2-Hydroxy-4-methoxybenzaldehyde inhibits the growth of Aspergillus flavus via damaging cell wall,cell membrane,manipulating respiration thus creating a promising antifungal effect on corn kernels

This study investigated the antifungal activity and the potential antifungal mechanisms of 2-hydroxy-4-methoxybenzaldehyde (HMB) against Aspergillus flavus (A. flavus). The minimum inhibitory concentration (MIC) of HMB in preventing spore germination was 70 μg mL⁻¹. HMB at MIC disrupted cell wall integrity by reducing the number of septa by 86.66% (P < 0.05) in mycelia and increased cell membrane permeability by about 14-fold (P < 0.05) evidenced by propidium iodide (PI) staining. Furthermore, HMB at MIC inhibited respiration by 33.33%. These results revealed that the antifungal activity of HMB against A. flavus could be attributed to the damaged cell wall integrity, cell membrane permeability and respiration metabolism. What’s more, A. flavus was completely restrained in corn kernels due to HMB. Therefore, HMB could be applied as an effective antifungal agent.     

Effect of UV-C irradiation on inactivation of Aspergillus flavus and Aspergillus parasiticus and quality parameters of roasted coffee bean (Coffea arabica L.)

ABSTRACT

This study investigated the antifungal effect of ultraviolet-C (UV-C) against Aspergillus flavus and Aspergillus parasiticus on roasted coffee beans. Also, any changes in the quality of the roasted coffee beans were measured after UV-C irradiation. As UV-C irradiation time increased (0–2 h), the number of surviving A. flavus and A. parasiticus spores significantly (P < .05) decreased. The reduction values of A. flavus in round part, crack part, and whole roasted coffee beans were 2.16, 0.71, and 1.58 log₁₀ CFU g^?1, respectively, and the reduction values of A. parasiticus in round part, crack part, and whole roasted coffee beans were 1.03, 0.37, and 0.72 log₁₀ CFU g^?1, respectively, after 2 h of UV-C irradiation. Field emission scanning electron microscopy showed that the morphology of A. flavus and A. parasiticus spores included expanded wrinkles that were deformed by UV-C irradiation. The Hunter colours were significantly reduced (P < .05). There was no significant change (P > .05) in moisture content, but the pH was significantly decreased (P < .05). Most of the sensory parameters did not change, but there was a significant difference (P < .05) in flavour. Based on this study, 2 h of UV-C irradiation was effective in reducing 90% of A. flavus, but it was not effective against A. parasiticus present on roasted coffee beans. Also, Hunter colour, pH, and sensory parameters (flavour) were changed by UV-C irradiation.     

黑曲霉孢子灭活前后红外消光特性

黑曲霉孢子是生物气溶胶的重要组成部分,质量消光系数是研究黑曲霉孢子电磁衰减特性的重要参数。采用压片法测量了灭活前后黑曲霉孢子2.5~15 um 波段的反射光谱,并利用Krames-Kronig(K-K)关系计算了黑曲霉孢子红外波段的复折射率。基于Mie 散射理论求出了灭活前后黑曲霉孢子红外波段的质量消光系数,并对结果进行了分析和讨论。分析结果表明:3~5 um 波段,灭活后平均质量消光系数降低了4.6%,8~14 um 波段,灭活后平均质量消光系数降低了89.5%,由此可知,保持活性对于提高黑曲霉孢子的电磁衰减能力具有重要的意义。     

Aflatoxin B1 and aflatoxins in ground red chilli pepper after drying

In this study, 180 red chilli pepper (RCP) berry samples were obtained from two different croplands of Gaziantep and Kahramanmara? (Turkey) in August, September and October. RCP berry samples were dried under sunlight and grinded. Ground red chilli pepper (GRCP) samples were analysed for aflatoxins (AFs, sum of B₁, B₂, G₁ and G₂) and AFB₁ contamination. According to the results, in 49 of 180 samples, AFB₁ and in 37 samples, AFs were higher than legal limits. The lowest amounts of AFs and AFB₁ were obtained in August and the highest amounts in October. χ² analysis showed that there were no significant differences (p > 0.05) between cities among 3 months according to number of samples with AFs and AFB₁ above legal limits. According to the Duncan multiple-range test, there was no significant difference between all months. Strict measures are necessary to produce high-quality GRCP. RCP berry must be treated to reduce moulds before production of GRCP.     

Identification of novel metabolites from Aspergillus flavus by high resolution and multiple stage mass spectrometry

The filamentous fungus Aspergillus flavus is one of the most important species in the Aspergillus genus and is distributed worldwide as a prevalent aflatoxin-producing food and feed contaminant. A. flavus contains more than 55 gene clusters that are predicted to encode proteins involved in secondary metabolite production. One of these, cluster 27, contains a polyketide synthase (pks27) gene that encodes a protein that is highly homologous to the aflatoxin cluster PKS. Comparative metabolomics, using ultra-high performance liquid chromatography (UHPLC) coupled to high resolution Orbitrap mass spectrometry (MS) was used to detect metabolites differentially expressed in the A. flavus wild-type and ?pks27 mutant strains. Metabolite profiling was aided by a statistical differential analysis of MS data using SIEVE software. This differential analysis combined with accurate mass data from the Orbitrap and ion trap multiple stage MS allowed four metabolites to be identified that were produced only by the wild-type culture. These included asparasone A (358 Da), an anthraquinone pigment, and related anthraquinones with masses of 316, 340 and 374 Da. These latter three compounds had similar fragmentation patterns to that of asparasone A. The 316 Da anthraquinone is particularly interesting because it is most likely formed by incorporation of seven malonyl-CoA units rather than the eight units required for the formation of asparasone A. The 340 and 374 Da metabolites are the dehydration and an oxy-derivative of asparasone A, respectively. Asparasone A was also identified in extracts from several other Aspergillus species.     

Delivery systems for biological control agents to manage aflatoxin contamination of pre-harvest maize

While soil application of a competitive non-toxigenic Aspergillus flavus strains is successful in reducing aflatoxin contamination in certain crops, direct application to aerial reproductive structures could be more effective for maize. A sprayable, clay-based water-dispersible granule formulation was developed to deliver non-toxigenic A. flavus strain K49 directly to maize ears. The efficacy of the K49 water-dispersible granule in mitigating aflatoxin in maize (Zea mays L.) was evaluated. Field studies were conducted to compare K49 colonization and effectiveness in reducing aflatoxin contamination when applied either as a soil inoculant or as a directed spray in plots infested with toxigenic strain F3W4. Fifty percent of non-toxigenic A. flavus was recovered from non-treated controls and from plots soil inoculated with K49 on wheat. In spray treatments with formulated or unformulated K49 conidia, over 90% of A. flavus recovered was non-toxigenic. Soil-applied K49 reduced aflatoxin contamination by 65% and spray applications reduced contamination by 97%. These findings suggest direct spray application of non-toxigenic A. flavus strains may be better than soil inoculation at controlling maize aflatoxin contamination and that a water-dispersible granule is a viable delivery system for maintaining viability and efficacy of the biological control agent, K49.     

Response of Aspergillus flavus,Aspergillus niger and Penicillium citrinum to oxidative stress induced by Fenton’s reagent

The presence of fungi in water systems represents a threat to human health. Hydrogen peroxide is known for its disinfecting properties and easy decomposition to water and oxygen. Its activity can be enhanced by the addition of iron as a catalyst, a reagent known as Fenton?s reagent. In the present study, different Fenton concentrations were investigated on the spores of Aspergillus flavus, Aspergillus niger and Penicillium citrinum at different time intervals. The results indicate that complete inactivation of spores was noticed after 60 min of exposure to both 2 and 3% H₂O₂ catalyzed by 0.025 g Fe²⁺/100 ml for A. niger, and 3% H₂O₂ catalysed by 0.075 g Fe²⁺/100 ml for P. citrinum. The activity of two antioxidant enzymes, superoxide dismutase (SOD) and catalase (CAT), was determined in mycelial mat harvested after 7 days. Their activities were either highly increased or reached their minimum values prior to inactivation of spores.     

超声波对黑曲霉细胞破壁作用的研究

用均匀设计法考察了超声时间、超声温度和超声功率对黑曲霉细胞破壁效果的影响．实验结果表明最优条件为：超声时间50min,超声温度60℃,超声功率200W,超声法与高压均质法比较,超声法破壁效果较好。