Alkaline phosphatase and microbial inactivation by pulsed electric field in bovine milk

The effects of pulsed electric field (PEF) treatments at field intensities of 25–37 kV cm^− 1 and final PEF treatment temperatures of 15 °C and 60 °C on the inactivation of alkaline phosphatase (ALP), Total Plate Count (TPC), Pseudomonas and Enterobacteriaceae counts were determined in raw skim milk. At 15 °C, PEF treatments of 28 to 37 kV cm^− 1 resulted in 24–42% inactivation in ALP activity and < 1 log reduction in TPC and Pseudomonas count, while the Enterobacteriaceae count was reduced by at least 2.1 log units to below the detection limit of 1 CFU mL^− 1. PEF treatments of 25 to 35 kV cm^− 1 at 60 °C resulted in 29–67% inactivation in ALP activity and up to 2.4 log reduction in TPC, while the Pseudomonas and Enterobacteriaceae counts were reduced by at least 5.9 and 2.1 logs, respectively, to below the detection limit of 1 CFU mL^− 1. Kinetic studies suggested that the effect of field intensity on ALP inactivation at the final PEF treatment temperature of 60 °C was more than twice that at 15 °C. A combined effect was observed between the field intensity and temperature in the inactivation of both ALP enzyme and the natural microbial flora in raw skim milk.Industrial relevanceMilk has been pasteurised to ensure its safety and extend its shelf life. However, the need for retaining heat-sensitive nutrient and sensory properties of milk has resulted in interest in the application of alternative technologies. The results of the current study suggest that PEF as a non-thermal process can be employed for the treatment of raw milk in mild temperature to achieve adequate safety and shelf life while preserving the heat-sensitive enzymes, nutrients and bioactive compounds.     

Evaluation of pulsed electric field and minimal heat treatments for inactivation of pseudomonads and enhancement of milk shelf-life

Pulsed Electric Field (PEF) treatment of milk provides the opportunity to increase the shelf-life of fresh milk for distribution to distant markets. PEF treatments were evaluated in sterile (UHT) milk to determine the inactivation of added spoilage Pseudomonas isolates and the subsequent gains in microbial shelf-life (time taken to reach 10⁷ CFU mL^− 1). Little inactivation of Pseudomonas was achieved at 15 or 40 °C compared with 50 or 55 °C. The greatest inactivation (> 5 logs) was achieved by processing at 55 °C with 31 kV cm^− 1 (139.4 kJ L^− 1). Heat treatment at the application temperature without PEF treatment caused minimal inactivation of Pseudomonas (only 0.2 logs), demonstrating that the inactivation of the Pseudomonas was due to the PEF treatment rather than the heat applied to the milk. At added Pseudomonas levels of 10³ and 10⁵ CFU mL^− 1, the microbial shelf-life of PEF-treated milk was extended by at least 8 days at 4 °C compared with untreated milk. The total microbial shelf-life of the PEF-treated milk was 13 and 11 days for inoculation levels of 10³ and 10⁵ CFU mL^− 1 respectively. The results indicate that PEF treatment is useful for the reduction of pseudomonads, the major spoilage bacteria of milk.Industrial relevancePseudomonads are the major psychrotrophic spoilage microflora of refrigerated, stored HTST pasteurised milk. Long-life (UHT) products are an important component of milk sales in South-East Asia, but in recent years there has been an increasing demand for less processed milk products with extended shelf-life. The recent practice of shipping fresh bulk milk from Australia to South-East Asian countries has necessitated additional heat treatment prior to export and on arrival, to achieve the required shelf-life. Pulsed electric field treatment of HTST milk, applied alone or in combination with mild heat under optimised conditions, offers the opportunity of shelf-life extension, while limiting the reduction in quality attributes of milk associated with more severe additional heat treatments.     

Modeling the inactivation kinetics of fruit bromelain in pineapple during high-pressure and thermal treatments

The stability of fruit bromelain (FBM) in pineapple pulp was studied within a high-pressure domain of 0.1–600 MPa/30–70 °C/1 s–30 min. The pulse effect was quantified as a function of pressure, temperature, pressure build-up and decompression times. A maximum of 60% reduction in FBM activity was obtained after a single pulse of 600 MPa/70 °C. Upon applying nth order model, the obtained reaction order (n) for thermal (0.1 MPa/30–70 °C) and high-pressure (100–600 MPa/30–70 °C) inactivation was 1.1 and 1.2, respectively. The inactivation rate constant (k) ranged from 1.2 to 45.0 × 10^− 3 U^n − 1 min^− 1. The activation energy was nonlinearly dependent on pressure (P); whereas, the activation volume was linearly related to temperature (T). The nonlinear dependence of k on P and T was modeled by an empirical equation. The D-values obtained from the empirical model appeared to be more realistic than those from the log-linear kinetics.Industrial relevancePineapple fruit bromelain (FBM) has numerous health benefits and therapeutic effects. It is a protease enzyme that helps in digestion. Processing of pineapple pulp needs attention towards retaining the maximum FBM activity in it. A detailed kinetic study of FBM within a broad range of pressure–temperature–time domain will help in designing a high-pressure process for the pineapple pulp with respect to its bromelain stability.     

Comparison of the effect of pulsed electric field or high voltage electrical discharge for the control of sweet white must fermentation process with the conventional addition of sulfur dioxide

The present work discusses the efficiency of pulsed electrical treatments for the inactivation of yeasts. The application of pulsed electric fields (PEFs) and high voltage electrical discharges (HVEDs) as alternatives to sulfites, which are used as anti-microbial to stop the fermentation of sweet white wine, was investigated. The influence of sulfite concentration (from 0 mg·L^− 1 to 500 mg·L^− 1), PEF (from 4 kV·cm^− 1 to 20 kV·cm^− 1; from 0.25 ms to 6 ms) and HVED (40 kV/cm; 1 ms or 4 ms) treatments on the inactivation of total yeasts and non-Saccharomyces yeasts was determined. The addition of SO₂ (250 mg·L^− 1) resulted in 8 log total yeast reduction. The maximum yeast inactivation obtained with PEF and HVED was respectively 3 and 4 logs. The use of SO₂, HVED and PEF allows decreasing the non-Saccharomyces yeast level by 7, 5 and 4 logs respectively. However, the wine browning was less pronounced for the samples treated by PEF in comparison with HVED and SO₂ treatments. PEF seems to be the most suitable alternative technique to sulfite addition.     

Effect of thermosonication,pulsed electric field and their combination on inactivation of Listeria innocua in milk

The impact of thermosonication (TS) and pulsed electric field (PEF), individually and combined, on the survival of Listeria innocua 11288 (NCTC) in milk was investigated. TS (400 W, 160 s) without pre-heating reduced L. innocua by 1.2 log₁₀ cfu mL^?1, while shorter treatment times produced negligible inactivation, suggesting TS to be a hurdle rather than an effective standalone treatment. PEF (30 and 40 kV cm^?1, 50 μs) at 10 °C caused a reduction of L. innocua of 1.1 and 3.3 log cycles, respectively. The highest field strength (40 kV cm^?1) combined with TS (80 s) led to 6.8 log₁₀ cfu mL^?1 inactivation. Milk pre-heated to 55 °C (over 60 s) prior to TS followed by PEF (30 and 40 kV cm^?1) showed inactivation between 4.5 and 6.9 log₁₀ cfu mL^?1, the latter being comparable (P > 0.05) with thermal pasteurisation. The data indicate that TS followed by PEF represents a valid alternative for L. innocua inactivation in milk.     

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.     

Survival of Listeria monocytogenes in Galotyri,a traditional Greek soft acid-curd cheese,stored aerobically at 4°C and 12°C

Galotyri is a traditional Greek soft acid-curd cheese, which is made from ewes’ or goats’ milk and is consumed fresh. Because cheese processing may allow Listeria monocytogenes post-process contamination, this study evaluated survival of the pathogen in fresh cheese during storage. Portions (0.5 kg) of two commercial types (<2% salt) of Galotyri, one artisan (pH 4.0±0.1) and the other industrial (pH 3.8±0.1), were inoculated with ca. 3 or 7 log cfu g⁻¹ of a five-strain cocktail of L. monocytogenes and stored aerobically at 4°C and 12°C. After 3 days, average declines of pathogen's populations (PALCAM agar) were 1.3–1.6 and 3.7–4.6 log cfu g⁻¹ in cheese samples for the low and high inocula, respectively. These declines were independent (P>0.05) of the cheese type or the storage temperature. From day 3, however, declines shifted to small or minimal to result in 1.4–1.8 log cfu g⁻¹ of survivors at 28 days of storage of all cheeses at 4°C, indicating a strong “tailing” independent of initial level of contamination. Low (1.2–1.7 log cfu g⁻¹) survival of L. monocytogenes also occurred in cheeses at 12°C for 14 days, which were prone to surface yeast spoilage. When ca. 3 log cfu g⁻¹ of L. monocytogenes were inoculated in laboratory scale prepared Galotyri of pH ≅4.4 and ≅3% salt, the pathogen died off at 14 and 21 days at 12°C and 4°C, respectively, in artisan type cheeses fermented with the natural starter. In contrast, the pathogen survived for 28 days in cheeses fermented with the industrial starter. These results indicate that L. monocytogenes cannot grow but may survive during retail storage of Galotyri despite its low pH of or slightly below 4.0. Although contamination of Galotyri with L. monocytogenes may be expected low (<100 cfu g⁻¹) in practice, that long-term survival of the pathogen in commercial cheeses was shown to be unaffected by the artificial contamination level (3 or 7 logs) and the storage temperature (4°C or 12°C), which should be a concern.     

Effect of ultrasound on the mass transfer and physical changes in brine bell pepper at different temperatures

Mass transfer and physical attributes of red bell pepper were evaluated. Pepper strips were placed into brine of constant concentration at different temperatures (25–55 °C) with immersion times ranging from 15 to 480 min with and without ultrasound treatment. Diffusion coefficients were evaluated for calcium, sodium, citric acid, soluble and total solids, impregnation and water loss. Firmness, kinetic coefficients and color were determined for each treatment. Ultrasound increased the uptake of solutes (p < 0.05) with the exception of calcium, sodium ions, and acidity, where diffusion coefficients did not significantly differ among treatments. Loss of water, total and soluble solids in tissue significantly increased at 55 °C with 47 kHz, with diffusion coefficients of 13.23 × 10⁻¹⁰ m²/s, 7.26 × 10⁻¹⁰ m²/s and 14.42 × 10⁻¹⁰ m²/s, respectively. These increases may be attributed to increased cell wall permeability, facilitating transport of water and solute, as evidenced by product firmness, where ultrasound treatments had a negative effect on firmness.     

Hard surfaces decontamination of enteropathogenic and Shiga toxin-producing Escherichia coli using bacteriophages

Three Myoviridae phages (DT1, DT5 and DT6) specific for pathogenic Escherichia coli were studied, either individually or as cocktails, for their lytic activity on in vitro challenge tests. Also, cocktail ability to reduce artificial contamination on hard surfaces (glass coverslips and stainless steel coupons) by three pathogenic Escherichia coli strains (EPEC920, non-O157 STEC ARG4827 and O157:H7 STEC464) was tested. Assays of phage stability during refrigerated storage showed that the three phages evaluated retained a high viability after two months at 4 °C. Challenge tests showed high reductions in viable cells, of up to 6.4 log CFU ml^− 1, for all tested strains at 37 °C. Efficiency was somewhat lower at 4 °C, though biocontrol levels were still good, reaching values of up to 3.8 log CFU ml^− 1. Considering only results obtained at 37 °C, phage cocktails produced the highest reduction in most cases. Treatments with phage cocktails produced complete inactivation (ca. 5–6 log CFU ml^− 1) of EPEC920 and O157:H7 STEC464 on glass coverslips, and of EPEC920, non-O157 STEC ARG4827 and O157:H7 STEC464 on stainless steel coupons, at both temperatures (4 °C and 37 °C) and multiplicity of infection (ca. 10³ and 10⁷) tested. However, some strains not detected at 3 h were sometimes detected at 24 h, and inactivation of non-O157 STEC ARG4827 on glass coverslips was never accomplished; viable cell reductions in all these cases ranged from 1.2 to 5.4 log CFU ml^− 1. Our results suggest that lytic phages, either individually or as a cocktail, may be useful for reducing contamination on hard materials used in food processing surfaces. To our knowledge, this is the first study focused on the use of bacteriophages to reduce contamination of food processing surfaces by EPEC and non-O157 STEC strains.     

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.     

Salmonella typhimurium resistance on pulsed electric fields associated with membrane fluidity and gene regulation

Effects of different growth temperatures on cytoplasmic membrane fluidity and phospholipids phase transition temperature (T_m) of Salmonella typhimurium and resistance to pulsed electric field (PEF) inactivation, as well as the expression of stress-related genes and fatty acid biosynthesis-associated genes were investigated. Results indicated that the PEF resistance of S. typhimurium increased as growth temperature increased. S. typhimurium cultivated at 10 °C exhibited the lowest PEF resistance with the reduction of 4.23 log₁₀ CFU/mL, while the reduction of 2.10 log₁₀ CFU/mL was found in S. typhimurium cultivated at 45 °C under the same PEF treatment, due to the up-regulation of the expression of fabA gene, which was characterized by the lowest T_m of membrane phospholipids and the greatest membrane fluidity. Although the expression of alternative sigma factors were altered by growth temperature, these genes were not essential for S. typhimurium to develop PEF resistance, suggesting that the PEF resistance modified by growth temperature could be caused by alterations in membrane fluidity.Industrial relevancePulsed electric fields (PEF) treatment has been widely applied in nonthermal pasteurization and increasingly focused on synergistic combinations with other techniques such as thermal treatment, sonication and antibacterial agents to improve the efficacy of PEF to inactivate micro-organisms. Our results indicated that S. typhimurium cultivated at relatively lower temperature was easily inactivated by PEF, due to the up-regulation of the expression of fabA gene, which was characterized by the lowest phase transition temperature of cytoplasmic membrane phospholipids and the greatest membrane fluidity. Therefore, the underlying mechanism of alterations in PEF resistance of S. typhimurium induced by growth temperature was explored to achieve better understanding of microbial inactivation by PEF.     

Time–temperature study of the kinetics of migration of DPBD from plastics into chocolate,chocolate spread and margarine

Migration of low molecular weight substances into foodstuffs is a subject of increasing interest and an important aspect of food packaging because of the possible hazardous effects on human health.The migration of a model substance (diphenylbutadiene) from low-density polyethylene (LDPE) was studied in foodstuffs with high fat contents: chocolate, chocolate spread and margarines (containing 61% and 80% fat).A simplifying mathematical model based on Fick’s diffusion equation for mass transport processes from plastics was used to derive effective diffusion coefficients which take also kinetic effects in the foods into account and to determine partition coefficients between plastic and food. With this model migration levels obtainable under other storage conditions can be predicted. The effective diffusion coefficients for both margarines stored at 5 °C (3.0–4.2 × 10⁻¹⁰ cm² s⁻¹) and at 25 °C (3.7–5.1 × 10⁻⁹ cm²  s⁻¹) were similar to each other, lower than for chocolate spread stored at 5 °C (9.1 × 10⁻¹⁰ cm² s⁻¹) and higher than the diffusion coefficient for chocolate stored at 25 °C (2.9 × 10⁻¹⁰ cm² s⁻¹). Good agreement was found between the experimental and the estimated data, allowing validation of this model for predicting diffusion processes in foodstuffs with high fat contents.     

Effect of freezing under electrostatic field on selected properties of an agar gel

The objective of this study was to investigate the effects of electrostatic freezing on the quality attributes of freeze-thaw agar gel. Agar gels were frozen under static electric field 0–5.8 × 10⁴ V m^− 1 at − 20 °C. Freezing rate and energy consumption were monitored during the freezing process and microstructures of the formed ice crystals were also analyzed by light microscopy techniques. Agar gel quality changes (syneresis and texture) were evaluated after thawing the frozen samples at + 4 °C. Results showed that the energy used by a DC high voltage generator was negligibly small as compared to the energy consumption by a freezer, and the freezing rate was not significantly influenced by electrostatic freezing (ESF). ESF also reduced the size of ice crystals but did not cause obvious changes in syneresis and texture of the samples.Industrial relevanceThe effects of electrostatic field freezing on the quality attributes of agar gel have been investigated. The results showed that the electrostatic freezing can be used as a potential tool to improve the microstructure of foodstuffs during freezing.     

Microbiological conditions of moisture-enhanced pork before and after cooking

Substantial numbers of aerobic bacteria but few coliforms or Listeria spp. and no Escherichia coli were recovered from both swab samples and brines circulated in cleaned equipment used for injecting pork loins. After meat was processed for 30 or 60 min, the numbers of aerobic bacteria in brines had increased by >1 log unit, to about 4.5 log cfu ml⁻¹, but coliforms were <2 and E. coli and Listeria spp. were <1 log cfu ml⁻¹. The numbers of bacteria on the surfaces of pork loins before and after injection of the meat were similar. No bacteria were recovered from the deep tissues of the uninjected meat, but aerobic bacteria were recovered at log-mean numbers of 2.1 log cfu g⁻¹ and coliforms at log-total numbers of 1.2 log cfu 25 g⁻¹ from 25 samples of deep tissues of injected meat. Aerobic bacteria were recovered at log total numbers of 1.0 log cfu 25 g⁻¹ from 25 samples of injected pork cooked to a central temperature of 61 °C, but no bacteria were recovered from the deep tissues of meat cooked to 70 °C. The findings suggest that moisture-enhanced pork cooked to a medium rare condition can be microbiologically safe.     

Developing an antimicrobial packaging of ready-to-eat pomegranate arils based on vapors of brandy or distillery ethanol

Despite the increasing pomegranate consumption, the ready-to-eat (RTE) arils are highly perishable and this negatively impacts their commercialization. Nowadays, mild pre-packaging decontamination interventions (washing with sanitizing agents or exposure to ultraviolet light) in sequence or not with modified atmospheres packaging technologies are applied. Even though, the latter combination of methods provides them a shelf-life of 10–14 days at cold storage, several negative effects have been also reported (i.e., degradation of anthocyanins). Thus, the aim of the study was to evaluate the effect of alternative, mild antimicrobials such as the vapors of distillery ethanol and brandy on microbial, physical, textural, sensorial, and multispectral imaging attributes of RTE arils during storage at different temperatures in perforated bags. Lactic acid bacteria (LAB) and yeasts/moulds were the dominant spoilage microbiota of RTE arils, regardless of storage temperature and antimicrobial. Vapors produced by both volatile antimicrobials significantly inhibited (p < 0.05) the growth of LAB and yeasts/moulds, at all storage temperatures. For instance, at 4 °C, when population of TVC on controls was 6.9 log CFU g^− 1 (day 23), the respective counts on arils treated with distillery ethanol or brandy followed the order: 4.9 log CFU g^− 1 (1 mL of ethanol) > 3.9 log CFU g^− 1 (1 mL of brandy) > 2.2 log CFU g^− 1 (2 mL of ethanol) > 1.2 log CFU g^− 1 (2 mL of brandy). Moreover, arils exposed to distillery ethanol and brandy vapors showed lower weight loss (%) compared to controls, while the firmness was reduced, regardless of treatment and storage temperature. Color measurements and evaluation of multiple sensory attributes revealed that arils exposed to brandy vapors showed more intense red color and look fresher compared to controls for longer storage time. The latter observation was also validated by multispectral image analysis, since the results suggested that arils packaged with distillery ethanol or brandy maintained their anthocyanin and carotenoids content at higher levels than controls, at 4 °C. Thus, such preservation methods may open new perspectives on mild antimicrobial packaging in order to extend shelf-life of perishable minimally processed fruits, like pomegranate RTE arils.     

Effect of ohmic heating on texture,microbial load,and cadmium and lead content of Chilean blue mussel (Mytilus chilensis)

The effect of ohmic heating (OH) on the texture, microbial load, and cadmium (Cd) and lead (Pb) content was evaluated in Chilean blue mussel (Mytilus chilensis) at shucking and subsequent canning. Mussel samples were processed by OH and blanching (BLAN) at 50 ± 1 °C, 70 ± 1 °C and 90 ± 1 °C for shucking and then canning at 115 °C for 20 min. The Cd and Pb content in fresh mussels was 2.47 ± 0.18 μg g^− 1 and 5.26 ± 0.55 μg g^− 1 dry weight (dw). The greatest reduction in Cd content was reached at 90 ± 1 °C by OH with 1.67 ± 0.06 μg g^− 1 (dw) and 1.69 ± 0.08 μg g^− 1 (dw) by BLAN. At the same temperature, the Pb content was reduced to 4.18 ± 0.24 μg g^− 1 dw for OH and 4.14 ± 0.30 μg g^− 1 dw for BLAN. The cutting strength of fresh samples (21.35 ± 2.44 N) significantly decreased in samples processed by OH (15.65 ± 1.36 N) at 90 ± 1 °C compared with BLAN samples (20.41 ± 3.16 N) at the same temperature. The initial mean count for mesophilic aerobic microorganisms and Enterobacteriaceae was 3.8 log cfu/g and 2.5 log cfu/g, respectively. The mesophilic aerobic microorganism count was reduced by 1.7 logarithmical units, while Enterobacteriaceae counts were reduced to undetectable levels by OH at 90 ± 1 °C.Industrial relevanceHigh temperature short time (HTST) processes rely on rapid convection heat transfer and are thus well suited to liquid foods. But, they are, however, limited in application to particulates since, for particles more than a couple of millimeters thick, the processing time is insufficient for heat to transfer to the center to give sterility. Ohmic heating is an emerging technology and very promising in food industries. It is a thermal process in which heat is generated internally in food and acts as a resistance to the flow of alternating electric current. This type of treatment prevents overheating by producing less deterioration in food components. It is a rapid procedure that allows food to conserve its natural properties; microorganisms and enzymes are also inactivated. The purpose of the present work was to evaluate the effect of Ohmic heating on mechanical properties, microbial load, Cd and Pb content in the opening and subsequent canning of Chilean blue mussel (Mytilus chilensis). This information could be used for the seafood industries in order to improve thermal heating processes in mussels.     

Influence of relative humidity on carbon dioxide sorption in wheat gluten films

The influence of relative humidity (RH) on carbon dioxide sorption at 10⁵ Pa in wheat gluten films (WGF) was investigated in the range of 0–96% RH at 25 °C. The amount of water sorbed by these protein based films reached up to 60% of the dry weight at 96% RH. Carbon dioxide sorption increased with water content, ranging from 2.8 × 10⁻⁴ to 1.9 × 10⁻² mol Pa⁻¹ m⁻³ respectively at 0% and 96% RH. This behavior was tentatively explained on the grounds that sorbed water enhanced carbon dioxide accessibility to protein active sorption sites. The dependence of both the solubility and the diffusivity coefficients of CO₂ and O₂ on WGF water content explains the very good permselectivity of these films observed at high RH values (22 at 93% RH and 25 °C).     

A comparative study of polyphenoloxidases from taro (Colocasia esculenta) and potato (Solanum tuberosum var. Romano)

Taro (C. esculenta) is a staple food in many tropical regions. A comparative study of crude polyphenoloxidases from taro (tPPO) and potatoes (pPPO) was carried out to provide information useful for guiding food processing operations. Crude PPO was prepared by cold acetone precipitation using ascorbic acid as antioxidant. The PPO content of taro acetone powder was 770±17 units (mg protein)⁻¹ as compared with 3848±180 units (mg protein)⁻¹ in potato acetone powder. The pH-activity optimum was pH 4.6 for tPPO and pH 6.8 for pPPO. Both enzymes retained >80% activity after incubation at pH 4.5–8 but there was rapid activity loss at pH < 4. The temperature-activity optimum (T_opt) was 30°C for tPPO and 25°C for pPPO with 75 and 27% of their respective maximum activity retained at 60°C. Both tPPO and pPPO were irreversibly inactivated by 10 min heating at 70°C. The activation enthalpy (ΔH^#) and activation entropy (ΔS^#) for tPPO heat-inactivation were 87.4 (±0.1) kJ mol⁻¹ and −56.2 (±4) J mol⁻¹ K⁻¹, respectively. For pPPO, ΔH^# was 59.1 (±0.1) kJ mol⁻¹ whilst ΔS^# was −141 (±4) J mol⁻¹ K⁻¹. The apparent substrate specificity was established from values V_max/K_m as: 4-methylcatechol>chlorogenic acid>dl-dopa>catechol>pyrogallol> dopamine>>caffeic acid for tPPO. There was no detectable activity towards caffeic acid. The substrate specificity for pPPO was: 4-methylcatechol>caffeic acid>pyrogallol>catechol>chlorogenic acid >dl-dopa>dopamine. According to the order of inhibitor effectiveness (sodium metabisulphite>ascorbic acid>NaCl≈ (EDTA), there was a significant lag-phase before increases occurred in the absorbance at 420 nm. Preincubation of PPO with inhibitors increased the extent of inhibition, indicating a direct effect on the structure of the enzyme.     

The inactivation of Listeria monocytogenes by pulsed electric field (PEF) treatment in a static chamber

An experimental analysis of the effect of pulsed electric field (PEF) energy on the inactivation of Listeria monocytogenes was conducted using a custom-designed static chamber and a gel suspension medium for treatment. This allowed PEF energy to be delivered to the suspension under near isothermal conditions. The effects of variations in the number of pulses (5–50 pulses), electric field strength (15–30 kV/cm), temperature (0–60°C) and media bases (water and skim milk) on the inactivation of L. monocytogenes were examined. At temperatures less than 50°C a maximum of 1 log reduction was obtained for L. monocytogenes regardless of pulse number or electric field strength within the ranges examined. In skim milk no reduction occurred. At 50°C and 55°C synergy between PEF and thermal energy was observed. The experimental approach separated the contribution of PEF and thermal energy to total kill and thus allowed this synergy to be quantified. At 55°C the kill due to PEF energy increased to 4.5 logs with another 4.5 logs reduction attributable to thermal energy. It appears that under the conditions of this study PEF alone has a very limited effect on the reduction of L. monocytogenes. However, the addition of thermal energy not only contributed to the kill, but also increased the susceptibility of L. monocytogenes to PEF energy.     

Partial renneting of pasteurised bovine milk: Casein micelle size,heat and storage stability

The effects of partial renneting at low temperature on the casein micelle (CM) size and the storage stability of milk were investigated. Low chymosin concentrations (≤ 0.03 IMCU mL^− 1) was applied to pasteurised skim milk at 4 °C and enzyme activity was terminated by thermal application at 60 °C/3 min and 85 °C/30 min, referred to as low heat (LHT) and high heat (HHT) treatment milk, respectively. The addition of rennet with concentrations of 0.01, 0.02 and 0.03 IMCU mL^− 1 for 15 min resulted in κ-casein hydrolysis of 10, 20 and 25%, respectively. Moreover, mean CM size of milk was reduced by up to 10 nm. For LHT milk, the renneted micelles appeared to be stable for up to 17 days, especially in response to the application of 0.01 IMCU mL^− 1 and at a storage temperature of 4 °C. Severe heating at 85 °C/30 min to inactivate the enzyme caused an increase in CM size.