High pressure–low temperature processing of beef: Effects on survival of internalized E. coli O157:H7 and quality characteristics

High pressure–low temperature (HPLT) processing was investigated to achieve Escherichia coli O157:H7 inactivation in non-intact, whole muscle beef while maintaining acceptable quality characteristics. Beef semitendinosus was internally inoculated with a four strain E. coli O157:H7 cocktail and frozen to − 35 °C, then subjected to 551 MPa for 4 min (HPLT). Compared to frozen, untreated control (F), HPLT reduced microbial population by 1.7 log colony forming units (CFU)/g on selective media and 1.4 log on non-selective media. High pressure without freezing (551 MPa/4 min/3 °C) increased pH and lightness while decreasing redness, cook yield, tenderness, and protein solubility. Aside from a 4% decrease in cook yield, HPLT, had no significant effects on quality parameters. It was demonstrated that HPLT treatment reduces internalized E. coli O157:H7 with minimal effect on quality factors, meaning it may have a potential role in reducing the risk associated with non-intact red meat.Industrial relevanceIn the current work, high pressure (551 MPa, 4 min) was applied to beef semitendinosus while it was at subfreezing temperatures (<− 30 °C). Most studies utilizing this high pressure–low temperature (HPLT) process employ subzero capable thermostatic high pressure equipment, which currently has no commercial equivalent. Successful HPLT runs were completed in this study using more conventional temperature control (1–3 °C) on pilot scale (20 L) high pressure processing equipment. The process yielded E. coli O157:H7 reductions of 1.4–1.7 log colony forming units (CFU)/g, which, while lower than conventional high pressure processing (HPP), may be sufficient to eliminate O157 populations typical of non-intact, whole muscle beef. Various quality factors, including color, purge losses and cooked tenderness, were unaffected by HPLT, while an equivalent HPP process at nonfreezing temperatures (551 MPa, 3 °C) induced color change (loss of redness), increased cook losses and decreased cooked tenderness compared to the control and HPLT beef. Producers of non-intact, whole muscle (blade tenderized or brine injected) meat, especially those that ship and sell frozen products, may look to HPLT processes to improve food safety.     

Cycled high hydrostatic pressure processing of whole and skimmed milk: Effects on physicochemical properties

In this study, we compare the effects of single- and double-cycle HP treatments at 600 MPa on inactivation of the natural microflora and physicochemical properties of whole and skimmed milk of high bacterial load. The results show that two-cycled HP (2 × 2.5 min) was more effective (P < 0.05) on microbial inactivation, and caused similar or slightly less changes (P > 0.05) in physicochemical properties of milk in comparison to single cycled HP (1 × 5 min). In addition to the expected milk protein structure changes, HP at 600 MPa caused only slight effects on milk fat and lactose. Minor decreases in levels of short chain fatty acids were observed with the cycled treatments, and the volatiles in general decreased after HP treatment, depending mostly on the pressure time but also on cycling in skimmed milk. The study confirmed the superior effect of two-cycle HP on microbial inactivation, and shows a slightly better preservation of the physical-chemical milk quality.Industrial relevanceMulti-cycling HP has been shown to be advantageous for microbial inactivation, but limited information is available regarding the effect on milk components in whole milk or skimmed milk. The present study compares the psychochemical properties of whole and skimmed milk processed by multi-cycling in comparison to single cycle HP treatment. Double cycled HP presented a superior effect on microbial inactivation and slightly better preservation of milk quality than one continuous HP.     

Compression Heating and Temperature Control for High-Pressure Destruction of Bacterial Spores: An Experimental Method for Kinetics Evaluation

High-pressure (HP) processing is considered as an alternative technique for thermal sterilization of high quality foods. Adiabatic compression during pressurization allows for quick increase in temperature of food products, which is reversed when the pressure is released, thereby providing rapid heating and cooling conditions and hence short process times. However, during the pressure holding time, the product experiences a temperature drop as a result of heat loss to the vessel. The temperature variation during the process and the synergistic effect of temperature and pressure make it difficult to get the required accurate data on microbial spore destruction kinetics. In this study, a polyoxymethylene (POM)-insulated chamber was evaluated for temperature control in the test sample during pressure treatment. Temperature variations in the HP system were measured in milk test samples inside the POM insulator and pressure medium in the HP vessel under various conditions of pressures (500–900 MPa) and initial temperatures (20–80 °C). Results demonstrated that the POM chamber had good thermal-insulation characteristics under pressure and was able to maintain stable operating conditions for microbial spore destruction kinetics. Based on the measured adiabatic temperature change, the required initial temperatures for the test sample and pressure medium were generated as a quadratic function of pressure and temperature. The setup was then verified for pressure inactivation of Clostridium sporogenes (PA 3679) spores in ultra-heat-treated milk. The better temperature stability of test samples during treatment provided a means to gather accurate data on HP destruction kinetics of the microbial spores.     

Effect of high pressure - low temperature processing on composition and colloidal stability of casein micelles and whey proteins

The aim of this study was to identify the impact of high pressure treatments at sub-zero temperatures (high pressure - low temperature; HPLT) on milk proteins. Whey protein solutions, micellar casein dispersions and two mixtures (micellar caseins:whey proteins, 80:20 and 20:80, w/w) were pressure treated (100–600 MPa) at pH 7.0 or 5.8 at −15 °C, −35 °C and ambient temperature. Solubility data showed that whey proteins could only be affected by HPLT treatments at pH 7.0 if caseins were present, while effects could be induced at pH 5.8 without the presence of caseins. The caseins formed on the one hand large aggregates (flocs) and on the other hand the solubility was increased by the creation of smaller micelles. The formation of flocs could only be observed for HPLT treated samples, which indicates the formation of different protein interactions in milk protein based samples compared with common HP treatments.     

Effect of high isostatic pressure on the peptidase activity and viability of Pseudomonas fragi isolated from a dairy processing plant

To produce safe and high quality processed milk, high pressure (HP) technology was tested to inactivate undesired microorganisms and their caseinolytic activity. A Pseudomonas fragi strain, isolated from the inner surface of a cheese-making machine from a dairy plant, was shown to harbour the aprX gene and cause casein proteolysis. Single-cycle HP processing of P. fragi-spiked milk at 450 MPa and 25 °C for 20 min decreased bacteria viability to lower levels and reduced peptidase activity by 14%. However when HP processing was performed at 50 °C, a synergistic effect on peptidase was observed, reaching 40% inactivation. Multiple HP treatment cycles at 450 MPa and 25 °C were less effective and reduced peptidase activity by only 23%. HP treatment could aid in the challenge to reduce AprX peptidase activity produced by microbial contaminants, but partial inactivation of peptidase was not effective in preventing UHT milk coagulation during storage at room temperature.     

Melting endothermic technique for establishing different phase diagram pathways during high pressure treatment of liquid foods

The principle of endothermic melting was used to trace the path of phase diagram of foods covering Ice I and Ice III. Fitting the experimental data by parameters of the Simon-Like equations for pure water, R² values of 0.999 and 0.952 for Ice I and Ice III, respectively, were obtained with a mean error less than 5%. Using this method, phase diagrams of fruit juice and milk in Ice I and Ice III were then obtained, and R² values in Ice I and Ice III of 0.990 & 0.583 for fruit juice, and 0.991 & 0.886 for milk, respectively, were obtained. Similarly, based on the principle of the melting endothermic of glucose solution and sodium chloride solution under high pressure, pure water and milk could be cooled to pass through different phase transitions regimes. The developed concept and experimental set up are currently can be used for evaluating microbial destruction kinetics as influenced by phase transition HP treatment.Industrial relevanceThis paper uses the principle of melting endotherm to experimentally obtain the phase diagram of juice and milk, and realize the self-cooling of water and milk. The food (water and milk) can be cooled by the melting endotherm of cooling solution using a simple cooling set-up, and achieve different phase transition profiles with any ordinary high pressure treatment vessel that can operate at 400 MPa. This method overcomes the limitation of previous research studies which rely on more sophisticated and expensive high-pressure- equipment with jacketing and cooling of the pressure chamber with an add on refrigeration source. The developed technique can be used to evaluate microbial destruction as influenced by phase transition, greatly simplifying the experimental process and equipment requirement.     

A microbiological perspective of raw milk preserved at room temperature using hyperbaric storage compared to refrigerated storage

The effects of hyperbaric storage (HS, 50–100 MPa) at room temperature (RT) on endogenous and inoculated pathogenic surrogate vegetative bacteria (Escherichia coli, Listeria innocua), pathogenic Salmonella enterica and bacterial spores (Bacillus subtilis) were assessed and compared with conventional refrigeration at atmospheric pressure for 60 days. Milk stored at atmospheric pressure and refrigeration quickly surpassed the acceptable microbiological limit within 7 days of storage, regarding endogenous microbiota, yet 50 MPa/RT slowed down microbial growth, resulting in raw milk spoilage after 28 days, while a significant microbial inactivation occurred under 75–100 MPa (around 4 log units), to counts below 1 log CFU/mL throughout storage, similar to what was observed for B. subtilis endospores. While inoculated microorganisms had a gradually counts reduction in all HS conditions. Results indicate that HS can not only result in the extension of milk shelf-life but is also able to enhance its safety and subsequent quality.Industrial relevanceThis new preservation methodology could be implemented in the dairy farm storage tanks, or during milk transportation for further processing, allowing a better microbial control, than refrigeration. This methodology is very promising, and can improve food products shelf-life with a considerable lower carbon foot-print than refrigeration.     

Assessing freeze–thaw and high pressure low temperature induced damage to Bacillus subtilis cells with flow cytometry

The effect of high pressure low temperature (HPLT) treatment of Bacillus subtilis PS832 in the domain of Ice I–III was studied. Flow cytometry (FCM) forward and sideward scatter measurements gave no indication for HPLT induced complete rupture of cells. The single cell population was gated using FCM in combination with propidium iodide (PI) and carboxyfluorescein diacetate. Results show that membrane damage was inflicted upon a significant subpopulation of cells. Of the remaining cells an increase in severely stressed and ghost cells was found. Positive PI staining was indicative for nearly complete loss of viability, while impaired esterase activity was not indicative for absence of viability. We confirmed that Ice I–Ice III phase transition, characteristic for a ? 25 °C/250 MPa treatment led to a > 4 log inactivation of vegetative B. subtilis. However, such a treatment did not influence the robustness of survivors. Finally, cells that survived either freeze–thaw or HPLT did not sporulate upon entry into stationary phase.Industrial relevanceThe single cell physiology data represented here, underpin that industrial application of this preservation technology is best done at conditions where Ice I–Ice III phase transitions occur. Importantly, the data also shows that compared to (just) a freeze–thaw cycle at ? 25 °C, such treatment does not lead to less robustness (outgrowth capability) of survivors.     

High-pressure calorimetric evaluation of ice crystal ratio formed by rapid depressurization during pressure-shift freezing of water and pork muscle

The amount of ice nuclei formed during the pressure release is important for the final formation and development of ice crystals in pressure shift freezing (PSF) frozen products. In this study, a high-pressure (HP) calorimeter was used to evaluate the ratio of ice crystals instantaneously formed by rapid depressurization during PSF of pure water and pork muscle tissue. Experiments were carried out initial pressure levels of 62, 115, 157 and 199 MPa, with corresponding phase change temperatures of −5, −10, −15 and −20 °C, respectively (slightly higher than phase change point of water–ice I). The ice crystal ratio was determined based on calorimetric peak measured and heat balance. The evaluated regression relationship between observed ice crystal ratio (R_ice in %) and pressure (P, MPa) was R_ice–water = 0.115P + 0.00013P² (R² = 0.96, n = 9) for pure water, and R_ice–pork = 0.080P + 0.00012P² (R² = 0.95, n = 11) for pork muscle. Compared to other methods, the calorimetric evaluation does not require any of the pressure-related properties of the test sample. HP calorimetry can thus be used to evaluate ice crystal ratio for PSF of foods even though their pressure related properties may be unknown.     

High-pressure destruction kinetics of Clostridium sporogenes ATCC 11437 spores in milk at elevated quasi-isothermal conditions

The high-pressure sterilization establishment requires data on isobaric and isothermal destruction kinetics of baro-resistant pathogenic and spoilage bacterial spores. In this study, Clostridium sporogenes 11437 spores (10⁷ CFU/ml) inoculated in milk were subjected to different pressure, temperature and time (P, T, t) combination treatments (700–900 MPa; 80–100 °C; 0–32 min). An insulated chamber was used to enclose the test samples during the treatment for maintaining isobaric and quasi-isothermal processing conditions. Decimal reduction times (D values) and pressure and temperature sensitivity parameters, Z_T (pressure constant) and Z_P (temperature constant) were evaluated using a 3 × 3 full factorial experimental design. HP treatments generally demonstrated a minor pressure pulse effect (PE) (no holding time) and the pressure hold time effect was well described by the first order model (R² > 0.90). Higher pressures and higher temperatures resulted in a higher destruction rate and a higher microbial count reduction. At 900 MPa, the temperature corrected D values were 9.1, 3.8, 0.73 min at 80, 90, 100 °C, respectively. The thermal treatment at 0.1 MPa resulted in D values 833, 65.8, 26.3, 6.0 min at 80, 90, 95, 100 °C respectively. By comparison, HP processing resulted in a strong enhancement of spore destruction at all temperatures. Temperature corrected Z_T values were 16.5, 16.9, 18.2 °C at 700, 800, 900 MPa, respectively, which were higher than the thermal z value 9.6 °C. Hence, the spores had lower temperature sensitivity at elevated pressures. Similarly, corrected Z_P values were 714, 588, 1250 MPa at 80, 90, 100 °C, respectively, which illustrated lower pressure sensitivity at higher temperatures. By general comparison, it was concluded that within the range operating conditions employed, the spores were relatively more sensitive to temperature than to pressure.     

High-pressure homogenisation of raw bovine milk. Effects on fat globule size distribution and microbial inactivation

Whole raw milk was processed using a 15 L h⁻¹ homogeniser with a high-pressure (HP) valve immediately followed by a cooling heat exchanger. The influence of homogenisation pressure (100–300 MPa) and milk inlet temperature T_in (4°C, 14°C or 24°C) on milk temperature T₂ at the HP valve outlet, on fat globule size distribution and on the reduction of the endogenous flora were investigated. The T_in values of 4–24°C led to milk temperatures of 14–33°C before the HP valve, mainly because of compression heating. High T_in and/or homogenisation pressure decreased the fat globule size. At 200 MPa, the d_4.3 diameter of fat globules decreased from 3.8±0.2 (control milk) to 0.80±0.08 μm, 0.65±0.10 or 0.37±0.07 μm at T_in=4, 14°C or 24°C, respectively. A second homogenisation pass at 200 MPa (T_in=4°C, 14°C or 24°C) further decreased d_4.3 diameters to about 0.2 μm and narrowed the size distribution. At all T_in tested, an homogenisation pressure of 300 MPa induced clusters of fat globules, easily dissociated with SDS, and probably formed by sharing protein constituents adsorbed at the fat globule surface. The total endogenous flora of raw milk was reduced by more than 1 log cycle, provided homogenisation pressure was ⩾200 MPa at T_in=24°C (T₂∼60°C), 250 MPa at T_in=14°C (T₂∼62°C), or 300 MPa at T_in=4°C (T₂∼65°C). At all T_in tested, a second pass through the HP valve (200 MPa) doubled the inactivation ratio of the total flora. Microbial patterns of raw milk were also affected; Gram-negative bacteria were less resistant than Gram-positive bacteria.     

Clostridium sporogenes-ATCC 7955 Spore Destruction Kinetics in Milk Under High Pressure and Elevated Temperature Treatment Conditions

Clostridium sporogenes (ATCC 7955) spores inoculated in milk (2% fat) were subjected to high-pressure (HP) treatments (700–900 MPa) and at elevated temperatures (80–100 °C) for selected times up to 32 min. Samples were sealed in 1-mL plastic vials and placed in a specially constructed insulated chamber to prevent temperature drop during the treatment. Both pressure pulse (with no hold time) and pressure hold techniques were employed for treatment. Pressure pulse resulted in a small, but consistent, destruction (up to 0.5 log kill) of spores. During the pressure hold treatment, the destruction followed a first-order model (R ² > 0.90). The kinetic data were compensated for the small variations in temperature during the treatment. As expected, higher pressures and higher temperatures resulted in a faster rate of spore destruction. Temperature-corrected D values ranged from 13.6 to 2.4 min at 700 MPa and 7.0 to 1.3 min at 900 MPa, respectively, with process temperatures set at 90 and 100 °C. In comparison, thermal treatments gave D values ranging from 156 min at 90 °C to 12.1 min at 100 °C. The temperature sensitivity Z _P values (16.5 to 20.3 °C) under high pressure (700–900 MPa) were higher than under conventional thermal processing (9.0 °C), indicating the spore’s thermal resistance to increase at HP processing conditions. The pressure sensitivity Z _T values varied between 450 and 680 MPa under the elevated temperature (80–100 °C) processing conditions. Overall, C. sporogenes 7955 spores were relatively more sensitive to temperature than pressure.     

Pressure-induced inactivation of bacteria through pressure-assisted thawing using a thermal buffer zone.

Effect of thermal buffer zone was examined on the microbial inactivation through a pressure-assisted thawing. A plastic bag of bacterial suspension enclosed with a thermal buffer zone was frozen at − 50 °C, and treated for 20 min with a pressure-assisted thawing in water of 4 °C. A reduction of 8-log cycle was obtained at 200 MPa for the stationary growth phase cells of Escherichia coli that was suspended in 1% skim milk and enclosed with wheat flour/water paste and two polytetrafluoroethylene plates. When 100% ethanol was used as a thermal buffer and the samples were pressured at 194 MPa in 1% skim milk, levels of E. coli and Listeria monocytogenes were reduced by 6-log cycle and 7-log cycle, respectively. Staphylococcus aureus decreased by 4-log cycle.Industrial relevanceThis work will contribute to new developments in the pressure processing of foods, since the use of a thermal buffer zone in pressure-assisted thawing was very effective in enhancing the level of pressure-induced microbial inactivation.     

Kinetics of destruction ofEscherichia coliandPseudomonas fluorescensinoculated in ewe's milk by high hydrostatic pressure

Ewe's1999199919991999 Academic PressAcademic PressAcademic PressAcademic Pressmilk standardized to 6% fat was inoculated with Escherichia coliand Pseudomonas fluorescensat a concentration of 10⁷and 10⁸ cfu ml⁻¹respectively, and treated by high hydrostatic pressure. Treatments consisted of combinations of pressure (50-300 MPa), temperature (2, 10, 25 and 50°C), and time (5, 10 and 15 min). Violet red bile agar and crystal-violet-tetrazolium count were used to determineE. coliandP. fluorescensrespectively. Pressurization at low and moderately high temperatures produced higher P. fluorescensinactivation than treatments at room temperature, while pressurization at only moderately high temperature produced high E. coliinactivation; low and room temperatures produced similar reductions. On E. coli,reductions of 6.055 log units were produced with 300 MPa for 15 min at 50°C, while on P. fluorescens,reductions of 5.059 log units were produced with 250 MPa for 15 min at 50°C. Both micro-organisms showed a first-order kinetics of destruction in the range 0-30 min, with D-values (at different temperatures and pressures from 150 to 300 MPa) between 2.055 and 18.058 min for E. coli,and 2.058-23.053 min for P. fluorescens.Abaroprotective effect of ewe's milk (6% fat) on both micro-organisms was observed, in comparison with other studies using different means and similar pressurization conditions.     

Cycling versus Continuous High Pressure treatments at moderate temperatures: Effect on bacterial spores?

The advantage of using high pressure (HP) cycling treatment compared with continuous HP treatment was investigated for the inactivation of bacterial spores. The effects of parameters such as pulse number, pressure level, treatment temperature, compression and decompression rates, and time between pulses were evaluated. For this purpose, Bacillus subtilis and B. cereus spores (10⁸ and 10⁶ CFU/mL respectively) were suspended in 2-(N-morpholino) ethanesulfonic acid (MES) buffer solution, tryptone salt (TS) buffer solution, or infant milk and treated by HP cycling at 300–400 MPa, at 38–60 °C, for 1–5 pulses. Pressure cycling reduced the number of viable spores by 1.8 and 5.9 log respectively for B. subtilis and B. cereus species. Continuous HP treatments were performed at the same pressure and temperature for similar treatment durations. Our results showed that the spore inactivation ratio was correlated with the cumulative exposure time to pressure rather than to effects of the cycling process. Greater spore inactivation caused by HP cycling was observed only when faster compression and decompression rates were applied, probably due to adiabatic heating. A three-step kinetic model was developed, which seemed to support our hypothesis regarding the mechanisms of inactivation by pressure cycling and continuous HP treatments.Industrial relevanceThe resistance of bacterial spores to HP limits the industrial applications to refrigerated food products. In this study, we investigated the use of pressure cycling as a means to improve spore baroinactivation at moderate temperatures (T < 60 °C). We showed that cycling pressure does not significantly increase bacterial spore inactivation in comparable treatment duration, but certainly increases material fatigue in HP vessels. Thus, under moderate temperature, cycling pressure treatment is not industrially relevant.     

High hydrostatic pressure effects on bacterial bioluminescence

The mechanism that leads to microbial inactivation by high hydrostatic pressure remains elusive. In this study, a high-pressure system interfaced with a photomultiplier tube (PMT) was developed to monitor cellular metabolism in situ using bioluminescent bacterial strains. Preliminary characterization of the system was performed using Pseudomonas fluorescens 5RL expressing lux proteins from Vibrio fischeri. Stepwise increases in pressure at 34 MPa and above resulted in decreased bioluminescence. Square wave exposure to pressures of 69, 103 and 138 MPa showed bioluminescence reductions greater than 95%, but when cells were returned to ambient pressure bioluminescence returned to 51, 38, and 4% of initial bioluminescence values, respectively. An Escherichia coli strain expressing lux proteins from V. fischeri was constructed to determine whether this reversible effect could be observed in another bacterial genus. Square wave perturbations of 69, 103 and 138 MPa resulted in bioluminescence reductions of about 94% at the highest pressure treatment. Upon decompression, bioluminescence returned to 74, 58 and 30% of the initial bioluminescence values for cells treated at 69, 103 and 138 MPa, respectively. These results suggest that square wave exposure to pressure up to 138 MPa induces reversible cell damage in P. fluorescens 5RL and E. coli VF lux.     

HIGH-PRESSURE DIFFERENTIAL SCANNING CALORIMETRY: EVALUATION OF PHASE TRANSITION IN PORK MUSCLE AT HIGH PRESSURES

High‐pressure (HP) differential scanning calorimetry (DSC) was used to investigate phase‐transition behavior of water in pork muscle at elevated pressures. Fresh pork (rib portion) muscle samples (0.62–0.72 g, vacuum‐packaged in polyethylene pouches) were tested through isothermal pressure‐scan (P‐scan, 0.3 MPa/min) and isobaric temperature‐scan (T‐scan, 0.15C/min) techniques. By using P‐scan testing procedure, the relationship between phase‐transition temperature (T) of frozen pork and the weighted‐average pressure during the phase‐change period (P?_1?2) was found to be T = ?1.17 ? 0.102P?_1?2 ? 0.00019P? (R² = 0.998, n = 10). Comparing with similar temperature pressure relationship classically established for pure water, it was observed that the depression of phase‐change temperature was much more pronounced in pork muscle than in pure water, and the degree of depression increased with an increase in pressure level. The ice content was evaluated with P‐scan at various constant calorimetric temperatures and compared with similar data from conventional DSC. Differences between the two were statistically insignificant (P > 0.05). T‐scan tests demonstrated phase‐transition behavior at constant pressure, but results were not very satisfactory. Overall, HP DSC seems a powerful technique for phase‐transition characterization of water in real foods during HP process.     

Combined effects of high pressure,moderate heat and pH on the inactivation kinetics of Bacillus licheniformis spores in carrot juice

The objective of this research was to evaluate the combined effect of high pressure processing (temperature, pressure and time) and product (pH) related variables on destruction kinetics of spores of Bacillus licheniformis in carrot juice. A 3-level factorial experimental design was used with the microbial spores inoculated into carrot juice at the natural pH (6.2) and acidified pH (4.5 and 5.5), pressure (400, 500 or 600 MPa), temperature (40, 50, and 60 °C) and time (0–40 min) conditions. D values found varied from 0.6 to 14.1 min based on the temperature, pressure and pH level combinations. The corresponding temperature and pressure dependency of D values were in the range 23.3 to 31 °C and 241 to 465 MPa, respectively. The destruction pattern was also dependent on pH, with lower pH contributing to higher destruction rate. Conventional log-linear model and Weibull model were used to describe the survivor curves and for predicting processing time to achieve a 5D spore reduction. The survivor curves exhibited slightly upward concavity and therefore better described by a Weibull than the log-linear model. Treatment combinations showed significant (p ≤ 0.05) effects on D and z values of log-linear model and rate parameter (α) of Weibull model. The 5D spore count reduction times estimated using Weibull model parameters were longer than those from the log-linear model, generally demonstrating an over-treatment. Overall, the pH reduction of low acid foods showed a significant enhancement of rate of destruction of B. licheniformis spores.     

Comparison of the quality characteristics of abalone processed by high-pressure sub-zero temperature and pressure-shift freezing

This study investigated the effects of high pressure sub-zero temperature (HPST) and pressure-shift freezing (PSF) on the quality characteristics of abalone. Each process was conducted within 0.1–200 MPa. HPST caused high drip loss relative to the control, whereas drip generation was effectively prevented by PSF at 150 MPa. The shear force of abalone treated by HPST exhibited a significant decrease with increasing pressure, whereas abalone treated by PSF maintained shear force values similar to the control. With respect to color, HPST resulted in high redness (a*) without changes in lightness (L*) or yellowness (b*) relative to control. The a* and b* of PSF-treated abalone were similar to control, although low L* was observed in PSF-treated abalone. Regardless of the processing methods, increasing pressure levels tended to decrease the aerobic colony count (ACC) of abalone. Consequently, the results suggested that PSF effectively minimized the quality damage caused by the abalone freezing process and that 150 MPa was the optimal condition for PSF for abalone.Industrial relevancePressure-shift freezing has been recognized as the most rapid freezing technique. Currently, high pressure low temperature (HPLT) processing is adopted by means of long time storage of biomaterials. Nevertheless, one of the problem to apply these technique in actual industry is that the materials have to be kept at normally 200 MPa at which the materials can cooled down to around − 20 °C. Based on this study, it is possible to reduce the processing pressure level (~ 100 MPa) which would provide a practical advantage of HPLT processing as well as industrial applicability.     

Yield, composition and rheological characteristics of cheddar cheese made with high pressure processed milk

High Pressure (HP) treatment of milk prior to cheese-making was shown to increase the yield of cheese due to increased protein and moisture retention in cheese. Cheeses were made with raw milk or milk treated with high temperature short-time (HTST) pasteurization, and HP treatments at two levels (483 and 676 MPa) at 10 °C, 483 MPa HP at 30 °C, and 483 MPa HP at 40 °C. Cheese yield, total solids, protein, fat and salt contents were evaluated, and fat and protein recovery indices were calculated. Cheeses from HP treatments of 676 MPa at 10 °C and 483 MPa at 30 °C exhibited wet yields of 11.40% and 11.54%, respectively. Protein recovery was 79.9% for HP treatment of 676 MPa at 10 °C. The use of slightly higher pressurization temperatures increased moisture retention in cheese. Visco-elasticity of cheeses was determined by dynamic oscillatory testing and a creep-recovery test. Rheological parameters such as loss (G″) and storage (G′) moduli were dependent on oscillation frequency. At high (173 rad/s) and low (2.75 rad/s) angular frequencies, cheeses made from milk treated at 483 MPa at 10 °C behaved more solid-like than other treatments. Creep tests indicated that cheeses from milk treated with 483 MPa HP at 10 °C showed the smallest instantaneous compliance (J_o), confirming the more solid-like behavior of cheese from the 483 MPa at 10 °C treatment compared to the behavior of cheeses from other treatments. Cheeses made with pasteurized milk were more deformable, exhibited less solid-like behavior than cheeses made with HP treated milk, as shown by the J_o value. With more research into bacteriological implications, HP treatment of raw milk can augment Cheddar cheese yield with better curd formation properties.