Modeling the protective effect of aw and fat content on the high pressure resistance of Listeria monocytogenes in dry-cured ham

High pressure processing (HPP) is a promising food preservation technology as an alternative to thermal processing for microbial inactivation. The technological parameters, the type of microorganism, and the food composition can greatly affect the microbicidal potential of HPP against spoilage and pathogenic microorganisms. Presently, the number of available models quantifying the influence of food characteristics on the pathogen inactivation is scarce. The aim of this study was to model the inactivation of Listeria monocytogenes CTC1034 in dry-cured ham, as a function of pressure (347–852 MPa, 5 min/15 °C), water activity (a_w, 0.86–0.96) and fat content (10–50%) according to a Central Composite Design. The response surface methodology, based on the equation obtained with a stepwise multivariate linear regression, was used to describe the relationship between bacterial inactivation and the studied variables. According to the best fitting polynomial equation, besides pressure intensity, both a_w and fat content exerted a significant influence on HP-inactivation of L. monocytogenes. A clear linear piezoprotection trend was found lowering the a_w of the substrate within the whole range of tested pressure. Fat content was included in the model through the quadratic term and as interaction term with pressure, resulting in a particular behavior. A protective effect due to the presence of high fat content was identified for pressure treatments above ca. 700 MPa. At lower pressure, higher inactivation of L. monocytogenes occurred by increasing the fat content above 30%. The results emphasize the relevant influence of intrinsic factors on the L. monocytogenes inactivation by HPP, making necessary to assess and validate the effectiveness of HPP on specific food products and consequently set process criteria adjusted to each particular food product.     

Antioxidant properties of plum concentrates and powder in precooked roast beef to reduce lipid oxidation

Boneless beef roasts (Semimembranosus + Adductor) were injected (20%) with a brine containing (1) no plum ingredient (control), (2) 2.5 or 5% fresh plum juice concentrate (FP), (3) 2.5 or 5% dried plum juice concentrate (DP), or (4) 2.5 or 5% spray dried plum powder (PP). Whole roasts were cooked, vacuum-packaged and stored at <4.0 °C for 10 wk. At 2 wk intervals, evaluations were performed on sliced product to determine vacuum-packaged purge, Allo-Kramer shear force, lipid oxidation (TBARS), color space values, and sensory attributes. All plum ingredients reduced TBARS values and had minimal effects on tenderness, sensory characteristics, color and appearance. Small changes in purge, color values, TBARS and some sensory properties were found during storage. These results indicate that 2.5% FP or DP could be incorporated into precooked beef roasts to reduce lipid oxidation and potentially, warmed-over flavor (WOF).     

Ready-to-eat chickpea flour purée or cream processed by hydrostatic high pressure with final microwave heating

It was shown that high hydrostatic pressure (HHP) induces either starch gelatinization or protein aggregation in chickpea flour (CF) slurries. The aim of this work was to develop a new “ready-to-eat” semi-solid CF product by using HHP at 600 MPa and 50 °C for 15 or 25 min combined with final microwave heating prior to consumption. Eight combinations with a formulation that includes raw or toasted CF, with or without lemon juice, were evaluated using physicochemical (color and protein content, mechanical and rheological behavior), microbiological and sensory analyses. All the CF products were microbiologically safe and stable during two months at refrigerated storage. Mainly, the HHP-treated CF products differed in their texture depending on the CF used, the holding time and the presence of lemon juice, whereby each individual product could be classified as a CF purée or a cream. Moreover, all the formulations showed similar very high sensory quality.Industrial relevanceHHP at 600 MPa and 50 °C, applied for 15 or 25 min to chickpea flour (CF) slurries formulated with raw or toasted CF, water in which chickpeas had been cooked, extra virgin olive oil, soy milk, salt, and, optionally, lemon juice induced starch gelatinization (HHP-induced gelatinization) and microbiological preservation that was sustained for two months in refrigerated storage at 4 °C. After microwave heating prior to consumption, CF products with the rheology and texture characteristic of purée or cream were obtained. The development of these refrigerated gluten-free HHP-induced semi-solid CF products which can be given a quick final heating in a microwave oven would be commercially interesting and foreseeably successful, providing the catering industry and consumers with various new CF products with high protein content, thus also helping to increase consumption of pulses and their contribution to food and nutritional safety.     

Effects of high hydrostatic pressure on physicochemical properties,enzymes activity,and antioxidant capacities of anthocyanins extracts of wild Lonicera caerulea berry

Wild Lonicera caerulea berries were subjected to five different high hydrostatic pressure (HHP) treatments (which resemble the conditions of active component extraction and commercial sterilization). The content of anthocyanins and total phenolics increased by 6.84% and 14.35% (p < 0.05), respectively after treatment at 200 MPa for 5 and 10 min. As HHP increased, a higher loss of active component was observed. The total phenolic contents did not differ significantly between the control and the 400 MPa/20 min treated group (p > 0.05); HHP processing demonstrated better sterilization effect but severely destroyed enzymes. Polyphenol oxidase (PPO) and peroxidase (POD) activity were activated at lower HHP, such as 200 MPa, and decreased at 400–600 MPa. Superoxide dismutase (SOD) maintained good stability under HHP processing. The antioxidant capacities of anthocyanins extracts of wild L. caerulea berry were evaluated by 3 different methods (DPPH assay, oxygen radical absorbance capacity assay, and cellular antioxidant activity assay).Industrial RelevanceFactors such as color, luster, and nutrition often affect consumer choice in food. However, the color and nutrition of foods tend to be destroyed during processing and storage. The demand for healthier and more nutritious food while retaining the color and flavor after processing highlights the need to develop novel and gentler technologies for fruit processing. Recently, high hydrostatic pressure (HHP) technologies have been used in different branches of the food industry. In the present study, the content of active component in blue honeysuckle fruit pulps such as anthocyanins and polyphenols showed tendency to increase and then decrease with increasing pressure at room temperature. Five different HHP treatment groups (resembling the conditions of active component extraction conditions and commercial sterilization) were compared to the control (fresh fruit) and heat-treated group to determine the effects of HHP processing on L. caerulea berry pulps. The aim of this study was to investigate the changes in active component particularly the content and composition of anthocyanins under different high-pressure treatment at room temperature; the color and physicochemical indexes were also analyzed at the same conditions. Low HHP for a long period of time (400 MPa/20 min) demonstrated better results than that with high HHP for a short time (600 MPa/10 min), as indicated by the higher contents of anthocyanins and phenols and stronger antioxidant capacities. Therefore, Low HHP conditions can be used as an auxiliary means of active component extraction. The conditions of HHP processing at low HHP for a long period of time (400 MPa/20 min) can be altered to retain active components during food processing.     

High pressure carbon dioxide combined with high power ultrasound processing of dry cured ham spiked with Listeria monocytogenes

Traditionally, thermal treatments for the inactivation of Listeria monocytogenes in meat products involve undesirable changes of the product quality. In recent years, efforts have been carried out to develop alternative methods to inactivate L. monocytogenes without affecting the product quality attributes. In this context, the feasibility of combined high pressure carbon dioxide and high power ultrasound (HPCO₂ + HPU) treatment to inactivate L. monocytogenes inoculated on the surface of dry cured ham was investigated. Inactivation data were determined at 6, 8 and 12 MPa, as a function of temperature (22, 35, 45 °C) and treatment time (0.5 to 30 min), and compared to those obtained after thermal and HPCO₂ treatments.Color, pH and acidity changes of the samples after both thermal and HPCO₂ + HPU treatments were measured and compared, sensorial profile of the treated samples was evaluated by a sensory panel and shelf-life was determined by a storage study for 4 weeks at 4 °C.The results clearly revealed that HPU alone was not able to induce any microbial inactivation while HPCO₂ + HPU treatment always assured a certain level of inactivation, variable with the process temperature used: the inactivation efficiency was demonstrated higher at 35 °C rather than 22 °C and no enhancement was observed at 45 °C compared to 35 °C. Process conditions of 12 MPa, 35 °C, at 10 W for 5 min assured inactivation to undetectable level of L. monocytogenes spiked on the surface of the product with an initial concentration of about 10⁹ CFU/g. No differences were detected between acidity, pH, color and sensory attributes of the untreated and HPCO₂ + HPU treated dry cured ham surface, while slight differences were measured between the values obtained for the untreated and thermally treated samples. Additionally, the storage study demonstrated that a full microbial and quality shelf-life was assured for 4 weeks at 4 °C. The results obtained may open the doors to the application of such an innovative process at industrial level, in particular to treat ham-type or meat products.     

Antioxidant capacity,phenolic composition and microbial stability of aronia juice subjected to high hydrostatic pressure processing

The aim of this study was to characterize the effect of high hydrostatic pressure (200–600 MPa/15 min) and storage (4 °C/80 days) on aronia juice quality. The total antioxidant capacity, phenolic content and composition were assessed using an updated analytical strategy. Microbial growth was also analyzed following juice storage. Among all the analyzed juices, the untreated aronia juice had the greatest reduction (36%) in total polyphenols over the entire storage period. At the end of the storage period, the pressurized juices demonstrated ABTS and FRAP values higher by 14% and 5% as compared to the untreated juices. The main antioxidants identified in the aronia juice were: chlorogenic acid; neochlorogenic acid; cyanidin 3-galactoside; cyanidin 3-xyloside; cyanidin 3-arabinoside; cyanidin 3-glucoside. Cyanidin 3-glucoside was the most stable compound during juice storage. Microorganism growth in juices pressurized at 400–600 MPa was below the detection limit (< 1 CFU mL^− 1) upon storage.Industrial relevanceAronia berries are rarely consumed fresh since they give off several negative sensory attributes. Multiple health-promoting properties of aronia berries make them a valuable raw material for juice production. However, processing involves pasteurization or hot-filling strongly diminishes the product quality due to the changes in quantity and quality of thermolabile phytochemicals. The objective of this work was to characterize the effect of high hydrostatic pressure on the antioxidant capacity, polyphenol content and composition and microbial stability of aronia juice. Results of this study may be useful for the juice industry commercialize this technology for the development healthy, nonclarified aronia juices with desired level of quality.     

Inactivation of Escherichia coli O157:H7 and Listeria monocytogenes in milk by caprylic acid and monocaprylin

Listeria monocytogenes and Escherichia coli O157:H7 are major foodborne pathogens implicated in various outbreaks involving pasteurized or unpasteurized milk, and various dairy products. The objective of this study was to determine the antibacterial effect of caprylic acid (CA, C_8:0) and its monoglyceride, monocaprylin (MC) on L. monocytogenes and E. coli O157:H7 in whole milk. A five-strain mixture of E. coli O157:H7 or L. monocytogenes was inoculated in autoclaved milk (10⁶ CFU/ml) containing 0, 25, or 50 mM of CA or MC. At 37°C, all the treatments, excepting 25 mm CA, reduced the population of both pathogens by approximately 5.0 log CFU/ml in 6 h. At 24 h of storage at 8°C, MC at both levels and CA at 50 mM decreased L. monocytogenes and E. coli O157:H7, respectively by >5.0 log CFU/ml. At 48 h of 4°C storage, populations of L. monocytogenes and E. coli O157:H7 were decreased to below detection level (enrichment negative) by 50 mm of MC and CA, respectively. Results indicate that MC could potentially be used to inhibit L. monocytogenes and E. coli O157:H7 in milk and dairy products, but sensory studies need to be conducted before recommending their use.     

Considerations for post-lethality treatments to reduce Listeria monocytogenes from fully cooked bologna using ambient and pressurized steam

During processing of ready-to-eat (RTE) deli meats, any secondary processing procedures such as peeling and cutting introduce the distinct possibility of cross-contamination between equipment, personnel, and food. To eliminate or reduce pathogens such as Listeria monocytogenes and ensure food safety, RTE deli meats can be pasteurized prior to or after packaging. In this study, ambient steam in-package pasteurization was compared with pressurized steam prepackaging pasteurization to reduce L. monocytogenes from fully cooked RTE bologna. The bologna (14 cm diameter×1.5 cm thickness) samples were surface-inoculated to contain about 8 log₁₀ of L. monocytogenes. To achieve 2 log reductions for L. monocytogenes, the bologna samples needed to be treated for about 10 s in pressurized steam at 131 °C or for about 2.5 min in ambient steam at 100 °C. The pasteurization time using pressurized steam treatment was about 75–90% shorter than using ambient steam treatment. Pressurized steam treatment may be integrated into a vacuum packaging unit to effectively eradicate L. monocytogenes from RTE meats just prior to sealing the retail packages to further reduce the treatment time, avoid post-treatment recontaminations by pathogens, and improve food safety without detrimentally affecting meat quality.     

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 food spoilage bacteria and Escherichia coli O157:H7 in phosphate buffer and orange juice using dynamic high pressure

This study aimed to evaluate the potential of dynamic high pressure (DHP) technology to inactivate pathogenic and spoilage microflora in orange juice. Escherichia coli O157:H7 ATCC 35150, Lactobacillus plantarum ATCC 14917, Leuconostoc mesenteroides ATCC 23386 and two orange juice isolates: Saccharomyces cerevisiae and Penicillium ssp. were subjected individually to different DHP treatments. The effectiveness of DHP treatment was first evaluated in phosphate buffered saline (PBS) before application in orange juice samples. The inactivation efficacy of DHP depended on the pressure applied and the number of passes. It was more efficient against Gram-negative strains than Gram-positives. Complete inactivation and 5 log reduction of E. coli O157:H7 were achieved in orange juice at 200 MPa after 5 and 3 passes at 25 °C, respectively. Lower inactivation was obtained with Penicillium ssp. (4 log), S. cerevisiae (2.5 log), L. plantarum (2.3 log) and L. mesenteroides (1.6 log). The gathered results revealed the potential of DHP to inactivate all the tested microorganisms and then, it could constitute a promising alternative technology for cold pasteurization of fruit juices.     

A Predictive Modelling Study for Using High Hydrostatic Pressure,a Food Processing Technology,for Protein Extraction

The aim of this study is to fit a response model to one response, extracted protein concentration by using high hydrostatic pressure, a food processing technology, as a function of two particular controllable factors of extraction procedure. These factors are “pressure” (applied in MPa) and the “extraction solvent”. Data were taken from a previously published data, where the minimum and maximum values chosen for pressure were 100 MPa and 300 MPa with a center point of 200 MPa. The solvents were PBS, TCA-Acetone and Tris-HCl. Protein concentration values were the mean values of 3 replicates.Firstly, a regression statistics were conducted by the data mentioned above to identify coefficients for intercept, pressure and solvents. The coefficients for intercept, pressure and solvents were identified as 34.29753333, 0.008442 and 0.85425 respectively with p-values of 0.03 for pressure and 0.10 for solvents.A predictive analysis model was fitted to the protein concentration response by using the predictive analysis model proposed with the analysis conducted.     

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 heat shock on thermal tolerance and susceptibility of Listeria monocytogenes to other environmental stresses

In the present study, Listeria monocytogenes Scott A, V7 and CCRC 14930 were first subjected to heat shock at 45°C for 1 h or at 48°C for 10 min. Thermal tolerance at 55°C and survival of the heat shocked as well as non-heat shocked cells of L. monocytogenes in the presence of 25% NaCl, 0.01% crystal violet, 0.1% H₂O₂, and 18% ethanol were examined.It was found that heat shock response of L. monocytogenes varied with strains, the condition of heat shock treatment and type of subsequent stress. Compared with the non-heat shocked cells, the 45°C-1 h heat shocked cells of strains Scott A and V7 showed an increased survival after exposure to 55°C for 60 min. Meanwhile, survival of the 48°C-10 min heat shocked L. monocytogenes cells, regardless of strain, exhibited no significant difference (p>0.05) with their respective control cells. Generally, heat shocking at 45°C for 1 h increased the tolerance of L. monocytogenes to NaCl, ethanol and crystal violet. On the other hand, heat shocking at 48°C for 10 min although increased the resistance of L. monocytogenes to NaCl reduced its resistance to H₂O₂ and crystal violet.     

Identification and characterization of antioxidant peptides from sweet potato protein hydrolysates by Alcalase under high hydrostatic pressure

Sweet potato protein hydrolysates (SPPH) were generated by Alcalase under high hydrostatic pressure (HHP, 100, 200 and 300 MPa). HHP significantly improved the degree of hydrolysis (DH) and antioxidant activity, and increased the < 3 kDa fraction content of SPPH (P < 0.05). SPPH by Alcalase at 300 MPa for 60 min exhibited the highest DH and antioxidant activity and was separated into three fractions by ultrafiltration. The most active fraction FIII (< 3 kDa) was further separated into fifty four fractions by semi-preparative RP-HPLC and measured using the ORAC assay. In addition, more active fractions were examined by LC–MS/MS, and diverse peptides were identified, matching sequences of Sporamins A and B. To evaluate the structure–activity dependences, twenty sequences were synthesized, of which the antioxidant activity was assessed. Five peptides showed good activity: HDSASGQY ≥ YYMVSA ≥ HDSESGQY ~ YYIVS ~ RYYDPL, with the contribution of His and Tyr.Industrial relevanceThis study will give a novel technique for using industrial waste slurry, a byproduct in the process of sweet potato starch manufacturing, which contains various bioactive components (such as protein, minerals, etc.) since most of them are normally discarded. The present study is focused on assessing the effects of enzymatic hydrolysis by Alcalase under high hydrostatic pressure (HHP) on the release of antioxidant peptides from sweet potato protein (SPP). The results of this work provide a potential application of enzymatic hydrolysis assisted by HHP on the development of ingredients from SPP in functional foods.     

High hydrostatic pressure processing on microstructure of probiotic low-fat yogurt

The effect of milk processing on the microstructure of probiotic low-fat yogurt was studied. Skim milk fortified with skim milk powder was subjected to three treatments prior to innoculation: thermal treatment at 85 °C for 30 min, high hydrostatic pressure at 676 MPa for 5 min, and combined treatments of high hydrostatic pressure (HHP) and heat. The processed milk was then fermented by using two different starter cultures containing Streptococcus thermophilus, Lactobacillus delbrueckii ssp. bulgaricus, Lactobacillus acidophilus, and Bifidobacterium longum. The microstructure of heat-treated milk yogurt had fewer interconnected chains of irregularly shaped casein micelles, forming a network that enclosed the void spaces. On the other hand, microstructure of HHP yogurt had more interconnected clusters of densely aggregated protein of reduced particle size, with an appearance more spherical in shape, exhibiting a smoother more regular surface and presenting more uniform size distribution. The combined HHP and heat milk treatments led to compact yogurt gels with increasingly larger casein micelle clusters interspaced by void spaces, and exhibited a high degree of cross-linking. The rounded micelles tended to fuse and form small irregular aggregates in association with clumps of dense amorphous material, which resulted in improved gel texture and viscosity.     

Supercritical carbon dioxide-treated blood orange juice as a new product in the fresh fruit juice market

The work described here deals with the effectiveness of using high-pressure carbon dioxide treatment (HPCD) to stabilise freshly squeezed blood orange juice. Technical planning of a continuous high-pressure supercritical carbon dioxide pilot system, suitable for development on an industrial scale, was carried out in our lab. To determine the optimal operating conditions (temperature, pressure, and CO₂/juice ratio), three different experimental trials were carried out. The first trial was conducted at 230 bar, 36 ± 1 °C, 5.08 L/h juice flow rate, and 3.91 L/h CO₂ flow rate, corresponding to a g_CO2/g_juice ratio of 0.770. The second trial utilised the same conditions except that the operative pressure was reduced (130 bar). The third trial was carried out at 130 bar, 36 ± 1 °C, 5.08 L/h juice flow rate, 1.96 L/h CO₂ flow rate, corresponding to a 0.385 g_CO2/g_juice ratio. The effects of processing were evaluated by determining physicochemical, antioxidant, and microbiological parameters of the treated juices. In addition, once the best operative parameters had been determined, physicochemical, antioxidant, microbiological and sensory evaluation of fresh blood orange juice stabilised by HPCD treatment was carried out during refrigerated storage of juices at 4 ± 1 °C for thirty days. The results showed that HPCD treatment cannot be considered as an alternative to traditional thermal methods but as a new mild technology for producing a stabilised blood orange juice with a shelf-life of 20 days.Industrial relevanceBlood oranges are the main cultivated varieties of Citrus sinensis (L.) Osbeck in Italy. Freshly squeezed blood orange juice exert a high antiradical and antioxidant activity, due to its rich phenolic profile, but its preservation is usually assured by thermal treatment which affects its nutritional and sensory value. In this study we proposed a “milder” continuous HPCD process suitable for implementation on an industrial scale. The HPCD stabilised juice retains its physicochemical, antioxidant, and sensory properties and could be placed within a new retail framework, namely, that of fresh juices with a shelf-life of 20 days.     

Use of Weibull frequency distribution model to describe the inactivation of Alicyclobacillus acidoterrestris by high pressure at different temperatures

The survival curves of Alicyclobacillus acidoterrestris by high hydrostatic pressure were obtained at two pressures (350 and 450 MPa) and three temperature levels (35, 45 and 50 °C) in BAM broth. Tailing (upward concavity) was observed in all survival curves. Weibull model was fitted to these data and goodness of fit of this model was investigated. Regression coefficients (R²), root mean square (RMSE) values and residual plot strongly suggested that Weibull model produced good fit to the data. A better fit was observed for the data at lower pressure (350 MPa). Shape factors of the Weibull model (n values) for 350 MPa at 35, 45 and 50 °C were significantly different from each other (P < 0.05). Two linear emprical equations were obtained for scale factors (b values) at the temperature values studied for 350 and 450 MPa. Such pressure–temperature inactivation models form the engineering basis for design, evaluation and optimization of high hydrostatic pressure processes as a new preservation technique.     

Modelling of red abalone (Haliotis rufescens) slices drying process: Effect of osmotic dehydration under high pressure as a pretreatment

Simultaneous application of osmotic dehydration and high pressure as a pretreatment to drying process on red abalone (Haliotis rufescens) slices was studied. During drying process the process time was reduced by increasing temperature from 40 to 60 °C along with the application of different pretreatments: high pressure (350 and 550 MPa), pressure time (5 and 10 min), and osmotic solution (10 and 15% NaCl). Effective moisture diffusivity was determined and varied from 4.35 to 9.95 × 10^− 9 m²/s, for both control and pretreated samples (R² ≥ 0.97). The Weibull, Logarithmic and Midilli–Kucuk models were applied to drying experimental data, where Midilli–Kucuk model was found to be the best fitting model. Furthermore, all drying curves were normalized and then modelled by the same three above models showing a R² ≥ 0.96. As to energy consumption and efficiency values for drying processes were found to be in the range of 777–1815 kJ/kg and 8.22–19.20%, respectively. Thus, knowledge on moisture transfer kinetics, energy consumption and data normalization, is needed to manage and control efficiently drying process under different pretreatment conditions.Industrial relevanceThis article deals with the mass transfer modelling and energy consumption during simultaneous high hydrostatic pressure treatment and osmotic dehydration as a pretreatment to drying process of abalone slices. Water and salt transfer during this combined process was satisfactorily simulated with the Midilli–Kucuk model. Results indicated that application of this combined innovative technology improved abalone slices dehydration rates compared to atmospheric pressure operation resulting in a dried abalone with intermediate moisture content ready to be used as input material of further processes. Furthermore, the different energetic features were determined in order to realize the importance of the changes that can influence to alter process time.     

Antimicrobial activity of lactic acid bacteria against Listeria monocytogenes on frankfurters formulated with and without lactate/diacetate

Contamination by Listeria monocytogenes has been a constant public health threat for the ready-to-eat (RTE) meat industry due to the potential for high mortalities from listeriosis. Lactic acid bacteria (LAB) have shown protective action against various pathogenic bacteria. The aim of this study was to evaluate the antilisterial activity of a combination of three LAB strains (Lactiguard®) on L. monocytogenes. The combination of the LAB was inhibitory to L. monocytogenes inoculated onto frankfurters not containing lactate/diacetate after 8 weeks of refrigerated storage (0.6 log reduction compared to L. monocytogenes only control), and when a cell free extract (CFS) of the LAB was added with LAB even more inhibition was obtained (1.2 log reduction compared with L. monocytogenes only). In frankfurters containing lactate/diacetate the LAB and the LAB plus CFS were more effective in reducing growth of L. monocytogenes after 8 weeks of refrigerated storage (2 and 3.3 log reductions respectively).     

Reduction effect of the selected chemical and physical treatments to reduce L. monocytogenes biofilms formed on lettuce and cabbage

As people shift their attention away from unhealthy foods, healthy fresh produce has become popular. However, fresh produce has contributed to many outbreaks of Listeria monocytogenes, which can form a mature biofilm within 24 h. Recent control strategies have proved ineffective in ensuring safe food production. This study focuses on L. monocytogenes biofilms formed on lettuces and cabbages using a viable plate count method and field emission electron microscopy. We investigated the reduction efficacy of treatment with 200 parts per million (ppm) chlorine, 2% each of citric, lactic, and malic acids, 32 Hz ultrasonication (US), 390 mJ/cm² ultraviolet-C (UV-C), or 750 mJ/cm² cold oxygen plasma (COP) on L. monocytogenes biofilms. Following treatment, the quality of the vegetables was analyzed with standard procedures. UV-C and COP showed the best CFU reduction, regardless of the nature of the vegetable surface, while US failed to produce any significant reduction (P > 0.05). Furthermore, chemical treatments reduced count by < 1 log colony forming unit (CFU)/cm² on lettuces, whereas a > 2 log reduction was observed on cabbages. The effect of chemical treatment largely depended on the particular vegetable, while UV-C and COP achieved high reduction regardless of the vegetable, and had no effect on quality. We, therefore, speculate that UV-C and COP show promise in overcoming L. monocytogenes biofilms on food produce.