Combined antibacterial activity of green tea extract with atmospheric radio-frequency plasma against pathogens on fresh-cut dragon fruit

The objective of this research was to observe the combined effect of green tea extract (at a tea: water; g ml⁻¹, ratio of 2.5–10.0%) and cold plasma (20 W and 40 W) against bacteria pathogens (Escherichia coli, Salmonella typhimurium, and Listeria monocytogenes) that can be found on the fresh-cut dragon fruit. The change in pathogens after plasma treatment of a fresh-cut dragon fruit treated with green tea at 4 ± 1 °C was also investigated. Dragon fruit's nutritional value, mineral, total phenolic content, and sensory within and without plasma and green tea was determined. It was found that atmospheric radio-frequency (RF) plasma at 40 W could extend the protection against all pathogen growth on the surface of fresh-cut dragon fruit treated with at a 5.0% of green tea to at least 15 days. Without the plasma treatment, green tea of 2.5–10.0% could not inhibit all bacterial growth. In addition, higher values of total phenolic content, crude protein, crude fat and crude fibre were observed in the fresh-cut dragon fruit with green tea after the plasma (p < 0.05) treatment; however, no change was found (p > 0.05) regarding the minerals Fe, Cu, and Mn and the sensory test. The research indicated that green tea extract and atmospheric RF plasma in combination could protect against the growth of pathogens on fresh-cut dragon fruit and extend its shelf-life.     

Synergetic antibacterial efficacy of cold nitrogen plasma and clove oil against Escherichia coli O157:H7 biofilms on lettuce

This study aims to evaluate the antimicrobial effects of cold nitrogen plasma (CNP) and clove oil against Escherichia coli O157:H7 (E. coli O157:H7) biofilm on lettuce. Both clove oil (1 mg/mL, 2 mg/mL and 4 mg/mL) and CNP (400–600 W) displayed significant eradication effect on E. coli O157:H7 biofilms in vitro (p < 0.001). Subsequently, the antibiofilm effect of combined treatment was studied as well. Compared with the respective treatment, combined treatment exhibited remarkable synergistic effect on eradicating E. coli O157:H7 biofilms. The confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM) had also visually testified that the antibacterial effects of clove oil on E. coli O157:H7 biofilms (in vitro and on lettuce) were enhanced by CNP at 400 W for short treatment duration. The results of sensory evaluation indicated that combined treatment has mild negative effect on lettuce quality. Moreover, the synergetic antibacterial mechanism of clove oil and CNP against E. coli O157:H7 was concluded as that they could damage the bacterial cell wall and the outer membrane, leading to leakage of cellular components, such as nucleic acid and ATP.     

Antifungal activity of Michelia alba oil in the vapor phase and the synergistic effect of major essential oil components against Aspergillus flavus on brown rice

The objectives of this study were to investigate the effect of essential oil (Michelia alba) vapor on the spore germination and mycelium growth of Aspergillus flavus on brown rice and to perceive the shelf life of the brown rice could be extended to a longer storage time. Different volumes (150, 300, 450 μl) of M. alba and a 300 μl linalool/caryophyllene combination at ratios of 10:1, 1:1, and 1:10 were first absorbed into plant absorbent material (Φ∼20 mm) before being put into a closed glass box (1L) containing A. flavus spore and the mycelium (Φ∼5 mm) in a Malt Extract Agar (uncovered plate). Mold testing was also carried out on brown rice with A. flavus spore suspension before being incubated at 25° C and 100% RH for 16 weeks. Quality tests e.g. texture, a sensorial evaluation (hedonic scale) of brown rice were also conducted. Results indicated that the vapor phase of M. alba at ≥ 300 μl L⁻¹ air could inhibit both spore germination and A. flavus mycelium. Antifungal activity of M. alba in air was strongly correlated with the linalool/caryophyllene combination at the ratio of 10:1 in 300 μl L⁻¹ air. In addition, M. alba vapor at 300 μl L⁻¹ air was found to extend the shelf-life of the brown rice by four times (16 weeks) in comparison with the control treated without essential oil (4 weeks). After being cooked, the hardness of brown rice with volatile essential oil was found to be reduced by one third (compared to the control brown rice). The hedonic value (overall liking) of cooked brown rice packed with M. alba vapor at 300 μl for 1 week and then stored for 16 weeks was a 7, rated as “like moderately”. Therefore, this study has demonstrated the good potential of M. alba vapor to control mold growth on the surface of brown rice.     

Antimicrobial peptides derived from hen egg lysozyme with inhibitory effect against Bacillus species

In food industry, Bacillus species are encountered in deteriorating many food products thus shortening their shelf-life. Moreover, Bacillus cereus and the subtilis group (Bacillus subtilis, Bacillus licheniformis, and Bacillus pumilus) have been recognized as food poisoning agents. Lysozyme peptides preparation (LzP) is a commercially available as a natural food preservative. Although, LzP derived from lysozyme yet it showed only 11% of the lysozyme lytic activity. LzP at a concentration of 100 μg ml⁻¹ completely inhibited B. subtilis, B. licheniformis, B. megaterium, B. mycoides, B. pumilus, B. coagulans, B. amyloliquefaciens, B. polymexa and B. macerans. However, B. cereus and B. stearothermophilus showed a slightly higher resistance. Interestingly, LzP at concentration ⩾10 μg ml⁻¹ showed inhibitory effect on both vegetative and spore forms of B. subtilis. Moreover, LzP was stable at 95 °C for 30 min and at different pH values (4.5–7). In conclusion, LzP may be useful to control growth of Bacillus spoilage organisms.     

Degradation of fumonisin B1 by cinnamon essential oil

Fumonisins are group of mycotoxins produced mainly by Fusarium verticillioides and Fusarium proliferatum. They frequently contaminate corn and corn based products, and cause several diseases in humans and animals. Fumonisin B₁ (FB₁) is the most prevalent fumonisin and is highly toxic to human and animal. The essential oils from plants offer a hope in the prevention and detoxification of these mycotoxins. The present study investigates the degradation effect of cinnamon, citral, Litsea cubeba, clove, eucalyptus, anise, spearmint and camphor oils on FB₁. The degradation level of FB₁ was determined by ELISA. Cinnamon oil proves to be effective essential oil in reducing FB₁, followed by citral, eugenol oil, eucalyptus oil, anise oil and camphor oil. The effects of incubation time, and temperature with respect to the concentration of cinnamon oil on their degradation effect on FB₁ by cinnamon oil were investigated. Results showed that at 120 h time with the 280 μg/ml concentration of cinnamon oil, under 30 °C is optimal for FB₁ reduction. Under optimal condition, FB₁ was reduced from 15.03 to 0.89 μg/ml (94.06%). Cinnamon oil could be a promising candidate in the detoxification and control of FB₁ in corn based products.     

Effects of Zataria multiflora Boiss. essential oil and nisin on Bacillus cereus ATCC 11778

The effects of different concentrations of Zataria multiflora Boiss. essential oil (EO, 0.0%, 0.005%, 0.015%, 0.03% and 0.045%) and nisin (N, 0.0, 0.25, 0.5, 1.5 and 2.5 μg ml⁻¹), pH values (7.4, 6.5 and 6.0), temperatures (Ts, 10, 20 and 30 °C) and storage times (Ds, up to 43 days) on log₁₀ probability percentage of growth initiation (log P%) of one vegetative cell of Bacillus cereus in brain heart infusion broth were evaluated in a factorial design study. The log P% of the organism was significantly affected (P < 0.01) by the values of EO, N, pH, T and D.The combinations of T ⩾ 20 °C, EO ⩽ 0.03% and pH values (7.4, 6.5 and 6.0) could not obviously affect the growth of the organism in this study. Whereas, the strong inhibitory action was observed by increasing EO concentration to 0.045 at T ⩾ 20 °C and selected pH values (7.4, 6.5 and 6.0) and by decreasing temperature to 10 °C at EO ⩾ 0.015% and pH values used in this study. The inhibitory effect of N also was enhanced by decreasing storage temperature to 10 °C at the selected pH values (7.4, 6.5 and 6.0) in this study.The growth of the organisms was strongly affected by increasing EO concentration to 0.03% in combination with N concentrations used at the selected temperatures in this study. The growth of the organism was completely inhibited at combinations EO ⩾ 0.015%, N ⩾ 1.5 μg ml⁻¹, T ⩽ 30 °C and pH ⩽ 7.4 during 43 days of storage in this study. This synergistic effect of EO and N was enhanced in lower pH values (6.5 and 6.0) in the present study. The growth of organism was completely inhibited at combinations of EO ⩾ 0.005 and N ⩾ 1.5 μg ml⁻¹ at pH = 6.0, and EO ⩾ 0.03 and N ⩾ 0.5 μg ml⁻¹ at pH ⩽ 6.5 during the study at the selected Ts (30, 20 and 10 °C).     

Antimicrobial activity of clove (Syzgium aromaticum) oil in inhibiting Listeria monocytogenes on chicken frankfurters

The ability of Listeria monocytogenes to survive and grow at refrigeration temperature in some ready to eat (RTE) poultry products is a public health concern. The inhibitory effect of clove oil (1% and 2%, v/w) applied to the surface of RTE chicken frankfurters was determined on seven strains of L. monocytogenes inoculated at low (10²–10³ cfu/g) or high cell numbers (10⁴–10⁶ cfu/g), and stored at 5 °C for 2 weeks or at 15 °C for 1 week. All strains of L. monocytogenes survived and grew on control frankfurters at 5 °C and 15 °C but growth was inhibited under both storage conditions in the presence of either 1% or 2% clove oil. Depending on the sensory considerations, the addition of clove oil to frankfurters may be an effective strategy to control L. monocytogenes in chicken frankfurters.     

Inactivation kinetics for Salmonella Enteritidis in potato omelet using microwave heating treatments

The aim of this study was to model the inactivation of Salmonella enterica serovar Enteritidis in pasteurized omelet internally inoculated at different microwave heating treatments (300 W; 450 W, 600 W and 800 W). Results indicated a non significant change in Salmonella populations during the first 30 s treatment at 300 W and 450 W, being log reductions lower than 0.5 log CFU g⁻¹. However, after 40 s treatment, log reductions had risen to 4.8 log CFU g⁻¹ at 800 W. Inactivation rates were higher at 600 W and 800 W (0.67 and 0.63 s⁻¹) than at 300 W and 450 W (<0.34 s⁻¹). The temperature-dependent parameters of a Weibull model obtained by Mattick, Legan, Humphrey & Peleg (2001) were evaluated. It was concluded that combinations characterized by a temperature equal or above 70 °C ensured a minimum 4 log reduction of Salmonella population (i.e. 300 W-80 s; 450 W-60 s or 600 W/800 W-40 s). These results may be of value in food service establishments, as target treatments for microwavable potato omelet portions.     

Biotransformation of patulin to hydroascladiol by Lactobacillus plantarum

Growth of Penicillium expansum, an ubiquitous mould found in stored fruit globallyt, was significantly restricted by exposure to 48 h cell-free supernatant of two strains of Lactobacillus plantarum (p < 0.001). In addition, the biotransformation of patulin, a toxic secondary metabolite formed by P. expansum, on exposure to L. plantarum cells and cell-free supernatant highlights the potential of this GRAS microbe as a biocontrol agent. Up to 80% of patulin was biotransformed following a 4 h incubation with 10¹⁰ cells ml⁻¹ (37 °C) forming E- and Z-ascladiol. The formation of these products was more pronounced at elevated pH and cell density. Exposure to cell free supernatant or sonicated cells resulted in complete patulin biotransformation with heat treatment inhibiting this effect. The ascladiol isomers were then further transformed over a 4-week cell-free incubation (4 °C) into the novel metabolite hydroascladiol (5-(2-hydroxyethyl)-4-(hydroxymethyl) furan-2(5H)-one) which produced a 2 amu difference across the main tandem mass fragments (113.1, 129.0, 139.0), compared to ascladiol (111.1, 127.0, 137.0). This suggests hydroascladiol could be a better biomarker of initial patulin levels in some food commodities. The in vitro biotransformation data and resistance of L. plantarum to highly elevated concentrations of patulin (≥100 μg ml⁻¹) suggest L. plantarum is a potential candidate for food preservation or remediation strategies and future work with fruit products is proposed.     

In vitro antibacterial activity of Australian native herb extracts against food-related bacteria

The antibacterial activities of water, ethanol and hexane extracts of five Australian herbs (Backhousia citriodora, Anetholea anisata, Eucalyptus staigerana, Eu. olida and Prostanthera incisa) against seven food-related bacteria (Enterococcus faecalis, Escherichia coli, Listeria monocytogenes, Pseudomonas aeruginosa, Salmonella Enteritidis, Sal. Typhimurium and Staphylococcus aureus) were determined by the microtitre broth microdilution assay. The water extracts of all the herbs displayed no or low antimicrobial activity against all of the bacteria tested with the exception of S. aureus. Relatively high levels of activity (minimum inhibitory concentrations of 125–15.6 μg ml⁻¹) against this pathogen were present in water extracts from all herbs except P. incisa. The ethanol and hexane extracts of all herbs displayed some activity against a number of the bacteria tested, with no one particular herb displaying an obviously higher level or range of activity. Staphylococcus aureus proved to be the most sensitive of the bacteria tested against the solvent extracts with all extracts displaying activity ranging from 125 to 7.8 μg ml⁻¹, while E. coli and L. monocytogenes, on the other hand, proved the least sensitive with only five of 15 herb/extract combinations displaying any activity against these pathogens. The extracts of the Australian native herbs examined in this study have potential for application in foods to increase shelf-life or promote safety.     

Growth inhibition and morphological alterations of Fusarium verticillioides by cinnamon oil and cinnamaldehyde

Fusarium verticillioides is a filamentous fungus and a widely distributed pathogen having the ability to infect and cause destruction in economically important crops and grains by producing fumonisin mycotoxins. In the present study, the inhibitory effect of cinnamon, citral, Litsea cubeba oil, clove, eucalyptus, anise, spearmint and camphor oils on F. verticillioides was investigated, and cinnamon oil proves to be the most effective in inhibition. The antifungal effect of cinnamon oil was studied with special reference to its mechanism of inhibition of F. verticillioides growth at the morphological and ultrastructural levels. For F. verticillioides, the minimal inhibitory concentrations (MICs) of cinnamon oil (85% cinnamaldehyde), natural cinnamaldehyde (95%), and synthetic cinnamaldehyde (99%) were 60, 50, and 45 μL/L, respectively. The antifungal activity of cinnamon oil was proportional to its cinnamaldehyde concentration. Scanning electron microscopy and transmission electron microscopy of F. verticillioides exposed to MIC of cinnamaldehyde showed irreversible deleterious morphological and ultrastructural alterations, such as lack of cytoplasmic contents, loss of integrity and rigidity of the cell wall, plasma membrane disruption, mitochondrial destruction, folding of the cell. These modifications induced by cinnamaldehyde may be due to its interference with enzymatic reactions of cell wall synthesis, thus affecting the morphogenesis and growth of the fungus. These results further emphasized the toxicity of cinnamon oil against F. verticillioides attacking grains, and that cinnamon oil could be safely used as an alternative to chemical fungicides during grain storage and in the field.     

Occurrence of four mycotoxins in cereal and oil products in Yangtze Delta region of China and their food safety risks

A total of 76 cereal and oil products collected from Yangtze Delta region of China were analyzed for occurrences of aflatoxins (AFs), aflatoxin B₁ (AFB₁), ochratoxin A (OTA), deoxynivalenol (DON) and zearalenone (ZEN). The mycotoxins were determined by the standard detection procedures using immunoaffinity column clean-up coupled with fluorometer (or HPLC-UV). ZEN was the most prevalent toxin, with the incidence of 27.6% (range = 10.0–440.0 μg kg⁻¹), and 9.2% of the evaluated samples were contaminated with a concentration higher than that of the legislation limit of China (60 μg kg⁻¹). AFs and AFB₁ were detected in 14.5% of the samples analyzed, the concentrations ranging 1.1–35.0 μg kg⁻¹ for AFs, and 1.0–32.2 μg kg⁻¹ for AFB₁; 4.0% of the samples had the concentrations of AFs and AFB₁ higher than that of the corresponding legislation limits of China (5.0, 10.0 and 20.0 μg kg⁻¹ for different products). OTA was detected in 14.5% of the cereal and oil products collected; the concentrations ranged 0.51–16.2 μg kg⁻¹. Only 2 samples showed OTA levels higher than that of the legislation limit of China (5.0 μg kg⁻¹). DON was detected in 7.9% of the samples; the concentrations ranged 100–700 μg kg⁻¹, and none of the samples showed DON concentration higher than that of the legislation limit of China (1.0 mg kg⁻¹). A total of 15.8% cereal and oil products were contaminated with at least two mycotoxins (multiple contaminations with different combinations including AFs-ZEN, AFs-OTA-ZEN, OTA-ZEN, ZEN-DON, OTA-ZEN-DON). The dietary exposure assessment results indicated that AFs (AFB₁), OTA, DON and ZEN from cereal-based products represented a series health risk to both adults and children in Yangtze Delta region of China. This is the first report of safety evaluation associated with major mycotoxins for the area.     

Application of solid phase extraction and two-dimensional gas chromatography coupled with time-of-flight mass spectrometry for fast analysis of polycyclic aromatic hydrocarbons in vegetable oils

A fast and simple solid-phase extraction (SPE) method followed by comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC × GC–TOFMS) has been developed for analysis of 15 + 1 carcinogenic polycyclic aromatic hydrocarbons (PAHs) in vegetable oils. Of three critically assessed sample preparation approaches – (i) gel permeation chromatography (GPC), (ii) GPC followed by silica based SPE, and (iii) SPE employing PAHs-dedicated molecularly imprinted polymers (MIPs), the latter one was selected as the best option. Recoveries of the overall analytical procedure ranged from 70 to 99%, with repeatabilities in the range of 2–11%. Limits of quantitation (LOQs) ranging for individual PAHs from 0.1 to 0.3 μg kg⁻¹, were fairly below the maximum level 2 μg kg⁻¹ established for the PAHs representative, benzo[a]pyrene (BaP), by EU Legislation for this commodity. Within the mini-survey in which the new method was employed for examination of 35 samples of various kinds of vegetable oils collected at the Czech market, the highest PAH4 levels, i.e. the sum of BaP, benz[a]anthracene (BaA), benzo[b]fluoranthene (BbFA) and chrysene (CHR) were found in sea buckthorn (708 μg kg⁻¹) followed by rapeseed oil (99.8 μg kg⁻¹). Altogether 8 samples from 35 examined vegetable oils exceeded the maximum limit 2 μg kg⁻¹ for BaP and 10 samples exceeded 10 μg kg⁻¹ set for PAH4 which is fixed by Commission Regulation (EU) no 835/2011 for oils.     

Validation of a method of high performance liquid chromatography with fluorescence detection for melamine determination in UHT whole bovine milk

A method of high performance liquid chromatography with fluorescence detection (HPLC-Fluo), based on previous studies of the natural fluorescence emission of melamine (250/365 nm), was developed and validated for melamine determination as an adulterant of bovine UHT whole milk. The clean up treatment of milk samples by deproteinization was thoroughly optimized. No matrix effect was observed and a linear range from 0.05 to 10.0 μg mL⁻¹ was obtained, with a value of R² equal to 0.9998. The limits of detection and quantification of melamine were 0.0081 and 0.027 μg mL⁻¹ respectively, or 0.023 and 0.076 μg g⁻¹ of milk, respectively, considering the sample dilution during extraction. Extracts of milk samples fortified with melamine at three concentration levels, two of which corresponded to the levels established by WHO for melamine in foods, led to an overall mean recovery of 95.4 ± 1.2% (n = 9). This recovery value satisfies the performance criteria established by the Codex Alimentarius for analytical methods suitable for determination of food residues, demonstrating the usefulness and effectiveness of the proposed method.     

Essential oil composition and biological/pharmacological properties of Salmea scandens (L.) DC

Salmea scandens (L.) DC is an indigenous edible plant whose stem bark is traditionally used as food by people of Oaxaca, México. Proximate analysis of the edible stem bark revealed abundant amounts of fiber (43.67%) and protein (9.27%). GC and GC-MS analyses demonstrated that the essential oil from leaves contained high levels of germacrene D (47.1%) and elemol (15.3%), whereas that of the stem bark contained the alkylamides N-Isobutyl-(2E,4E,8Z,10E/Z)-dodecatetraenamide isomers (39.7%). Levels of these compounds in the essential oil from both organs were in similar concentrations in all seasons except winter. The HPLC purified N-Isobutyl-(2E,4E,8Z,10E/Z)-dodecatetraenamide isomers produced a non-competitive inhibition on porcine pancreatic lipase. The enzymatic assays with these compounds revealed a modification on V_max (0.0431–0.0533 mM min⁻¹) whereas the K_m value (0.880–0.881 mM) was not significantly changed. Essential oil from the stem bark showed a high anti-microbial activity against some phytopathogenic microorganisms. The MIC's in μg mL⁻¹ for Pseudomonas syringae pathovars were tabaci 56.1, tomato 91.2 and phaseolitica 196.4, for Clavibacter michiganensis 35.8 and Erwinia carotovora 48.1. The fungi Fusarium oxysporum and Phytophthora infestans had MIC's in μg mL⁻¹ of 3.3 and 2.4 respectively. Same essential oil was highly effective against larvae from Aedes aegypti (LC₅₀ = 0.3 μg mL⁻¹) and Anopheles albimanis (LC₅₀ = 2.5 μg mL⁻¹).     

Effect of pesticide residues in grapes on alcoholic fermentation and elimination of chlorothalonil inhibition by chlorothalonil hydrolytic dehalogenase

The effect of different kinds of pesticide residues in grapes on alcoholic fermentation by Saccharomyces cerevisiae was evaluated. Among four types of pesticides added into the grape slurry, omethoate, triadimefon and cyhalothrin did not inhibit the alcoholic fermentation at their proposed spraying concentration of 0.21, 0.10 and 0.10 g L⁻¹, respectively, whereas chlorothalonil concentration above 0.03 g L⁻¹ behaved significantly negative influence on both S. cerevisiae growth and alcoholic fermentation efficiency. When the chlorothalonil concentration was lower than 0.01 g L⁻¹, the fermentation proceeded smoothly without any degradation of chlorothalonil. Considering the cumulative toxicity and adverse effect of chlorothalonil on fermentation, chlorothalonil hydrolytic dehalogenase (Chd) extracellularly expressed from the recombinant Bacillus subtilis WB800 was used to pretreat the chlorothalonil-contaminated grape slurry. After treatment by the Chd enzyme in an activity of 7.25 mU L⁻¹ slurry for 60 min, the inhibition effect could be substantially eliminated even at an initial concentration of 0.10 g L⁻¹ chlorothalonil. This study provides a potential approach for solving the conflict in fermentation industry with pesticides inhibition.     

A survey of mycotoxins in random street-vended snacks from Lagos,Nigeria, using QuEChERS-HPLC-MS/MS

A survey in African snacks was carried out in order to evaluate the intake of 23 mycotoxins. The African snack samples were purchased from street vendors within Lagos metropolis (Nigeria) and evaluated for the presence of 23 mycotoxins using a modified QuEChERS procedure coupled with liquid chromatography-triple quadrupole linear ion trap mass spectrometer. The snacks included akara, baked coconut, coconut candy, donkwa, groundnut cake (kulikuli), lafun, milk curd (wara), fresh and dried tiger-nuts, and yam flour. Only three mycotoxins were detected in 23.8% of the studied snacks, and at concentrations ranging from 6 to 54 μg kg⁻¹. The concentrations of aflatoxin B₁ (AFB₁) and AFB₂ reached 23 μg kg⁻¹ and 3 μg kg⁻¹, respectively. Moreover a sample of baked coconut contained α-zearalenol (α-ZOL), which was up to 54 μg kg⁻¹ in coconut candy. As considers prevalence, aflatoxins and α-ZOL were not detected in lafun and groundnut-based snacks (donkwa and kulikuli), whereas each of the three mycotoxins contaminated 12.5% (1/8) of the coconut-based samples. This is the first report of α-ZOL in cassava and coconut, and their products. AFB₁ and total aflatoxins (TAFs) concentrations exceeded the maximum allowable limit recommended by National Agency for Food and Drug Administration and Control Nigeria (NAFDAC) in one sample of baked coconut (AFB₁ = 23 μg kg⁻¹ and TAFs = 26 μg kg⁻¹) and donkwa (AFB₁ = 19 μg kg⁻¹ and TAFs = 21 μg kg⁻¹).     

Influence of cold plasma on fungal growth and aflatoxins production on groundnuts

In this study, influence of cold plasma on the Aspergillus parasiticus and Aspergillus flavus growth and aflatoxins productions have been investigated as an alternative to chemical free and thermal treatments. Artificially inoculated fungal species onto the groundnuts were treated with air plasma at 40 W and 60 W power levels at various time intervals. After the plasma treatment, inactivation of A. parasiticus and A. flavus was examined and the concentration of aflatoxins produced was analyzed using high performance liquid chromatography. There is 97.9% and 99.3% reduction in the growth of A. parasiticus and A. flavus respectively, when treated at 60 W powers. Electron microscopy was also used to study the effect of cold plasma on the cellular membranes of the spores. Results showed complete disintegration of fungal spore membrane due to electroporation and etching caused by the reactive species of plasma. In 40 W 15 min and 60 W 12 min plasma treated samples more than 70% and 90% reduction in aflatoxin B1 content was observed. These results suggest that cold plasma may be considered as alternative methods for disinfestation of foods due to its strong potential for microbial inactivation.     

Effects of a partially digested whey protein concentrate on Salmonella enterica serotype Typhimurium adhesion to Caco-2 cells: Prevention of Salmonella adhesion to Caco-2 cells using whey

The effect of a partially lipase-digested whey protein concentrate (WPD) containing free fatty acids on the adherence of Salmonella enterica serovar Typhimurium to Caco-2 cells was investigated. A short concurrent exposure of the Caco-2 monolayers and WPD caused dose-dependent inhibition of bacterial adhesion. Pre-treatment of S. Typhimurium with WPD resulted in inhibition of adhesion equivalent to that with concurrent administration, whereas treatment with WPD did not significantly inhibit adhesion. WPD was not bactericidal towards S. Typhimurium at up to 50 mg ml⁻¹ for up to 1 h, but was bacteriostatic over 12 h. High concentrations of WPD (>20 mg ml⁻¹) were cytotoxic to newly-confluent cell monolayers, depending on the duration of exposure. Lactoferrin (LF), caseinoglycomacropeptide (CGMP), and gamma globulins all significantly inhibited S. Typhimurium adhesion.     

Determination of aflatoxins in walnut sujuk and Turkish delight by HPLC-FLD method

This study aims to assess the risk of aflatoxins (AFs) in traditional confectionery products (walnut sujuk and Turkish delight) of Turkey. A high performance liquid chromatography coupled with fluorescence detection (HPLC-FLD) method was used for the determination of AFs. Evaluation of the method showed good selectivity, linearity, recovery and precision. The limit of quantification (LOQ) ranged from 0.106 to 0.374 μg kg⁻¹. The expanded measurement uncertainty was less than 40% for all target analytes. The validated method was successfully applied to the determination of AFs in 112 traditional confectionery products containing nuts (hazelnuts and walnuts). AFs were detected in 43.8% of walnuts and 60.9% of hazelnuts used as ingredients in walnut sujuk and Turkish delight and at levels ranging from 0.58 to 15.2 μg kg⁻¹ and 0.43–63.4 μg kg⁻¹, respectively. This means that AFs levels in walnut sujuk and Turkish delight were up to levels of 6.1 and 9.5 μg kg⁻¹, respectively. Six walnut samples and twenty-one hazelnut samples were above the EU maximum limits (MLs) of 2 and 5 μg kg⁻¹ for aflatoxin B₁ (AFB₁), respectively.