Antimicrobial activity of 405 nm light-emitting diode (LED) in the presence of riboflavin against Listeria monocytogenes on the surface of smoked salmon

This study investigated the antimicrobial activity of 405 nm light-emitting diode (LED) with and without riboflavin against Listeria monocytogenes in phosphate buffered saline (PBS) and on smoked salmon at different storage temperatures and evaluated its impact on food quality. The results show that riboflavin-mediated LED illumination in PBS 25 °C significantly inactivated L. monocytogenes cells by 6.2 log CFU/mL at 19.2 J/cm², while illumination alone reduced 1.9 log CFU/mL of L. monocytogenes populations at 57.6 J/cm². L. monocytogenes populations on illuminated smoked salmon decreased by 1.0–2.2 log CFU/cm² at 1.27–2.76 kJ/cm² at 4, 12, and 25 °C, regardless of the presence of riboflavin. Although illumination with and without riboflavin caused the lipid peroxidation and color change in smoked salmon, this study demonstrates the potential of a 405 nm LED to preserve the smoked salmon products, reducing the risk of listeriosis.     

A detection method of Escherichia coli O157:H7 based on immunomagnetic separation and aptamers-gold nanoparticle probe quenching Rhodamine B’s fluorescence: Escherichia coli O157:H7 detection method based on IMS and Apt-AuNPs probe quenching Rho B’ s fluorescence

This research aimed to detect Escherichia coli O157:H7 in milk based on immunomagnetic probe separation technology and quenching effect of gold nanoparticles to Rhodamine B. Streptavidin-modified magnetic beads (MBs) were combined with biotin-modified antibodies to capture E. coli O157:H7 specifically. Gold nanoparticle (AuNPs) was incubated with sulfhydryl-modified aptamers (SH-Aptamers) to obtain the Aptamers-AuNPs probe. After magnetic beads captured target bacteria and formed a sandwich structure with the gold nanoprobe, Rhodamine B was added into complex to obtain fluorescent signal changes. Our results demonstrated that the established method could detect E. coli O157:H7 in the range of 10¹–10⁷ CFU/mL, and the limit of detection (LOD) was 0.35 CFU/mL in TBST buffer (pH = 7.4). In milk simulation samples, the LOD of this method was 1.03 CFU/mL. Our research provides a promising approach on the detection of E. coli O157:H7.     

Recovery of hesperidin and narirutin from waste Citrus unshiu peel using subcritical water extraction aided by pulsed electric field treatment

The objective of this study was to identify whether the efficacy of extracting hesperidin and narirutin from Citrus unshiu peel by-products can be increased by combining pulsed electric field (PEF) and subcritical water extraction (SWE). The samples were treated with a PEF at a strength of 3 kV/cm for 60 and 120 s. Subsequent SWE was conducted at extraction temperatures of 110–190 °C for 3–15 min. The concentration of hesperidin was highest at 46.96 ± 3.37 mg/g peel (dry basis) after PEF treatment at 120 s, combined with SWE at 150 °C for 15 min, while that of narirutin peaked at 8.76 ± 0.83 mg/g after PEF treatment at 120 s, integrated with SWE at 190 °C for 5 min. The concentrations of both hesperidin and narirutin increased with PEF treatment time. The PEF increased the amounts of hesperidin and narirutin extracted by 22.1% and 33.6%, respectively. This study demonstrate the potential of PEF pretreatment for enhancing the SWE of flavonoids from C. unshiu peel.     

Accelerated inactivation of Geobacillus stearothermophilus spores by ohmic heating

Until recently, ohmic heating was commonly thought to kill microorganisms through a thermal effect. However a growing body of evidence suggests that non-thermal effects may occur. Our aim was to determine the kinetics of inactivation of Geobacillus stearothermophilus spores (ATCC 7953) under ohmic and conventional heating using a specially constructed test chamber with capillary sized cells to eliminate potential sources of error and ensure that identical thermal histories were experienced both by conventionally and ohmically heated samples. Ohmic treatments at frequencies of 60 Hz and 10 kHz were compared with conventional heating at 121, 125 and 130 °C for four different holding times. Both ohmic treatments showed a general trend of accelerated spore inactivation. It is hypothesized that vibration of polar dipicolinic acid molecules (DPA) and spore proteins to electric fields at high temperature conditions may result in the accelerated inactivation.     

Degradation kinetics of anthocyanins in acerola pulp: Comparison between ohmic and conventional heat treatment

Degradation kinetics of monomeric anthocyanins in acerola pulp during thermal treatment by ohmic and conventional heating was evaluated at different temperatures (75–90 °C). Anthocyanin degradation fitted a first-order reaction model and the rate constants ranged from 5.9 to 19.7 × 10⁻³ min⁻¹. There were no significant differences between the rate constants of the ohmic and the conventional heating processes at all evaluated temperatures. D-Values ranged from 116.7 to 374.5 for ohmic heating and from 134.9 to 390.4 for conventional heating. Values of the free energy of inactivation were within the range of 100.19 and 101.35 kJ mol⁻¹. The enthalpy of activation presented values between 71.79 and 71.94 kJ mol⁻¹ and the entropy of activation ranged from −80.15 to −82.63 J mol⁻¹ K⁻¹. Both heating technologies showed activation energy of 74.8 kJ mol⁻¹ and close values for all thermodynamic parameters, indicating similar mechanisms of degradation.     

Pulsed Ligh inactivation of Listeria innocua on food packaging materials of different surface roughness and reflectivity

Inactivation of Listeria innocua on food packaging materials by Pulsed Light (PL) treatment was investigated. Coupons of low density polyethylene (LDPE), high density polyethylene (HDPE), polyethylene-laminated ultra-metalized polyethylene terephthalate (MET), polyethylene-coated paperboard (TR), and polyethylene-coated aluminum foil paperboard laminate (EP) were inoculated with L. innocua cells in stationary growth phase. Inoculated coupons (∼8 CFU/coupon) were treated with Pulsed Light fluence of up to 8.0 J/cm², and survivors were determined. Reductions up to 7.2 ± 0.29, 7.1 ± 0.06, 4.4 ± 0.85, 4.5 ± 1.32, and 3.5 ± 0.82 log CFU/coupon were obtained on LDPE, HDPE, MET, TR, and EP, respectively. Inactivation data were used to determine Weibull kinetic parameters and predict inactivation in a wide range of fluence. Increasing surface reflectivity and surface roughness appeared to induce lower inactivation. Minimal surface heating was observed for all materials except MET, on which significant heating occurred. These results demonstrate the potential of Pulsed Light as an effective method for decontaminating food packaging materials.     

Supercritical Carbon Dioxide Processing of Dry Cured Ham Spiked with Listeria monocytogenes: Inactivation Kinetics, Color, and Sensory Evaluations

The feasibility of supercritical carbon dioxide (SC-CO₂) treatment to inactivate Listeria monocytogenes inoculated on the surface of dry cured ham was investigated. A multibatch apparatus was used. Inactivation kinetics were determined at 8 and 12 MPa, as a function of temperatures (35–50 °C), treatment times (5–60 min), and initial microbial loads (10³–10⁷ colony-forming units [CFU]/g). Color changes of the sample were determined by measuring the reflectance spectra and L*, a*, and b* parameters. A new spectroscopic technique was developed for this. Sensory quality of the product before and after the SC-CO₂ treatment was evaluated by a sensory panel. Treatment at 50 °C, 12 MPa for 15 min resulted in total inactivation of L. monocytogenes with an initial microbial load of 10⁷ CFU/g. Less severe conditions, e.g., 45 °C, 12 MPa, 5 min, were sufficient to reach total inactivation if the initial microbial load was 10³ CFU/g. The process slightly influenced the color and sensory attributes of the sample. The results demonstrated the efficiency and the potential of SC-CO₂ as a technology for the pasteurization of the surface of foods, in particular ham-type meat products.     

A comparative study on the effectiveness of chlorine dioxide gas, ozone gas and e-beam irradiation treatments for inactivation of pathogens inoculated onto tomato, cantaloupe and lettuce seeds

The increase in reported food-borne outbreaks linked with consumption of raw fruits and vegetables has motivated new research focusing on prevention of pre-harvest produce contamination. This study evaluates and compares the effectiveness of three non-thermal technologies, chlorine dioxide gas, ozone gas and e-beam irradiation, for inactivation of Salmonella enterica and Escherichia coli O157:H7 on pre-inoculated tomato, lettuce and cantaloupe seeds, and also their corresponding effect on seeds germination percentage after treatments. Samples were treated with 10 mg/l ClO₂ gas for 3 min at 75% relative humidity, with 4.3 mg/l ozone gas for 5 min and with a dose of 7 kGy electron beam for 1 min. Initial load of pathogenic bacteria on seeds was ~ 6 log CFU/g. Results demonstrate that all treatments significantly reduce the initial load of pathogenic bacteria on seeds (p < 0.05). In particular, after ozone gas treatments 4 log CFU/g reduction was always observed, despite the seeds and/or microorganisms treated. ClO₂ and e-beam treatments were noticeably more effective against Salmonella on contaminated tomato seeds, where 5.3 and 4.4 log CFU/g reduction were respectively observed. Germination percentage was not affected, except for cantaloupe seeds, where the ratio was significantly lowered after ClO₂ treatments. Overall, the results obtained show the great applicability of these non-thermal inactivation techniques to control and reduce pathogenic bacteria contamination of seeds.     

Characterization of native microbial populations on Swiss chard (Beta vulgaris,type cicla) cultivated by organic methods

The native microflora of fresh Swiss chard (Beta vulgaris, type cicla) cultivated by organic methods was quantified and characterised. The concentration of the different microorganism groups presented less variability among different lots than results found on chard leaves produced by conventional methods. These results would indicate a greater degree of homogeneity among the different samples of chard produced by organic procedures.The microbial populations on Swiss chard leaves produced by organic methods were 6.8×10⁵ CFU/g for mesophilic microorganisms, 3.9×10³ CFU/g for psycrotrophic microorganisms, 1.4×10⁴ CFU/g for lactic acid microorganisms, 5.1×10³ CFU/g for total coliforms and 1.66×10³ CFU/g for Staphylococcus spp. Neither fecal coliforms nor human pathogens were identified. Immersion of organic Swiss chard leaves in tap water at 18°C for 4 min reduced microbial populations but did not accomplish more than 70% removal in any of the populations under study.     

Inactivation of Bacillus cereus spores using a combined treatment of UV-TiO2 photocatalysis and high hydrostatic pressure

Bacillus cereus spores are resistant to high hydrostatic pressure (HHP) processing treatment. A combination of UV-TiO₂ photocatalysis (UVTP for 10 min) and two cycles of 600 MPa HHP treatment for 10 min for the first cycle and 1 min for the second cycle (UVTP-2HHP) at ambient temperature was applied to inactivate B. cereus spores inoculated on a solidified agar matrix (SAM) used as a model matrix. Two cycles of HHP treatment were used as a strategy for induction of spore germination, followed by inactivation. UVTP and 2 cycles of HHP resulted in a 5.0-log CFU/cm² spore reduction (initial spore count was 6.6 log CFU/cm²), including an approximate 0.8-log CFU/cm² reduction due to a synergistic effect. The inactivation mechanism of UVTP pretreatment was related to lipid peroxidation of the spore membrane based on the level of malondialdehyde (MDA) making spores susceptible to the HHP treatment. Flow cytometry and transmission electron microscopic (TEM) analyses showed severe physiological alteration and structural damage to spores after the combined treatment. UVTP and 2 cycles of HHP showed potential for effective inactivation of B. cereus to ensure food safety from B. cereus spores on food products.Practical applicationsInactivation of bacterial spores remains a technical challenge for HHP and other interventions because spores are highly resistant to high pressure. Pretreatment with UVTP followed by two cycles of HHP resulted in reduction in B. cereus spores due to a synergistic effect. This hurdle technology of UVTP and HHP can help food industry in ensuring food safety against the Bacillus spores.     

Experimental and computational analysis of microbial inactivation in a solid by ohmic heating using pulsed electric fields

Pulsed electric field technology (PEF) has traditionally been used as a technique to inactivate microorganisms in liquid foods at temperatures below those used in heat treatments; however, application of high-intensity PEF (E>1 kV/cm) at high frequencies (>10 Hz) can allow rapid and volumetric solid food electrical heating in order to replace traditional convection/conduction heating that progresses from the heating medium to the inside of the product. This investigation is the first one to evaluate the inactivation of Salmonella Typhimurium 878 in a solid product (cylinder of technical agar used as reference solid) by applying PEF treatments (2.5 and 3.75 kV/cm, and up to 9000 microseconds) at 50 Hz. The evolution of temperature in different locations of the agar cylinder was measured by observing the variability of heating rates depending on location and PEF intensity. Microbial inactivation was determined and compared with isothermal heat treatments that predicted similar inactivation values, but did not detect additional inactivation. Computational analysis enabled us to predict temperature and microbial inactivation for any spatial and temporal distribution of the cylinder agar by detecting the coldest point in the transition zone between the high-voltage electrode, the agar, and the plastic container of the treatment chamber. In order to evaluate the variability of the temperature, computational predictions were done each 0.5-mm. The difference between the coldest and the hottest point (e.g. at the center of the cylinder) resulted in around 10 ^∘C and 10 second variation in temperature and processing time, respectively. In any case, it was possible to obtain 5-log₁₀-reductions after 60 s of PEF treatments when using 2.5 kV/cm and 50% reduction for 3.75 kV/cm. These results suggested the potential of PEF technology as a rapid heating system based on ohmic heating for microbial inactivation in solid food products.     

Effect of cooking procedures of kiymali pide,a traditional Turkish fast-food,on destruction of Escherichia coli O157:H7

The objective of the present study was to obtain data about cooking time and temperature of kiymali pide in the restaurants and to investigate thermal inactivation of E. coli O157:H7 during experimental kiymali pide making. A field study was conducted in randomly selected 23 of 87 pide restaurants. Processing parameters including oven temperature, cooking period and post-cooking temperature were determined. Kiymali pide samples were prepared using ground beef filling experimentally inoculated with E. coli O157:H7 (7.6 log₁₀ CFU/g). Pide samples were cooked at a conventional oven at 180 °C for 180, 240, 270, 300 and 330 s. Results of the current study suggest that cooking kiymali pide at 180 °C for at least 330 s (5.5 min) may provide sufficient food safety assurance (≥ 6 log₁₀ CFU/g) for E. coli O157:H7.     

Inactivation of Escherichia coli in orange juice using ozone

This research investigated the efficacy of gaseous ozone for the inactivation of Escherichia coli ATCC 25922 and NCTC 12900 strains in orange juice. Orange juice inoculated with E. coli (10⁶ CFU mL^− 1) as a challenge microorganism was treated with ozone at 75–78 µg mL^− 1 for different time periods (0–18 min). The efficacy of ozone for inactivation of both strains of E. coli was evaluated as a function of different juice types: model orange juice, fresh unfiltered juice, juice without pulp, and juice filtered through 500 µm or 1 mm sieves. Fast inactivation rates for total reduction of E. coli were achieved in model orange juice (60 s) and in juice with low pulp content (6 min). However, in unfiltered juice inactivation was achieved after 15–18 min. This indicated that juice organic matter interferes with antibacterial activity of gaseous ozone. The effect of prior acid (pH 5.0) exposure of E. coli strains on the inactivation efficacy of ozone treatment was also investigated. There was a strain effect observed, where prior acid exposure resulted in higher inactivation times in some cases by comparison with the control cells. However, the overarching influence on inactivation efficacy of ozone was related to the pulp content. Generally, the applied gaseous ozone treatment of orange juice resulted in a population reduction of 5 log cycles.

Industrial relevance

To facilitate the preservation of unstable nutrients many juice processors have investigated alternatives to thermal pasteurisation, including un-pasteurised short shelf life juices with high retail value. This trend has continued within the European Union. However within the US recent regulations by the FDA have required processors to achieve a 5-log reduction in the numbers of the most resistant pathogens in their finished products. Pathogenic E. coli may survive in acid environments such as fruit juices for long periods. This study demonstrates that the use of ozone as a non-thermal technology is effective for inactivation of E. coli and acid exposed E. coli in orange juice. Information on the design of the ozone treatment for inactivation of E. coli which results into safe juice products is also among the main outputs of this work. Ozone auto-decomposition makes this technology safe for fruit juice processing.     

Influence of electron beam treatment on naturally contaminated red pepper (Capsicum annuum L.) powder: Kinetics of microbial inactivation and physicochemical quality changes

This study reported the impact of electron beam (e-beam) treatment on microbiota and mycotoxins naturally present in red pepper powder and physicochemical quality changes. Treatment at 6 kGy indicated significant (p < 0.05) decontamination of yeasts and molds by 3.0 and 4.4 log CFU/g, respectively. A reduction of 4.5 log CFU/g of total plate counts (TPC) was observed at 10 kGy for 23 s. Fungal inactivation followed first-order kinetics while TPC better fitted with Gompertz function (R² = 0.9912). E-beam treatment was not efficient for the degradation of aflatoxins but indirectly controlled their production by inactivation of mycotoxigenic molds. Indeed, reduction of 25% ochratoxin A was recorded at 30 kGy retaining >85% of total phenols, carotenoids and antioxidants activity. Moreover, treatment impact on total color difference (ΔE*) indicated ‘slight differences’. Overall, e-beam treatments up to 10 kGy were efficient in decontaminating the natural microbiota without detrimental effects on the physicochemical qualities of red pepper powder.     

Brewing of glucuronic acid-enriched apple cider with enhanced antioxidant activities through the co-fermentation of yeast (Saccharomyces cerevisiae and Pichia kudriavzevii) and bacteria (Lactobacillus plantarum)

Co-fermentation using yeast (Saccharomyces cerevisiae and Pichia kudriavzevii) and the bacteria (Lactobacillus plantarum) as starters isolated from spontaneous sourdough was conducted for the brewing of glucuronic acid (GlcA)-enriched apple cider. The concentration of GlcA in the apple cider co-fermented for 14 d with commercial S. cerevisiae and L. plantarum was 37.7 ± 1.7 mg/mL while a concentration of 62.8 ± 3.1 mg/mL was recorded for fermentation with P. kudriavzevii and L. plantarum, which was higher than the corresponding single yeast fermentation. The co-fermented apple cider revealed higher 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity of 171.67 ± 0.79 µg trolox equivalents (TE)/mL using P. kudriavzevii and L. plantarum, compared to the control (143.89 ± 7.07 µg TE/mL) just using S. cerevisiae. Thus, the co-fermentation of S. cerevisiae and L. plantarum and P. kudriavzevii and L. plantarum provided a new strategy for the development of GlcA-enriched apple cider with enhanced antioxidant capacity.     

Proofing of bread dough assisted by ohmic heating

Proofing of bread dough was studied under ohmic heating for a target temperature of 35°C. An experimental device based on PLC monitoring was developed to study the effect of heating rates and voltages on the proofing process. Conventional and ohmic heating-assisted proofing were compared; the results showed that the process itself had no impact on the proofing when identical heating rates (0.065°C·min^− 1) were used. However, increasing the heating rate could significantly reduce the time needed to reach an expansion ratio of 3 (from 122 min during conventional proofing to 65–70 min during ohmic heating in the range of 1–10°C·min^− 1). This was due to the shortening of the lag phase at the beginning of proofing (from 58 min during conventional heating to 20 min at 10°C·min^− 1 in ohmic heating). Results also showed that the voltage intensity had no significant effect on the proofing kinetics in the range of 50–150 V. The evolution of expansion ratios with proofing time could be fitted by a Gompertz model with a very high accuracy (R² > 0.999)     

Pasteurization of citrus juices with ohmic heating to preserve the carotenoid profile

This study was carried out to assess, for the first time, the effect of ohmic heating on the carotenoid profile of two citrus fruit juices: grapefruit and blood orange. Two heat treatments were designed to obtain pasteurization values of 50 and 150 min (Tref = 70 °C and z-value = 10 °C) with ohmic heating as compared to conventional heating. The results showed that xanthophyll losses could reach 70% for epoxyxanthophylls (cis-violaxanthin and cis-antheraxanthin) and 40% for hydroxyxanthophylls (β-cryptoxanthin, lutein, and zeaxanthin) with conventional heating, but losses were under 30% and 20%, respectively, with ohmic heating. Carotene species (lycopene and β-carotene) were stable regardless of the treatment. No negative non-thermal effects of ohmic heating were shown on carotenoids. Loss simulations of the studied carotenoids showed that the high temperatures reached with ohmic heating during pasteurization could substantially increase the organoleptic and nutritional quality of acid carotenoid-rich juices.Industrial relevanceCitrus are the top fruit crops in terms of world trade. This craze for them -particularly orange and grapefruit- is notably due to their high content in organoleptic and nutritional compounds of interest and among them carotenoids. About 50% of the Citrus production is processed in juice. From the growing variety of products, minimal processed juices now have a significant market share. This work assessed for the first time the effect of ohmic heating, a thermal method for stabilizing juices while minimizing the impact on the juice quality, on the carotenoid profiles of blood orange and grapefruit juice. Pasteurization with ohmic heating was proven to be a very good alternative for protecting carotenoids and especially xanthophylls compared to conventional heating. These results will help in designing ohmic heating process parameters for optimizing the overall quality of carotenoid-rich fruit juices.     

Inactivation of Escherichia coli by ozone treatment of apple juice at different pH levels

This research investigated the efficacy of gaseous ozone on the inactivation of Escherichia coli ATCC 25922 and NCTC 12900 strains in apple juice of a range of pH levels, using an ozone bubble column. The pH levels investigated were 3.0, 3.5, 4.0, 4.5 and 5.0. Apple juice inoculated with E. coli strains (10⁶ CFU/mL) was treated with ozone gas at a flow rate of 0.12 L/min and ozone concentration of 0.048 mg/min/mL for up to 18 min. Results show that inactivation kinetics of E. coli by ozone were affected by pH of the juice. The ozone treatment duration required for achieving a 5-log reduction was faster (4 min) at the lowest pH than at the highest pH (18 min) studied. The relationship between time required to achieve 5 log reduction (t_5d) and pH for both strains was described mathematically by two exponential equations. Ozone treatment appears to be an effective process for reducing bacteria in apple juice and the required applied treatment for producing a safe apple juice is dependant on its acidity level.     

Quality of shelf-stable low-acid vegetables processed using pressure–ohmic–thermal sterilization

Pressure ohmic thermal sterilization (POTS) involves ohmic heating of foods by applying an electric field under elevated pressure. Experiments were conducted using a custom made POTS apparatus using carrot as the model food. The samples were processed at a target temperature of 105 °C at 600 MPa and treated for 0, 1, 3, and 5 min by regulating the electric field (30 V/cm). POTS treated carrot sample quality attributes were compared against those processed using ohmic heating (0.12 MPa, 30 V/cm, 105 °C) and pressure-assisted thermal processing (PATP; 600 MPa, 0 V/cm, 105 °C). Within the experimental conditions of the study, the thermal come-up time of the POTS, Ohmic and PATP were 1.45 min, 3.58 min and 6.84 min respectively. PATP come-up time also included the pre-heating time (≈6 min). Results indicate the POTS samples had the least textural damage due to minimal thermal exposure. POTS samples had higher crunchiness index (CI) of 0.76 compared to PATP (CI = 0.57) and ohmic heated (CI = 0.62) carrots. All the technologies investigated had minimal impact on product color. This study demonstrates the potential to produce high quality shelf stable low-acid vegetable products using POTS.     

Decontamination of chokeberries (Aronia melanocarpa L.) by cold plasma treatment and its effects on biochemical composition and storage quality of their corresponding juices

To improve the microbiological quality of chokeberries, corona discharge plasma jet (CDPJ) was employed as a decontaminating agent. The mean levels of aerobic bacteria and yeast and molds contaminants in chokeberries were 4.78 and 4.87 log CFU/g, respectively; the viable counts were decreased by 2.09 and 1.83 log units following CDPJ treatment for 3 min, respectively. A first-order kinetic model was well-suited for explaining the inactivations. The concentration of total polyphenols of chokeberries was unaffected (up to 3 min treatment), whereas DPPH radical scavenging activity was significantly decreased by CDPJ treatment (2 min and more). CDPJ treatment (all tested times) of chokeberries led to a significant decrease of monomeric anthocyanin content of their corresponding juices, whereas soluble solids content (Brix) and pH were unaffected. After storage at 4 °C for 72 h, juices obtained from CDPJ-treated berries possessed relatively low levels of contaminants with no significant alterations in pH and soluble solids content when compared with controls. In conclusion, CDPJ treatment for 2 min was optimal to improve the microbiological quality of the berries without negatively affecting biochemical qualities of their corresponding juices.