Biodegradable Polymeric Films Incorporated with Nisin: Characterization and Efficiency against <Emphasis Type="Italic">Listeria monocytogenes</Emphasis>

Nisin (0.2 IU per cm² films) containing biodegradable films were produced from pea protein isolate (PPI), whey protein isolate (WPI), and polylactic acid (PLA). Nisin was released over 4 h at 22 °C and 8 h at 4 °C. PPI released more nisin compared to other films suppressing the growth of Listeria monocytogenes (P?<?0.05) based upon diffusion into agar and liquid culture media. The population of bacteria after 48 h in liquid media was 6 CFU/mL (1 log₁₀ increase) in PPI, 8.47 CFU/mL (3.47 log₁₀ increase) in WPI and 9 CFU/mL (4 log₁₀ increase) in PLA, which was significantly lower in protein based films compared to PLA (P?<?0.05). The inhibition zone in agar test was significantly higher (P?<?0.05) in PPI and WPI, compared to PLA film, which might be due to the higher hydration in protein based films. Fourier transform infrared spectroscopy (FTIR) showed that nisin altered the intensity of amide I peaks in protein based films suggesting that nisin can bind to the protein functional groups in PPI and WPI. Thermogram showed that nisin did not influence the glass transition and melting temperatures of the films. Nisin containing films exhibited significantly lower enthalpy compared to control films (P?<?0.05). PeakForce Quantitative Nano Mechanical Property Mapping (PeakForce QNM) was applied to extract material and mechanical properties in PPI, WPI and PLA films with and without nisin. Results showed significant reductions in material and mechanical properties of protein based films containing nisin compared to PLA films.     

Modeling the Inactivation of <Emphasis Type="Italic">Listeria innocua</Emphasis> and <Emphasis Type="Italic">Escherichia coli</Emphasis> in Fresh-Cut Tomato Treated with Pulsed Light

The effectiveness of pulsed light (PL) treatments to inhibit microorganisms on fresh-cut tomatoes (Lycopersicon esculentum Mill., cv. Daniela) was investigated. Tomato slices inoculated with Escherichia coli or Listeria innocua were exposed to PL treatments (4, 6, or 8 J cm^?2 fluence) and kept cold at 4 °C for 20 days. L. innocua and E. coli counts, gases in the headspace of the containers (O₂ and CO₂), pH, titratable acidity, and soluble solid content were monitored throughout the cold storage. The PL treatments reduced significantly (p < 0.05) initial loads of both microbes. The effect of the PL fluence on the survival number of microoganisms was described by a log-linear model (R ² = 0.849–0.999). At any fixed time within the cold storing, the microbial counts for untreated samples were always higher than those cut tomatoes that had been previously PL-treated. The behavior of L. innocua and E. coli during the storage were well adjusted (R ² > 0.930) by Gompertzian models; the studied microorganisms exhibited different patterns during the storage period. On the other hand, O₂ and CO₂ partial pressures in containers with fresh-cut tomatoes were also significantly affected by PL treatments (p < 0.05). The highest PL fluence caused the greatest changes of O₂ and CO₂ contents. In addition, the application of PL triggered an acceleration of the O₂ consumption during the cold stage. PL treatments might be used to effectively extend the safety of fresh-cut tomatoes over 12 days of storage against E. coli and L. innocua growth.     

Comparative Study on the Inactivation and Photoreactivation Response of <Emphasis Type="Italic">Listeria monocytogenes</Emphasis> Seafood Isolates and a <Emphasis Type="Italic">Listeria innocua</Emphasis> Surrogate after Pulsed Light Treatment

The inactivation and photoreactivation response of six seafood-isolated Listeria monocytogenes and one Listeria innocua strain after pulsed light (PL) treatment was evaluated. The lower inactivation levels found after exposure of treated samples to daylight during the first 90 min of storage confirmed that both L. innocua and L. monocytogenes have the capability to photorepair PL-induced DNA damage upon appropriate conditions. Photoreactivation levels from 0.2 to 2.1 log CFU cm^?2 were observed depending on treatment intensity (fluence) and Listeria strain. Complete photorepair of PL-caused damage was not found even after treatments inducing low inactivation levels. Photoreactivation increased up to 2.1 log with the applied fluence up to a threshold able to cause between 2.4 and 5.4 log reductions under dark storage. Photorepair was not avoided but lower photoreactivation was observed after higher fluence inducing more than 6 log reductions under dark storage. Both L. innocua and L. monocytogenes serotype 1/2b exhibited the highest photoreactivation levels whereas serotypes 1/2a showed the lowest ones. The overall inactivation and photoreactivation responses of tested Listeria strains were comparable indicating that L. innocua may be a good surrogate for the safe evaluation, optimization and validation of PL technology to control L. monocytogenes in food products and food processing facilities.     

A Gompertz Model Approach to Microbial Inactivation Kinetics by High-Pressure Processing Incorporating the Initial Counts,Microbial Quantification Limit,and Come-Up Time Effects

During come-up time (CUT), the time to reach a desired processing pressure, isobaric-isothermal conditions cannot be assumed in the estimation of kinetic parameters for the design of commercial high-pressure processing (HPP) treatments. Since CUT effects on microbial population, enzyme activity, and chemical concentration are often ignored, kinetic models incorporating the non-isobaric and non-isothermal conditions prevailing during CUT were the objective of this work. The analysis of peer-reviewed data on the HPP inactivation of bacteria (counts observations n = 919, 60 survival curves) and bacterial spores (n = 273, 12 curves) showed that a Gompertz model (GMPZ) approach is an effective alternative. The GMPZ parameter A was fixed as the difference between the initial population (log₁₀ N _o ) and the lower quantification limit of microbial counts (log₁₀ N _lim), while exponential equations were used to describe pressure effects on the lag time (λ) and the maximum inactivation rate (μ_max). In low-acid media (pH > 4.5), λ decreased exponentially with pressure, allowing the identification of a theoretical pressure level (P _λ) sufficient to initiate microbial inactivation during CUT. The parameter μ_max exponentially increased with pressure for all evaluated datasets. Dynamic pressure effects during CUT were simplified by assuming isobaric conditions during CUT (t _CUT), allowing to obtain GMPZ parameter estimates using only nonlinear regression (R ² ～ 0.938, σ ² = 0.030–0.604). The proposed approach is a simpler, promising tool for a more informative analysis of the kinetics of microbial inactivation by HPP and should be further validated with additional experimental data.     

Development and characterization of reconstituted hydrogel from <Emphasis Type="Italic">Aloe vera</Emphasis> (<Emphasis Type="Italic">Aloe barbadensis</Emphasis> Miller) powder

Structural and rheological characterization of reconstituted hydrogels developed from A. vera non-fibrous alcohol insoluble residue (NFAIR) powder using different methods [viz., shaking (S), heating-shaking (HS), and heating (H)] and concentrations (viz., 0.2–1.6 %, w/v) was carried out. Functional group distribution by FTIR spectroscopy and Congo red (CR) method revealed the presence of acetylated acemannan in A. vera powder. Dynamic oscillation studies of A. vera (NFAIR) fluids at all concentrations of 0.2–1.6 %, w/v, showed gel strength in the order of H > HS > S method. However, in H method, increase in concentration from 0.2 to 1.6 %, w/v showed the conformational transition from semi-diluted solution to weak gel nature. Rheological models described the effect of heating temperatures (HT); 30–90 °C, and times (Ht); 15–60 min on viscoelastic behavior in reconstituted A. vera fluids. The reconstituted A. vera hydrogel prepared with a concentration of 1.6 %, w/v using 50 °C (HT) and 30 min (Ht) condition showed a good agreement with the Power law (storage modulus, G′) and Weak gel model (complex modulus, G*) fitted data (R² > 0.94) resulting higher viscoelastic moduli intercepts; G′₀ (71.5 Pa s ^n′), G″₀ (33.5 Pa s ^n″), lower slopes; n′ (0.22), n″ (0.06), higher network strength (A _F , 121.3 Pa s^1/z ) and number of network (z, 5.3) values. The obtained results suggested that heating at 50 °C/30 min can develop aqueous weak gel networks of A. vera with enhanced gel strength which may be utilized as a novel gelling agent for wide variety of targeted applications in food and pharmaceutical sectors.     

Thermal transition and thermo-physical properties of potato (<Emphasis Type="Italic">Solanum tuberosum L</Emphasis>.) var. Russet brown

Potatoes are an important food in many regions of the world and are commonly used in a variety of food products. Thermal transition and thermo-physical properties of potatoes are important in order to design efficient food processes and select appropriate storage conditions. In this study, we determined the thermal transitions and thermophysical properties of raw and blanched/par-fried potato for a temperature range of ??32 to 21.1 °C. Using differential scanning calorimetry, we found an initial freezing point (T_f) at ??1.8?±?0.1 °C, an onset of melting (T_m^′) at ??9.9?±?0.2 °C and an unfreezable water content (X^′_w) for maximally freeze-concentrated raw potato at 0.21 kg water/kg potato. Corresponding values for blanched/par-fried potatoes were ??0.9?±?0.1 °C, ??11.0?±?0.2 °C and 0.18 kg water/kg potato. Results show that an increase in solids content decreased T_f of both raw and blanched potatoes. We modelled the relationship between them using the Chen model. The apparent specific heat (C_app) increased around T_f to 31.7?±?1.13 kJ/kg K for raw potato and 26.7?±?0.62 kJ/kg K for blanched/par-fried potato. For frozen raw potato at ??32 °C, thermal diffusivity (α) was 0.89?±?0.01?×?10?^?6 m²/s and thermal conductivity (k), 1.82?±?0.14 W/m K, respectively. These values were higher for frozen raw potato than for the unfrozen raw potato (0.15?±?0.01?×?10?^?6 m²/s and 0.56?±?0.08 W/m K, respectively at 21.1 °C). The apparent density (ρ) of frozen raw potato (992?±?4.00 kg/m³ at ??32 °C) was less than that for unfrozen raw potato (1053?±?4.00 kg/m³ at 21.1 °C), and a similar trend was obtained for blanched/par-fried potato (993?±?2.00 kg/m³ at ??32 °C and 1188?±?7.00 kg/m³ at 21.1 °C, respectively). This study established a correlation between thermo-physical properties and temperature. Findings may be used to inform the design and optimization of freezing processes and frozen storage for potato products.     

<Emphasis Type="Italic">Listeria</Emphasis> Inactivation by the Combination of High Hydrostatic Pressure and Lactocin AL705 on Cured-Cooked Pork Loin Slices

The effect of the bacteriocin lactocin AL705 in combination with high hydrostatic pressure (HHP) on the inactivation of Listeria innocua 7, a nonpathogenic indicator for Listeria monocytogenes, deliberately inoculated (ca. 6.4 log CFU/g) onto the surface of ready-to-eat (RTE) sliced cured-cooked pork loin, was evaluated. Nontreated pork slices (control) and treatments subjected to lactocin AL705 (105 AU/ml) and/or HHP (400 or 600 MPa) were prepared. L. innocua 7 was monitored at days 1, 20, and 40 of storage at 4 °C. The results showed a complete inhibition of L. innocua 7 after the combined treatment with lactocin AL705 and 600 MPa and no regrowing of cells up to 40-day storage. The treatment at 600 MPa alone was not enough to avoid regrowth of L. innocua. Ultrastructural cell damage was observed at the cytoplasm and cell membrane/wall levels with all treatments; however, complete cell lysis was observed only with the combined treatment. HHP in combination with lactocin AL705 provided a wider margin of safety as post-processing listericidal treatment of RTE cured-cooked meat products.     

A Case Study on Optimization of Biomass Flow During Single-Screw Extrusion Cooking Using Genetic Algorithm (GA) and Response Surface Method (RSM)

In the present study, response surface method (RSM) and genetic algorithm (GA) were used to study the effects of process variables like screw speed, rpm (x ₁), L/D ratio (x ₂), barrel temperature (°C; x ₃), and feed mix moisture content (%; x ₄), on flow rate of biomass during single-screw extrusion cooking. A second-order regression equation was developed for flow rate in terms of the process variables. The significance of the process variables based on Pareto chart indicated that screw speed and feed mix moisture content had the most influence followed by L/D ratio and barrel temperature on the flow rate. RSM analysis indicated that a screw speed?>?80 rpm, L/D ratio?>?12, barrel temperature?>?80 °C, and feed mix moisture content?>?20% resulted in maximum flow rate. Increase in screw speed and L/D ratio increased the drag flow and also the path of traverse of the feed mix inside the extruder resulting in more shear. The presence of lipids of about 35% in the biomass feed mix might have induced a lubrication effect and has significantly influenced the flow rate. The second-order regression equations were further used as the objective function for optimization using genetic algorithm. A population of 100 and iterations of 100 have successfully led to convergence the optimum. The maximum and minimum flow rates obtained using GA were 13.19?×?10^?7 m³/s (x ₁?=?139.08 rpm, x ₂?=?15.90, x ₃?=?99.56 °C, and x ₄?=?59.72%) and 0.53?×?10^?7 m³/s (x ₁?=?59.65 rpm, x ₂?=?11.93, x ₃?=?68.98 °C, and x ₄?=?20.04%).     

A mathematical model for moisture movement during continous and intermittent drying of <Emphasis Type="Italic">Eucalyptus saligna</Emphasis>

A modified diffusion-based mathematical model is proposed to describe the moisture movement during continuous and intermittent drying of Eucalyptus saligna. This model includes the temperature change, the surface drying coefficient (β _n ) and 2 diffusion coefficients [from green to FSP (D _f ) and from FSP to dry condition (D _o )] as important parameters. The final model expression obtained was M?=?exp (??25 β _n ² D _t /l²) with the β _n used was 1.5807 kg m^?2 s^?1, the D _f was 2.26?×?10^?11 m² s^?1, and the D _o was 5.85?×?10^?12 m² s^?1. The range of temperature change between heating and non-heating phases in the intermittent drying regimes was from 24.9 to 31.8 °C. The R² values obtained when the model was fitted into the drying data of different intermittent regimes ranged from 71.5 to 85.9%. The R² value was 87.4% when the model was fitted into continuous trial data. The high values of R² indicate that the model can be used to understand the moisture reduction both in intermittent and continuous regimes.     

A Novel Staphylococcal Enterotoxin Q Immunosensor Prepared with Self-Assembly Method Based on Horseradish Peroxidase and Double-Layer Gold Nanoparticles

A novel and green electrochemical immunosensor for detection of Staphylococcal enterotoxin Q (SEQ), a toxic superantigen that can induce severe food poisoning and even fatal conditions, was developed by fixing double-layer gold nanoparticles (AuNPs), horseradish peroxidase, and thionin-chitosan composite membrane on the glassy carbon electrode surface. Under optimal conditions, the developed immunosensor showed a wide linear range from 0.1 to 100 pg mL^?1 (R ² = 0.992) for SEQ with a low detection limit of 0.046 pg mL^?1 (S/N = 3). The immunosensor had good specificity (no significant cross reaction with lipopolysaccharides, bovine IgG, Escherichia coli, or other common biological components), and remained fairly stable (over 87 % of the original signal response after stored for 20 days at 4 °C). In addition, the immunosensor was successfully applied to milk sample detection and demonstrated with high recoveries (from 91 to 113 %). In conclusion, the developed electrochemical immunosensor can supply a green and feasible tool for detection of SEQ in food.     

Smart NMR Method of Measurement of Moisture Content of Vegetables During Microwave Vacuum Drying

Microwave drying is usually combined with vacuum environment in conjunction with hot air flow to draw the moisture rapidly. The moisture content of the vegetables undergoing drying is hard to measure online. This research designed a microwave vacuum drying (MVD)-low-field nuclear magnetic resonance (NMR) smart device and investigated the feasibility of NMR method for online measurement of state of moisture during MVD. The relation between the signal amplitude (A ₂) and the true moisture content (M ₁) of six kinds of vegetables (mushroom, carrot, potato, lotus, edamame, vegetable corn) was fitted to estimate if NMR can measure the M ₁ of vegetables directly. Results showed that A ₂ and M ₁ of different fresh vegetables had no single empirical mathematical model to fit. However, for each kind of these vegetables, the A ₂ and corresponding M ₁ in different MVD stages showed a significant linear relationship. The predicted moisture content (M ₂) of mushroom: M ₂ = 5.25351 × 10^?4 A ₂ ? 0.34042, R = 0.996; carrot: M ₂ = 5.78756 × 10^?4 A ₂ ? 0.14108, R = 0.998; potato: M ₂ = 3.10019 × 10^?4 A ₂ ? 0.10612, R = 0.991; lotus: M ₂ = 2.32415 × 10^?4 A ₂ ? 0.01573, R = 0.998; edamame: M ₂ = 3.13310 × 10^?4 A ₂ ? 0.4198, R = 0.996; vegetable corn: M ₂ = 1.69461 × 10^?4 A ₂ ? 0.09063, R = 0.995. The linear models between M ₂ and A ₂ were able to estimate the end point (M ₁ < 8%) of MVD with a high accuracy (P > 0.950).     

Purification and characterization of <Emphasis Type="Italic">β</Emphasis>-glucosidase from <Emphasis Type="Italic">Oenococcus oeni</Emphasis> 31MBR

This study was designed to characterize a β-glucosidase from Oenococcus oeni 31MBR, a strain widely used in Chinese winemaking. An intracellular β-glucosidase (EC 3.2.1.21) was partially purified using a combination of ammonium sulfate precipitation and chromatographic methods. A single band was obtained in SDS-PAGE electrophoresis, indicating that the enzyme was highly purified and had an estimated molecular mass of 38.9 kDa. The enzyme exhibited highest activity at pH 4.5–5.0. The optimum temperature was 45 °C. Ethanol promoted the activity of this enzyme up to three times. Among the several metal ions assayed, only Mn²⁺ exhibited a partial promotion effect. The K _m and V _max values for p-nitrophenyl-β-d-glucopyranoside were 1.05 mmol/L and 0.957 nmol/min, respectively. Up to now, this study contains the first characterization of a native β-glucosidase purified from crude extracts of O. oeni 31MBR.     

Effect of Solids Concentration on the Physicochemical and Flow Properties of Cactus Pear Juices of Two Varieties (<Emphasis Type="Italic">Opuntia ficus-indica</Emphasis> and <Emphasis Type="Italic">Opuntia streptacantha</Emphasis>)

Juices from two varieties of cactus pear, a green (Opuntia ficus-indica) and a red (Opuntia streptacantha), were obtained and concentrated by evaporation. Both fruit varieties and their juices at different concentrations were characterized. Green cactus pears had significantly higher amount of pulp than red cactus pears; the peel of O. ficus-indica represented only 38 versus 52 % of the fruit for the O. streptacantha. Both varieties had no significant differences on moisture, density, pH, and titratable acidity, in contrary to soluble solids. Juice was concentrated under vacuum conditions to reach a final concentration of 42, 53–55, and 58–60 °Brix, respectively, and stored under refrigeration (10 °C) during 4 weeks. Physicochemical properties of the pears and juices were determined as fresh items (time zero) and every week for the concentrate juices through storage; similarly, flow parameters were measured at 10 and 25 °C. Concentrate density (1160–1283 kg/m³) was mainly affected by final soluble solids, while pH and acidity were affected differently depending on the variety. Concentrated juices at 42 °Brix were considered with Newtonian behavior with a viscosity of 2–22 mPa s, while those at higher concentrations were of pseudoplastic nature (n < 1.0 and K > 69 mPa sⁿ). Power Law model fitted better the flow behavior than Herschel-Bulkley model of concentrates of both varieties. Temperature, solid concentration, and/or storage time affected the consistency coefficient (K) and flow index (n) depending on the cactus pear variety. Overall, those concentrated juices from O. streptacantha were more stable and exhibited lower apparent viscosity.     

Steaming time effects on the moisture migration and structural properties of Chinese Northern-style steamed bread

The aim of this study was to investigate the steaming time effects on proton transverse relaxation behavior with low field 1H nuclear magnetic resonance and structural properties of Chinese Northern-style steamed bread (CNSB). Three proton populations could be distinguished at the first 4 min: T_2b (0.1–1 ms) corresponded to rigid and exchangeable protons; T₂₂ (9–21 ms) was associated with the water protons in small and large meshes of the dough microstructure; T₂₃ (69–300 ms) was assigned to the water protons on the surface of samples. The starch gelatinization began and the water turned into the integral part of the biopolymer at 6 min, forming T₂₁ (1–3 ms) fraction. The gelatinization effect was strengthened up to 8 min and supplied a more mobile microenvironment, resulting in the increase of T₂₁, A₂₁ and M₂₁. However, the gelatinization process ended at 8 min, bringing about the stabilization of T₂₁, A₂₁ and M₂₁ until 25 min. T₂₂ fraction accounted for the largest proportion during all the steaming process. All variation trends on structural properties of CNSB and T₂ relaxation parameters including T_i, A_i (relative intensity of T_i), and M_i (population abundance of T_i) indicated that 6 and 8 min were the two transitions. The gluten matrix began to be disrupted at 6 min and was quite damaged up to 8 min by scanning electron microscopy. The peaks at 15°, 18°, 20°, and 23° in X-ray diffraction patterns appeared in the first 6 min but were lost up to 8, 10, and 25 min.     

Deposit Generation During Camel and Cow Milk Heating: Microstructure and Chemical Composition

The aim of this study is to identify the chemical composition and the microstructure of the deposits obtained after heating camel and cow milks at 80 °C for 60 min using a laboratory-scale device. Like cow milk, camel milk was affected by heat treatment with the reduction of the non-casein nitrogen content reflecting the denaturation of camel whey proteins. The composition of the deposits generated during heating camel and cow milks at 80 °C for 60 min revealed that while camel deposit contained 57 % w/w protein, cow deposit showed a higher protein content of 69 % w/w. The mineral content was 35 % w/w for camel deposit which was higher than that of cow sample, which was 28 % w/w. SEM of both deposits showed a familiar structure of a protein deposit with large clumps composed of smaller aggregates. Camel deposit showed an amorphous structure due to its deficiency in β-lactoglobulin.     

Multi-Element (C,N, H,O) Stable Isotope Ratio Analysis for Determining the Geographical Origin of Pure Milk from Different Regions

In order to identify the geographical origin of pure milk, different proteins and milk water were extracted from pure milk originated from Australia and New Zealand, Germany and France, the USA, and China. Then, δ ¹³C and δ ¹⁵N values of the extracted proteins and δ ²H and δ ¹⁸O values of milk water were determined by element analyzer-isotope ratio mass spectrometry (EA-IRMS). The results indicated that pure milk from these regions could be potentially discriminated by using analyte δ ¹³C, δ ¹⁵N, δ ²H, and δ ¹⁸O. The P value analysis of them was highly significant (P?<?0.01) considering the origins. 3D distribution of δ ¹³C, δ ¹⁵N, δ ²H, and δ ¹⁸O can also clearly present regional concentration phenomena according to the regions of pure milk. Therefore, it can be concluded that δ ¹³C, δ ¹⁵N, δ ²H, and δ ¹⁸O analysis could potentially be rapid and routine for origin discrimination of pure milk.     

Antioxidant Activity and Determination of Phenolic Compounds from <Emphasis Type="Italic">Eugenia involucrata</Emphasis> DC. Fruits by UHPLC-MS/MS

Fruits have been the focus of several studies aimed at finding new antioxidant sources for protection against the damage caused by reactive species. In this study, the antioxidant activity and the presence of phenolic compounds in all parts (peel, pulp, and seeds) of Eugenia involucrata DC. fruits were evaluated. DPPH^·, ABTS^·+, and ORAC methods were used to determine the antioxidant activity, and an UHPLC-MS/MS method was developed for determining the phenolic compounds (gallic, chlorogenic, ferulic, p-coumaric and ellagic acids, quercetin, and myricetin). In the determination of both antioxidant activity and phenolic composition, the efficiency of solvents with different polarities—methanol/H₂O (80:20, v/v), ethanol/H₂O (80:20, v/v), methanol/acidified water with phosphoric acid pH 3.00 (80:20, v/v), and ethyl acetate—for the extraction of the phenolic compounds, was also evaluated. All parts of E. involucrata fruits showed antioxidant activity, in the range of 36.68 ± 1.44 to 873.87 ± 18.24 μmol TE g^?1, being the highest values found in the seeds and peel when more polar extraction solvents were used. Six, five, and three phenolic compounds were identified and quantified in the pulp, peel, and seeds, respectively, with the highest abundance as p-coumaric acid (14 ± 2 mg kg^?1) in the pulp, quercetin (47 ± 5 mg kg^?1) in the peel, and gallic acid (74 ± 4 mg kg^?1) in the seeds, also when more polar solvents were used. Although antioxidant activity methods suggested that the peel and seeds have more antioxidant potential, a wider variety of compounds were determined in the pulp.     

Chlorophyll Fluorescence Imaging for Monitoring the Effects of Minimal Processing and Warm Water Treatments on Physiological Properties and Quality Attributes of Fresh-Cut Salads

In this study, chlorophyll fluorescence imaging (CFI) was used to monitor plant stress induced by cutting of mini romaine lettuce (Lactuca sativa L. var. longifolia) and by cutting and washing of endive (Cichorium endivia L.) during storage. Regarding the more detailed study of endive fresh-cut salads, we additionally monitored respiratory activity, phenylalanine ammonia lyase (PAL) activity, contents of plant pigments, and cut edge browning. Determination of maximum quantum efficiency F _v/F _m was feasible through sealed consumer-sized film bags, thus, enabling the non-invasive monitoring of both fresh-cut salad types in the corresponding modified atmosphere during storage. Cutting of romaine lettuce provoked a partially reversible drop of F _v/F _m during the first 24 h. Subsequently, F _v/F _m of cut romaine strongly decreased with elapsing shelf life, whereas intact leaves exhibited only a slight decline. Regarding minimally processed endive, warm water washing progressively reduced F _v/F _m with increasing heat exposure, while respiratory activities and the content of accessory pigments remained unaffected. The heat-dependent decrease of F _v/F _m was correlated to the inhibition of the PAL activity. Mildly warm washing (40 °C, 120 s; 45 °C, 60 s) reduced PAL activities, while F_v/F_m remained widely unaffected and visual quality was only partially improved. However, warm water washing at elevated temperatures (45 °C, 120 s; 50 °C, 30–60 s) enabled maximum visual quality retention, accompanied by a significant decrease of F _v/F _m. CFI may represent a useful tool to monitor the stress conditions due to cutting and warm water treatments, hence, allowing the systematic improvement of fresh-cut produce.     

Effect of Low-pressure Cold Plasma (LPCP) on the Wettability and the Inactivation of <Emphasis Type="Italic">Escherichia coli</Emphasis> and <Emphasis Type="Italic">Listeria innocua</Emphasis> on Fresh-Cut Apple (<Emphasis Type="Italic">Granny Smith</Emphasis>) Skin

The aim of this study was to investigate the effect of low-pressure cold plasma (LPCP) on the inactivation of Escherichia coli and Listeria innocua on fresh-cut apple skin and its influence on wettability. Cold plasma treatments have shown to be effective to decontaminate foods, but their effect on the wettability has not been well studied. Surface-inoculated apple samples were treated with argon (Ar), nitrogen (N2), oxygen (O₂), and argon-oxygen (Ar-O₂) cold plasma using a commercial LPCP unit. Three different models were used to fit bacterial survival curves after the LPCP treatments. Changes in surface wettability were also determined by measuring the contact angle. The LPCP treatments using Ar, O₂, or Ar-O₂ mixture for 20 min were the most effective to inactivate E. coli with O₂, while the LPCP treatment with N2 for 20 min reduced L. innocua the most for (p?<?0.05). The highest increase in surface wettability was observed in samples treated for 20 min with O₂ and Ar-O₂. Different LPCP treatments have not great effectivity on the inactivation of E. coli and L. innocua on fresh-cut apple surface, but the all treatments changed the surface wettability of apples, making it more hydrophilic. This can be considered as a negative effect of the LPCP treatment because it can facilitate the adhesion and proliferation of re-contaminating microorganisms. More research should be undertaken to explore the use of other gases and complex surfaces.     

Biological activities of lactobacilli relevant to cardiovascular health in skim milk

In this study, skim milk was fermented using 14 Lactobacillus strains for 16 h at 42 °C or for 48 h at 25 °C. On conclusion of fermentation, the proteolytic, angiotensin converting enzyme-inhibitory (ACE-I), and antioxidant activities as well as the inhibition of thrombin and cholesterol micellar solubility were determined. The results revealed that Lb. paracasei B-4564 exhibited the highest ACE-I activity (68.11%) under the 42 °C for 16 h condition, while Lb. rhamnosus B-1445 demonstrated the highest ACE-I activity (92.23%) under the 25 °C for 48 h condition. Lb. paracasei B-4564 exhibited the highest inhibition rate of thrombin (42.43 and 48.10%) and cholesterol (68.60 and 87.01%) under the 42 °C for 16 h and 25 °C for 48 h conditions, receptively. Lb. rhamnosus B-442 exhibited the highest DPPH radical scavenging activity of 95.63 and 62.89% under the 42 °C for 16 h and 25 °C for 48 h conditions, receptively. Lb. rhamnosus B-1445 demonstrated the highest Fe²⁺ chelating activity and reducing power under both the tested fermentation conditions.