Effects of combining ultraviolet and mild heat treatments on enzymatic activities and total phenolic contents in pineapple juice

Ultraviolet (UV) is able to inactivate most microorganisms in fruit juices with a low absorption coefficient but its effect is limited in inactivating undesired enzymes. The aim of this study was to overcome limitation of ultraviolet light (UV) by combining mild heat with UV. Pineapple juice was treated with mild heat (temperature: 50, 55 and 60 °C; holding time: 10, 20 and 30 min) and subsequently exposed to UV (5.61, 7.55 and 11.23 mJ·cm^− 2). The effects of these combined treatments on pectin methylesterase (PME), bromelain activities and total phenolic content (TPC) were determined. Both enzymatic activities were reduced by mild heat but not by UV treatment. Increasing holding time and UV dosage led to higher depletion of TPC. Treating pineapple juice with mild heat at 55 °C for 10 min and UV at 5.61 mJ·cm^− 2 decreased PME by 60.53% whilst retaining 61.57 ± 0.21% and 72.80 ± 0.33% of bromelain and TPC, respectively.Industrial relevanceAs opposed to traditional heat pasteurisation, ultraviolet (UV) treatment has the potential to produce pineapple juice with added value, such as high amount of health benefiting phenols and bromelain. Despite being known for being economically feasible, this technology is not widely adapted by the industry due to its inability to inactivate pectin methylesterase (PME). To overcome the limitation of UV, mild heat (MH) is introduced as hurdle technology. This study demonstrates that combining UV and MH could be able to effectively inactivate the PME in pineapple juice whilst preserving relatively high amount of bromelain and phenols.     

High-pressure and temperature effects on the inactivation of Bacillus amyloliquefaciens,alkaline phosphatase and storage stability of conjugated linoleic acid in milk

Milk rich in conjugated linoleic acid (CLA, 42 ± 3 mg g^− 1 fat) was used to evaluate the impact of high-pressure sterilization (HPS). The pressure, temperature and time needed to reduce 7-log of Bacillus amyloliquefaciens endospores were determined in the presence of nisin (4–64 mg L^− 1). In addition, the inactivation of alkaline phosphatase was evaluated. After HPS treatment, the remaining CLA and formation of hydroperoxides were monitored during storage up to 60 d at 25 °C. The addition of nisin (≥ 16 mg L^− 1) to milk significantly enhanced the inactivation of B. amyloliquefaciens (7-log reduction) after treatment at 600 MPa, 120 °C and 5 min of holding time. These conditions were selected to evaluate the impact of HPS on the CLA retention and hydroperoxides formation. Milk with the addition of nisin and treated with HPS delivered higher retention of CLA and a lower concentration of hydroperoxides compared with the UHT equivalent process (125 °C/15 s and 135 °C/10 s).Industrial relevanceHigh-pressure sterilization is a valuable alternative to produce superior quality milk products in cases where traditional thermal treatments have failed. This study evaluated the impact of processing conditions on the conjugated linoleic acid content at conditions where commercial sterilization has been achieved (7-log reduction of B. amyloliquefaciens). The outcomes of this study are considered as a step further for the development of high-pressure sterilized milk.     

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.     

The impact of high pressure on glucosinolate profile and myrosinase activity in seedlings from Brussels sprouts

The potential of high pressure (HP) to control bioactive components using seedlings of Brussels sprouts as a simple non-chopped vegetable system was examined. Enzyme activity in situ compared to purified enzyme and residual enzyme substrate in situ are used as three complementary measures for the HP effect. Purified myrosinase and seedlings of Brussels sprouts were submitted to HP 200–800 MPa at 5 °C for 3 min. The myrosinase activity decreased for both myrosinase systems upon increasing pressure to 800 MPa. Applying first-order kinetic to determine activation volumes revealed a linear relationship from 400 to 600 (ΔV^# = − 19.04 mL/mol) and 450–600 MPa (ΔV^# = − 37.79 mL/mol) for seedlings and purified myrosinase, respectively, indicating a protective effect of the plant matrix against enzyme inactivation. Purified myrosinase was activated at 200 MPa but at 800 MPa the glucosinolate degradation due to pressure induced disruption of the plant matrix seems to be partly counter-acted by myrosinase inactivation.Industrial relevanceHigh Pressure (HP) processing is an effective non-thermal preservation treatment for liquid and solid food. Moreover, over the last years, the potential of this technology to improve health and safety attributes of foods has been demonstrated. In particular, the ability of HP to preserve bioactive compounds has been established. There are only few studies evaluating the impact of HP on the complex bioactive glucosinolates-myrosinase. Therefore, this study opens the doors through the application of HP to preserve the bioactive glucosinolates in cruciferous vegetables by creating new processing solutions through controlled enzyme inactivation. Thus, HP could be an effective tool to achieve more effective solutions to obtain the new generation of convenient food and meet the need for new bioactive food products.     

Colour and texture of apples high pressure processed in pineapple juice

Cubes of Granny Smith and Pink Lady apples were vacuum packed in barrier bags with 0% to 50% (v/v) pineapple juice (PJ) at 20°Bx and subjected to high pressure processing (HPP) at 600 MPa for 1–5 min (22 °C). The in-pack total colour change (ΔE) was observed over 4 weeks at 4 °C. Within <1 week of storage at 4 °C, texture, polyphenoloxidase, pectinmethylesterase activities, changes in ΔE and visual browning after opening the bags during air exposure (22 °C; 21% O2 ) for 5 h were also monitored. During the 4 weeks storage in bag visible colour changes were not observed. Texture and ΔE after 5 h air exposure were significantly affected by the apple variety, HPP time and % PJ used. The combined treatment significantly reduced residual PPO activity while PME activity was not affected in both varieties. Pineapple juice in combination with HPP could be used as a natural preservation system for minimally processed apples.Industrial relevanceBrowning upon opening the packs and during air exposure can adversely affect the quality of fresh-cut fruits. Combined treatment of high pressure processing (HPP) and use of pineapple juice has the potential to prevent browning for several hours giving sufficient time for presentation and use in domestic and foodservice environment where high quality fresh-like fruit is required.     

Effect of combinations of high-pressure treatment and bacteriocin-producing lactic acid bacteria on the survival of Listeria monocytogenes in raw milk cheese

The combined effect of high-pressure (HP) treatment and bacteriocin-producing lactic acid bacteria (BP-LAB) on the survival of Listeria monocytogenes Scott A in cheeses made from raw milk that was inoculated with the pathogen at 4.80 log cfu mL⁻¹, a commercial starter and one of seven strains of BP-LAB was investigated. On day 3, the counts of L. monocytogenes were 7.03 log cfu g⁻¹ in a control cheese (without BP-LAB, not HP treated), 6.06–6.74 log cfu g⁻¹ in cheeses with BP-LAB, 6.13 log cfu g⁻¹ in a cheese without BP-LAB and treated on day 2 at 300 MPa, 2.01 log cfu g⁻¹ in a cheese without BP-LAB and treated on day 2 at 500 MPa, 3.83–5.43 log cfu g⁻¹ in cheeses with BP-LAB and treated on day 2 at 300 MPa, and 1.81 log cfu g⁻¹ or less in cheeses with BP-LAB and treated on day 2 at 500 MPa. HP treatment was more effective on day 51 than on day 2.     

Pressure–ohmic–thermal sterilization: A feasible approach for the inactivation of Bacillus amyloliquefaciens and Geobacillus stearothermophilus spores

The efficacy of a pressure–ohmic–thermal sterilization (POTS) for Bacillus amyloliquefaciens and Geobacillus stearothermophilus spore inactivation was investigated. Spores (2.5 × 10⁸ cfu/ml) were inoculated in 0.1% NaCl solution (pH 5.0 and 7.0), green pea puree (pH 6.1), carrot puree (pH 5.0) or tomato juice (pH 4.1). Samples were ohmically (50 V/cm) treated at 600 MPa and 105 °C for various holding times using a laboratory-scale high-pressure processor. B. amyloliquefaciens and G. stearothermophilus spores suspended in 0.1% NaCl solution (pH 7.0) were inactivated by 4.6 and 5.6 log, respectively, for a 30-min holding time. B. amyloliquefaciens and G. stearothermophilus spores in tomato juice were reduced by 3.1 and 4.8 log, respectively, for a 10-min holding time. Spore germination was highest in the G. stearothermophilus suspended in 0.1% NaCl solution (pH 7.0). POTS treatment appears to be a potent method for inactivating pressure–thermal resistant bacterial spores.Industrial RelevanceFood industry is interested in developing superior quality low-acid shelf-stable foods. This study evaluated the pressure–ohmic–thermal sterilization (POTS) for the inactivation of Bacillus amyloliquefaciens and Bacillus stearothermophilus endospores. The impact of food matrices and acidity on the spore resistance was also investigated. Knowledge gained from the study will help the food processors for understanding the importance of various POTS treatment parameters for sterilization of low-acid foods.     

Microbial shelf-life of high-pressure-homogenised milk

The anti-bacterial effect of high pressure homogenisation (HPH) on milk is widely reported but the shelf-life of HPH-treated milk, as reported in this communication has not been studied thus far. Raw whole milk was homogenised at 200 or 250 MPa at 55 or 70 °C and counts of total bacteria (TBC), psychrotrophs, pseudomonads, coliforms, lactobacilli, Bacillus cereus and Staphylococcus aureus were determined throughout subsequent storage for 14 days at 4 °C. Immediately after HPH treatment, counts of all bacteria were below the level of detection but after storage for 14 days at 4 °C, TBC, psychrotroph and pseudomonad counts had reached ∼10⁸ cfu mL⁻¹ in all samples treated with HPH. The limited shelf-life obtained indicates that HPH of milk at these processing parameters it is not a suitable alternative to pasteurisation for extending the shelf-life of milk.     

Inactivation of bacteriophages by thermal and high-pressure treatment

Dairy companies commonly experience fermentation failures due to bacteriophages that are spread mainly by milk, whey or air. Heat or high-pressure treatment may potentially reduce the phage titre, but further knowledge about the inactivation kinetics is desirable. Inactivation experiments were carried out with the commonly occurring lactococcal phages P001 and P008. Phage suspensions in calcium-enriched M17-broth were heated at 55–80 °C, or high-pressure treated at up to 600 MPa. Kinetic analysis showed that the order of inactivation reaction was above 1; thus, inactivation kinetics were approximated by a non-linear regression model. The Arrhenius parameters, rate constant, k_p,T, and activation energy, E_A (for heat treatments), and the volume of activation, ΔV^# (for pressure treatments) were calculated. Both measured and calculated results indicate that phage P008 was the more heat- and pressure-resistant of the two. By combining the results from heat and pressure inactivations, a pressure–temperature diagram for phage P008 was established.     

High-pressure-induced changes in the rennet coagulation properties of bovine milk

The mechanism of high-pressure (HP)-induced changes in rennet coagulation properties of milk, particularly the role of whey protein-casein micelle associations, was studied. Treatment at 100 or 250 MPa reduced the rennet coagulation time (RCT) of raw skimmed bovine milk, compared with untreated milk. Treatment at 400 MPa had little effect, but at 600 MPa, RCT increased considerably. HP-induced increases in RCT did not occur in serum protein-free milk or milk treated with the sulphydryl-oxidising agent KIO₃, which prevents association of denatured β-lactoglobulin with casein micelles. Treatment at 5 or 10 °C at 250–600 MPa resulted in shorter RCT than treatment at 20 °C. In milk without KIO₃, coagulum strength was highest after treatment at 250 or 400 MPa, whereas in milk with KIO₃ it was highest after treatment at 400 MPa. These results indicate the significance of HP-induced association of whey proteins with casein micelles for rennet coagulation properties of milk.     

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.     

Antibiotic resistance and susceptibility to some food preservative measures of spoilage and pathogenic micro-organisms from spices

Antibiogram of 84 strains of Bacillus cereus, 26 strains of Clostridium perfringens, four strains of Staphylococcus aureus, 51 strains of Enterobacteriaceae, two strains of each of Salmonella and Shigella; isolated from spices, were studied against 20 different antibiotics that are commonly used against foodborne diseases, mainly gastroenteritis. All the tested strains of B. cereus, Cl. perfringens, Staph. aureus, Escherichia coli, Salmonella and Shigella were found resistant to at least 3, 4, 7, 6, 10 and 9 antibiotics, respectively. In brain–heart infusion broth supplemented with glucose, the D_100°C-values for B. cereus were 3.5–5.9 min, and the z-values were 17–18°C. The D_100°C-values for Cl. perfringens in fluid thioglycolate medium were higher (10.0–19.8 min) than those of B. cereus. The minimum inhibitory concentrations (MICs) of sodium chloride were 45–80 mg ml⁻¹. While the MIC of benzoic acid for Cl. perfringens, tested on perfringens agar (pH 7.3) plates by incubating anaerobially at 35°C for 24 h, was 1.9–2.2 mg ml⁻¹, for others, tested on nutrient agar (pH 6.8) plates by incubating at 35°C for 18 h in static aerobic condition, it was much less. Similarly, the MIC of sorbic acid for all the tested isolates, excepting Cl. perfringens, was 0.6–1.1 mg ml⁻¹. Of the eight isolates of Cl. perfringens, only three were inhibited at 2.0 mg sorbic acid ml⁻¹, while others were resistant. Sixty percent and 75% of the respective strains of B. cereus and Cl. perfringens were resistant to 5000 IU Nisaplin ml⁻¹, whereas the MIC values of Staph. aureus were between 3000 and 5000 IU ml⁻¹. While studying combined effect of selected hurdles on the growth of enterotoxigenic Cl. perfringens 16-C2, the judicious combination considered was low acid (pH 6.0), 30 mg sodium chloride ml⁻¹ and 1.25 mg benzoic acid ml⁻¹.     

Assessing the acid tolerance and the technological robustness of probiotic cultures for fortification in fruit juices

The suitability of probiotic cultures as fruit juice supplements was examined by assessing their acid tolerance and technological robustness. Survival of Lactobacillus and Bifidobacterium strains in orange juice (OJ), pineapple juice (PJ) and cranberry juice (CJ) was monitored. Results revealed that extensive differences exist among probiotic strains regarding their acid resistance. All of the strains screened survived for longer in OJ and PJ compared to CJ. L. casei DN-114 001, L. rhamnosus GG and L. paracasei NFBC43338 displayed the greatest robustness surviving at levels above 10⁷ cfu ml^− 1 in OJ and above 10⁶ cfu ml^− 1 in PJ for at least 12 weeks. Probiotic tolerance to thermal and non-thermal processing was studied to determine the feasibility of their addition to OJ prior to pasteurisation. OJ fortified with probiotic cultures was subjected thermal pasteurisation at 76 °C for 30 s and 90 °C for 1 min in addition to a high pressure treatment of 400 MPa for 5 min. Results indicated no strain was capable of withstanding treatments necessary to achieve a stable juice at levels > 10⁶ cfu ml^− 1. The outcome of the overall study points to L. rhamnosus GG, L. casei DN-114 001 and L. paracasei NFBC43338 as having promising potential for exploitation as functional supplements in fruit juices due to their impressive tolerance in acidic environments; however, fortification post processing is recommended.Industrial relevanceThe ability of health-promoting cultures to survive for at least 12 weeks in orange juice and pineapple juice at commercially critical levels renders them suitable strains for exploitation. Their inclusion may enhance the market potential of these already successful beverages.     

Inactivation of hepatitis A virus,poliovirus and a norovirus surrogate by high pressure processing

Hepatitis A virus (HAV), feline calicivirus (FCV, a surrogate for non-culturable norovirus), and poliovirus (PV), suspended in buffered cell culture media, were treated with pressures ranging from 200 to 600 MPa at ambient temperature for between 30 and 600 s. HAV was inactivated by > 1-log₁₀ tissue culture infectious dose 50% mL^− 1 (TCID₅₀ mL^− 1) and > 2-log₁₀ TCID₅₀ mL^− 1 after 600 s treatment with 300 and 400 MPa, respectively, and was undetectable (> 3.5-log₁₀ TCID₅₀ mL^− 1 reduction) within 300 s treatment with 500 MPa. FCV was inactivated by 3.6-log₁₀ TCID₅₀ mL^− 1 after 120 s treatment with 300 MPa, and was undetectable after 180 s treatment with 300 MPa. PV was the most resistant with little or no substantial reduction in titre after 300 s treatment with 600 MPa. The studies were designed to determine the efficacy of using high pressure to inactivate enteric viruses and generate inactivation data to assist in determining appropriate process criteria for safe shellfish production.Industrial relevanceThe high pressure treatment of raw oysters has proved commercially successful, due in part to a marked increase in the product’s shelf life, yet little alteration of its organoleptic properties. Illnesses from human enteric viruses such as hepatitis A virus and norovirus have traditionally been associated with shellfish consumption, and for this reason, studies have examined the stability of enteric viruses under high pressure. However, kinetic data on enteric virus stability under pressure is needed by processors to better understand the response of viruses throughout the entire treatment time. The kinetic data obtained in this study may be useful for processors wishing to alter high pressure processing conditions to ensure a high quality product in terms of organoleptic and microbiological properties.     

Modeling the inactivation of pectin methylesterase in pineapple puree during combined high-pressure and temperature treatments

The inactivation of pectin methylesterase (PME) in pineapple puree was studied within the domain of 0.1–600 MPa/30–70 °C/1 s–40 min. The combined effect of pressure-build up and decompression, as characterized by pulse inactivation (PI value), was modeled by the artificial neural network (ANN) through a tan-sigmoidal function of target pressure, target temperature, compression, and decompression time. Besides, nth order kinetic model was fitted during the isobaric-isothermal hold period. The extent of pulse inactivation of PME ranged from 15% (200 MPa/30 °C) to 67% (600 MPa/70 °C) and it increased at a higher temperature and/or pressure. The inactivation orders (n) during thermal (0.1 MPa/30–70 °C) and high pressure (100–600 MPa/30–70 °C) treatments were 1.15 and 1.3, respectively. The rate constant (k) ranged within 4.0 to 71.2 × 10⁻³ Uⁿ⁻¹·min⁻¹. A nonlinear model considering the pressure dependency of activation energy, and temperature dependency of activation volume was developed which adequately described the inactivation behavior of PME within the domain.Industrial relevancePectin methylesterase (PME) in the pineapple puree results in a product with a modified texture and consistency that is usually not entertained by the consumer. Therefore, pineapple puree has to be processed to inactivate PME to avoid the cloud loss. Now-a-days, high-pressure processing is being used for fruit products to retain the heat sensitive nutrients. In this sense, a model capable of predicting the exact inactivation behavior of PME during the treatment is very much obligatory for process design. This combined model developed in the study will help the food industry to come-up with the exact pressure-temperature-holding time combination achieving a certain degree of PME inactivation.     

Temperature effect on the biological activity of Bifidobacterium longum CRL 849 and Lactobacillus fermentum CRL 251 in pure and mixed cultures grown in soymilk

The influence of temperature on the growth and biological activity of two probiotic strains (Bifidobacterium longum CRL 849 and Lactobacillus fermentum CRL 251) as pure and mixed cultures in soymilk (SM) were evaluated. Maximum growth was observed at 37°C in both mixed and pure cultures. In a product prepared with the mixed culture (1:1) at 37°C, the amount of lactic acid produced was approximately 55 mmol l⁻¹ after 24 h with a slow production rate (2.8 mmol l⁻¹ h⁻¹); the formation of acetic acid was higher with respect to pure cultures (82.01 mmol l⁻¹ after 24 h), and final pH (24 h) was 5.0. About 85% of the total amount of sugars in SM was reduced, mainly sucrose. Stachyose was reduced (71%) after 4 h of incubation. Maximum activity of alpha-galactosidase (alpha-gal) (13.2 U ml⁻¹) was observed after 6 h. At 37°C the bifidobacterium strain was viable in mixed culture throughout the period assayed. At lower (30°C) or higher (42°C) temperatures, mixed culture showed slower growth and lower acid production in SM but the alpha-gal activity was stimulated at 30°C.     

Free radical-scavenging activity of Aloe vera (Aloe barbadensis Miller) extracts by supercritical carbon dioxide extraction

The free radical-scavenging activities of extracts of Aloe vera of leaf skin by supercritical CO₂ extraction and solvent extraction were determined. An orthogonal array design matrix of L₉ (3⁴) was considered to optimize supercritical carbon dioxide extraction processing at a CO₂ flow rate of 12–36 l h⁻¹, 35–45 MPa and 32–50 °C. The optimum extracted yield of 1.47% was provided at 50 °C 36 l h⁻¹, 35 MPa and 20% of modifier of methanol. These four factors were all demonstrated to be significantly crucial in the supercritical carbon dioxide extraction operation, as two-variable interactions. The extracts of A. vera rind by supercritical carbon dioxide extraction and solvent extracts provided significantly higher free radical-scavenging activities of 33.5% and 39.7%, respectively, than extracts of A. vera gel extracted by ethanol with a free radical-scavenging activity of 14.2%. The inhibition percentage of extracts of A. vera and reference antioxidants followed the decreasing order: Trolox (76.8%) > ethanol extracts of A. vera skin (39.7%) > BHT (35.9%) > the extract of supercritical carbon dioxide extraction (33.5%) >α-tocopherol (25.6%) > ethanol extracts of A. vera pulp (14.2%). Compared to BHT and α-tocopherol, the extracts of A. vera skin, by supercritical carbon dioxide extraction and ethanol, showed stronger antioxidant activities. Components in the rind of A. vera are responsible for the higher antioxidant activity of A. vera extracts.     

The effect of high hydrostatic pressure on the flow behaviour of skim milk–gelatin mixtures

The flow behaviour of aqueous solutions of gelatin, and skim milk–gelatin mixtures treated by high-pressure processing (HPP) were investigated. HPP was carried out at 5 °C for 15 min, at 150 MPa, 300 MPa, 450 MPa and 600 MPa, and the gelatin concentrations were varied from 0 to 1 wt.%. Viscosity measurements showed that the HPP treatment did not affect the flow behaviour of gelatin alone, nor that of the skim milk–gelatin mixtures made with < 0.4 wt.% gelatin. However, at gelatin concentration > 0.4 wt.%, the mixtures treated with 300 and 450 MPa exhibited a peculiar flow behaviour, where at intermediate shear rates the viscosity was higher than that of the non-treated mixture or the mixtures treated at 150 MPa and 600 MPa. Particle size measurements showed that for gelled mixtures (> 0.4 wt.% gelatin) 300 MPa HPP treatment resulted in an increase in the particle size, while at all other pressure treatments (> 150 MPa), a shift in particle size distribution to lower sizes was observed. Confocal microscopy showed that these skim milk–gelatin mixtures were phase-separated with a gelatin continuous phase, this was confirmed by dynamic rheological measurements which showed that qualitatively the viscoelastic properties of the mixtures were the same. A mechanism of the effect of high-pressure treatment on the casein micelle in skim milk–gelatin mixtures is proposed.Industrial relevanceThis fundamental work, dealing with the effect of high pressure on the physicochemical properties skim milk–gelatin mixtures could be relevant to the industry in several ways. Firstly, skim milk–gelatin mixtures are widely used in the dairy industry, particularly in yoghurt manufacture, where gelatine is used as a stabiliser. In addition the application of High Hydrostatic Pressure to such a system is also relevant, as this technology could be used as a substitute to the conventional heat treatment processes. Secondly, an important finding of this study is that under certain conditions of high pressure and gelatine concentration, an increase in viscosity is observed at intermediate shear-rate (between 10 and 100 s^?1). This is highly relevant to Industry if the system requires subsequent pumping. Thirdly, from a sensory view point, this range of shear rates (10 and 100 s^?1) is comparable to that experienced by a food bolus during swallowing. Thus, this effect of high pressure on the viscosity can influence sensory attribute of the skim milk–gelatin food system.     

Effect of thermal and high pressure processing on antioxidant activity and instrumental colour of tomato and carrot purées

Total antioxidant activity, levels of bio-active compound groups and instrumental colour of tomato and carrot purée subjected to high pressure treatment (400–600 MPa/15 min/20 °C) and thermal treatments (70 °C/2 min) were measured. Antioxidant activity in tomato and carrot purée was significantly higher (p < 0.05) than in untreated or thermally processed samples. High pressure treatments at 600 MPa retained more than 90% of ascorbic acid as compared to thermal processing in tomato purées. Heat treatments caused a rapid decrease in ascorbic acid (p < 0.05). Phenolic contents were in general un-affected by thermal or high pressure treatments. Colour parameters were significantly affected (p < 0.05) by thermal and high pressure processing. Principal component analysis (PCA) revealed that the first two components represented 97% and 92% of the total variability in instrumental colour parameters with respect to processing for tomatoes and carrots respectively.Industrial relevanceThis research paper provides scientific evidence of the potential benefits of high pressure processing in comparison to thermal treatments in retaining important bioactive compounds. Antioxidant activity (ARP), ascorbic acid, and carotenoids after exposure to high pressure treatments (400–600 MPa) were well retained. Our results also show that redness and colour intensity of purées were better preserved by high pressure processing than conventional thermal treatment. It would appear from a nutritional prospective, high pressure processing is an excellent food processing technology which has the potential to retain compounds with health properties in foods. Therefore high pressure processed foods could be sold at a premium over their thermally processed counterparts as they will have retained their fresh-like properties.     

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.