Effects of temperature,solid content and pH on the stability of black carrot anthocyanins

Anthocyanin stability of black carrots was studied at various solid contents (11, 30, 45 and 64° Brix) and pHs (4.3 and 6.0) during both heating, at 70–90 °C, and storage at 4–37 °C. Monomeric anthocyanin degradation fitted a first-order reaction model. Degradation of monomeric anthocyanins increased with increasing solid content during heating, while it decreased during storage. For example, at pH 4.3, half-life periods for anthocyanins at 30, 45 and 64° Brix were, respectively, 8.4, 6.9 and 5.2 h during heating at 80 °C and 18.7, 30.8 and 35.9 weeks during storage at 20 °C. At 30–64° Brix, increasing pH from 4.3 to 6.0 enhanced the degradation of anthocyanins during heating. The effect of pH on thermal stability of anthocyanins was also studied at six different pHs (2.5–7.0) in citrate-phosphate buffer solutions and significant decrease in anthocyanin stability was observed at pHs above 5.0. Higher activation energies (E_a) were obtained during heating than during storage with increasing solid contents. At 30–64° Brix, E_a values ranged from 68.8 to 95.1 kJ mol⁻¹ during heating and from 62.1 to 86.2 kJ mol⁻¹ during storage. Q₁₀ values at 20–37 °C were as high as 3.1 at 45° Brix and 3.6 at 64° Brix.     

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.     

The survivability of Bacillus anthracis (Sterne strain) in processed liquid eggs

In this study, we investigated the survival and inactivation kinetics of a surrogate strain of Bacillus anthracis (Sterne strain) in whole egg (WE), egg white (EW), sugared egg yolk (YSU), and salted egg yolk (YSA) at low (−20, 0, and 5 °C), moderate (15, 20, 25, 30, 35, and 40 °C), and high storage temperatures (45, 50, 55, and 60 °C). Outgrowth of the spores was measured as lag phase duration (LPD). Replication of vegetative cells was measured in terms of growth rate (GR) and maximum population density (MPD). Spore inactivation was recorded as inactivation rate and percent reduction in viable count. In general, spore viability decreased at low and high temperatures and increased at moderate temperatures. At 0 and 5 °C, a 60–100% reduction in spore viability was seen within 2–3 weeks in WE and YSU, 0–30% in YSA, and 50–100% in EW. At −20 °C, however, no drop in spore titer was observed in YSU and EW but a 20% drop in titer was seen in YSA and 50% in WE within 2–3 weeks. At high temperatures, WE, EW, and YSA produced a 20–50% drop in the spore titer within 1–4 h whereas YSU showed 100% inactivation within 0.75 h. At moderate storage temperatures, as the temperature increased from 15 to 40 °C, LPD decreased from 13.5 to 0.75 h and MPD reached 0.27–2.2 × 10⁹ CFU/ml in YSU and WE, respectively. Markedly lower growth was observed in YSA (LPD = 24–270 h, MPD = 9 × 10⁵ CFU/ml) and spores were inactivated completely within 1–6 h in EW. The survivability and inactivation data of B. anthracis in liquid egg products reported in this investigation will be helpful in developing risk assessment models on food biosecurity.     

Stability and colour characteristics of PEF-treated cyanidin-3-glucoside during storage

The stability and colour characteristics of PEF (pulsed electric field)-treated cyanidin-3-glucoside (Cy-3-glu) was investigated during storage at 4, 24 and 37 °C. The degradation of Cy-3-glu was analyzed using a first reaction kinetics while its colour characteristics was evaluated using colour indices such as colour density (CD) and CIE L^∗a^∗b^∗ parameters. PEF had no post-effect on the stability and colour characteristics of Cy-3-glu during storage while the storage temperature had a significant effect (p < 0.05). The degradation of PEF-treated Cy-3-glu during storage conformed to the first-order reaction kinetics with regression coefficients R² greater than 0.9300. Corresponding to 4, 24 and 37 °C, the degradation rate constant k in Cy-3-glu significantly increased in the exponential order level of 10⁻⁴, 10⁻³ and 10⁻², while the t_1/2 (the time that 50% Cy-3-glu degradation would take) and D-value (the time that 90% Cy-3-glu degradation would take) of Cy-3-glu during storage decreased in the exponential order level of 10³, 10² and 10. The reduction of CD was closely related to the Cy-3-glu content in this study, the Cy-3-glu content was perfectly predicted using CD with a higher coefficient R² > 0.9999. A significant decrease in b^∗ and H⁰ value was obtained at all storage temperature (p < 0.05). A positive correlation was found between the Cy-3-glu content and b^∗ value or H⁰ value with a coefficients R² > 0.8400 during storage. ΔE increased significantly, ΔE was less than 2 at 4 °C while it was greater than 2 at 24 and 37 °C.     

Effect of high pressure processing on the stability of anthocyanin,ascorbic acid and color of Chinese bayberry juice during storage

The stability of anthocyanin (Cy3Gl) and ascorbic acid (AA) of pressure treated Chinese bayberry (Myrica rubra Sieb. et Zucc.) juice was investigated during storage at temperature of 4 °C and 25 °C. Samples of Chinese bayberry juice (350 mL each, packed with a polyethylene bag) were processed at 400, 500, 600 MPa in room temperature for 10 min. The retention ratio of Cy3Gl and AA content after pressure treatment was more than 98% and 96%, respectively. Both Cy3Gl and AA of pressure treated juice were more stable during storage as compared to those of the untreated control juice. The degradation of Cy3Gl and AA of samples during storage could be described using first order kinetic model. It was observed that there was a significant (p < 0.01) correlation between changes of Cy3Gl and AA content for all tested samples of Chinese bayberry juice during storage.     

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.     

Ascorbic acid degradation kinetics of sonicated orange juice during storage and comparison with thermally pasteurised juice

Ascorbic acid degradation kinetics of sonicated orange juice during storage were determined and compared to thermally pasteurised samples. Acoustic energy densities (AED) ranging from 0.30 to 0.81 W/mL and treatment times of 2-10 min were investigated. The degradation kinetics of sonicated samples followed first-order kinetics (R² ≥ 0.91) during processing. During storage ascorbic acid degradation of sonicated samples followed the Weibull model (R² ≥ 0.97) with β values ranging from 0.662 to 0.697. Comparatively, first-order degradation kinetics were observed during storage for thermally pasteurised (R² = 0.98) and control samples (R² = 0.96). Increased shelf life based on ascorbic acid retention was found for sonicated samples compared to thermally pasteurised samples. Predicted shelf life for sonicated orange juice ranged from 27 to 33 days compared to 19 days for thermally pasteurised juice during storage at 10 °C. These results indicate that sonication results in enhanced retention of ascorbic acid in orange juice during storage compared to thermal processing.     

Microencapsulation by spray drying of bioactive compounds from cactus pear (Opuntia ficus-indica)

Bioactive compounds of pulp (CP) and ethanolic (CE) extracts of the cactus pear (Opuntia ficus-indica) were encapsulated with maltodextrin (MD) or inulin (I). A 2² statistical factorial design was then used to study the stability of the powders obtained at the optimal conditions for each system (CP–MD, CP–I, CE–MD and CE–I) at 60 °C in the dark. The 3:1 ratio of core/coating material and 140 °C inlet air temperature were the optimal conditions for CP–MD and CE–MD systems; whereas, for CP–I and CE–I, the ratios were 3:1 and 5:1, respectively, and 120 °C was used for the inlet air temperature for both systems. An increase of phenolic compounds was observed in all systems during storage at 60 °C. Indicaxanthins in all systems showed a slow degradation during storage at 60 °C and were more stable than betacyanins. The microcapsules described in this study represent an interesting food additive for incorporation into functional foods, due to both the presence of antioxidants and as a red colourant.     

Total phenolics,ascorbic acid,and antioxidant capacity of noni (Morinda citrifolia L.) juice and powder as affected by illumination during storage

Total phenolics, ascorbic acid, and antioxidant capacity of noni (Morinda citrifolia L.) juice and powder were determined during storage at 24 °C. After 2 weeks of storage, illuminated noni juice lost 32% of total phenolics, 89% of ascorbic acid, and 46–65% of antioxidant capacity—about 8%, 22%, and 9–15% more than unilluminated juice. Both illuminated and unilluminated juice lost 97% of ascorbic acid by 4 weeks. The difference in antioxidant characteristics between illuminated and unilluminated juice became insignificant at 12 weeks. After 12 weeks, illuminated noni powder lost 21% of total phenolics, 17% of ascorbic acid, and 23–36% of antioxidant capacity—about 13%, 4%, and 7–19% more than the unilluminated powder. Noni powder in brown bottles retained antioxidant characteristics significantly greater than that in clear bottles. Protection from light effectively reduced degradation of antioxidant characteristics of noni juice for only 2 weeks but those of noni powder for at least 3 months.     

Kinetics of tocols degradation during the storage of einkorn (Triticum monococcum L. ssp. monococcum) and breadwheat (Triticum aestivum L. ssp. aestivum) flours

The kinetics of tocols degradation in wholemeal and white flours from einkorn cv Monlis and bread wheat cv Serio were studied during storage at five different temperatures (−20, 5, 20, 30 and 38 °C) up to 242 days. Tocols decreased as a function of time and temperature, following first-order kinetics. Degradation rates and their dependence upon temperature were similar for the two Triticum species studied. Tocols decrease was quicker in white flour than in wholemeal flour (on average for total tocols at 38 °C, k = 7.79 × 10⁻³ days⁻¹ vs 3.15 × 10⁻³ days⁻¹, respectively). The temperature-dependent degradation was similar for all homologues (Ea = 34.3–49.4 kJ/mol) except for α-T, less thermostable in white flours (Ea = 61.2 kJ/mol in einkorn and Ea = 54.7 kJ/mol in bread wheat).     

Fate of post-processing inoculated Listeria monocytogenes on vacuum-packaged pepperoni stored at 4, 12 or 25 °C

If present, Listeria monocytogenes may not be eliminated during processing of pepperoni or may be introduced during peeling, slicing, or packaging. We evaluated the fate of the pathogen on sliced inoculated pepperoni during vacuum-packaged storage, and potential differences in survival among three types of inocula, including nonacid-adapted, acid-adapted and pepperoni extract-habituated cultures. Commercial pepperoni (two replicates, three samples per treatment) was sliced and inoculated (3 to 4 log CFU/cm²), before vacuum-packaging and storage for up to 180 days at 4, 12 or 25 °C. Samples were periodically analyzed for pathogen counts (PALCAM agar) and total bacterial counts (tryptic soy agar with 0.6% yeast extract). The pH of the product was relatively stable (4.50–4.81) throughout storage. Overall, levels of the pathogen (all inocula) and total counts decreased continuously during storage at all temperatures. The pathogen died slower at 4 °C than at 12 and 25 °C, while at 12 and 25 °C the death rates were similar. Death rates depended on type of inoculum and generally decreased in the order: acid-adapted, extract-habituated and nonacid-adapted inoculum. At day 60, pathogen levels were below the detection limit and remained undetectable throughout the rest of the 180-day storage period, regardless of inoculum type and storage temperature. Therefore, storage of sliced vacuum-packaged pepperoni, especially at ambient temperature, prior to consumption may reduce the potential risk of listeriosis.     

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.     

Influence of storing time and temperature on the viscosity of an egg yolk

The influence of storing time and temperature on rheological behavior of egg yolk was investigated. The eggs of two brown egg-laying breeds (Bar Plymouth Rock and Rhode Island Red) were stored for 1, 2, 3, 4, and 8 weeks at constant temperatures: 4 °C, 8 °C, 12 °C, and 16 °C. The apparent viscosity was measured by a rotational viscometer as a function of shear rate. It was found that yolk samples exhibited shear-thinning (pseudoplastic) behavior. The shear-thinning behavior was fitted well into Herschel–Bulkley model (with a satisfying correlation of R² > 0.95). For the selected shearing rate, viscosity was measured in relation to shearing time. The time-dependant viscosity decreased rapidly with time and, at lower share rates, reached an equilibrium state. The time-dependant viscosity was also found to decrease with storage time. The value of pH changed (increased) during storing. No clear dependence between pH value and viscosity was confirmed.     

High pressure–temperature degradation kinetics of polyacetylenes in carrots

The present study assessed the effect of high pressure–temperature (HPT) processing on the levels of three polyacetylenes in carrot disks immediately after processing in comparison to sous-vide processing. The degradation kinetics of these compounds following processing at HPT was also investigated. The highest pressure–temperature combination which gave maximum retention during the time 10–30 min, for falcarinol it was 400 MPa, at 50 and 60 °C for 10 min; for falcarindiol it was 400 MPa, at 50 °C for 10 min and for falcarindiol-3-acetate was 400 MPa, at 50 °C for 10 min, respectively. Falcarindiol-3-acetate was found to be most barosensitive and falcarindiol was found to be most thermosensitive of the three polyacetylenes studied. When compared with sous-vide (SV) processed carrot disks, HPT processed samples showed higher retention of polyacetylenes. The changes in the levels of polyacetylenes during HPT treatment were adequately described by Weibull model function.     

Analysis of volatile nitrosamines from a model system using SPME–DED at different temperatures and times of extraction

Solid-phase microextraction (SPME) coupled to a direct extraction device (DED) was evaluated as a method for extracting nitrosamine (NA) standard mix containing nine volatile nitrosamines from a solid food model system using several temperatures and times of extraction. The efficacy of extraction, the linearity of response and the sensitivity of this method for analysis of NA were determined at refrigeration (4 °C) and room (25 °C) temperature. Several extraction times (15, 30, 60,120 and 180 min) were also tested. Analysis was carried out with gas chromatography–mass spectrometry (GC–MS) in selected ion monitoring (SIM) mode. At 4 °C all NA were detected at all concentrations studied (ranged from 1 to 50 ng ml⁻¹) except for N-nitrosopyrrolidine (NPYR), N-nitrosomorpholine (NMOR) and N-nitrosodiphenilamine (NDPheA). Better results were obtained at 25 °C in terms of efficacy of extraction, linearity values (regression coefficients, R²) and sensitivity values (limit of detection, LOD). Only 15 min of extraction time were enough to extract all NA from gelatines (10 ng ml⁻¹) at 25 °C. None of the NA reached the equilibrium, even when long times of extraction (20 and 24 h) were evaluated. SPME–DED appears to be a rapid and suitable technique for extracting NA from model food system at both refrigeration and room temperatures.     

Effects of fining treatment and storage temperature on the quality of clarified banana juice

The clarified banana juice was subjected to different treatment namely bentonite, combination of gelatin and bentonite and control and stored at 4, 25 and 37 °C for 24 weeks. The effects of fining treatment, storage temperature and storage time on turbidity, total polyphenol, browning index, microbiological, and sensory quality of clarified banana juice were evaluated during storage. Fining treatment, storage temperature and storage time had a significant (p<0.001) effect on turbidity, total polyphenol and browning index of clarified banana juice. Turbidity and browning index of juice were reduced by fining treatment with bentonite and a combination of gelatin and bentonite but increased with storage temperature and storage time. A significant decrease in total polyphenol content and increase in turbidity and browning index were detected for all juice samples during storage. However, it was noted that changes were significantly greater in control juice stored at higher temperature than in juice stored at 4 or 25 °C for up to 6 months. Sensory evaluation revealed that juices treated with bentonite or a combination of gelatin and bentonite and stored at 4, 25 or 37 °C were acceptable for up to six months, whereas untreated juice stored at 37 °C was only acceptable for up to 16 weeks.     

Effectiveness of a polyamide film releasing lactic acid on the growth of E. coli O157:H7, Enterobacteriaceae and Total Aerobic Count on vacuum-packed beef

The suitability of a polyamide 6 monolayer film containing lactic acid for use as an antimicrobial package for fresh beef cuts was studied. The release of lactic acid in an aqueous environment was immediate (within 1 h) and was from approx. 55 μg lactic acid/cm² film at 0–8 °C to approx. 67 μg lactic acid/cm² film at 12–20 °C. Beef was contaminated with an Escherichia coli O157:H7 isolate with known minimum inhibitory concentration against lactic acid (0.09% v/v), then wrapped with the lactic-acid polyamide film and vacuum packaged. During storage at 12 °C, the numbers of E. coli were 1 log unit lower than that of a control (untreated polyamide film) and decreased by an additional 1 log during storage for 14 days.     

Relevance of season and nucleotide catabolism on changes in fillet quality during chilled storage of raw Atlantic salmon (Salmo salar L.)

Farmed 5–6 kg Atlantic salmon were pre-rigor filleted, vacuum packed and subsequently analysed after 1, 9 and 13 days of storage at 4 °C. The study was repeated in February, April, August and October. The conversion of hypoxanthine (Hx) showed the highest seasonal variation among the nucleotide metabolites, with an inverse relationship with sea temperature at harvesting (R² = 0.95–0.96). The Hx content was inversely related to fresh odour and flavour (R² = 0.81–0.83), but positively to tenderness (R² = 0.87). Hence, these results suggest that salmon reared in seawater of 11–15 °C (August–October) maintain a superior sensory quality for a longer period post-mortem than salmon reared at 6–8 °C (February–April). The colour intensity increased from days 1 to 9 post-mortem, probably due to rigor contraction. The highest increase in drip loss was observed in October and the lowest in April. It is proposed that seawater temperature significantly influences the storage life of raw salmon, and that Hx is a valuable biomarker for sensory quality.     

Detection of Rhyzopertha dominica larvae in stored wheat using ELISA: The impact of myosin degradation following fumigation

Hard red winter wheat kernels were infested with eggs of Rhyzopertha dominica. After 20 d, when the larvae reached the fourth instar, they were killed by exposing the infested kernels to phosphine gas for 24 h. The infested kernels were then divided into four portions and treated as follows: one portion was immediately frozen at −80 °C to avoid myosin degradation; the other three portions were kept at 32 °C and 65% relative humidity, and then frozen at −80 °C after 14, 28, and 56 d post-fumigation, respectively. Each treatment was replicated five times. Myosin was measured using a commercial enzyme linked immunosorbent assay (ELISA) method that specifically detects this protein (Biotect^®, Austin, TX). Myosin degradation was most rapid in the first 2 weeks after the larvae were killed, decreasing from 1.672 to 0.695 ng/well during this period (a 58.4% reduction). There were no significant differences in myosin degradation between samples that were 14, 28, and 56 d post-fumigation. Grain is often fumigated to control insects. Frequently, this occurs many weeks before the grain is milled and may be repeated during the storage period. Therefore, estimates using the ELISA test may underestimate internal insect infestation because of myosin degradation. Insect fragment estimates for previously fumigated grain could be underestimated by as much as 58%.     

Kinetic and prediction studies of ascorbic acid degradation in normal and concentrate local lemon juice during storage

Kinetics of the loss of ascorbic acid (AA) in local lemon juice of 9° and 50° Brix stored at 25, 35, and 45 °C for 4 months have been investigated. The results indicate that increases of concentrations and temperatures increase the rate of AA degradation. The calculated values of activation energies (E^≠) and frequency factors (A) at different Brix imply that the concentration of juice does not change the mechanism of degradation. Thermodynamic functions of activation (ΔG^≠, ΔH^≠, ΔS^≠ and K^≠) have been determined and considered briefly. A direct equation for estimation of the shelf life of stored juice with respect to first-order losses of AA, at any specific temperature and degradation ratio, has been derived and programmed successfully.