Analytical performance and characterization of antibody immobilized magnetoelastic biosensors

This article presents the results of an investigation into the enhancement of sensitivity and thermal stability of polyclonal antibody immobilized magnetoelastic biosensors. The Langmuir–Blodgett (LB) monolayer technique was employed for antibody (specific to Salmonella sp.) immobilization on rectangular shaped strip magnetoelastic sensors. Biosensor performance was investigated by exposing to graded concentrations (5 × 10¹–5 × 10⁸ cfu mL⁻¹) of Salmonella typhimurium solutions in a flow through mode. Bacterial binding to the antibody on the sensor surfaces changed the resonance parameters, and these changes were quantified by the sensor’s resonance frequency shift. An increase in the sensitivity from 159 Hz decade⁻¹ for a 2 mm sensor to 246 Hz decade⁻¹ for a 1 mm sensor was observed during the dose–response measurements. The stability of the biosensor was also investigated by storing the biosensor at 25, 45 and 65 °C. The binding activity of the stored biosensor was estimated by measuring the changes in resonance frequency after exposure to the bacterial solutions (10⁹ cfu mL⁻¹). Binding activity was also confirmed by counting bound S. typhimurium cells on the sensor surface using Scanning Electron Microscopy (SEM) micrographs. The results show that at each temperature, the binding activity of the biosensor gradually decreased over the testing period. Degradation of biosensor accelerated at higher storage temperatures. The activation energy of biosensor system degradation was determined to be 7.7 kcal mol⁻¹.     

Effects of supercritical carbon dioxide treatment against generic Escherichia coli, Listeria monocytogenes, Salmonella typhimurium, and E. coli O157:H7 in marinades and marinated pork

This study was conducted to evaluate the effects of supercritical carbon dioxide (SC-CO₂) treatment on soy sauce and hot-pepper paste marinades, as well as in marinated pork products, for the inhibition of generic Escherichia coli, Listeria monocytogenes, Salmonella typhimurium, and E. coli O157:H7. SC-CO₂ was more effective at destroying foodborne pathogens when it was applied to the marinades than the marinated products. SC-CO₂ treatment at 14 MPa and 45 °C for 40 min resulted in a greater reduction in soy sauce (2.52–3.47 log CFU/cm²) than in hot-pepper paste marinade (2.12–2.72 log CFU/cm²). In the case of the marinated pork, when SC-CO₂ was applied at 14 MPa and 45 °C for 40 min, the reduction levels of L. monocytogenes were 2.49 and 1.92 log CFU/cm² in soy sauce and hot-pepper paste marinated pork, respectively. The results should be useful in the meat industry to help increase microbial safety and assure the microbial stability of marinades and marinated products.     

Inactivation of Escherichia coli O157:H7, Salmonella typhimurium,and Listeria monocytogenes on Stored Iceberg Lettuce by Aqueous Chlorine Dioxide Treatment

ABSTRACT: Inactivation of Escherichia coli O157:H7, Salmonella typhimurium, and Listeria monocytogenes in iceberg lettuce by aqueous chlorine dioxide (ClO₂) treatment was evaluated. Iceberg lettuce samples were inoculated with approximately 7 log CFU/g of E. coli O157:H7, S. typhimurium, and L. monocytogenes. Iceberg lettuce samples were then treated with 0, 5, 10, or 50 ppm ClO₂ solution and stored at 4 °C. Aqueous ClO₂ treatment significantly decreased the populations of pathogenic bacteria on shredded lettuce (P < 0.05). In particular, 50 ppm ClO₂ treatment reduced E. coli O157:H7, S. typhimurium, and L. monocytogenes by 1.44, 1.95, and 1.20 log CFU/g, respectively. The D₁₀‐values of E. coli O157:H7, S. typhimurium, and L. monocytogenes in shredded lettuce were 11, 26, and 42 ppm, respectively. The effect of aqueous ClO₂ treatment on the growth of pathogenic bacteria during storage was evaluated, and a decrease in the population size of these pathogenic bacteria was observed. Additionally, aqueous ClO₂ treatment did not affect the color of lettuce during storage. These results suggest that aqueous ClO₂ treatment can be used to improve the microbial safety of shredded lettuce during storage.     

Viability of multi-strain mixtures of Listeria monocytogenes, Salmonella typhimurium, or Escherichia coli O157:H7 inoculated into the batter or onto the surface of a soudjouk-style fermented semi-dry sausage

The fate of Listeria monocytogenes, Salmonella typhimurium, or Escherichia coli O157:H7 were separately monitored both in and on soudjouk. Fermentation and drying alone reduced numbers of L. monocytogenes by 0.07 and 0.74 log₁₀ CFU/g for sausages fermented to pH 5.3 and 4.8, respectively, whereas numbers of S. typhimurium and E. coli O157:H7 were reduced by 1.52 and 3.51 log₁₀ CFU/g and 0.03 and 1.11 log₁₀ CFU/g, respectively. When sausages fermented to pH 5.3 or 4.8 were stored at 4, 10, or 21 °C, numbers of L. monocytogenes, S. typhimurium, and E. coli O157:H7 decreased by an additional 0.08–1.80, 0.88–3.74, and 0.68–3.17 log₁₀ CFU/g, respectively, within 30 days. Storage for 90 days of commercially manufactured soudjouk that was sliced and then surface inoculated with L. monocytogenes, S. typhimurium, and E. coli O157:H7 generated average D-values of ca. 10.1, 7.6, and 5.9 days at 4 °C; 6.4, 4.3, and 2.9 days at 10 °C; 1.4, 0.9, and 1.6 days at 21 °C; and 0.9, 1.4, and 0.25 days at 30 °C. Overall, fermentation to pH 4.8 and storage at 21 °C was the most effective treatment for reducing numbers of L. monocytogenes (2.54 log₁₀ CFU/g reduction), S. typhimurium (5.23 log₁₀ CFU/g reduction), and E. coli O157:H7 (3.48 log₁₀ CFU/g reduction). In summary, soudjouk-style sausage does not provide a favorable environment for outgrowth/survival of these three pathogens.     

Magnetoelastic biosensor for the detection of Salmonella typhimurium in food products

In this article, a magnetoelastic sensor immobilized with polyclonal antibody for the detection of Salmonella typhimurium in food products is described. The remote query nature of magnetoelastic sensors enables the detection of bacterial species in sealed and opaque containers. Bacterial binding to the antibody on the sensor surfaces changed the resonance parameters, and these changes were quantified by the shift in the sensor’s resonance frequency. Response of the sensors to increasing concentrations (5 × 10¹–5 × 10⁸ cfu/ml) of S. typhimurium in three different food products (water, fat-free milk and apple juice) was studied and similar responses were observed. These results were also further ascertained by Scanning Electron Microscopy (SEM) studies. A detection limit of 5 × 10³ cfu/ml, with a sensitivity of 139 Hz/decade was obtained for the sensors tested in water samples, as compared to 129 Hz/decade in apple juice and 127 Hz/decade in fat free milk. A 2 × 0.4 × 0.015 mm sensor was employed in all the investigations. The dissociation constant K _d and the binding valencies for S. typhimurium spiked in water samples was 435 cfu/ml and 2.33 respectively; as compared to 309 cfu/ml and 2.38 for apple juice; and 1389 cfu/ml and 1.85 for fat free milk samples. Bacterial binding was specific and a divalent binding was observed.     

Combined treatment of fumaric acid with aqueous chlorine dioxide or UV-C irradiation to inactivate Escherichia coli O157:H7, Salmonella enterica serovar Typhimurium, and Listeria monocytogenes inoculated on alfalfa and clover sprouts

Effect of fumaric acid, chlorine dioxide (ClO₂), and UV-C treatment was examined on the inactivation of microorganisms in alfalfa and clover sprouts. Clover sprouts were irradiated with UV-C light (1–10 kJ/m²), and the treatment decreased the population of total aerobic bacteria by 1.03–1.45 log CFU/g. Clover sprouts inoculated with pathogenic bacteria were treated with various concentration of fumaric acid, and 0.5 g/100 ml fumaric acid treatment was the most effective. In addition, the combined treatment of fumaric acid (0.5 g/100 ml)/UV-C (1 kJ/m²) reduced the populations of Escherichia coli O157:H7, Salmonella enterica serovar Typhimurium, and Listeria monocytogenes inoculated on clover sprouts by 3.02, 2.88, and 2.35 log CFU/g. Alfalfa sprouts were treated with ClO₂, fumaric acid, and the combination of fumaric acid/ClO₂. The combined treatment was the most effective, and it reduced the total aerobic bacteria by 3.18 log CFU/g as well as the initial populations of E. coli O157:H7, S. typhimurium, and L. monocytogenes inoculated on alfalfa sprouts by 4.06, 3.57, and 3.69 log CFU/g. These results suggest that the combined treatment of fumaric acid with UV-C or ClO₂ can be useful for improving the microbial safety of alfalfa and clover sprouts.     

Detection of Salmonella typhimurium Grown Directly on Tomato Surface Using Phage-Based Magnetoelastic Biosensors

A phage-based magnetoelastic (ME) biosensor method is being developed for on-site pathogen detection in fresh fruits and vegetables. Salmonella typhimurium was directly grown with minimal nutrients on tomato surfaces in order to mimic natural environmental conditions. S. typhimurium was inoculated on the surface of fresh tomatoes, and ME biosensors were used to detect the bacteria. The populations of S. typhimurium after 24-h incubation time at 37°C and 100% relative humidity were 6.1 and 7.8 logCFU/cm² after starting with initial inoculations of 3.0 and 5.0 logCFU/cm², respectively. After evident growth, measurement sensors with E2 phage immobilized on their surfaces and control sensors devoid of E2 phage were placed on the inoculated tomato surfaces and the resonant frequency shifts were measured. As the population of S. typhimurium increased, the resonant frequency shifts of the measurement sensors significantly increased (P?<?0.01), exhibiting 6,680?±?665 and 9,384?±?457 Hz for the populations of 6.1 and 7.8 logCFU/cm², respectively. SEM images confirmed that the measurement sensor resonant frequency shifts were due to S. typhimurium binding with E2 phage. This study demonstrated that the ME biosensor method could detect S. typhimurium grown directly on tomato surfaces with limited sample preparation procedures. Therefore, the ME biosensor could be applied as a cost and time effective, relatively simple, practically suitable on-site detection method for S. typhimurium in fresh produce.     

Analysis and the potential applications of essential oil and leaf extracts of <Emphasis Type="Italic">Silene armeria</Emphasis> L. to control food spoilage and food-borne pathogens

The aim of this study was to analyze the chemical composition of essential oil isolated from the floral parts of Silene armeria L. by hydrodistillation and to test the efficacy of essential oil and the various leaf extracts against a diverse range of microorganisms comprising food spoilage and food-borne pathogenic bacteria. The chemical composition of essential oil was analyzed by the GC–MS. It was determined that 28 compounds, which represented 89.03% of total oil, were present in the oil. The oil contained mainly methylamine (21.48%), β-butene (17.97%), α-butene (46.40%), coumaran (0.22%), eugenol (0.21%), α-humulene (0.07%), farnesol (0.05%) and linalool (0.12%). The essential oil (5 μl/ml, corresponding to 1,000 ppm/disc) and various leaf extracts of methanol, ethyl acetate, chloroform and hexane (7.5 μl/ml, corresponding to 1,500 ppm/disc) exhibited promising antibacterial effect against Bacillus subtilis ATCC6633, Listeria monocytogenes ATCC19166, Staphylococcus aureus KCTC1916, S. aureus ATCC6538, Pseudomonas aeruginosa KCTC2004, Salmonella typhimurium KCTC2515, Salmonella enteritidis KCTC2021, Escherichia coli O157-Human, E. coli ATCC8739, E. coli O57:H7 ATCC43888 and Enterobacter aerogenes KCTC2190. The zones of inhibition of different concentrations of essential oil and the various leaf extracts against the tested bacterial pathogens were found in the range of 10–19 and 7–13 mm, respectively, along with their respective MIC values ranging from 125 to 1,000 and 250–2,000 μg/ml. Also, the essential oil had a potential effect on the viable count of the tested bacteria. The results of this study suggest that the essential oil and leaf extracts derived from S. armeria could be used for the development of novel types of antibacterial agents to control food spoilage and food-borne pathogens.     

Development of oscillation method for reducing foodborne pathogens on lettuce and spinach

In this study, the efficacy of an oscillator for reducing the numbers of foodborne pathogens on lettuce and spinach was tested. A cocktail of three strains each of Salmonella typhimurium, Escherichia coli O157:H7 and Listeria monocytogenes cells and of Bacillus cereus spores was inoculated onto lettuce and spinach leaves and followed by oscillation at 10 Hz and 20 Hz for up to 30 s. After treatment of inoculated lettuce leaf with an oscillator at 20 Hz for 30 s, 2.58, 2.82, 2.21 and 2.22 Log₁₀ CFU/g reductions were obtained with the cells of S. typhimurium, E. coli O157:H7 and L. monocytogenes and the spores of B. cereus, respectively. In the case of the oscillation treatment of spinach leaf, 2.89, 3.73, 2.46 and 2.25 Log₁₀ CFU/g reductions of those pathogens were achieved under the same condition. Statistically significant reductions were observed after oscillation treatment at 20 Hz for 5-10 s. The oscillation treatment at 10 Hz led to slightly less reductions of the pathogens tested as compared to the treatment at 20 Hz. In conclusion, the oscillation method developed shows to be highly efficacious in reducing foodborne pathogens on lettuce and spinach leaves.     

Investigation of Different Gas Sensor-Based Artificial Olfactory Systems for Screening <Emphasis Type="Italic">Salmonella typhimurium</Emphasis> Contamination in Beef

Two different electronic nose systems (metal oxide and conducting polymer based) were used to identify Salmonella typhimurium contaminated beef strip loin samples (stored at two temperatures). The sensors present in the two systems were ranked based on their Fisher criteria of ranking to evaluate their importance in discriminant analysis. The most informative sensors were then used to develop linear discriminant analysis and quadratic discriminant analysis-based classification models. Further, sensor signals collected from both the sensor systems were combined to improve the classification accuracies. The developed models classified meat samples based on the Salmonella population into “No Salmonella” (microbial counts < 0.7 log₁₀ cfu/g) and “Salmonella inoculated” (microbial counts ≥ 0.7 log₁₀ cfu/g). The performances of the developed models were validated using leave-1-out cross-validation. Classification accuracies of 80% and above were observed for the samples stored at 10 °C using the sensor fusion approach. However, the classification accuracies were relatively low for the meat samples stored at 4 °C when compared to the samples stored at 10 °C. The results indicate that the electronic nose systems could be effectively used as a first stage screening device to identify the meat samples contaminated with S. typhimurium.     

Active packaging of ground beef patties by edible zein films incorporated with partially purified lysozyme and Na2EDTA

In this study, antimicrobial activity of zein films incorporated with partially purified lysozyme and disodium ethylenediaminetetraacetic acid (Na₂EDTA) has been tested on selected pathogenic bacteria and refrigerated ground beef patties. The developed films containing 700 μg cm^?2 lysozyme and 300 μg cm^?2 Na₂EDTA showed antimicrobial activity on Listeria monocytogenes, Escherichia coli O157:H7, and Salmonella typhimurium. The application of lysozyme and Na₂EDTA incorporated zein films on beef patties significantly decreased total viable counts (TVC) and total coliform counts after 5 days of storage compared to those of control patties (P < 0.05). Zein films incorporated with lysozyme and Na₂EDTA or Na₂EDTA alone significantly slowed down the oxidative changes in patties during storage (P < 0.05). Redness indices of patties coated with zein films were significantly lower than those of uncoated control patties during storage (P < 0.05). This study demonstrated the potential usage of zein films containing lysozyme and Na₂EDTA for active packaging of refrigerated meat products.     

Sinapic acid derivatives in defatted Oriental mustard (<Emphasis Type="Italic">Brassica juncea</Emphasis> L.) seed meal extracts using UHPLC-DAD-ESI-MS<Superscript><Emphasis Type="Italic">n</Emphasis></Superscript> and identification of compounds with antibacterial activity

This study identified phenolic compounds from mustard seed meal and characterized their antibacterial activity. Phenolic compounds were extracted from defatted Oriental mustard (Brassica juncea L.) seed meal and characterized using ultra-high-performance liquid chromatography with diode array and electrospray ionization-mass spectrometric detection (UHPLC-DAD-ESI-MS ⁿ ). Sinapic acid and several sinapoyl conjugates were identified based on retention time, UV spectra, MS fragmentation pattern, and by comparison with the authentic sinapic acid reference substance. The crude extract and a purified phenolic fraction exhibited selective antibacterial effects against Gram-negative and Gram-positive spoilage bacteria including Staphylococcus aureus and Listeria monocytogenes; Lactobacillus plantarum was resistant. After alkaline hydrolysis, only sinapic acid could be detected, enabling quantification with the authentic reference substance. Alkaline hydrolysis released 2.66 ± 0.00 mg sinapic acid g⁻¹ dry matter defatted mustard seed meal. Minimum inhibitory concentrations of the hydrolyzed extract against Bacillus subtilis, Escherichia coli, L. monocytogenes, Pseudomonas fluorescens, and S. aureus were 0.1 g L⁻¹ or less. Growth of L. plantarum remained unaffected. Sinapic acid and sinapoyl esters are generally found in members of the Brassicaceae family. Methods for their fast identification will be useful in chemotaxonomic studies. The release of sinapic acid after alkaline hydrolysis not only allows for the quantification using the reference substances but also facilitates the standardization of the antibacterial activity of plant extracts for use as food preservative.     

Nano Zinc Oxide-Loaded Calcium Alginate Films with Potential Antibacterial Properties

In this work, zinc oxide nanoparticles-loaded calcium alginate films were investigated for their moisture uptake behavior at different temperatures. The equilibrium uptake data was interpreted quantitatively by GAB isotherm models. The monolayer moisture contents were 0.301 ± 0.003, 0.0214 ± 0.092, and 0.171 ± 0.102 at 20, 30, and 37°C, respectively. The water vapor transmission rate was found to be 0.816 ± 0.143, 1.42 ± 0.045, and 1.632 ± 0.064 g s⁻¹ m⁻² respectively. For the moisture content range of 0.2 to 0.6, the net ∆H and ∆S values were found to be 22.73 to 11.14 KJ/mol and 0.064 to 0.034 KJ/mol/K, respectively. The moisture uptake of films increased with water activity but showed negative temperature dependence. The enthalpy of sorption (∆H) and differential entropy (∆S) were determined at different moisture content values, ranging from 0.2 to 0.6 g/g db. The two parameters showed a higher degree of correlation. The equilibrium moisture content data was used to evaluate harmonic mean temperature T _hm. Finally, the biocidal action of films was tested against model bacteria Escherichia coli.     

Antimicrobial activity against foodborne pathogens of chitosan biopolymer films of different molecular weights

Antimicrobial activity against Listeria monocytogenes, Escherichia coli 0157:H7 and Samonella typhimurium of chitosan biopolymer films (CBFs) prepared with four different viscosities of chitosans (10, 40, 100 and 200 mPa s) were investigated by agar diffusion assay. The films were also characterized with measurements of color, tensile strength (TS), % elongation (EL), water vapor permeability and oxygen permeability. CBFs prepared with 100 mPa s chitosan showed an antimicrobial effect only on 10⁴ cfu/mL inoculation of L. monocytogenes while other viscosities showed an antilisterial effect on all concentrations (10⁴-10⁶ cfu/mL) of L. monocytogenes. CBFs prepared with 10 mPa s (CBF-10) and 40 mPa s (CBF-40) chitosans showed an inhibitory effect against E. coli 0157:H7 and S. typhimurium only at the 10⁴ cfu/mL concentration. CBFs prepared with the two higher viscosity chitosans did not show any effect regardless of bacterial level. TS and EL of the CBFs increased with increasing viscosity up to 100 mPa s. Molecular weight distribution was found to be positively correlated with viscosity. The oxygen permeability of the CBFs increased with increasing viscosity of chitosans, but water vapor transmission rate was not similarly affected. In conclusion, CBFs were more effective at inhibition of L. monocytogenes than S. typhimurium and E. Coli O157:H7. Molecular weight of chitosan must be chosen selectively to control the target foodborne pathogens.     

Bacterial inactivation and quality changes in fresh-cut avocado treated with intense light pulses

This study investigated the impact of intense light pulses (ILP) on inactivation of Listeria innocua and Escherichia coli as well as quality changes in fresh-cut avocado. Cylinders of avocado inoculated with L. innocua or E. coli were placed in plastic trays, which were sealed with a 64-μm-thick polypropylene film (oxygen permeability of 110 cm³ O₂ m⁻² bar⁻¹ day⁻¹ at 23 °C and 0% RH) and subjected to 15 or 30 pulses at fluencies of 0.4 J/cm² per pulse and then stored for 15 days at 5 °C. In addition to L. innocua and E. coli counts, the headspace atmosphere, pH, colour and firmness were measured. The growth of E. coli and L. innocua was more effectively inhibited when increasing treatment intensity. Hence, significant inactivation was obtained in samples treated with 15 and 30 pulses for L. innocua (2.61 and 2.97 log CFU/g, respectively) and E. coli (2.90 and 3.33 log CFU/g, respectively) just after processing. Oxygen concentrations were significantly reduced, whereas CO₂ and ethanol concentrations increased due to product respiration; however, ethylene production was decreased by the effect of ILP treatments. The use of 30 pulses affected the colour and firmness of fresh-cut avocado, causing browning and softening.     

Evaluation of Nano Zinc (ZnO) for Surface Enhancement of ATR–FTIR Spectra of Butter and Spread

The effect of nano zinc (ZnO) particles in surface enhancement of attenuated total reflection–Fourier transform mid-infrared spectroscopy (ATR–FTIR) has been studied in butter and spread. Due to the health implications associated with consumption of trans fats, the studies also included the determination of band corresponding to trans fats of butter/spread in the nano-zinc-treated samples. The FTIR spectra of nano-zinc-treated butter showed enhancement of bands related to (―C―O, ―CH₂―) at wave number 1,238 cm⁻¹ and (O―C―C) band of esters at wave number 1,100 cm⁻¹. Shifting in wave number to 1,150 cm⁻¹ and reduction in its peak intensity was observed with the band corresponding to 1,162 cm⁻¹ (―C―O stretch). Reduction in peak intensity of the bands at about 2,915 and 2,850 cm⁻¹ (C―H groups) was also observed. In the case of spread, nano zinc reduced the peak intensities of FTIR bands at 2,915 cm⁻¹, 2,850 cm⁻¹ (―C―H― (CH₂) stretches), 1,746 cm⁻¹ (―C═O ester), 1,465 cm⁻¹ (―C―H (CH₂, CH₃)), 1,375 cm⁻¹ (―C―H (CH₃)) and 1,156 cm⁻¹ (C―O, ―CH₂). Trans fats band corresponding to ═C―H stretch (trans bonds, 966 cm⁻¹), was observed in pure butter and spread. Trans fatty acids in butter and spread were quantified with the aid of calibration/validation standards using trielaidin and triolein and by using partial least squares regression analysis. However, the band at 966 cm⁻¹ was hindered in Zn-treated butter and reduced in Zn-treated spread.     

Properties of <Emphasis Type="Italic">Aspergillus subolivaceus</Emphasis> free and immobilized dextranase

Aspergillus subolivaceus dextranase is immobilized on several carriers by entrapment and covalent binding with cross-linking. Dextranase immobilized on BSA with a cross-linking agent shows the highest activity and considerable immobilization yield (66.7%). The optimum pH of the immobilized enzyme is shifted to pH 6.0 as compared with the free enzyme (pH 5.5). The optimum temperature of the reaction is resulted at 60 °C for both free and immobilized enzyme. Thermal and pH stability are significantly improved by the immobilization process. The calculated K _m of the immobilized dextranase (14.24 mg mL⁻¹) is higher than that of the free dextranase (11.47 mg mL⁻¹), while V _max of the immobilized enzyme (2.80 U μg protein⁻¹) is lower than that of the free dextranase (11.75 U μg protein⁻¹). The immobilized enzyme was able to retain 76% of the initial catalytic activity after 5.0 cycles.     

In situ hybridization of microcolonies using catalyzed reporter deposition with tetramethylbenzidine: a method for detecting low numbers of bacterial cells in drinking water

In this study, catalyzed reporter deposition in situ hybridization (CARD—ISH) with tetramethylbenzidine (TMB) was used for rapid detection of the food pathogens Salmonella typhimurium and Escherichia coli. The bacteria in a sample were concentrated by membrane filtration. The filter membranes with the cells thus removed were incubated on nutrient agar for 4–5 h to allow the formation of microcolonies. Instead of fluorescent tyramide, 3,3′,5,5′-tetramethylbenzidine (TMB), which yields a blue precipitate, was used for signal amplification after in situ hybridization. Microcolonies amplified with TMB produced blue signals, which were sufficiently intense to allow visual evaluation either using a stereomicroscope, or even with the naked eye. Therefore even low cell numbers of hygienically critical bacteria can be detected on the filter membrane without a protracted examination. This enables the detection of low cell numbers (<10 cfu) in a sample of 100 ml tap water within 9–10 h.     

Polycyclic aromatic hydrocarbons (PAHs) in traditional and industrial smoked beef and pork ham from Serbia

Smoked beef and pork ham samples were analysed during process of smoking (after packing and storing) for the presence of the 16 EU priority PAHs via Fast GC/HRMS method. This study showed that there are differences in PAH contents between final smoked beef ham samples from traditional smokehouse (TS) (3.9 μg kg⁻¹) and industrial smokehouse (IS), (1.9 μg kg⁻¹). Also there is a difference in PAH contents in final smoked pork ham samples (4.9 μg kg⁻¹, TS; 4.2 μg kg⁻¹, IS). In beef and pork ham samples from the same smokehouse different PAH contents were observed during smoking. The highest content of examined PAHs in all beef and pork ham samples during smoking showed benzo[c]fluorene (BcL) (beef ham: from 0.3 μg kg⁻¹ to 1.5 μg kg⁻¹; pork ham: from 0.2 μg kg⁻¹ to 2.1 μg kg⁻¹).The maximum level for benzo[a]pyrene (BaP) of 5 μg kg⁻¹ in smoked meat products was not exceeded in any samples. Correlation statistic analysis (P < 0.05) of obtained contents from samples both from TS and IS showed that BaP is a good marker both for 16 EU priority PAHs and 12 IARC probably and possibly carcinogenic PAHs (IS: R _BaP/Σ16PAHs = 0.95, R _BaP/Σ12PAHs = 0.96; TS: R _BaP/Σ16PAHs = 0.71, R _BaP/Σ12PAHs = 0.88).     

Effects of electron beam irradiation on microbial inactivation and quality of kimchi paste during storage

The effects of electron beam irradiation on microbial inactivation and quality of noninoculated and inoculated (Listeria monocytogenes) kimchi pastes were examined. Kimchi paste samples were irradiated at doses of 2, 4, 6, 8 and 10 kGy and stored for 21 days at 4 °C. Irradiation (10 kGy) reduced the populations of total aerobic bacteria, lactic acid bacteria, and yeast and moulds in the samples by 1.72, 2.24 and 0.86 log CFU g^?1, respectively, compared to the control. In particular, coliforms were not detected at 8 and 10 kGy, and the population of L. monocytogenes in inoculated samples was significantly decreased by 2.67 log CFU g^?1. Electron beam irradiation delayed the changes in O₂ and CO₂ concentrations, pH, acidity and reducing sugar content observed in kimchi paste during storage. These results suggest that electron beam irradiation can be used to improve the microbiological safety and shelf life of kimchi paste.