Combination of chitosan and ethanol to control gray mold of table grapes

Gray mold, caused by Botrytis cinerea, is the most important postharvest disease of table grapes. Chitosan, a natural biopolymer with antifungal and eliciting properties, and ethanol, a common food additive with antifungal properties, are both able to reduce postharvest decay of table grapes. The effectiveness of reduced doses of chitosan and ethanol, applied alone or in combination, to control gray mold of table grapes was evaluated. Artificially inoculated single berries or clusters were immersed in chitosan (0.1 and 0.5%), ethanol (10 and 20%), or their mixture. The combination of 0.5% chitosan with 10 or 20% ethanol improved decay control with respect to their single treatments, while combinations of 0.1% chitosan with 10 or 20% ethanol did not improve gray mold control compared to the treatments applied alone. On single berries stored 7 days at 151°C, the highest levels of decay control were observed on grapes treated with the combination of 0.5% chitosan and 10 or 20% ethanol (reductions of 94 and 97% on cv Autumn Seedless and 69 and 73% on Thompson Seedless, respectively, compared to controls). On small clusters stored 60 days at 0.51°C, the highest percent reduction was observed on grapes treated with the combination of 0.5% chitosan and 10 or 20% ethanol (reductions of 47 and 60% in Thompson Seedless, and 70 and 94% in Autumn Seedless, respectively, compared to controls). The tests with small clusters were carried out to simulate commercial prolonged cold storage of table grapes. The combination of reduced doses of chitosan and ethanol improved the control of gray mold of table grapes compared to their application alone, and the effect was at least additive and at times synergistic

Postharvest ethanol and potassium sorbate treatments of table grapes to control gray mold

Germination of Botrytis cinerea spores on potato dextrose agar after a 30 s immersion in 10 or 20% ethanol was 87 and 56%, respectively, compared to 99% among untreated controls. After similar immersion in 0.5 or 1.0% potassium sorbate, 84 and 68% of the spores germinated, respectively. Addition of 0.5 and 1.0% potassium sorbate to 10 and 20% ethanol solution significantly increased the inhibition of spore germination. The germination of spores after 30 s immersion in 20% ethanol plus 0.5% potassium sorbate was 9.7%. The incidence of gray mold, caused by B. cinerea, on detached berries of ‘Flame Seedless’ grapes immersed for 30 s in water, 10 and 20% ethanol, and 0.5 or 1.0% potassium sorbate was 55.2, 42.1, 31.0, 37.7, or 24.4 %, respectively. Addition of 0.5 and 1.0% potassium sorbate to 10 and 20% ethanol reduced decay to 10% or less and was more effective than either alone. After 30 days of storage at 1oC, the combination of 20% ethanol either with 0.5 or 1.0% potassium sorbate was equal in efficacy to commercial SO2 generator pads in reducing the incidence of gray mold on ‘Thompson Seedless’ grapes. None of the combinations of ethanol and potassium sorbate injured the berries

Decontamination of Bacillus subtilis var. niger spores on selected surfaces by chlorine dioxide gas*

Objective: Chlorine dioxide (CD) gas has been used as a fumigant in the disinfection of biosafety laboratories. In this study, some experiments were conducted to assess the inactivation of spores inoculated on six materials [stainless steel (SS), painted steel (PS), polyvinyl chlorid (PVC), polyurethane (PU), glass (GS), and cotton cloth (CC)] by CD gas. The main aims of the study were to determine the sporicidal efficacy of CD gas and the effect of prehumidification before decontamination on sporicidal efficacy. Methods: Material coupons (1.2 cm diameter of SS, PS, and PU; 1.0 cm×1.0 cm for PVC, GS, and CC) were contaminated with 10 μl of Bacillus subtilis var. niger (ATCC 9372) spore suspension in mixed organic burden and then dried in a biosafety cabinet for 12 h. The spores were recovered by soaking the coupons in 5 ml of extraction liquid for 1 h and then vortexing the liquid for 1 min. Results: The log reductions in spore numbers on inoculated test materials exposed to CD gas [0.080% (volume ratio, v/v) for 3 h] were in the range of from 1.80 to 6.64. Statistically significant differences were found in decontamination efficacies on test material coupons of SS, PS, PU, and CC between with and without a 1-h prehumidification treatment. With the extraction method, there were no statistically significant differences in the recovery ratios between the porous and non-porous materials. Conclusions: The results reported from this study could provide information for developing decontamination technology based on CD gas for targeting surface microbial contamination

Ocorrência, aspectos toxicológicos, métodos analíticos e controle da patulina em alimentos Occurrence, toxicological aspects, analytical methods and control of patulin in food

A patulina é uma micotoxina produzida por várias espécies de Penicillium, Aspergillus e Byssochlamys. Em experimentos com animais, ela demonstrou ter atividade mutagênica, carcinogênica e teratogênica. Tem sido freqüentemente encontrada em maçãs e derivados. A patulina é facilmente transferida da maçã para o suco durante o processamento devido a sua alta solubilidade em água. Essa micotoxina é muito estável ao aquecimento em meio ácido, como no suco de maçã. Assim, a presença de patulina em suco de maçã é um indicador da qualidade das maçãs utilizadas no processamento. Muitos métodos têm sido desenvolvidos para a determinação da patulina, principalmente baseados na extração líquido-líquido com acetato de etila e determinação por CLAE. É importante evidenciar a necessidade de legislação que regulamente limites dessa micotoxina em alimentos no Brasil. Esta revisão bibliográfica tem como objetivos descrever as principais características da patulina, a ocorrência, os aspectos toxicológicose os métodos desenvolvidos para sua detecção e controle durante os estágios da produção da maçã e suco.<br>Patulin is a mycotoxin produced by several Penicillium, Aspergillus and Byssochlamys species. Patulin is a highly toxic compound which has shown to be mutagenic, carcinogenic and teratogenic in experiments with animals. It has often been found in apples and apple products. Patulin is easily transfered into apple juice during processing due to its high solubility in water. This mycotoxin is very stable to heat in acidic medium as in apple juice. Thus, patulin content of apple juice is an indicator of the quality of the apples used to juice production. Many methods have been developed for the patulin determination mainly based on liquid-liquid extraction with ethyl acetate and use of HPLC for detection. It is important to show the need of legislation that imposes patulin limits in foods in Brazil. The objectives of this review are to describe the main patulin characteristics, occurrence, toxicological aspects, methods developed for patulin detection and control during the stages of apple and juice production

Água aquecida e radiação UV-C no controle pós-colheita de Cryptosporiopsis perennans em maçãs Heated water and UV-C radiation to postharvest control of Cryptosporiopsis perennans on apples

O objetivo deste trabalho foi avaliar a colonização de Cryptosporiopsis perennans na epiderme de maçãs e a eficiência da aplicação de água aquecida e radiação UV-C no controle desse patógeno. Em maçãs submetidas à inoculação de C. perennans, a colonização de lenticelas e das áreas adjacentes pelo patógeno foi avaliada por microscopia eletrônica de varredura. A sensibilidade dos conídios de C. perennans aos tratamentos foi avaliada em suspensão aquosa, às temperaturas de 28, 45, 50 e 55ºC, por 15 e 30 s, e às doses de radiação UV-C de 0,018, 0,037, 0,075, 0,150, 0,375, 0,750, 1,500 e 3,000 kJ m-2. Em maçãs submetidas à inoculação de C. perennans, foram avaliados os efeitos de 0,375, 0,750 e 1,500 kJ m-2 de radiação UV-C e da aspersão de água aquecida à 50ºC, por 15 e 30 s no controle do patógeno. O fungo produziu abundante micélio e conídios nas lenticelas e nas áreas adjacentes, na epiderme das maçãs. A água aquecida a 50ºC por 15 s e à dose de radiação de UV-C de 0,750 kJ m-2 reduzem em mais de 99% a sobrevivência de conídios. A aspersão de água aquecida a 50ºC por 15 s e à dose de radiação de UV-C de 0,375 kJ m-2, controlam C. perennans em maçãs.<br>The objective of this work was to assess the colonization of Cryptosporiopsis perennans in the epidermis of apples and the efficiency of heated water and UV-C radiation application to control this pathogen. In apples inoculated with C. perennans, the colonization of lenticels and adjacent areas by the pathogen was observed by electronic scanning microscopy. The sensitivity of C. perennans conidia was evaluated in aqueous suspension, at temperatures of 28, 45, 50 and 55ºC for 15 and 30 s, and at UV-C radiation doses of 0.018, 0.037, 0.075, 0.150, 0.375, 0.750, 1.500 and 3.000 kJ m-2. The effects of UV-C radiation doses at 0.375, 0.750 and 1.500 kJ m-2 and heated water at 50ºC, sprayed during 15 and 30 s were evaluated for controlling C. perennans in apples inoculated with the pathogen. The fungus produced abundant mycelium and conidia in lenticels and adjacent areas on the epidermis of the apples. The heated water at 50ºC during 15 s and a 0.750 kJ m-2 UV-C radiation dose reduced conidia survival in more than 99%. Heated water sprayed at 50ºC during 15 s and a UV-C radiation dose of 0.375 kJ m-2 control C. perennans in apples