Effect of high-pressure induced ice I/ice III-transition on the texture and microstructure of fresh and pretreated carrots and strawberries

The effect of pressure treatments at −25 °C between 150 and 300 MPa, indicated as high-pressure induced crystallization (HPIC) processes if formation of ice III occurs during pressurization, on the texture and structure of frozen strawberries and carrots were studied. The formation of ice III, which has been proven to inactivate the microbial load of a frozen food, occurred when pressure was increased to 250 MPa or higher. Volume changes related to the formation of ice III affected the cell wall integrity of infused frozen strawberries and caused a 42–46% reduction of the fruit’s hardness. These textural and structural changes were not affected by the pressure holding time (30 s versus 10 min), and thus by partial thawing during the pressure holding time, and were absent in frozen fruits treated at pressures lower than 250 MPa. The structure and texture of frozen carrots were respectively not and only slightly altered during high-pressure–low-temperature (HP–LT) treatments at all pressure levels studied. However, if carrots were blanched (30 min at 60 °C, 2 min at 90 °C and a combination of both) prior to freezing, structural damages during pretreatment and freezing made the tissue, in terms of both structural and textural quality, unsuitable for a post-freezing HP–LT treatment. These observations should be taken in mind when analyzing the possibilities of HPIC processes as a tool for post-freezing microbial reduction when applied to tissue based systems.     

Effect of temperature and growth media on the attachment of Listeria monocytogenes to stainless steel

Listeria monocytogenes ATCC 19111 cultivated in nutrient-rich medium (brain heart infusion, BHI) or starved in minimal medium (10% filter sterilized pond water and 90% sterilized distilled water) were investigated for their initial attachment to austenitic stainless steel No. 4 with satin finish at 4 °C, 20 °C, 30 °C, 37 °C, or 42 °C. A droplet (10 μl) containing  10⁷ CFU/ml of L. monocytogenes suspended in BHI or minimal medium was placed on the stainless steel surface. After holding in saturated humidity for 3 h at the desired temperature the surface was washed and prepared for scanning electron microscopy (SEM). Using SEM, attachment of L. monocytogenes was determined by counting cells remaining on the surface. When L. monocytogenes cultivated in BHI were used, with the exception of the number of attached cells being lower at 42 °C than at 37 °C and 30 °C, the number of attached cells increased with increasing temperature (P < 0.05). When L. monocytogenes starved in minimal medium were used, the number of attached cells also increased with increasing attachment temperature (P < 0.05), but the number of attached cells at 42 °C was lower than that at the other temperatures. The attachment of L. monocytogenes to stainless steel surface was greater when cultivated in rich medium of BHI vs starved in the minimal medium.     

Impact of sorbitol on the thermostability and heat-induced gelation of bovine serum albumin

The influence of sorbitol (0–40 wt.%) on the thermal denaturation and gelation of bovine serum albumin (BSA, pH 7.0) in aqueous solution has been studied. The effect of sorbitol on heat denaturation of 0.5 wt.% BSA solutions was measured using ultrasensitive differential scanning calorimetry. The unfolding process was irreversible and was characterized by the thermal denaturation temperature (T_m). As the sorbitol concentration increased from 0 to 40 wt.%, T_m increased from 73.0 to 80.9 °C. The rise in T_m was attributed to the increased thermal stability of the globular state of BSA relative to its native state. The dynamic shear rheology of 4 wt.% BSA solutions containing 200 mM NaCl was monitored as they were heated from 30 to 90 °C at 1.5 °C min⁻¹, held at 90 °C for 120 min, and then cooled back to 30 °C at −1.5 °C min⁻¹. Sorbitol increased the protein gelation temperature (ΔT_gel +10 °C for 40 wt.% sorbitol), decreased the isothermal gelation rate at 90 °C, but increased the final shear modulus of the gels cooled to 30 °C. The impact of sorbitol on gel characteristics was attributed to its ability to increase protein thermal stability, increase the attractive force between proteins and decrease the protein–protein collision frequency.     

Effects of pH and temperature on metmyoglobin solubility in a model system

From a series of experiments heating metmyoglobin solutions at pH 5.0 through 7.0, the effects of temperature and pH on the thermal stability of metmyoglobin were investigated. The percent metmyoglobin denatured at temperatures from 25 to 80 °C was determined. pHs lower than 6.5 caused metmyoglobin denaturation at various temperatures from 25 to 80 °C, but it was particularly apparent when pH was < 5.6. Thermal stability of metmyoglobin increased as pH increased. Metmyoglobin denaturation occurred at 55 °C at pH 5, however, denaturation did not occur until 60 °C at pHs from 5.3 to 7.0. A slower heating rate (0.9 °C/min) resulted in more metmyoglobin thermal denaturation than a faster heating rate (1.3 °C/min) when the temperature was above 55 to 60 °C. The denaturation caused by low pH alone was reversible, while that caused by high temperature was not. Techniques which increase muscle pH, such as the injection of sodium bicarbonate, could effectively improve the color condition of PSE meat.     

Investigation of desirable hydrostatic pressure required to sterilize Bacillus stearothermophilus IFO 12550 spores and its sterilization properties in glucose, sodium chloride and ethanol solutions

Desirable hydrostatic pressure required to sterilize Bacillus stearothermophilus IFO 12550 spores and its sterilization properties in glucose, sodium chloride and ethanol solutions were investigated. Spores were inactivated as treatment temperature (35 to 95°C) increased at 50 and 100 MPa. The Pz (pressure z) values were 29.32 MPa under the pressure ranged from 10 to 60 MPa and 545.6 MPa in under 60 to 100 MPa at 95°C. Therefore, 60 MPa was the desirable pressure to sterilize the spores at 95°C. Glucose, sodium chloride and ethanol respectively decrease the inactivation rate of the spores significantly (P<0.05) except for 6% glucose. The spores were inactivated at 60 MPa, 95°C for 420 to 540 min in the media with various food additives. The PD (pressure D) values ranged from 75.2 min (containing no food additives) to 86.2 min (containing 20% ethanol).     

Evidence on the role of protein biosynthesis in the induction of heat tolerance of Lactobacillus rhamnosus GG by pressure pre-treatment

It was the aim of this work to evaluate, whether and to which extent heat resistance of Lactobacillus rhamnosus GG is affected by mild pressure treatments prior to exposure to lethal temperatures, such as during spray-drying. It was observed that cells pressure pre-treated at 100 MPa at 37 degrees C for 10 min showed higher survival than untreated cells when exposed to heat challenge at 60 degrees C. To gain more insights on the cellular mode of action of pressure induced heat tolerance, flow cytometric analysis was applied in combination with functional dye LIVE/DEAD BacLight bacterial viability kit. Dot plot analysis showed that a lower degree of membrane damage was observed at pressure pre-treated cells upon heat treatment at 60 degrees C for 3 min. Evaluation of heat inactivation kinetics of cells pressure treated in the presence of chloramphenicol, a protein synthesis inhibitor, pointed out the potential contribution of pressure-induced protein biosynthesis in the enhancement of bacterial heat tolerance.     

Modeling the effect of inoculum size and acid adaptation on growth/no growth interface of Escherichia coli O157:H7

The objective of this study was to model with logistic regression the growth/no growth interface of different initial inoculation levels (10¹, 10³ and 10⁵ CFU/ml; study 1), or nonadapted vs acid-adapted (study 2) Escherichia coli O157:H7 as influenced by pH, NaCl concentration and incubation temperature. Study 1 was conducted with a mixture of four E. coli O157:H7 strains grown (35 °C, 24 h) in tryptic soy broth (TSB). Study 2 was conducted with the same mixture of four E. coli O157:H7 strains grown (35 °C, 24 h) in glucose-free TSB with 1% added glucose (final pH 4.83), or in diluted lactic acid meat decontamination runoff fluids (washings; final pH 4.92), or nonadapted cultures prepared in glucose-free TSB (final pH 6.45), or in water washings (final pH 6.87). Parameters included incubation temperature (10–35 °C), pH (3.52–7.32), and NaCl concentration (0–10% w/v). Growth responses were evaluated for 60 days turbidimetrically (610 nm) every 5 days in 160 (study 1) and 360 (study 2) combinations in quadruplicate samples, with a microplate reader. The lower the initial inoculum the higher were the minimum pH and a_w values permitting growth. Differences in the pH and a_w growth limits among inoculum concentrations increased at 15 and 10 °C. Acid-adapted cultures were able to grow at lower pH than nonadapted cultures, while at temperatures below 25 °C, growth initiation of nonadapted cultures stopped at higher a_w compared to acid-adapted cultures for the whole pH range of 3.52 to 7.32. A comparison with available data indicated that our model for acid-adapted E. coli O157:H7 in different environments may provide representative growth probabilities covering both nonadapted and stress-adapted contaminants.     

Effect of pressure treatments on the mechanical properties of pre- and post-rigor meat

Pressure-heat treatment of beef semitendinosus samples post-rigor gave shear and tensile results similar to those obtained with pressure treatment pre-rigor. Post-rigor pressure-heat treatment did not affect the contraction state, unlike pre-rigor pressure treatment which caused samples to contract by about 40%. Maximum tenderizing effect by pressure-heat treatment (150 M Nm⁻² at 60°C for 30 min) was achieved when samples were heated at 45°C for 45–180 min immediately before application of the treatment. As the pre-pressurization temperature was increased, the duration of heating became more critical until at temperatures ≥ 60°C the effects of subsequent pressure-heat treatment became very small. Pressure-heat treated samples did not show the increase in shear force values for cooking temperatures ≥ 60°C associated with myofibrillar hardening. It was concluded that pressure-heat treatment primarily affected the myofibrillar structure.     

Listeria innocua and aerobic mesophiles during chill storage of inoculated mechanically recovered poultry meat treated with high hydrostatic pressure

Mechanically recovered poultry meat (MRPM) was inoculated with Listeria innocua 910 CECT at a level of approximately 10⁸ CFU g⁻¹. Vacuum-packaged samples were treated by combinations of pressure (350, 400, 450 and 500 MPa), time (5, 10, 15 and 30 min) and temperature (2, 10 and 20°C) and later stored at 2°C for 2 months. Counts of L. innocua and aerobic mesophilic bacteria were determined 1, 4, 7, 15, 30 and 60 days after pressurisation. For mesophiles, in most treatments, pressurization at 2°C gave the significantly best results. High pressure caused a marked bactericidal effect on L. innocua: reductions higher than 7.5 log units were achieved in several cases. Some cells were just sublethally injured by pressure. Samples treated at 500 MPa for 30 min at 2°C had counts of only 2.3 log units after 60 days of chill storage. Noninoculated pressurised MRPM did not show Listeria growth throughout storage. These results suggest that high pressure processing can enhance the microbiological quality of MRPM.     

Influence of temperature and surfactant on Escherichia coli inactivation in aqueous suspensions treated by moderate pulsed electric fields

This research employed a conductometric technique to estimate the inactivation kinetics of Escherichia coli cells in aqueous suspensions (1 wt.%) during simultaneous pulsed electric fields (PEF) and thermal treatments. The electric field strength was E = 5 kV/cm, the effective PEF treatment time t_PEF was within 0–0.2 s, the pulse duration t_i was 10^− 3 s, the medium temperature was 30–50 °C, and the time of thermal treatment t_T was within 0–7000 s. The damage of E. coli was accompanied by cell size decrease and release of intracellular components. The synergy between PEF and thermal treatments on E. coli inactivation was clearly present. The non-ionic surfactant Triton X-100 additionally improved its inactivation. The characteristic damage time followed the Arrhenius law within the temperature range 30–50 °C with activation energies W = 94 ± 2 kJ mol^− 1 and W = 103 ± 5 kJ mol^− 1 with and without the presence of surfactant, respectively. Relations between cell aggregation, cell ζ-potentials and presence of surfactant were analysed.     

Physiological properties of Lactobacillus paracasei, L. danicus and L. curvatus strains isolated from Estonian semi-hard cheese

Growth and survival of Lactobacillus paracasei (six strains), L. danicus sp. nov. (four isolates, two strains) and L. curvatus (two strains) from semi-hard Estonian cheeses were comparatively studied in different environmental conditions of relevance for their growth in cheese and survival in gastric environment. Maximum specific growth rates for L. paracasei strains varied between 0.40 and 0.57 h⁻¹, and all strains were tolerant to low water activities, heating at 60 °C for 30 min and pH 3. The newly discovered genetically distinct species L. danicus was characterized by low maximum growth rates (0.26–0.38 h⁻¹) and low temperature optimum (<30 °C). It was acid and heat sensitive and inhibited at salt concentrations from 4% and water activities below 0.93. L. curvatus was characterized by the highest growth rates (0.65–0.70 h⁻¹), tolerance to high NaCl concentrations, but sensitivity to heating, bile salts and low pH. The study showed that genetically different LAB species isolated from cheese could be distinguished by simple cultivation experiments.     

Effect of water activity on inactivation of Listeria monocytogenes and lactate dehydrogenase during high pressure processing

The aim of this study was to investigate the effect of water activity (a_w) on the inactivation of Listeria monocytogenes and lactate dehydrogenase (LDH) during high pressure processing (HPP). For microbial inactivation lyophilized cells of L. monocytogenes 19,115 were left dry or were suspended in 10 ml of 0.1% peptone water, 10 ml of glycerol, or mixtures of glycerol and peptone water. All samples of various a_ws were high pressure (HP) processed at ambient temperature at 600 MPa for 300 s. Following HPP, samples were serially diluted in 0.1% peptone and spread-plated on Tryptic Soy agar supplemented with Yeast Extract. For enzyme inactivation, 4.2 mg of lyophilized LDH was suspended in 2 ml of 100 mM phosphate buffer (pH 7.4), 2 ml of peptone water or glycerol, or in 2 ml mixtures of glycerol and peptone water. A lyophilized sample with no added liquid was also included. All enzyme samples were subjected to HPP as described above. After HPP, LDH was diluted to 0.28 μg/ml in 100 mM phosphate buffer (pH 7.4). LDH activity was assessed by measuring the change in concentration of β-NADH as a function of time. Dynamic light scattering analysis (DLS) was performed to examine the size distribution, polydispersity, and hydrodynamic radius of LDH before and after HPP. No significant difference in CFU/g was observed between lyophilized cells not subjected to HPP and lyophilized cells subjected to 600 MPa for 300 s (P < 0.05). However, lyophilized cells that were suspended in 100% to 60% peptone water showed a ~ 7.5-log₁₀ reduction when subjected to HPP. Survival of L. monocytogenes following HPP significantly increased (P < 0.05) when the peptone water concentration was decreased below 60% (a_w ~ 0.8). DLS results revealed that LDH suspended in buffer underwent aggregation following HPP (600 MPa, 300 s). Inactivation rate constants obtained using a first-order kinetic model indicated that untreated and HP processed lyophilized LDH had similar activities. When LDH was subject to HPP in solutions containing glycerol, enzyme activity decreased as the water content increased (r² = 0.95). Lyophilization completely protected L. monocytogenes and LDH from inactivation by high pressure. Furthermore, enzyme activity and cell survival increased as water activity was decreased. We postulate low a_w results in protein stabilization, which prevents protein denaturation and cell death during HPP.     

Modeling the combined effects of pH, temperature and ascorbic acid concentration on the heat resistance of Alicyclobacillus acidoterrestis

In this study, thermal inactivation parameters (D- and z-values) of Alicyclobacillus acidoterrestris spores in McIlvaine buffers at different pH, apple juice and apple nectar produced with and without ascorbic acid addition were determined. The effects of pH, temperature and ascorbic acid concentration on D-values of A. acidoterrestris spores were also investigated using response surface methodology. A second order polynomial equation was used to describe the relationship between pH, temperature, ascorbic acid concentration and the D-values of A. acidoterrestris spores. Temperature was the most important factor on D-values, and its effect was three times higher than those of pH. Although the statistically significant, heat resistance of A. acidoterrestris spores was not so influenced from the ascorbic acid within the concentration studied. D-values in apple juice and apple nectars were higher than those in buffers as heating medium at similar pH. The D-values ranged from 11.1 (90 °C) to 0.7 min (100 °C) in apple juice, 14.1 (90 °C) to 1.0 min (100 °C) in apple nectar produced with ascorbic acid addition, and 14.4 (90 °C) to 1.2 min (100 °C) in apple nectar produced without ascorbic acid addition. However, no significant difference in z-values was observed among spores in the juices and buffers at different pH, and it was between 8.2 and 9.2 °C. The results indicated that the spores of A. acidoterrestris may survive in fruit juices and nectars after pasteurization treatment commonly applied in the food industry.     

Conventional freezing plus high pressure-low temperature treatment: Physical properties, microbial quality and storage stability of beef meat

Meat high-hydrostatic pressure treatment causes severe decolouration, preventing its commercialisation due to consumer rejection. Novel procedures involving product freezing plus low-temperature pressure processing are here investigated. Room temperature (20 °C) pressurisation (650 MPa/10 min) and air blast freezing (−30 °C) are compared to air blast freezing plus high pressure at subzero temperature (−35 °C) in terms of drip loss, expressible moisture, shear force, colour, microbial quality and storage stability of fresh and salt-added beef samples (Longissimus dorsi muscle). The latter treatment induced solid water transitions among ice phases. Fresh beef high pressure treatment (650 MPa/20 °C/10 min) increased significantly expressible moisture while it decreased in pressurised (650 MPa/−35 °C/10 min) frozen beef. Salt addition reduced high pressure-induced water loss. Treatments studied did not change fresh or salt-added samples shear force. Frozen beef pressurised at low temperature showed L, a and b values after thawing close to fresh samples. However, these samples in frozen state, presented chromatic parameters similar to unfrozen beef pressurised at room temperature. Apparently, freezing protects meat against pressure colour deterioration, fresh colour being recovered after thawing. High pressure processing (20 °C or −35 °C) was very effective reducing aerobic total (2-log₁₀ cycles) and lactic acid bacteria counts (2.4-log₁₀ cycles), in fresh and salt-added samples. Frozen + pressurised beef stored at −18 °C during 45 days recovered its original colour after thawing, similarly to just-treated samples while their counts remain below detection limits during storage.     

High pressure treatment decelerates the lipolysis in a caprine cheese

Garrotxa cheese, a cheese made of goat's milk, typical of the Catalonian region, has been high pressure-treated (400 MPa, 5 min, 14 °C) to accelerate the ripening. The volatile fraction of Garrotxa cheese was studied on treated and untreated samples at two ripening stages by SDE extraction with dichloromethane, and identified with GC–MS. Pressure treatment at 400 MPa for 5 min decelerated the lipolysis, having treated cheese lower amount of free fatty acids, and, in general, less volatile compounds showing a tendency to decrease differences during ripening. No new volatile compounds could be identified after pressure treatment. Humidity and content of non-casein nitrogen and non-protein were higher on pressurised cheese, but bacterial counts were significantly reduced after pressure treatment. High pressure-treated Garrotxa cheese was not substantially equivalent to the regular-ripened cheese, however the treatment presented in this paper could lead to new varieties of cheese.     

Temperature and relative humidity profiles during heat treatment of mills and its efficacy against Tribolium castaneum (Herbst) life stages

Heat treatment involves raising the temperature of a food-processing facility to 50–60°C and maintaining these elevated temperatures for 24–36 h to kill stored-product insects. The pilot feed and flour mills at Kansas State University, Manhattan, KS, were subjected to heat treatment using gas and steam heaters, respectively, during 4–8 August 2001 to characterize temperature and relative humidity profiles and to determine efficacy against developmental stages of the red flour beetle, Tribolium castaneum (Herbst). Temperature and relative humidity profiles in each mill were electronically monitored in 10 different locations. Susceptibility of eggs, young instars, old instars, pupae, and adults of T. castaneum to heat was determined at the same 10 locations within each mill. The number of hours required to reach the target temperature of 50°C, number of hours above 50°C, and maximum temperatures varied between the mills and among mill locations. Relative humidity decreased predictably with an increase in temperature, and was 21% in most locations at 50°C or above. Two separate three-parameter non-linear regression models best described temperature and relative humidity profiles observed in each mill. Despite non-uniform heating at the sample locations, mortality of T. castaneum life stages was 100% in most locations, except in areas where temperatures were <50°C. Old instars and pupae appeared to be relatively heat tolerant when compared with other life stages, especially in the flour mill where lethal temperatures were attained. Possible reasons for the non-uniform heating observed at mill locations and survival of certain T. castaneum developmental stages are discussed.     

Design, fabrication, and testing of a returnable, insulated, nitrogen-refrigerated shipping container for distribution of fresh red meat under controlled CO2 atmosphere

In today's market, fresh red meat is cut and packaged at both the wholesale and retail level. Greater economies could result if the wholesaler prepared all consumer cuts centrally, but the short storage life of meat limits distribution. Use of CO₂-controlled atmosphere, master packaging, and strict temperature control (−1.5±0.5°C) can enhance storage life and, therefore, distribution ease. An insulated shipping and storage container was designed and tested for its suitability to distribute master-packaged meat. Shelves in the container supported 36 master trays (508 × 381 × 60 mm), with the source of refrigeration being injected liquid nitrogen (N₂). Electric fans dispersed the N₂ gas throughout the container. To reduce costs, 36 saline water bags (10% w/v NaCl) were used to thermally simulate the meat. Temperatures of 20 bags were recorded during storage experiments. The container was tested at outside temperatures of 15, 0 and −15°C with 4 internal fans and at 30°C with 2, 4 and 6 fans. In all instances, bags cooled from 10°C to an equilibrium temperature of −1.5°C within 5.5 h. Minimum equilibrium temperatures during any 8 h trial were −2.6, −2.0 and −2.0°C for 2, 4 and 6 fans, respectively. Correspondingly, maximum temperatures were −0.2, −0.7 and −0.3°C. Initial chilling of the product required, on average, 19 kg of N₂, while equilibrium was maintained at a N₂ consumption rate of 5.5, 4.0, 2.6 and 0.93 kg/h at outside temperatures of 30, 15 0 and −15°C, respectively, with 4 fans. The N₂ use for 2 and 6 fans was 5 and 6.3 kg/h, respectively, at an outside temperature of 30°C. During simulated power failure or when the N₂-tank ‘ran dry', temperatures in the container rose 0.9 and 2.0°C/h, respectively. When the door to the container was opened long enough to remove three trays, temperature was restored within 5 min. Convective heat transfer coefficients between saline water bags and circulating N₂ were in the range of 80–100, 115–135, and 140–155 W/(m²·K) for 2, 4 and 6 fans, respectively. Heat transfer to meat will be limited by conduction in master packaged meat if similar convection coefficients prevail.     

Inactivation of polyphenol oxidases in cloudy apple juice exposed to supercritical carbon dioxide

The inactivation of polyphenol oxidase (PPO) in cloudy apple juice exposed to supercritical carbon dioxide (SCCO₂) treatment was investigated. Higher pressure, higher temperature, and longer treatment time caused more inactivation of PPO. The maximum reduction of PPO activity reached more than 60% at 30 MPa and 55 °C for 60 min. The experimental data followed first-order reaction kinetics; the kinetic rate constant k and the decimal reduction time D were closely related to the pressure and temperature of SCCO₂ treatment. Higher pressures or higher temperatures resulted in lower D values (higher k), the D value of PPO was minimized to 145 min treated by the combination of 30 MPa and 55 °C. Activation energy of 18.00 kJ /mol, was significantly reduced by SCCO₂ treatment at 30 MPa, as compared to activation energy of 72.0 kJ/mol for identical treatment at atmospheric pressure. Pressure and temperature sensitivity of kinetic parameters were studied. Z_P at 55 °C was 66.7 MPa and Z_T at 30 MPa was 108 °C.     

Post-mortem degradation of gap filaments at different post-mortem pHs and temperatures

Super-stretched muscle fiber bundles (<10 min post mortem) were incubated at one of four combinations of temperature and pH (pH 5.5, 37°C; pH 5.5, 0–4°C; pH 7.4, 37°C; pH 7.4, 0–4°C) for 1 h prior to fixation and embedding for transmission electron microscopy. These tissues were compared with controls fixed immediately after stretching. Disruption of gap filament ultrastructure was greatest in those muscle bundles incubated at pH 5.5 and 37°C. It was determined that pH had a greater influence upon gap filaments than did temperature and that pH 5.5 caused more gap filament disruption than pH 7.4. Other structural alterations of the stretched muscle included more glycogen granule disruption at pH 7.4 and pulling of groups of thick filaments toward the Z-lines within a sarcomere. A pulling of alternate thick filaments toward opposite Z-lines was not observed. It was concluded that gap filament disruption may occur very rapidly in post-mortem muscle.     

Anthocyanin condensation reactions under high hydrostatic pressure

The effects of temperature and/or high hydrostatic pressure on anthocyanin condensation reactions were studied. For this purpose, model solutions containing cyanidin-3-O-glucoside (Cy3gl) and pyruvate, in excess, were subjected to different combined temperature/pressure treatments. After a high hydrostatic pressure treatment of 600 MPa, at 70 °C during 30 min, about 25% of Cy3gl was degraded. Parallel to this decrease, a vitisin A-type derivative was formed. By contrast, the rate of condensation was only 5% when samples were heated (70 °C, 30 min). In both cases, the degradation kinetics fitted well to a first order reaction (R² = 0.99). The decrease in Cy3gl was correlated with a decrease in the antioxidant activity. Moreover, the chemical stability of wine subjected to a temperature/pressure treatment of 600 MPa, at 70 °C during 1 h was investigated. After this treatment, a decrease in the concentration of malvidin-3-O-glucoside (Mv3glu) was found. As a consequence, an increase in the concentration of several products of high molecular weight at 370 nm was observed. When wine was subjected to pasteurization conditions (600 MPa, 70 °C, 10 min), no significant changes in the chemical composition were found (P < 0.05).