degradation Kinetics of Anthocyanin of Traditional and Low-Sugar Blackberry Jam

The objective of this study was to monitor the stability of anthocyanin and phenolic compounds contained in two formulations of blackberry jam (traditional and low-sugar) during storage. For that purpose, jams were prepared with varying amounts of hydrocolloids and investigated as to pH, total soluble solids, water activity, total acidity, total anthocyanins and total polyphenols. In order to accompany and assess the levels of phenolic compounds and colour (L*, a* and b*) changes, the samples were stored for 180 days at two different temperatures (10 and 25 °C). The Arrhenius model was used to determine the relationship between the reaction rate (k) at the different storage temperatures, yielding activation energy values of 19 and 12 kcal/mol and Q ₁₀ values of 3.0 and 2.0 for traditional and low-sugar jams, respectively. The results show that by the end of the storage time investigated, the anthocyanin compounds had been partially degraded, with the greatest loss being observed in traditional jam stored at 25 °C. Colour stability was also lower in traditional jam as compared to the low-sugar product.     

Storage Changes in Anthocyanin Content of Red Raspberry Juice Concentrate

Anthocyanins from red raspberry juice concentrates were extracted with acidified ethanol and methanol and separated by high performance liquid chromatography. Six anthocyanin peaks were identified as cyanidin-3-sophoroside (cy-3-sop), cyanidin-3-glucorutinoside (cy-3-glru), cyanidin-3-glucoside (cy-3-gl), cyanidin-3-rutinoside (cy-3-ru), pelargonidin-3-sophoroside (pg-3-sop), and pelargonidin-3-glu-corutinoside (pg-3-glru). Relative proportions of individual anthocyanins were determined by comparing peak areas. The proportions of cy-3-sop, cy-3-glru and cy-3-gl in particular changed greatly on storage for 3 mo at + 20°C. Minor changes occurred when the raspberry juice concentrate was stored at ?20°C.     

Effect of packaging materials and storage temperature on the quality of sour cherry nectar

The purpose of this research was to determine the effects of the packaging materials and size on the stability of monomeric anthocyanins, polyphenols, antioxidant activity, ascorbic acid, colour index and hydroxyl methyl furfural (HMF) during the 12‐month shelf life of sour cherry nectars at 4 °C and 20 °C. Sour cherry nectars were aseptically filled out into packaging of different sizes and materials. The packaging included cartons of two different sizes (200 and 1000 mL) and aluminium cans (330 mL). Results showed that the nectars were of better quality when stored at lower temperatures. HMF generally increased significantly for all nectars during storage. Conversely, the total polyphenol content and the antioxidant activity of the nectars stored in aluminium cans and the larger‐sized carton packaging decreased during storage. Lower anthocyanin loss and colour change were found in the nectars stored in aluminium cans. However, the better packaging material was found to be the large‐sized carton package when HMF was analysed.     

Changes in anthocyanin,flavonoid and phenolic acid concentrations during development and storage of coloured potato (Solanum tuberosum L) tubers

Changes in the anthocyanin concentration of coloured potato tubers have been investigated in cultivars with coloured skin and coloured or white flesh. The biosynthesis of anthocyanins coincided with tuber initiation in cultivars with intensely coloured mature tubers and, after a slight increase as the smaller tubers increased in size, anthocyanin concentrations remained relatively constant. Thus, because tubers were increasing in weight, anthocyanin was being synthesised to maintain a more or less constant concentration. In cultivars with less coloured tubers, the developing tubers remained white for a longer time, with anthocyanin concentrations increasing gradually up to a maximum at a certain tuber weight depending on the cultivar. The concentration of flavonoids was lower than that of anthocyanins but followed a similar pattern. Phenolic acid levels were about twice those of the anthocyanins and reached their maximum at a slightly lower tuber weight than anthocyanins and flavonoids. During cold storage (4°C) the anthocyanin concentration in coloured tubers increased, whereas tubers stored at higher temperatures did not show this increase. The increased colour in cold‐stored tubers is discussed in terms of its relationship to ‘cold sweetening’ and the increased concentration of sugars in cold‐stored tubers. The distribution of anthocyanins altered during tuber development and also during cold storage. In very small developing tubers the anthocyanins appeared first at the stem end of the tuber whilst the bud end remained white. As the anthocyanin concentration increased during tuber development, it increased over the whole tuber, but the concentration at the stem end was always higher than that at the bud end, until the tuber reached maturity, when the concentration became approximately equal at both ends. After cold storage, tubers had a higher concentration of anthocyanin in the bud end than the stem end; the opposite to that found in developing tubers. © 1999 Society of Chemical Industry     

Anthocyanin stability studies in Tibouchina semidecandra L.

The effects of pH, storage period, temperature, light and dark conditions on the stability of anthocyanins extracted from Tibouchina semidecandra flowers of different developmental stages was evaluated. Fully formed but unopened flower bud had the highest amount of total anthocyanin extracted from fresh petals. The anthocyanin contents for all flower developmental stages were stable at pH 0.5–3.0 but the colour of the extracts faded at higher pH values. Degradation percentages of total anthocyanins in the extracts kept at 25 °C were 7–20% lower than that maintained at 31 °C. Extracts stored in darkness at 25 °C maintained their purple colour for 26 days while light exposure reduced it to an average of 10 days. The study shows that suitable storage condition for coloured anthocyanin pigments in extracted form is in acidic conditions in the dark. This implies the potential usage of coloured anthocyanins as natural food colourants and shelf life indicator for acidic foods.     

Process and storage stability of anthocyanins and non-anthocyanin phenolics in pectin and gelatin gels enriched with grape pomace extracts

Gelatin and pectin gels were supplemented with anthocyanin extracts obtained from grape pomace and stored either under neon light (20 ± 2 °C) or in the dark (20 ± 2 and 6 ± 2 °C, respectively) for a period of up to 24 weeks. During storage, antioxidant activities of the samples (FRAP and TEAC assays), total phenolic contents (Folin–Ciocalteu assay) and the amounts of monomeric and polymeric anthocyanins and of non-anthocyanin phenolics were monitored spectrophotometrically and by HPLC, respectively. Processing of the gels had the most significant effect on the total phenolic contents in all samples, resulting in total losses up to 24.6%. Light considerably decreased the phenolic compounds during storage, whereas the effect of temperature on their stability was less pronounced. Total phenolic contents of illuminated samples decreased from 243.6 to 82.6 mg/kg in the gelatin gels within 24 weeks of storage and from 279.8 to 139.5 mg/kg (pectin gel, 16 weeks of storage). In contrast, antioxidant activity of the samples was only slightly reduced or remained virtually unchanged. Thus, the model gels still exhibited brilliant colors and strong antioxidant capacity even after storage of 24 weeks at ambient temperature.     

Effect of Processing and Storage on The Antioxidant Activity of Frozen and Pasteurized Shadblow Serviceberry (Amelanchier canadensis)

Serviceberry fruits were pasteurised in glass jars at two temperatures, 85 and 100°C, while another batch was packed in polyethylene bags and frozen at a temperature of ?20 ± °C. Processed fruits were stored for 10 months: frozen fruit at ?20 ± 1°C; and pasteurised fruit at room temperature without access to light. Refrigerated storage and pasteurization lowered the DPPH antioxidant activity of serviceberry fruit. In the former, the change was not great, whilst pasteurisation caused an approximately twofold increase in EC50. On the basis of total anthocyanin content and total polyphenolic content measurements, it would appear that the antioxidant properties of serviceberry were affected mainly by anthocyanins. Pasteurising at 100°C allowed slightly better preservation of these compounds during long-term storage.     

Improving the keeping quality of pomegranate fruit by intermittent warming

 Mollar pomegranates (Punica granatum, Punicaceae) were stored at 0  °C or 5  °C and 95% relative humidity (RH) for 80 days. Intermittent warming (IW) cycles of 1 day at 20  °C every 6 days, during which time the fruit had been stored at 0  °C or 5  °C, followed by a shelf-life period of 7 days at 15  °C and 70% RH were applied. IW during storage at 0  °C was the best treatment for maintaining the red skin colour as at harvest. However the red colour of the arils (hue angle) was kept better under warming at 5  °C. Although significant changes in the individual anthocyanins were observed in all treatments, particularly after the shelf-life period, the total anthocyanin content of the juice at harvest was maintained. While storage at 0  °C avoided decay although increased the risk of chilling injuries such us pitting and husk scald, 5  °C-storage reduced these injuries but fungal attacks were not inhibited. After the shelf-life period, IW alleviated chilling injuries without any incidence of decay. Warming treatments gave very good results with respect to storage and the keeping quality of pomegranates, particularly when applied during storage at 0  °C. Received: 10 February 1998 / Revised version: 24 April 1998     

Cis-trans isomerisation of lycopene and colour stability of foam—mat dried tomato powder during storage

Tomato powder with ～3% moisture was obtained by foam-mat drying tomato paste (29% solids). Samples of powder were stored at various temperatures (?10° +2° +20° and +37°c), atmospheres (air, nitrogen) and humidities (with and without in-package desiccation), and colour changes were observed for periods of up to 1 year. The main cause of colour fading was the oxidation of lycopene. However, another phenomenon, trans—cis isomerisation of all-trans lycopene, can occur, with apparent loss of coloration, which is later restored by re-isomerisation. The existence of this mechanism was demonstrated by simultaneous measurements of total liposoluble colour at 420 nm and separations of carotenoid pigments by column chromatography on Al₂O₃. Neo-lycopene A (6-mono-cis-lycopene) and at least one other cis-lycopene isomer were found in fresh powder and in samples stored up to 5 months. cis-Isomers were more susceptible to oxidation. Colour changes depend upon the interplay of isomerisation and oxidation; in some cases, tomato powder was more intensively coloured after storage than when fresh. Storage at +20°c was more favourable for colour retention than storage at +2°c, or — 10°c. Excessive desiccation strongly promoted oxidation losses. Storage in an inert atmosphere improved colour retention. At +37°c non-enzymic browning, accompanied by formation of water, caused rapid darkening although carotenoid pigments were not lost to a great extent.     

Effect of Storage Conditions on Various Parameters of Colour and the Anthocyanin Profile of Rosé Wines

Colour compounds of rosé wines can be very sensitive to storage conditions because of the low levels of naturally-occurring protective compounds. This article deals with the effects of storing rosé wines under different temperature and light conditions, with regard to their colour characteristics and anthocyanin profile. Samples were taken seven times altogether over a period of 582 days. At the end of the storage period, the resulting differences in the wines were studied by μLC/MS. It was found that storing rosé wine at room temperature caused a reduction of 50% in the levels of anthocyanins compared to storing them at 3°C. Increasing the storage temperature to 45°C caused the total decomposition of all anthocyanins. Furthermore, during the maturation of the wine, a loss of sugar moiety, hydration of aglycone, and the formation of the corresponding chalcone or diketone were observed. Levels of pyranoanthocyanins in the wines were studied as well. Vitisins A and B, hydroxyphenyl-pyranomalvidin-3-glucoside, dihydroxyphenyl-pyranomalvidin-3-glucoside, and methoxyhydroxyphenyl-pyranomalvidin-3-glucoside were identified. The highest levels of both chalcones and pyranoanthocyanins were found in samples stored at room temperature. The effect of irradiation on the pigments also appeared to be significant but less important than the effect of high temperature.     

Chemical and microbial stability of high moisture dried apricots during storage

BACKGROUND: This study was conducted to determine the chemical and microbial stability of high moisture (HM) dried apricots during storage at 5, 20 and 30 °C for a period of 8 months. HM dried apricots were obtained by rehydrating dried apricots in ‘water’ and ‘water + H₂O₂’. RESULTS: Analysis of kinetic data suggested first‐order models for loss of SO₂ and non‐enzymatic browning reactions. Higher storage temperatures increased the rate of SO₂ loss and formation of brown colour in HM dried apricots. Results from extensive colour measurements (non‐enzymatic browning, reflectance colour and β‐carotene) revealed that the colour of HM dried apricots stored at 5 °C was almost unchanged during 8 months of storage. The colour of samples stored at 30 °C was unacceptable starting from 2 months of storage. Total mesophilic aerobic bacteria counts decreased 0.7, 1.1 and 1.5 log cycles after 8 months of storage at 5, 20 and 30 °C, respectively. For the same storage period, the decrease in mesophilic bacteria was 0.62 log cycle in samples rehydrated in ‘water + H₂O₂’ and stored at 20 °C. CONCLUSION: These results suggest that HM dried apricots should be stored at temperatures lower than 20 °C to preserve the characteristic golden yellow colour. A relatively low level of SO₂ (1458 mg kg^?1 at 200 g kg^?1 moisture level) was sufficient to prevent the growth of spoilage organisms in HM dried apricots at all three storage temperatures. Copyright © 2008 Society of Chemical Industry     

Degradation kinetics of pigment,colour and stability of the antioxidant capacity in juice model systems from six anthocyanin sources

Coloured model juices with extracts from several species of commonly consumed vegetables rich in anthocyanins (eggplant peel, strawberry, grape, bilberry, red raspberry and plum peel) were studied in detail. The model juices prepared at pH 4.5 were stored in darkness for 17 weeks at 20 °C. The kinetics of anthocyanin degradation, colour and stability of the antioxidant capacity were measured during storage. The anthocyanins were determined identifying delphinidins, cyanidins, petunidins, pelargonidins, peonidins and malvidins. The extraction yields ranged from 2.3% to 13.3%. The level of anthocyanins in the model juices prepared with the extracts ranged between 4 and 158 mg L^–1. The results showed a good correlation between the anthocyanin concentration and the time of storage, with determination coefficients varying from R² = 0.9470 to R² = 0.9855. The eggplant peel, grape and plum peel anthocyanins showed the highest half‐life and D values that were higher than those of 12 and 17 weeks, respectively. The antioxidant capacity showed a high stability during the time of storage for all the model juices, showing the eggplant peel model juice the highest values.     

Stability of anthocyanins in frozen and freeze-dried raspberries during long-term storage: in relation to glass transition

Abstract: Anthocyanins, natural plant pigments in the flavonoid group, are responsible for the red color and some of the nutraceutical benefits of raspberries. This study explores anthocyanin degradation in frozen and freeze‐dried raspberries during storage in relation to glass transition temperatures. Frozen raspberries were stored at ?80, ?35, and ?20 °C, while freeze‐dried raspberries were stored at selected water activity (a_w) values ranging from 0.05 to 0.75 at room temperature (23 °C) for more than a year. The characteristic glass transition temperatures (T′_g) of raspberries with high water content and glass transition temperature (T_g) of raspberries with small water content were determined using a differential scanning calorimeter. The pH differential method was used to determine the quantity of anthocyanins in frozen and freeze‐dried raspberries at selected time intervals. The total anthocyanins in raspberries fluctuated during 378 d of storage at ?20 and ?35, and ?80 °C. Anthocyanin degradation in freeze‐dried raspberries ranged from 27% to 32% and 78% to 89% at a_w values of 0.05 to 0.07 and 0.11 to 0.43, respectively, after 1 y. Anthocyanins were not detectable in freeze‐dried raspberries stored at a_w values of 0.53 to 0.75 after 270 d. First order and Weibull equations were used to fit the anthocyanin degradation in freeze‐dried raspberries. The 1^st‐order rate constant (k) of anthocyanin degradation ranged from 0.003 to 0.023 days^?1 at the selected water activities. Significant anthocyanin degradation occurred in both the glassy and rubbery states of freeze‐dried raspberries during long‐term storage. However, the rate of anthocyanin degradation in freeze‐dried raspberries stored in the glassy state was significantly smaller than the rate of anthocyanin degradation in the rubbery state.     

Effect of Storage on Anthocyanin Degradation in Black Mulberry Juice and Concentrates

Anthocyanins present in fruits and vegetables are receiving increased attention because of their potential antioxidant activity but are very susceptible to degradation during processing and storage. Effect of storage on kinetics of anthocyanin degradation and hydroxymethylfurfural (HMF) formation in black mulberry juice and concentrate was determined during 8 months of storage at temperatures of 5°, 20°, 30°, and 40 °C. The monomeric anthocyanin degradation was in accordance with the first-order reaction kinetics and the activation energies of anthocyanin degradation in black mulberry juice and concentrate were found as 56.48 and 49.75 kJ mol^?1, respectively. HMF formation in black mulberry juice and concentrate increased linearly with storage time and temperature and followed zero-order reactions. The activation energies of HMF formation in black mulberry juice and concentrate were found as 75.70 and 104.11 kJ mol^?1, respectively. The losses of antioxidant activity for black mulberry juice and concentrate during storage at different temperatures were in the ranges of 4.87–16.01 and 4.47–33.57 %, respectively. Antioxidant activity in black mulberry juice and concentrate was correlated with total monomeric anthocyanins.     

Minimal Processing and Modified Atmosphere Packaging Effects on Pigmentation of Pomegranate Seeds

The influence of different washings, temperatures, and packagings on anthocyanins of minimally processed pomegranate seeds was evaluated. No differences were found in anthocyanin composition after washing with different solutions, although a slight decrease in pigments occurred. Storage in perforated polypropylene bags preserved pigments and a slight increase in most anthocyanins occurred. During storage in modified atmospheres, anthocyanins increased at 1°C, but decreased at 8 and 4°C. The delphinidin derivatives were the most sensitive while cyanidin and pelargonidin derivatives were stable and increased slightly. The 3,5-diglucosides were more stable than 3-glucosides. Compared with storage at 1°C for 7 days in perforated OPP bags, unperforated OPP bags maintained the pigments better. However, stored an additional 4 days at 4°C to simulate domestic storage, they were better preserved in perforated films.     

Effect of high hydrostatic pressure and thermal processing on the nutritional quality and enzyme activity of fruit smoothies

Fruit smoothie samples were thermally (P₇₀ > 10 min) or high hydrostatic pressure (HHP) processed (450 MPa/20 °C/5 min or 600 MPa/20 °C/10 min) and the total antioxidant capacity (TAC), levels of antioxidant groups [total phenols (TP), anthocyanins and ascorbic acid], instrumental colour, polyphenol oxidase (PPO) enzyme activity and dissolved oxygen were examined over a storage period of 10 h at 4 °C. Thermal processing of smoothies reduced (p < 0.001) TAC and TP values, ascorbic acid and L and a colour attributes (lightness and redness respectively) compared to fresh and HHP-450 processed samples. Conversely, it did result in complete inactivation of PPO enzyme, with no activity detected. Of the HHP treatments, HHP-450 samples had higher (p < 0.001) levels of total antioxidant, phenols and anthocyanin content than HHP-600 samples. However, the latter was more effective in reducing (p < 0.001) the endogenous enzyme activity of the smoothies. .Ascorbic acid content degraded over the storage for all smoothies. HHP-600 samples had high initial values, which declined slowly over storage, while thermal samples had the lowest initial value (0.5 h) that fell below detectable limits by 10 h. Despite these data, less pronounced effects were observed for storage. No significant effects were observed for total anthocyanin and phenolic contents as well as L and colour change (ΔE) variables. Overall, HHP processing of smoothies at moderate temperatures may be a suitable alternative to traditional thermal processing.     

Effects of Juice Matrix and Pasteurization on Stability of Black Currant Anthocyanins during Storage

The effects of juice matrix and pasteurization on the stability of total phenols and especially total and individual anthocyanins were examined in black currant (BC) juice and mixtures with apple, persimmon, and peach juices at 4 °C and 20 °C. Total phenol content decreased in all juices at both temperatures but there was a trend to lower levels in unpasteurized over pasteurized juices. Differences in the decline of total anthocyanins between pasteurized and unpasteurized juices varied according to the juice type and the storage temperature. At 4 °C storage, anthocyanins declined in all juices according to pseudo 1st‐order kinetics and there were only small differences in the rates between pasteurized and unpasteurized juices. However, at 20 °C, although pasteurized and unpasteurized BC juices and pasteurized mixed juices followed pseudo 1st‐order kinetics, there was a different pattern in unpasteurized mixed juices; a rapid initial decline was followed by a slowing down. The effect of the added juice on anthocyanin decline was also different at either temperature. At 4 °C, the anthocyanins decreased faster in mixed juices than BC juice alone, but at 20 °C, at least in pasteurized mixed juices, the decline was similar or even slower than in BC juice; there were only small differences among the 3 mixed juices. At 20 °C, in pasteurized and unpasteurized BC juices, the rate of decrease was essentially the same for all 4 individual anthocyanins but in the mixed juices the 2 glucosides decreased significantly faster than the 2 rutinosides.     

Impact of enzymatic mash maceration and storage on anthocyanin and color retention of pasteurized strawberry purées

Strawberry purées were prepared using a commercial polygalacturonase (PG) and a highly purified pectinesterase (PE) preparation, respectively. To elucidate the effect of pectin on color stability following enzymatic pulp maceration, pectin composition was studied by isolating and fractionating the alcohol-insoluble residue from the strawberry purées. The purées were stored at +20 and +4 °C in the dark over a period of 24 weeks monitoring the amounts of monomeric and polymeric anthocyanins as well as antioxidant activities (FRAP, TEAC). Individual anthocyanins were analyzed by HPLC–DAD–MS ⁿ , and color measurements were obtained in the CIE L*a*b* system. Pectin composition was significantly modified following enzymatic maceration of the purées. While PG treatment generally resulted in pectin losses, oxalate-soluble pectins were increased in PE-treated purées. After 24 weeks of storage, the best anthocyanin retention was observed in PE-treated purées. Such products also revealed greatest anthocyanin half-life values and lowest proportion of polymeric pigments. Compared to an untreated control, enzymatic purée maceration using the PG was also beneficial for pigment retention, but less effective than PE. In contrast, color and antioxidant activity were independent of both enzymatic treatments. An initial heating step (90 °C, 10 s) for immediate inactivation of native enzymes such as polyphenoloxidases slightly improved pigment stability, while lowered temperature during mash maceration was less effective. However, by far best color and pigment retention were achieved when the purées were stored at 4 °C in the dark.     

Changes in anthocyanins in arils of chitosan-coated pomegranate (Punica granatum L. cv. Rabbab-e-Neyriz) fruit during cold storage

Edible coatings as chitosan treatments (0%, 1% and 2%) were applied to ‘Rabbab-e-Neyriz’ pomegranate (Punica granatum L.). The effect of chitosan coating on individual anthocyanins and colour parameters of the juice during storage at 2 °C or 5 °C was examined. Six predominant anthocyanins were identified in the juice, with up to 935 mg/L total anthocyanins at the time of harvest. Cyanidin 3,5-diglucoside (402 mg/L) was the major pigment. The total anthocyanin content and chroma decreased with storage time in all applied treatments, although lightness and hue angle increased. These changes were reduced with chitosan treatments and at lower storage temperature (2 °C as compared to 5 °C). Based on the obtained results, the diglucoside anthocyanins were more stable than the monoglucosides. Chitosan coating followed by cold storage delayed anthocyanin degradation and prevented colour deterioration in the pomegranate arils.