Effect of Hibiscus sabdariffa extract and Nigella sativa oil on the growth and aflatoxin B1 production of Aspergillus flavus and Aspergillus parasiticus strains

This study was undertaken to evaluate the inhibitory effect of Hibiscus sabdariffa calyx extract at concentrations of 5, 7.5, 10 and 12.5 g/100 ml and Nigella sativa oil at concentrations of 1, 2 and 3 ml/100 ml on the growth and aflatoxin B₁ production by Aspergillus parasiticus (CBS 921.7) and Aspergillus flavus (SQU 21) strains. The inhibition of aflatoxin B₁ production by the different concentrations of H. sabdariffa calyx ranged between 91.5-97.9% and 87.1-93.3% for A. flavus and A. parasiticus strains, respectively, whereas the inhibition by different concentrations of N. sativa oil ranged between 47.9 and 58.3% for A. flavus and 32-48% for A. parasiticus strains. The different concentrations of H. sabdariffa calyx and N. sativa oil had no significant effect on the growth of either Aspergillus species. Neither H. sabdariffa calyx nor N. sativa oil detoxified pure aqueous aflatoxin. Our results suggest that H. sabdariffa calyx and N. sativa oil extracted from seeds had metabolic effects on aflatoxin biosynthesis pathway of both Aspergillus species and can be used as an effective biocontrol and non-toxic biopreservatives in food industry against aflatoxin contamination.     

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.     

The potential of some spice essential oils in the control of A. parasiticus CFR 223 and aflatoxin production

Essential oils of sweet basil (Ocimum basilicum), cassia (Cinnamomum cassia), coriander (Coriandrum sativum) and bay leaf (Laurus nobilis) at 1–5% (v/v) concentration in palm kernel broth inoculated with spore suspension (10⁶/ml) of Aspergillus parasiticus CFR 223 were evaluated for their potential in the control of aflatoxigenic fungus A. parasiticus CFR 223 and aflatoxin production. Healthy sorghum grains (120/treatment) immersed in the oils and distributed in three petri dishes with wet cotton wool were also inoculated with spore suspension (10⁶/ml) of A. parasiticus CFR 223 and assayed for grain protection. Sweet basil oil at optimal protective dosage of 5% (v/v) was fungistatic on A. parasiticus CFR 223 and aflatoxins produced in vitro and on fungal development on sorghum grains (P ⩽ 0.05) with a residual effect that lasted for 32 days. In contrast, oils of cassia and bay leaf stimulated the mycelia growth of the fungus in vitro but reduced the aflatoxin concentration (B₁ + G₁) of the fungus by 97.92% and 55.21% respectively, while coriander oil did not have any effect on both the mycelia growth and aflatoxin content of the fungus. The combination of cassia and sweet basil oils at half their optimal protective dosages (2.5% v/v) completely inhibited the growth of the fungus. The feasibility of implementing the results of this study to control aflatoxins was examined by the addition of whole and ground dry basil leaves at 5% and 10% (w/w), respectively, to 10 g sorghum, groundnut, maize and melon seed after 35 days storage period. It was found that the addition of whole and ground basil leaves markedly reduced aflatoxin contamination; however, 10% (w/w) of whole leaves was more effective as the reduction in aflatoxin was between 89.05% and 91%.The findings showed that aflatoxins can be controlled by co-storing whole sweet basil leaves with aflatoxin infected foods. The economic value of the study lies in the simplified technique for control of aflatoxin contamination in agricultural products and the benefits derivable from the use of local resources.     

Aflatoxigenic fungi and aflatoxins occurrence in sultanas and dried figs commercialized in Brazil

The presence of aflatoxins, Aspergillus flavus and Aspergillus parasiticus in dried fruits was investigated. A total of 62 dried fruit samples were analyzed (24 black sultanas, 19 white sultanas and 19 dried figs). A total of 10 A. flavus isolates were found, nine in one white sultana sample (corresponding to 18% infection) and one isolate in dried figs (2%), and all of them were aflatoxin B₁ and B₂ producers. A. parasiticus was not found. Aflatoxins were detected in 3 of 19 (16%) white sultana samples analyzed and, the limits were not higher than 2.0 μg/kg. In dried figs 11 of 19 (58%) samples were contaminated with aflatoxins and, with exception of one sample that was contaminated with 1500 μg/kg of B₁ aflatoxin, the others had less than 2.0 μg/kg. Neither aflatoxigenic or aflatoxins contaminated black sultanas.     

Investigations on the essential oil of Lippia rugosa from Cameroon for its potential use as antifungal agent against Aspergillus flavus Link ex. Fries

Lippia rugosa essential oil was tested for its effectiveness against Aspergillus flavus on artificial growth media. The chemical composition of the oil was determined by gas chromatography–mass spectrometry (GC–MS). Geraniol (51.5%), nerol (18.6%) and geranial (10.4%) were the main components of Lippia oil. After 8 days of incubation on essential oil supplemented medium, mycelium growth of A. flavus was totally inhibited by 1000 mg l^?1 of L. rugosa essential oil. The effect of essential oil on aflatoxin B₁ synthesis was evaluated in SMKY broth. The medium supplemented with different essential oil concentrations, was inoculated with A. flavus mycelium and incubated at 25 °C. After 2, 4, 6 and 8 days, aflatoxin B₁ (AFB₁) was quantified in the supernatant using Enzyme Linked Immuno-Sorbent Assay (ELISA). Results showed that aflatoxin B₁ synthesis was inhibited by 1000 mg l^?1 of L. rugosa essential oil after 8 days of incubation. The effect of the EO on the H⁺-ATPase pumping membrane was also evaluated in the presence of several concentrations of oil (200–2000 mg l^?1) by monitoring glucose-induced acidification of the external medium. L. rugosa essential oil at the concentration of 2000 mg l^?1 completely inhibited the activity of this enzyme. These data suggest that the essential oil of L. rugosa is a fungicidal for A. flavus and its possible cellular target include the H⁺-ATPase.Results obtained in the present study indicate the possibility of exploiting Lippia rugosa essential oil in the fight against strains of A. flavus responsible for biodeterioration of stored foods products.     

Aflatoxin-producing Aspergillus spp. and aflatoxin levels in stored cassava chips as affected by processing practices

Cassava chips (cassava balls, and cassava pellets) are derived cassava products traditionally produced by farmers in sub-Saharan Africa following fermentation, and drying of fresh roots of cassava, and are widely consumed in Cameroon. Once produced, this food commodity can be stored for more than two months and contaminated by a wide array of harmful microbes. In order to assess persistence of toxigenic fungi in cassava chips, aflatoxin-producing fungi (Aspergillus flavus, Aspergillus nomius, and Aspergillus parasiticus) and aflatoxins were contrasted at regular intervals in home-stored cassava chips collected in two locations of southern Cameroon throughout a two-month monitoring period. Three hundred and forty-six isolates of aflatoxin-producing fungi were found to be associated with all samples. A. flavus contaminated more samples in both types of chips (267 isolates in 53 samples), followed by A. nomius (58 isolates in 15 samples), whereas A. parasiticus was rarest. A direct competitive Enzyme-linked immunosorbent assay (ELISA)-based method was implemented to quantify the content in aflatoxins. Eighteen of the samples contained some aflatoxins at detectable levels whereas 54 did not. The levels of aflatoxin ranged between 5.2 and 14.5 ppb. The distribution of aflatoxin in positive samples depended on 8 parameters including pH, moisture content, storage duration, types of chips, level of contamination by aflatoxin-producing fungi, processing practices and storage facilities. From analysis of variance results, only pH (p < 0.01), duration of storage (p < 0.01), population of aflatoxin-producing species (0.0001) and the chip type (p < 0.05) were significantly related to aflatoxin in positive samples. A stepwise regression analysis (forward selection procedure) indicated that aflatoxin levels were significantly (p < 0.01) correlated with processing practices, storage facilities, and storage duration of the chips.     

Mycological quality and mycotoxin contamination of Sri Lankan peppers (Piper nigrum L.) and subsequent exposure assessment

The aim of the study was to characterize the toxigenic moulds and to screen different mycotoxins in peppers (Piper nigrum L.) of Sri Lankan origin. Aspergillus flavus, Aspergillus parasiticus, Aspergillus niger and Penicillium spp. were found to be the most dominant fungi. Characterization of the moulds was carried out in A. flavus and parasiticus agar (AFPA) and malt extract agar (MEA) in 77 black pepper (BP) and 11 white pepper (WP) samples. In total, 73% of the BP and 64% of the WP samples were contaminated with A. flavus and/or A. parasiticus (AfAp). A BP sample with water activity (a_w) 0.70 recorded the highest count of AfAp (4.3*10⁴ CFU/g). Moreover, 75% of the BP samples exceeded the safe a_w limit (0.65) set by the European Spice Association (ESA). The frequency of occurrence of A. niger in BP was 62% with counts up to 1.3*10³ CFU/g. Penicillium spp. were found in 61% and 55% of the BP and WP samples, respectively. In BP 94% of the samples had a Penicillium contamination below 10³ CFU/g. Other Aspergillus spp, found in peppers included, Aspergillus terrus, Aspergillus tamarii, Aspergillus candidus, Aspergillus penicilloides, Aspergillus sydowii and Aspergillus fumigatus. Mould counts in BP (10²–10⁴ CFU/g) were significantly higher than that of WP (<10² CFU/g). Apart from the occurrence of “classical mycotoxins” of spices, aflatoxins (<LOQ-18 μg/kg) and ochratoxin A (<LOQ-79 μg/kg), other toxins including fumonisin B1 (<LOQ-135 μg/kg), sterigmatocystin (<LOQ-49 μg/kg) and citrinin (<LOQ-112 μg/kg) were detected in peppers. In total, 63% of the BP samples were contaminated with at least one mycotoxin. Mycotoxin contamination in WP was significantly less compared to BP. The exposure to aflatoxins and ochratoxin A by consuming pepper remains harmless considering the existing pepper dietary intake data of the Sri Lankan population.     

Mycoflora and absence of aflatoxin contamination of commercialized cassava chips in Benin, West Africa

Studies conducted in Benin, in which the main staple foods are maize, cassava, groundnuts and yams, showed high levels of aflatoxin residues in blood of the exposed population. The natural contamination with fungi and aflatoxins in cassava chips sold at markets in Benin, West Africa was investigated. A total of sixty samples were sampled from open markets in 11 districts of 3 agroecological zones and analyzed for the presence of mycoflora and aflatoxin B₁, B₂, G₁ and G₂. Fourteen genera of fungi were associated with marketed dried cassava chips. Within these, twenty- two isolates were identified to species level, whereas four were identified only to genus. The dominating fungal species isolated were Rhizopus oryzae, Nigrospora oryzae, Chrysonilia sitophila, Cladosporium resinae, Cladosporium herbarum, Apergillus niger and Aspergillus flavus. Fifty-four out of sixty samples were contaminated with A. flavus. The rate of occurrence in CFU/g of A. flavus fungi was lower than for all other fungal species together. Aflatoxin was not detected in any of the samples analyzed using HPLC with post-column photochemical derivatization and fluorescence detection. The limit of detection (LOD) was 0.1 μg/kg. Results from this study suggest cassava chips are unlikely to be a source of aflatoxin in Benin, and that other staples such as maize and groundnuts are more important in aflatoxin exposure. Therefore it can be speculated that staples like maize and groundnut are more important in aflatoxin exposure.     

Effect of water activity and temperature on the growth of Aspergillus flavus,the expression of aflatoxin biosynthetic genes and aflatoxin production in shelled peanuts

The contamination of peanuts with Aspergillus flavus and subsequent aflatoxins is considered to be one of the most serious safety problems in the world. Water activity (a_w) and temperature are limiting factors for fungal growth and aflatoxins production during storage. To optimize the practical storage parameter, the effect of a_w (0.85–0.99) and temperature (15–42 °C) on fungal growth, aflatoxin production and the expression of aflatoxin biosynthetic and regulatory genes in shelled peanuts was investigated. A. flavus grew at a lower rate when temperature ≤20 °C or a_w ≤ 0.85. For the growth of A. flavus in shelled peanuts, the optimum conditions were a_w was 0.98, and the optimum temperature was 37 °C. The maximum amount of AFB₁ in peanuts was obtained at 28 °C and a_w 0.96. Real-time analysis showed that 16 of 25 genes had highest expression levels at 28 °C under a_w 0.92, while 9 genes had highest expression levels at 37 °C under a_w 0.92. Compared with 37 °C, all aflatoxin biosynthetic pathway genes were down-regulated at 42 °C. All the pathway genes and laeA were up-expressed at a_w of 0.96 under 28 °C, compared to a_w 0.99. Furthermore, there was a good positive correlation between the ratio of aflS/aflR and AFB₁ production. The expression of laeA was also positively correlated with AFB₁ production while the expression of brlA was correlated with the A. flavus growth. The results of this study suggest that AFB₁ production in peanut kernels can occur over a wider range of a_w × temperatures levels compared to formula media and peanut media. Previous studies have showed that AFB₁ could not be produced on formula media at 37 °C without the expression of most aflatoxin structural genes. But, in the un-autoclaved shelled peanuts, high concentration of AFB₁ was produced at 37 °C with up-regulation of some aflatoxin biosynthetic genes. From a food safety point of view, the results can be used to optimize certain food technological processes and develop prevention strategies to control such carcinogenic natural metabolites in grains (such as peanuts, maize and rice) and derived products.     

Effects of high pressure processing on immunoreactivity and microbiological safety of crushed peanuts

Peanuts are a common economical food source consumed worldwide but exist health concern of food allergy and are particularly susceptible to infection by the mold fungus Aspergillus flavus during storage, accumulating highly toxic substance aflatoxin. In this study, the effect of high pressure treatments on peanut immunoreactivity, peanut amino acid composition, A. flavus growth and aflatoxin contents on crushed peanuts was evaluated. Results showed that immunoreactivity of peanuts treated with 600 MPa and 800 MPa for 10 min was significantly lower (P < 0.05) than those of the control group by 69.2 ± 5.3% and 73.3 ± 1.9%, respectively. High pressure treatment at 800 MPa decreased total essential amino acid content as well as two nutritional indexes, the chemical score and the essential amino acid index, by 32.4 ± 2.1% and 31.1 ± 3.2%, respectively. The growth of aflatoxigenic fungi was inhibited in peanuts with aflatoxin accumulation that were subjected to different levels of pressure treatments during 30 days of storage. Peanuts treated with 600 MPa and 800 MPa had considerably lower aflatoxin levels, 0.26 μg/g and 0.22 μg/g in wet basis, respectively, than the control peanut aflatoxin level (9.08 μg/g) on day 30. Results were demonstrated that high pressure treatment had a significant inhibitory effect on A. flavus growth in peanuts and this contributes to reduction of aflatoxin production and accumulation instead of directly destroy aflatoxin. Taken together, the findings of this study indicated that high pressure treatment could preserve peanut quality by reducing food immunoreactivity and by eliminating A. flavus in peanuts.     

Gaseous allyl isothiocyanate to inhibit the production of aflatoxins,beauvericin and enniatins by Aspergillus parasiticus and Fusarium poae in wheat flour

There is a growing concern about the presence of mycotoxins in foods, since up to 25% of cereals and cereal foods are contaminated with these compounds. Moreover, the general public is against the use of synthetic preservatives in foods and the use of natural antimicrobials in foods is a current trend. Allyl isothiocyanate (AITC) is a volatile antimicrobial derived from oriental and black mustard. The objective of this work was to evaluate the capacity of gaseous AITC in inhibiting the production of mycotoxins by Aspergillus parasiticus (aflatoxin producer) and Fusarium poae (beauvercin and enniatin producer) in wheat flour. Petri dish lids filled with 2 g of wheat flour were inoculated with 10⁴ conidia/g of A. parasiticus or F. poae and placed in a 1 L mason jar. AITC was added at 0.1, 1 or 10 µL/L in the gaseous phase. Jars were hermetically closed and kept at 23 °C for 30 d. Mycotoxins were identified and quantified by LC-MS/MS. Even 0.1 µL/L of AITC was able to produce 6.9–23% reduction of mycotoxin production. In general, synthesis of aflatoxins and beauvericin was more affected than enniatins. The use of AITC at 10 µL/L completely inhibited the production of all mycotoxins for 30 d. AITC at low doses could be added to flour packages in order to inhibit the production of potentially dangerous mycotoxins.     

Potential of botanicals and biocontrol agents on growth and aflatoxin production by Aspergillus flavus infecting rice grains

The potential of certain plant extracts and biocontrol agents for the reduction of aflatoxin B₁ (AFB1) in stored rice was investigated. Among the plant extracts tested, Syzigium aromaticum (5 g/kg) showed complete inhibition of Aspergillus flavus growth and AFB1 production. Curcuma longa, Allium sativum and Ocimum sanctum also effectively inhibited the A. flavus growth (65–78%) and AFB1 production (72.2–85.7%) at 5 g/kg concentration. Among the biocontrol agents, culture filtrate of Rhodococcus erythropolis completely inhibited the AFB1 production at 25 ml/kg concentration. The other biocontrol agents, Pseudomonas fluorescens, Trichoderma virens and Bacillus subtilis showed 93%, 80% and 68% reduction of A. flavus growth and 83.7%, 72.2% and 58% reduction of AFB1 at 200 ml/kg, respectively.     

Occurrence of aflatoxin B1 in food products derivable from ‘egusi’ melon seeds consumed in southwestern Nigeria

Aflatoxin, the toxic secondary metabolite of Aspergillus flavus and Aspergillus parasiticus has been considered as one of the most serious food safety problems in sub Saharan Africa. Egusi melon seeds is susceptible to these fungal infection during postharvest. Therefore, the content of aflatoxin B1 in three food products derivable from ‘egusi’ melon seeds ogiri’ (fermented melon seed condiment), ‘robo’ (melon ball snacks) and egusi soup destined for human consumption in Nigeria in 2005 and 2006 were determined. Aflatoxin B1 was analysed by thin layer chromatography (TLC) with fluorescent detection. The percentage of samples positive for aflatoxin B1 were for 25% robo, 31.8% for ogiri, and 19.5% for ‘egusi’ soup. Aflatoxin B1 ranged from 2.3 to 15.4 ppb in all samples. The overall mean levels of aflatoxin B1 were for 8.9 ppb for ogiri, 9.7 ppb for ‘robo’ and 7.2 ppb for ‘egusi soup’. All positive melon seeds derived food products analysed in this study contained aflatoxin B1 at concentrations much lower than the 20 ppb permissible limit recommended in Nigerian food and suggests that melon seed derived foods present less risk by human exposure to aflatoxin through their consumption. However, it is important to consider these levels in terms of their contribution to overall daily exposure to aflatoxin levels in food. This is the first report of aflatoxin determination in melon seed food products.     

Antifungal, aflatoxin inhibition and antioxidant activity of Callistemon lanceolatus (Sm.) Sweet essential oil and its major component 1,8-cineole against fungal isolates from chickpea seeds

The present investigation reports the extent of molds and aflatoxin contamination to Avarodhi, Kabuli, Pusa 256, Radha and Samrat varieties of chickpea seeds. The study also examines the chemical composition of Callistemon lanceolatus (Sm.) Sweet essential oil and its antifungal, antiaflatoxin and antioxidant activity. During standardization of chemical profile, a total of 8 compounds constituting 0.862 mg/mL of oil composition were analyzed by GC-MS analysis where 1,8-cineole was recorded as a major component (0.56 mg/mL). The antifungal activity of EO and 1,8-cineole was evaluated by contact assay on Czapek’s dox agar. The EO (0.227-0.908 mg/mL) and 1,8-cineole (0.918 mg/mL) showed remarkable antifungal effect against all the fungal isolates of chickpea. Their minimal inhibitory (MIC) and fungicidal (MFC) concentrations for Aspergillus flavus were lower than those of the prevalent systemic fungicide Nystatin. Aflatoxin B₁ (AFB₁) production by NKD-208 isolates of A. flavus was strongly inhibited even at the lower fungistatic concentration of EO and 1,8-cineole.There was no adverse effect of EO treatment on chickpea seed germination suggesting its non-phytotoxic nature. Based on the findings of present investigation, C. lanceolatus essential oil may be recommended as botanical preservative for the enhancement of shelf life of food items in- view of the adverse effect of synthetic preservatives and its strong antifungal, aflatoxin inhibition and antioxidant activity.     

In vitro antifungal activity of lactic acid bacteria against mycotoxigenic fungi and their application in loaf bread shelf life improvement

Food spoilage caused by mycotoxigenic fungi represents an important food safety problem. Lactic acid bacteria (LAB) are used as starter cultures in a larger number of food products. In this study, 16 strains of LAB were cultivated in MRS broth under anaerobiosis. Then, cell free supernatants were obtained by centrifugation and their antifungal activity against Aspergillus parasiticus and Penicillium expansum was tested using the disc-diffusion method. Furthermore, the LABs that showed in vitro antifungal activity were used in bread fermentation with yeast in order to study fungal growth inhibition and aflatoxin (AF) reduction in processed bread previously inoculated with A. parasiticus. The compounds present in the fermented medium of six LAB strains induced inhibition of P. expansum growth, whereas five probiotic strains produced antifungal compounds against A. parasiticus. The analysis by liquid chromatography coupled to mass spectrometry in tandem showed a reduction of the AF content in bread samples fermented with yeast and LABs. The reduction of AFs ranged from 84.1 to 99.9%. Moreover, bread sample studies showed a shelf life increase of about 3–4 days.     

Chemical composition and antiaflatoxigenic activity of Carum carvi L., Thymus vulgaris and Citrus aurantifolia essential oils

In order to find out plants useful to controlling aflatoxins (AFs) production, the essential oils (EOs) from 12 medicinal plants prepared by hydrodistillation were studied with special reference to the inhibition of Aspergillus parasiticus growth and AFs production. The toxigenic fungus was cultured in presence of various oils in 6-well microplates using a microbioassay technique. The mycelial mass was estimated as an index of fungal growth, while the aflatoxins B₁ (AFB₁) and G₁ (AFG₁) were measured by high performance liquid chromatography (HPLC). Among plants tested, Thymus vulgari and Citrus aurantifolia were found to inhibit both A. parasiticus and AF production. The EOs from Mentha spicata L., Foeniculum miller, Azadirachta indica A. Juss, Conium maculatum and Artemisia dracunculus were only inhibited fungal growth, while Carum carvi L. effectively inhibited AF production without any obvious effect on fungal growth. The other plants including Ferula gummosa, Citrus sinensis, Mentha longifolia and Eucalyptus camaldulensis had no effect on A. parasiticus growth and AF production at all concentrations used. The IC₅₀ values of T. vulgaris, C. aurantifolia and C. carvi for AF inhibition were reported as 93.5, 285.6, and 621.9 μg/ml for AFB₁, while they were calculated as 11.7, 50.1, and 56.0 μg/ml for AFG₁. These results indicate that the EOs of some medicinal plants may be considered as potential candidates to protect foods and feeds from toxigenic fungus growth and subsequent AF contamination.     

In vitro and in vivo activity of essential oil from dill (Anethum graveolens L.) against fungal spoilage of cherry tomatoes

The objectives of present study were to determine the antifungal activity in vitro of the essential oil extracted from the seeds of dill (Anethum graveolens L.) and to evaluate its antifungal activity in vivo as a potential food preservative. The antifungal activity of this oil was tested by poisoned food technique against Aspergillus flavus, Aspergillus oryzae, Aspergillus niger and Alternaria alternata. The wet and dry mycelium weight of the tested fungi was also determined in a liquid culture to evaluate the antifungal activity. The minimum inhibitory concentration of oil for the four tested fungi was found to be 2.0 μl/ml, and the mycelial growth inhibition was determined at day 9. Observations on the microstructure of A. niger using light and scanning electron microscopes revealed degenerative alterations in the conidial heads and hyphal morphology after oil treatment, including distorted conidial heads, decreased hyphal diameters, shriveled hyphal aggregates, and swelling of the hyphal wall. The effect of the essential oil on inhibition of decay development on cherry tomatoes was tested in vivo by exposing inoculated and control fruit to essential oil vapor at 120 μl/ml and 100 μl/ml concentrations, respectively. Thus, the essential oil of dill could be used to control food spoilage as a potential source of food preservative.     

Inactivation of aflatoxigenic fungi (Aspergillus spp.) on granular food model,maize, in an atmospheric pressure fluidized bed plasma system

Atmospheric plasma provides the advantages of high microbial inactivation that can be performed under ambient conditions; therefore, it is regarded as a potential alternative to traditional food preservation methods. The present work presents the results of a critical study conducted on the efficiency of a non-thermal atmospheric pressure fluidized bed plasma (APFBP) system used for decontamination of maize. Maize grains that were artificially contaminated with Aspergillus flavus and Aspergillus parasiticus spores were treated in APFBP system for 1–5 min at two differently designed fluidized bed reactors with air and nitrogen. Results indicate maximum significant reductions of 5.48 and 5.20 log (cfu/g) in Aspergillus flavus and A. parasiticus after 5 min air plasma treatment. The native microbial flora of the maize grains decreased to more than 3 log after 3 min APFBP treatment, and no viable cells were counted. During the storage of plasma treated maize samples at 25 °C for 30 days, the Aspergillus spp. spores log reduction was maintained with no occurrence of re-growth. Overall, this study shows that plasma treatment has a fungicidal effect on A. flavus and A. parasiticus spores associated with alterations in spore surface morphology and loss of spore integrity. APFBP can inactivate aflatoxigenic spores on maize grains and could be optimized to improve the safety and quality of produce.     

Use of citrus flavanones to prevent aflatoxin contamination using response surface methodology

The aim of this study was to analyze the possible utilization of flavanones obtained as by-products of the citrus industry, naringin (NAR), hesperidin (HES) and neohesperidin (NEO), to inhibit the production of aflatoxins (AFs) from Aspergillus flavus. Response Surface Methodology (RSM) was applied to optimize experimental conditions in terms of the different flavanones concentrations used. Through this methodology these optimal combinations were calculated: HES-NAR: 0.206–0.037 mM, HES-NEO: 0.156–0.283 mM and NAR-NEO: 0.035–0.195 mM. The theoretical concentrations obtained by RSM were assayed, achieving total inhibition of AFB₁ and AFB₂ production. Moreover, the use of these flavanones, obtained at low cost from the residues of citric industry, presents an interesting option for improving the profitability of these industries.     

Safety of a street vended traditional maize beverage,ice-kenkey,in Ghana

Ice-kenkey is a chilled cereal beverage sold as street food in some open markets in Ghana. It is produced by mashing and sweetening kenkey, a stiff dumpling produced from fermented maize meal. The safety of street vended ice-kenkey was assessed by microbiological, elemental and myco-toxicological analysis of ice-kenkey and intermediary products obtained from 16 producers in four open markets in the Accra and Tema metropolis. A tenfold increase in counts of aerobic mesophiles, and yeast and moulds were recorded during the production of ice-kenkey. Coliform bacteria, E. coli and Staphylococcus aureus which were not detected in the starting materials were found partway through production or in the final product. The mean microbial counts in the packaged ice-kenkey were 10⁶–10⁷ CFU/g for aerobic mesophiles, 10⁴–10⁵ CFU/g for yeast and moulds, 10–1000 CFU/g for total coliforms and 10–100 CFU/g for S. aureus. E. coli counts of 10 CFU/g were recorded in samples from three out of the four markets. The microbial load could be eliminated by pasteurizing ice-kenkey at 80 °C for 15 min. The mean concentration in mg/kg of Fe was between 15.97 and 29.48, Cu, 0.57 to 1.41, Mn, 0 to 2.55, Pb 0 to 1.25 and Zn 0.47 to 6.17. Total aflatoxins content in samples ranged from 7.04 to 22.17 μg/kg and included a range of 7.01–20.54 for aflatoxin B₁, 0.51 to 1.63 for aflatoxin B₂ and 0–0.47 μg/kg for aflatoxin G_I. Aflatoxin G₂ was not detected in any of the samples. A simplified training module based GMP, GHP and a HACCP plan was developed and used to train ice-kenkey producers in Accra in collaboration with municipal authorities.