Stability of black carrot anthocyanins in various fruit juices and nectars

Fruit juices (apple, grape, orange, grapefruit, tangerine and lemon) and nectars (apricot, peach and pineapple) were coloured with black carrot juice concentrate and stability of black carrot anthocyanins in these matrices was studied during heating at 70–90 °C and storage at 4–37 °C. Anthocyanin degradation, in all coloured juices and nectars, followed first-order reaction kinetics. During heating, black carrot anthocyanins in apple and grape juices showed higher stability than those in citrus juices at 70 and 80 °C. High stability was also obtained for the anthocyanins in peach and apricot nectars at these temperatures. Black carrot anthocyanins were the least stable in orange juice during both heating and storage. During storage, degradation of anthocyanins was very fast at 37 °C, especially in pineapple nectar. Refrigerated storage (4 °C) markedly increased the stability in all samples. Activation energies for the degradation of black carrot anthocyanins in coloured juices and nectars ranged from 42.1 to 75.8 kJ mol⁻¹ at 70–90 °C and 65.9–94.7 kJ mol⁻¹ at 4–37 °C.     

Effects of light,temperature and water activity on the kinetics of lipoxidation in almond-based products

Lipoxidation in almond-derived products was investigated using the chemiluminescence (CL) and thiobarbituric acid-reactive substances (TBARS) methods to detect the first and later reaction products, respectively. The effects of light during storage at 5 °C, 22 °C and 40 °C were studied, as well as the effects of combined heat/water activity treatments in the 60–120 °C and 0.38–0.72 range. During storage, light was found to enhance the CL and TBARS values, and specific responses were observed in almond paste and the final Calisson product. During the heating of almond paste, as the initial water activity (a_w) increased, the CL rate constants increased during heating to 60 °C and 80 °C, but interestingly, these values decreased during further heating to 120 °C, whereas the maximum TBARS rate constants occurred at a_w 0.57 at all the heating temperatures tested. The activation energies, based on the CL and TBARS values, decreased specifically when the a_w increased from 0.38 to 0.72, giving overall values ranging from110 kJ mol⁻¹ to 60 kJ mol⁻¹. Likewise, in the same water activity range, the temperature-dependent rate constant enhancing factor (Q₁₀) decreased from 3.3 to 1.6.     

The effect of pre-treatment on the anthocyanin and flavonol content of black currant juice (Ribes nigrum L.) in concentration by reverse osmosis

Reverse osmosis process for the concentration of black currant juice was carried using AFC-99 tubular membrane at 30 °C and 45 bar. The contents of selected flavonols and anthocyanins were analyzed after centrifugation; enzyme treatment by Panzym Super E and by Rohapect berry followed by centrifugation; and ultrafiltration black currant juices and juice concentrates. The total soluble solid (TSS) content of the juices increased from the initial 17.6–17.9 °Brix to 24–24.8 °Brix in the case of the centrifuged juice in the concentration process. Similarly, it increased from 14.5–15.5 °Brix to 23.1–23.4 °Brix for the Panzym Super E treated juice, and from 16.1–16.9 °Brix to 22.5–23.1 °Brix for the Rohapect berry treated black currant juices. The ultrafiltered juice had the lowest initial TSS content between 14.1 and 14.9 °Brix and it increased to 22.1–23.1 °Brix. The average permeate fluxes during the concentration process were 7.3 L m⁻² h⁻¹ for the centrifuged juice, 11.9 L m⁻² h⁻¹ for the Panzym Super E treated juice, 9.2 and 13.1 L m⁻² h⁻¹ for the Rohapect berry treated and ultrafiltered juice, respectively. Analysis indicated that the enzymatic treatment resulted in the increase of anthocyanin and flavonol content of the juices. The centrifugation process decreased the amount of anthocyanins and flavonols to some extent. The juice clarified by ultrafiltration had significantly lower concentrations of anthocyanins and flavonols, while the juices treated by Panzym Super E had the highest levels of these flavonoids. This study recommends enzymatic pre-treatment by Panzym Super E, since it improves the permeate flux in reverse osmosis during the concentration process, and results in a juice concentrates highest in anthocyanins and flavonols.     

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.     

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.     

Chemical stability of açai fruit (Euterpe oleracea Mart.) anthocyanins as influenced by naturally occurring and externally added polyphenolic cofactors in model systems

The influence of different classes of naturally occurring and externally added polyphenolic cofactors on the phytochemical and colour stability of anthocyanins in açai fruit (Euterpe oleracea) was investigated. Model systems were based on anthocyanin isolates from açai fruit, rich in cyanidin-3-rutinoside (311 ± 27 mg/l) and cyanidin-3-glucoside (208 ± 18 mg/l), and isolated groups of naturally occurring polyphenolic cofactors in açai fruit (phenolic acids, procyanidins, and flavone-C-glycosides, each adjusted to ∼50 mg/l). Anthocyanin degradation kinetics were assessed as a function of pH (3.0, 3.5, and 4.0) and storage temperature (5, 20 and 30 °C). During storage, anthocyanins experienced pH and temperature-dependent losses, and the half life cyanidin-3-rutinoside (t_1/2 = 2.67–210 days) was consistently longer than cyanidin-3-glucoside (t_1/2 = 1.13–144 days). The presence of flavone-C-glycosides induced significant hyperchromic shifts and enhanced anthocyanin stability at all pH and temperature combinations, while no significant effects were attributed to the presence of phenolic acids or procyanidins. Additional models using externally added cofactors from rooibos tea, also rich in flavone-C-glycosides, resulted in up to 45.5% higher anthocyanin colour and up to 40.7% increased anthocyanin stability compared to uncopigmented anthocyanin isolates and had similar copigmentation effects to a commercial rosemary-based colour enhancer. Results suggest flavone-C-glycosides offer potential for their use as colour enhancers and stabilizing agents in products rich in cyanidin glycosides, particularly açai fruit-containing foods, juice blends, and beverages.     

Anthocyanins and hydroxycinnamic acids of Lambert Compact cherries (Prunus avium L.) after cold storage and 1-methylcyclopropene treatment

Sweet cherries cv. Lambert Compact were treated with 1-methylcyclopropene (1-MCP) at 0, 180 and 360 nL/L for 2 h at 25 °C and then stored at 2–4 °C in refrigerator. Their quality was measured after 12 days of storage in terms of the contents of total and individual anthocyanins and hydroxycinnamic acids, occurrence of rot, and colour change. Colour change was monitored at three day intervals during storage in the CIE L*, a*, b* colour space. 1-MCP did not retard colour change. The contents of total and individual anthocyanins and hydroxycinnamic acids showed no correlation with the colour behaviour of the cherries. All cherries lost their initial shiny red colour on storage, regardless of the treatment. 1-MCP reduced sweet cherry rot at the highest concentration used (360 nL/L) – only 6% were rotten after 12 days in the refrigerator. This differed significantly (P < 0.05) from untreated fruits and those treated with 180 nL/L 1-MCP which resulted on average in 14 and 20% rot (not statistically different P < 0.05), respectively. The occurrence of rot was shown to be correlated with anthocyanin accumulation, (R = 0.62, P < 0.10). The profile of individual anthocyanins and hydroxycinnamic acids in sweet cherry was not affected neither by cold storage nor 1-MCP treatment.     

Phloridzin and other phytochemicals in apple pomace: Stability evaluation upon dehydration and storage of dried product

Apple pomace (mixed Red Delicious and Golden Delicious varieties) obtained from the industrial production of puree was both vacuum-dried at 40 °C and air-dried at 60 °C, ground and stored at water activity (a_w) in the range 0.11–0.75, for 9 months, at 30 °C. The aims were to investigate the effect of drying and long-term storage on phytochemical contents. Air-drying at 60 °C was better than vacuum-drying at 40 °C in terms of anthocyanin and flavanol retention; no adverse effect of drying was observed for flavonols, dihydrochalcones and hydroxycinnamic acids. The maximum stability occurred for all apple phytochemicals at the lowest a_w. At a_w 0.75 degradation of all phytochemicals occurred with the following stability ranking: phloridzin > chlorogenic acid > quercetin 3-O-galactoside > epicatechin > procyanidin B2 and cyanidin 3-O-galactoside. A promising feature of pomace is its exclusive high content of phloridzin, which showed relatively high stability during long-term storage.     

Degradation kinetics of anthocyanins in acerola pulp: Comparison between ohmic and conventional heat treatment

Degradation kinetics of monomeric anthocyanins in acerola pulp during thermal treatment by ohmic and conventional heating was evaluated at different temperatures (75–90 °C). Anthocyanin degradation fitted a first-order reaction model and the rate constants ranged from 5.9 to 19.7 × 10⁻³ min⁻¹. There were no significant differences between the rate constants of the ohmic and the conventional heating processes at all evaluated temperatures. D-Values ranged from 116.7 to 374.5 for ohmic heating and from 134.9 to 390.4 for conventional heating. Values of the free energy of inactivation were within the range of 100.19 and 101.35 kJ mol⁻¹. The enthalpy of activation presented values between 71.79 and 71.94 kJ mol⁻¹ and the entropy of activation ranged from −80.15 to −82.63 J mol⁻¹ K⁻¹. Both heating technologies showed activation energy of 74.8 kJ mol⁻¹ and close values for all thermodynamic parameters, indicating similar mechanisms of degradation.     

Effect of ripeness and postharvest storage on the evolution of colour and anthocyanins in cherries (Prunus avium L.)

The relationship between colour parameters and anthocyanins of four sweet cherry cultivars, Burlat, Saco, Summit and Van was studied. The colour (L^∗, a^∗, b^∗, chroma and hue angle parameters) and anthocyanins were analysed during two different years at two different ripening stages (partially ripe, and ripe, respectively). The cherries were analysed at harvest and after storage at 1.5 ± 0.5 °C and 15 ± 5 °C for 30 and 6 days, respectively. The colour was measured by tristimulus colourimetry (CIELAB system) directly on the fruits, while anthocyanins were quantified by HPLC-DAD analysis on methanolic extracts of freeze-dried samples of the fresh cherries and on the differently stored cherries. L^∗, chroma, and hue angle values were always lower for the ripe than for the partially ripe cherries. All of the cultivars were found to contain cyanidin-3-rutinoside and cyanidin-3-glucoside as the major anthocyanins. The total anthocyanin content in fruits of the different cultivars varied in the order Burlat > Saco > Van > Summit. The concentration of anthocyanins increased at both temperatures of storage in both ripe and partially ripe cherries, but the extent of increase varied among cultivars. Cherries stored at 15 ± 5 °C showed higher reduction of L^∗, chroma and hue angle than fruits stored at 1.5 ± 0.5 °C. L^∗, a^∗, b^∗, chroma and hue angle correlated negatively (P < 0.001) with the total anthocyanins levels, but not with the total phenols. These results show that chromatic functions of chroma and hue correlate closely with the evolution of colour and anthocyanins levels during storage of sweet cherries and indicate that colour measurements can be used to monitor pigment evolution and anthocyanin contents of cherries (and vice versa).     

Determination of the degradation kinetics of anthocyanins in a model juice system using isothermal and non-isothermal methods

The effect of temperature on the degradation of blackcurrant anthocyanins in a model juice system was determined over a temperature range of 4–140 °C. The thermal degradation of anthocyanins followed pseudo first-order kinetics. From 4–100 °C an isothermal method was used to determine the kinetic parameters. In order to mimic the temperature profile in retort systems, a non-isothermal method was applied to determine the kinetic parameters in the model juice over the temperature range 110–140 °C. The results from both isothermal and non-isothermal methods fit well together, indicating that the non-isothermal procedure is a reliable mathematical method to determine the kinetics of anthocyanin degradation. The reaction rate constant (k) increased from 0.16 (±0.01) × 10⁻³ to 9.954 (±0.004) h⁻¹ at 4 and 140 °C, respectively. The temperature dependence of the rate of anthocyanin degradation was modelled by an extension of the Arrhenius equation, which showed a linear increase in the activation energy with temperature.     

Changes in strawberry phenolics, anthocyanins, and antioxidant capacity in response to high oxygen treatments

Changes in fruit quality, decay, phenolic and anthocyanin content, and antioxidant capacity of strawberries (Fragaria × ananassa Duch. cv. Allstar) stored under air and high oxygen atmospheres at 5 °C were investigated. Freshly harvested strawberries were placed in jars and ventilated continuously with air or with 40, 60, 80, or 100 kPa O₂ at 5 °C for up to 14 days. Samples were taken initially, and after 3, 7, 10 and 14 days of storage. While fruit quality parameters such as titratable acidity, total soluble solids and surface color were only slightly affected by differing levels of O₂, the higher oxygen concentration treatments significantly reduced decay. Oxygen concentrations higher than 60 kPa also promoted increases in ORAC values, total phenolics and total anthocyanins as well as individual phenolic compounds analysed by HPLC during the initial 7 days of storage. However, this effect diminished with prolonged storage. No significant differences in ORAC values, total phenolics, total anthocyanins, or the individual phenolic compounds were observed among the high O₂ and air-stored fruits after 14 days of storage. These results indicate that high oxygen treatments exert the most effects on fruit quality and antioxidant capacity of strawberry fruit in the first 7 days of storage.     

Effect of low temperature storage on physical and physiological characteristics of eggplant fruit (Solanum melongena L.)

Eggplant (Solanum melongena L.) is a perishable and chilling-sensitive tropical fruit. The chilling injury (CI) symptoms as well as some physical and physiological implications were studied in eggplants Money Maker No. 2 stored at 0 and 10 °C for 15 days. Eggplants stored at 10 °C were not damaged by temperature, whereas fruit stored at 0 °C suffered CI. Eggplant stored at 0 °C exhibited a decrease in L₀ (lightness) and ΔL (oxidation potential), increase of pH and electrolyte leakage after CI symptoms are manifested. At this temperature, flesh tissue revealed ultrastructural damage. On the other hand, skin from upper fruit section showed more lightness, reddish colouration, and lower content of anthocyanins than the central fruit section at harvest and over the entire storage period at 0 °C. In fruit stored at this temperature and in upper section, changes of anthocyanin content with time were closely proportional to the Chroma evolution (lower content of anthocyanin, lower saturation of colour).     

Kinetics of the formation of radicals in meat during high pressure processing

The kinetics of the formation of radicals in meat by high pressure processing (HPP) has been described for the first time. A threshold for the radicals to form at 400 MPa at 25 °C and at 500 MPa at 5 °C has been found. Above this threshold, an increased formation of radicals was observed with increasing pressure (400–800 MPa), temperature (5–40 °C) and time (0–60 min). The volume of activation (ΔV^#) was found to have the value −17 ml mol⁻¹. The energy of activation (E_a) was calculated to be 25–29 kJ mol⁻¹ within the pressure range (500–800 MPa) indicating high independence on the temperature at high pressures whereas the reaction was strongly dependent at atmospheric pressure (E_a = 181 kJ mol⁻¹). According to the effect of the processing conditions on the reaction rate, three groups of increasing order of radical formation were established: (1) 55 °C at 0.1 MPa, (2) 500 and 600 MPa at 25 °C and 65 °C at 0.1 MPa, and (3) 700 MPa at 25 °C and 75 °C at 0.1 MPa. The implication of the formation of radicals as initiators of lipid oxidation under HPP is discussed.     

Effect of ohmic heating and vacuum impregnation on the quality and microbial stability of osmotically dehydrated strawberries (cv. Camarosa)

The combined effect of osmotic dehydration/ohmic heating (OD–OH) and vacuum impregnation/ohmic heating (VI–OH) on physicochemical and quality parameters of strawberry (a_w, color, firmness and microstructure), as well as on microbial stability of storage samples at 5 and 10 °C, was analyzed. Treatments were carried out with a 65% (w/w) sucrose solution at 30 °C, and ohmic heating at 9.2, 13, and 17 V/cm electric field strengths, corresponding to applied voltages of 70, 100, and 130 V. Dehydrated samples showed that water loss was greater in OD–OH treatments at 17 V/cm. The greatest solute gain, least firmness loss and least color loss were obtained in the VI–OH treatment at 13 V/cm. The shelf-life of strawberries treated with VI–OH at 13 V/cm and stored at 5 °C was extended from 12 d (control samples) to 25 d. Furthermore, the VI–OH treatment at 13 V/cm was the best processing condition for dehydrating strawberries.     

Characteristics of submicron emulsions prepared by ultra-high pressure homogenisation: Effect of chilled or frozen storage

Model O/W pre-emulsions at an initial temperature of 24 °C and pH 6.3, and containing (w/w) 4.3% whey proteins plus 15, 30 or 45% peanut oil were processed using a ∼15 L/h homogeniser with a high pressure (HP) valve immediately followed by cooling heat exchangers. The effect of ultra-high pressure homogenisation (UHPH) between 100 and 300 MPa (P₁) or of recycling (1–3 homogenisation passes) at 200 MPa was investigated on the droplet size distribution, size indices and viscosity. Fluid temperatures were measured at the inlet (T₁) and outlet (T₂) of the HP-valve, and after immediate cooling downstream of the HP-valve (T₃) as they varied throughout UHPH. Short-life heating phenomena and mechanical energy involved in droplet processing were clearly influenced by emulsion composition. Oil droplet diameters decreased when (P₁) increased from 100 to 300 MPa leading to submicron droplets at ≥200 MPa. Monomodal distributions with droplets well below 0.3 μm were obtained after recycling at 200 MPa for the three oil contents, with a peak at 138 nm (distribution in volume) or 60–70 nm (in number frequency). The emulsion behaviour varied from fluid (and quite Newtonian) to thick (and shear thinning) depending on the droplet size reduction and the oil volume fraction. Emulsions displayed an excellent stability vs. creaming and coalescence after 9 d storage at 5 °C. Freezing followed by 13 d storage at −24 °C then thawing, induced an increase in particle sizes depending both on the oil volume fraction and (P₁). After UHPH at 200–225 MPa (±recycling), the freezing/thawing process maintained most of oil droplet size below 1 μm at 15% (w/w) oil, and induced mainly oil droplet aggregation through SDS-labile interactions at higher oil contents.     

Thermal degradation kinetics of anthocyanins and visual colour of Urmu mulberry (Morus nigra L.)

Urmu mulberry (Morus nigra L.) juice was concentrated from 15.02 to 45.20 °Brix by rotary vacuum evaporator at 40 °C. The objectives of this study were to determine the titratable acidity, soluble solid content, antioxidant capacity, total monomeric anthocyanins and total phenolic matter in prepared concentrate, to investigate the thermal degradation kinetics of anthocyanins and Hunter colour parameters (L^∗, a^∗, b^∗) and total colour difference (TCD^∗) and to develop a relationship between visual colour and anthocyanin during thermal processing at 60, 70 and 80 °C. Monomeric anthocyanin degradation showed a first order reaction kinetics. The zero order, first order and a combined kinetics model were applied to the changes in Hunter colour parameters (L^∗, a^∗ and b^∗) and total colour difference (TCD^∗). All colour parameters followed an apparent combined kinetics model. The degradation of anthocyanins showed positive correlation with a^∗, b^∗ and L^∗ and negative correlation with TCD^∗.     

Approaches to understanding the contribution of anthocyanins to the antioxidant capacity of pasteurized pomegranate juices

Influence of processing and storage conditions on anthocyanin stability and antioxidant activity of clarified and cloudy juices from arils of the ‘Mollar’ pomegranate variety was studied. Clarification process reduced the content of total monomeric and individual anthocyanins, and increased the antioxidant activity of pomegranate juice. Thermal treatments (65 and 90 °C for 30 or 5 s) decreased the percentage of polymeric anthocyanin form, increasing on the contrary the monomeric one. In any case, storage temperature was the main factor affecting all the parameters tested. Cyanidin 3-O-glucoside (Cy3G) was more instable than delphinidin 3,5-di (Dp3,5dG) and cyaniding 3,5-diglucosides (Cy3,5dG). A linear relationship was observed between oxygen radical absorbance capacity (ORAC) and total monomeric anthocyanins, suggesting that they contributed strongly to the antioxidant capacity. Results presented in this study show that hurdle technology (heating plus refrigeration) may help to reduce anthocyanin degradation in pasteurized pomegranate juice, avoiding a dramatic impact on its colour and preserving the beneficial effects of this specific bioactive compounds on human health.     

Properties of polyphenol oxidase from Anamur banana (Musa cavendishii)

Polyphenol oxidase (PPO) was extracted from Anamur banana, grown in Turkey, and its characteristics were studied. The optimum temperature for banana PPO activity was found to be 30 °C. The pH-activity optimum was 7.0. From the thermal inactivation studies, in the range 60–75 °C, the half-life values of the enzyme ranged from 7.3 to 85.6 min. The activation energy (E_a) and Z values were calculated to be 155 kJ mol⁻¹ and 14.2 °C, respectively. K_m and V_max values were 8.5 mM and 0.754 OD₄₁₀ min⁻¹, respectively. Of the inhibitors tested, ascorbic acid and sodium metabisulphite were the most effective.