Mass transfer dynamics during high pressure brining of chicken breast

The objectives of this study were to investigate the changes in mass transfer, textural properties and water holding capacity of chicken breast when brine treated under different pressures. Chicken breasts were treated for up to 20 min in 4% sodium chloride solution under five pressures: 50, 100, 150, 200, and 300 MPa at 25 ± 1 °C. The results indicated that the total weight and water uptake of the chicken breast increased with increasing pressure up to 150 MPa, and then decreased with further pressure increase up to 300 MPa. Chicken breast samples brined at 150 MPa, with a sodium chloride effective diffusivity value of 2.96 × 10⁻⁸ m²/s, exhibited minimum hardness and maximum water holding capacity. In general, pressure treatment at 150 MPa was found to be the most suitable level for curing based on its higher yield, effective diffusivity and improved texture and water holding capacity.     

Assessing the suitability of polylactic acid flexible films for high pressure pasteurization and sterilization of packaged foodstuff

Effects of high pressure (HP) pasteurization and sterilization processes on the properties of commercial biodegradable polylactic acid (PLA), used as packaging material, have been investigated. HP treatments have been performed at pressures of 200, 500 and 700 MPa on PLA pouches, containing different types of food, i.e. tap water, solid carrots, carrot juice and carrot puree. Process temperature was in the ranges 25–40 and 90–110 °C, respectively for HP pasteurization and HP sterilization.     

Effects of high hydrostatic pressure and varying concentrations of sodium nitrite from traditional and vegetable-based sources on the growth of Listeria monocytogenes on ready-to-eat (RTE) sliced ham

The objective of this study was to determine the effect the source of added nitrite and high hydrostatic pressure (HHP) had on the growth of Listeria monocytogenes on ready-to-eat (RTE) sliced ham. Use of 600 MPa HHP for 3 min resulted in an immediate 3.9–4.3 log CFU/g reduction in L. monocytogenes numbers, while use of 400 MPa HHP (3 min) provided less than 1 log CFU/g reduction. With the 600 MPa HHP treatment, sliced ham with a conventional concentration of sodium nitrite (200 ppm) was not different in L. monocytogenes growth from use with 50 or 100 ppm of sodium nitrite in pre-converted celery powder. Instrumental color values as well as residual nitrite and residual nitrate concentrations for cured (sodium nitrite and nitrite from celery powder) and uncured ham formulations are discussed.     

Quality of selected cheeses fortified with vegetable and animal sources of omega-3

Queso fresco, cheddar, and mozzarella were fortified with omega-3 from flaxseed oil (FO) and microencapsulated fish oil (MFO) at specific stages in cheese-making process. The highest omega-3 retention (8.69 mg/g MFO; 5.08 mg/g FO) was observed in cheddar when added during salting; 50-100 g of cheddar would supply the daily recommended amount of omega-3 needed in diets to prevent cardiovascular disease. Some variations observed in the studied cheeses physicochemical properties were in pH and moisture content, and increased weight (cheddar, around 10 g); changes in weight and moisture could be related to the water-holding capacity of rennet when omega-3 is incorporated. Texture Profile Analysis indicated new texture behavior in cheddar after fortification, showing increased hardness, chewiness and gumminess. Cheeses were stored at 4 °C; after 16 d microbial counts were mostly high (9 log). Sensory evaluation (5-point hedonic scale) showed similar color acceptability for all three cheeses regardless of omega-3 source. However, scores ranged from 2.43 to 3.6 for aroma, the lowest score being for MFO cheddar. Flavor of cheese with added FO was preferred by panelists more than MFO fortified cheese. Overall, omega-3 is an excellent nutrient that can be easily added to cheese with only minor changes.     

The effect of high hydrostatic pressure,sodium nitrite and salt concentration on the growth of Listeria monocytogenes on RTE ham and turkey

Growth of Listeria monocytogenes was evaluated for up to 182 days after inoculation on ready-to-eat (RTE) sliced ham and turkey breast formulated with sodium nitrite (0 or 200 ppm), sodium chloride (1.8% or 2.4%), and treated (no treatment or 600 MPa) with high hydrostatic pressure (HHP). HHP at 600 MPa for 3 min resulted in a 3.85–4.35 log CFU/g reduction in L. monocytogenes. With formulations at similar proximate analyses, one of the evaluation days (day 21) without HHP showed significantly greater growth of L. monocytogenes in ham than in turkey breast, but there were no significant differences on other evaluation days or with HHP. There were no differences in growth of L. monocytogenes due to sodium chloride level. Sodium nitrite provided a small, but significant inhibition of L. monocytogenes without HHP, but addition of sodium nitrite did not significantly affect growth of L. monocytogenes with use of HHP.     

Effect of high pressure/high temperature processing on cell wall pectic substances in relation to firmness of carrot tissue

Thermal processing for food preservation results in undesired softening of fruits and vegetables. To explore the potential of high pressure sterilization in food processing, the effects of combined high pressure/high temperature (HP/HT) treatments on carrot pectic polysaccharides and the related textural properties were investigated and compared with that of samples thermally processed at atmospheric pressure. Disks of fresh carrot (Daucus carota var. Yukon) tissue were subjected to three different treatments (80 °C–0.1 MPa, 100 °C–0.1 MPa and 80 °C–600 MPa) for varying time intervals. Subsequently, the residual texture and microstructural changes of the carrots were evaluated. Alcohol-insoluble residues were prepared from the samples and sequentially fractionated with water, cyclohexane-trans-1,2-diamine tetra-acetic acid (CDTA) and Na₂CO₃ solutions. Thermal treatments at 0.1 MPa caused extensive tissue softening. This was marked by increased cell separation, an increase in water soluble pectin (WSP) paralleled by a decrease in chelator (CSP) and sodium carbonate (NSP) soluble pectin. HP/HT treated carrots showed minimal softening and negligible changes in intercellular adhesion. This was accompanied by a significant reduction in the degree of methyl esterification of pectin, low WSP in contrast to the high CSP and NSP fractions, minor changes in the different pectin fractions during treatment, and a substantial amount of pectin in the fractionation residue. There was a clear difference between HP/HT and thermally processed carrot pectin; HP/HT showing pronounced texture preservation.     

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.     

Evaluation of high pressure (HP) treatment for rapid and uniform pH reduction in carrots

Acidification (pH < 4.6) of marginally low acid foods allows them to be treated like high acid foods and, hence, has the potential to improve quality and reduce energy costs by lowering the severity of processing conditions. The objective of this study was to evaluate high pressure (HP) treatment for rapid and uniform pH reduction of low acid foods using carrot. Three organic acids (citric, malic and glucono-delta-lactone) were used in the study. Conventional acidification tests were carried out at atmospheric pressure at different temperatures (36–48 °C) and different treatment times (0–36 min). HP treatments were given at room temperature (maximum process temperature <32 °C) with different pressures (200–300 MPa) and treatment times (0–14 min). Time dependent acid infusion and the resulting pH reduction were used to evaluate the acidification kinetics. Results showed that the pH reduction rates were described by a first order kinetic model. No significant differences (p > 0.05) in acidification rates were observed between the acidifying agents either in conventional or HP acidification process. Pressure (HP acidification) and temperature (conventional acidification) significantly (p < 0.05) reduced decimal reduction time (D) for pH drop. The associated D values were 2.4–4.4 times higher in conventional (slower) as compared with HP acidification. For conventional acidification, the z values (temperature sensitivity) were 34–44.8 °C and for HP acidification, the z values (pressure sensitivity) were 206–222 MPa. HP acidification provided more rapid and uniform pH reduction as compared to conventional method.     

Comparison of the inactivation kinetics of pectin methylesterases from carrot and peach by high-pressure carbon dioxide

The inactivation of pectin methylesterases (PMEs) from carrot and peach in buffer by high-pressure carbon dioxide (HPCD) at 55 °C was investigated. The two PMEs were effectively inactivated by HPCD, their residual activity (RA) decreasing with increasing pressures. The RA of the two PMEs exhibited a fast decrease firstly and reached a constant after a prolonged treatment time; their inactivation kinetics was adequately modelled by a fractional-conversion model. The non-zero RA(A_∞)of the two PMEs was 6–7%, with increasing pressures the kinetic rate constant, k, increased and the decimal reduction time, D, decreased for the HPCD-labile fraction of the two PMEs. The labile fraction of carrot PME was more susceptible to HPCD than that of peach PME; the activation volume, V_a, and Z_P (the temperature increase needed for a 90% reduction of D) was −1079.37 cm³/mol and 5.80 MPa for carrot PME, and −130.51 cm³/mol and 48.31 MPa for peach PME.     

A note on the relationships between cured-cooked and dry-cured ham processing yields

Right and left hams from 353 pigs slaughtered at around 100 kg body weight were processed into cured-cooked hams and dry-cured hams, respectively. Weights and yields at various stages of each process, carcass lean content and fresh meat quality traits were registered. Technological yield of cured-cooked processing (saleable cooked ham weight/defatted–deboned fresh ham weight) was more closely correlated to ultimate pH (r = 0.51, p < 0.001) than to carcass leanness (r = −0.13, p < 0.05) whereas the reverse situation – r = 0.15 (p < 0.01) and r = −0.62 (p < 0.001), respectively – was found for technological yield of dry-cured processing (saleable dry ham weight/trimmed fresh ham weight). The correlation between the two technological yields was significantly positive but of fairly moderate magnitude (r = 0.36). The correlation between the overall yields (saleable processed ham weight/entire fresh ham weight) of the two processes revealed to be very close to zero (r = −0.01).     

High pressure–temperature degradation kinetics of polyacetylenes in carrots

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

Synergistic action of transglutaminase and high pressure on chicken meat and egg gels in absence of phosphates

The effects of simultaneous application of microbial transglutaminase (MTGase) and high pressure (HP) (500, 700 and 900 MPa/40 °C/30 min), only pressure under the same conditions or heat (75 °C/30 min) were investigated on chicken batters with the addition of egg components and without phosphates. MTGase gels (700 and 900 MPa) showed marked increases in textural parameters compared to gels without enzyme (NE) or those obtained by heat. The addition of enzyme did not show differences between gels obtained at 700–900 MPa; however, gels obtained at 500 MPa were darker and more reddish than those obtained by heat. MTGase gels were more homogeneous and compact. Thermal analysis revealed that pressure levels above 700 MPa caused as much denaturing as did heat. The microstructure and texture of MTGase gels suggest that a higher amount and heterogeneity of crosslinks was produced when meat and egg proteins were treated in the presence of MTGase under specific conditions of pressure.     

Aroma development in high pressure treated beef and chicken meat compared to raw and heat treated

Chicken breast and beef muscle were treated at 400 and 600 MPa for 15 min at 5 °C and compared to raw meat and a heated sample (100 °C for 15 min). Vacuum-packed beef meat with a smaller fraction of unsaturated fatty acids showed better oxidative stability during 14 days of cold storage, as shown by a low steady-state level of hydroperoxide values, than vacuum-packed chicken meat. Accordingly, the critical pressures of 400 MPa and 600 MPa for chicken breast and beef sirloin, respectively, were established. Volatiles released after opening of the meat bags or during storage of open meat bags, simulating consumer behaviour, were measured under conditions mimicking eating. Quantitative and olfactory analysis of pressurised meat gave a total of 46 flavour volatiles, mainly alcohols (11), aldehydes (15), and ketones (11), but all in low abundance after 14 days of storage. Overall, beef meat contained less volatiles and in lower abundance (factor of 5) compared to chicken meat. The most important odour active volatiles (GC-O) were well below the detection thresholds necessary to impart a perceivable off-flavour. Lipid oxidation was significantly accelerated during 24 h of cold storage in both cooked chicken and beef when exposed to oxygen, while the pressurised and oxygen-exposed chicken and beef meat remained stable. Pressure treatment of beef and chicken did not induce severe changes of their raw aroma profiles.     

Rheology and melt characterization of low-fat and full fat Mozzarella cheese made from microfluidized milk

Microfluidization of cheese milk at different temperatures and pressures altered the meltability and rheological properties of Mozzarella cheese. Pasteurized milks, standardized to 1.0 (low-fat (LF)) or 3.2 (full fat (FF)) g fat/100 g milk, heated to 10, 43, or 54 °C, and then microfluidized at pressures of 34, 103, or 172 MPa, were used to manufacture Mozzarella cheese. Cheeses made from nonmicrofluidized milks served as controls. During the hot water step, only control cheeses and cheeses made with milk microfluidized at 10 °C could be stretched while all others had short curds that did not fuse together. Cheese responses to different stresses (heat, compression, torsion, and oscillatory shear) were measured after 1 and 6 weeks of storage. FF cheeses made with the control milks and milks processed at 10 °C/34 MPa or 10 °C/103 MPa were softer and less rigid, and had the lowest visco-elastic properties and the highest meltabilities of all the cheeses. Microfluidization of the cheese milk did not improve the melt or rheology of LF cheeses. Microfluidization of milk with fat in the liquid state at higher pressures resulted in smaller lipid droplets that altered the component interactions during the formation of the cheese matrix and resulted in LF and FF Mozzarella cheeses with poor melt and altered rheology.     

Effect of foliar application of selenium on its uptake and speciation in carrot

Carrot (Daucus carota) shoots were enriched by selenium using foliar application. Solutions of sodium selenite or sodium selenate at 10 and 100 μg Se ml⁻¹, were sprayed on the carrot leaves and the selenium content and uptake rate of selenium were estimated by ICP–MS analysis. Anion and cation exchange HPLC were tailored to and applied for the separation of selenium species in proteolytic extracts of the biological tissues using detection by ICP–MS or ESI–MS/MS. Foliar application of solutions of selenite or selenate at 100 μg Se ml⁻¹ resulted in a selenium concentration of up to 2 μg Se g⁻¹ (dry mass) in the carrot root whereas the selenium concentration in the controls was below the limit of detection at 0.045 μg Se g⁻¹ (dry mass). Selenate-enriched carrot leaves accumulated as much as 80 μg Se g⁻¹ (dry mass), while the selenite-enriched leaves contained approximately 50 μg Se g⁻¹ (dry mass). The speciation analyses showed that inorganic selenium was present in both roots and leaves. The predominant metabolised organic forms of selenium in the roots were selenomethionine and γ-glutamyl-selenomethyl-selenocysteine, regardless of which of the inorganic species were used for foliar application. Only selenomethionine was detected in the carrot leaves. The identity of selenomethionine contained in carrot roots and leaves was successfully confirmed by HPLC–ESI–MS/MS.     

Sensory,physical and chemical characteristics of cooked ham manufactured from rapidly chilled and earlier deboned M. semimembranosus

Effects of rapid chilling of carcasses (at − 31 °C in the first 3 h of chilling, and then at 2–4 °C) and earlier deboning (8 h post-mortem), compared to rapid (till 24 h post-mortem) and conventional chilling (at 2–4 °C, till 24 h post-mortem), on quality characteristics of pork M. semimebranosus and cooked ham were investigated. Quality measurements included pH value, colour (CIEL*a*b* values) and total aerobic count of M. semimebranosus, as well as sensory (colour, juiciness, texture, and flavour), physical (pH value, colour – CIEL*a*b* values and texture – Warner–Bratzler shear and penetration forces) and chemical (protein, total fat, and moisture content) characteristics of cooked ham. The cooked ham was manufactured from pieces of M. semimebranosus with ultimate lightness (CIEL* value) lower than 50. Rapid chilling and earlier deboning significantly increased quantity of M. semimebranosus desirable for cooked ham manufacturing. Earlier start of pork fabrication did not affect important quality characteristics of cooked ham.     

The effect of NaCl-free processing and high pressure on the fate of Listeria monocytogenes and Salmonella on sliced smoked dry-cured ham

NaCl is an important multifunctional ingredient applied in dry-cured ham elaboration. However, its excessive intake has been linked to serious cardiovascular diseases causing a recent increase in the development of reduced salt products. In the present study Listeria monocytogenes and Salmonella, food-borne pathogens which can cross-contaminate post processed products, were spiked with < 100 CFU/g on slices of both standard (S) and NaCl-free processed (F) (elaborated with KCl + potassium lactate instead of NaCl) smoked dry-cured ham. Although L. monocytogenes and Salmonella counts decreased faster in S ham, pathogens were present in both types of non-pressure treated ham during the entire refrigerated storage period (112 days). Pressurisation at 600 MPa for 5 min caused the elimination of both pathogens in S ham after 14 days. In contrast, Salmonella and L. monocytogenes were present in F ham until days 28 and 56, respectively, indicating that the NaCl-free processed dry-cured ham had lower stability than standard smoked dry-cured ham.     

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

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

Antimicrobial effect of κ-carrageenan-based edible film containing ovotransferrin in fresh chicken breast stored at 5 °C

The antimicrobial activity of κ-carrageenan-based film (κCF) containing ovotransferrin (OTf) against Escherichia coli, Salmonella typhimurium, Staphylococcus aureus, and Candida albicans was investigated. The effects of packaging with κCF–OTf on fresh chicken breast were also investigated during storage at 5 °C. The κCF–OTf showed a slight antimicrobial activity against E. coli (diameter of inhibition zone was <2 mm), but the effect was increased synergistically in the presence of 5 mM EDTA (diameter of inhibition zone is 2–5 mm). However, there were only weak inhibitory effects against S. aureus and S. typhimurium (diameter of inhibition zone was <2 mm). The growth of total microbes and E. coli in fresh chicken breast wrapped with κCF showed 1.8 and 2.7 decimal reductions by the addition of 5 mM EDTA or 5 mM EDTA in combination with 25 mg of OTf (P < 0.05), respectively, when compared to that of control at day 7. The chicken breast wrapped with κCF–PS–EDTA was also inhibited the growth of total microbes and E. coli during storage period. However, the addition of either 25 mg of OTf alone or 10 mg of potassium sorbate alone slightly inhibited the growth of microorganisms in chicken breast. Based on the obtained results, the κ-carrageenan-based film containing ovotransferrin combined with EDTA can be used for extending shelf life of fresh chicken breast.     

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.