Ochratoxin A (OA)-producing fungi were identified in coffee at different stages of maturation. The toxin was quantified in coffee during terrace drying and in coffee stored in barns. By direct plating, a high level of contamination (100%) was found in the coffee beans studied, with the genus Aspergillus representing 33.2%, of which Aspergillus ochraceus and Aspergillus niger represented 10.3 and 22.9%, respectively, of the strains isolated from the coffee beans. The capacity to produce ochratoxin was determined in 155 strains of A. ochraceus and A. niger using both the agar plug method and extraction with chloroform, giving positive results for 88.1% of the A. ochraceus strains and 11.5% of the A. niger strains. Analysis for OA in the terrace and barn coffee samples showed that, independent of cultivar, year harvested, or production region, all except one of the samples analyzed showed mycotoxin levels below the limit suggested by the European Common Market (8 microg/kg), thus indicating that the problem is restricted and due to severe faults in harvesting and storage practices.
Bacteriocins produced by fifteen strains of Lactococcus lactis (14 L. lactis subsp. lactis and one L. lactis subsp. cremoris) were heat resistant, sensitive to several proteolytic enzymes and active over a wide range of pH. Their resistance to the heating was greatly influenced by the pH. Only the strain L. lactis subsp. lactis ITAL 383 produced a bacteriocin with a wide activity spectrum, similar to nisin of L. lactis subsp. lactis ATCC 11454. This bacteriocin inhibited closely related species and other Gram-positive microorganisms including Listeria monocytogenes and Staphylococcus aureus, but it was not active against the Gram-negative bacteria tested. The identification of partially purified antimicrobial compounds by SDS-PAGE showed that bacteriocin produced by strain ITAL 383 had the same molecular weight of nisin produced by L. lactis subsp. lactis ATCC 11454.
O Brasil utiliza a irradiação em especiarias e condimentos para a comercialização. No entanto, além de grãos, frutas e flores, a carne de frango é particularmente outro produto nacional com enorme potencial para o emprego da irradiação. Dados divulgados pela União Brasileira de Avicultura [37], posicionaram o Brasil como terceiro maior produtor mundial (5,9 milhões de toneladas) e segundo maior exportador de carne de frango, no ano de 2000 (907 mil toneladas).Em carnes de frango, o crescimento de microrganismos e as atividades enzimáticas são os principais fatores limitantes da vida-útil, freqüentemente prolongada com a proteção das embalagens e aplicação de agentes descontaminantes. A umidade, a composição de voláteis, e principalmente, os lipídeos podem ser alterados de acordo com o material utilizado na embalagem [3]. Da mesma forma, os agentes descontaminantes, associados ao efeito bactericida, devem manter a aparência e o sabor do alimento sem deixar resíduos prejudiciais à saúde [4].O prolongamento da vida-útil de carcaças de frango é uma preocupação constante da indústria avícola. Nos abatedouros, as carcaças são geralmente resfriadas por imersão em água para minimizar o crescimento bacteriano. Apesar de reduzir o índice de crescimento, isso também pode gerar contaminação cruzada entre as carcaças. Ressalta-se que o crescimento de microrganismos durante o armazenamento refrigerado ocorre principalmente no tecido muscular lesado, sendo as contaminações dependentes do tipo de músculo e do pH. Estudos realizados por LAMUKA et al. [22] mostraram que o uso da irradiação em carnes de frango pode retardar a deterioração bacteriana e diminuir a incidência de microrganismos patogênicos e deteriorantes. RESUMOCaixas de papelão contendo cortes de peito de frango sem pele e sem ossos, previamente acondicionadas em bandejas de polietileno expandido, com aproximadamente 200 gramas por bandeja e recobertas por filme de polietileno, foram submetidas à irradiação com 60 Co, utilizando-se equipamento Nordion JS 7500. As amostras foram expostas a doses de 1,5; 3,0 e 7,0kGy, sendo irradiadas na modalidade estática a 0 o e 180 º em relação ao feixe de irradiação. Para avaliar a homogeneidade das doses de irradiação um conjunto de 18 dosímetros de alanina+parafina por tratamento foi colocado dentro das caixas com as amostras. Outro conjunto de dosímetros foi irradiado na faixa de 1 a 10kGy para elaboração da curva de resposta . Após a irradiação, os peitos de frango foram armazenados a 5±1ºC durante 39 dias, sendo submetidos a análises microbiológicas (contagem total de bactérias aeróbias psicrotróficas, bactérias aeróbias mesófilas, bolores e leveduras, Pseudomonas spp, enterobacteriáceas totais, bactérias lácticas e NMP de E.coli) em 10 períodos diferentes ao longo do armazenamento. Os resultados obtidos revelaram um comportamento linear dos dosímetros de alanina+parafina na faixa de 1 a 10kGy de irradiação. Com base nas avaliações microbiológicas as amostras controle tiveram vida-útil de 5 dias, observandose um ganho na vid...
One hundred sixty seven strains of Lactococcus lactis were screened for bacteriocin production by well diffusion assay of GM17 agar. Fourteen (8.4%) produced antimicrobial activity other than organic acids, bacteriophages or hydrogen peroxide. The frequency of bacteriocin production ranged from 2% in L. lactis subsp. cremoris up to 12% in L. lactis subsp. lactis. Antimicrobial activities were not observed in any strain of L. lactis subsp. lactis var. diacetylactis. Among thirteen bacteriocin-producing strains and two nisin-producing strains (L. lactis subsp. lactis ATCC 11454 and L. lactis subsp. lactis CNRZ 150), eight (53%) were characterized as lactose-positive (Lac + ) and proteinase-negative (Prt -). The bacteriocin-producing cultures were also characterized on the basis of plasmid content. All strains had 2 to 7 plasmids with molecular weights varying from 0.5 to 28.1 Mdal. Four strains (ITAL 435, ITAL 436, ITAL 437 and ITAL 438) showed identical profiles and the other were quite distinct.
Microbiological and chemical changes were evaluated in freshwater prawn stored under refrigeration at 0°C and 5°C during 10 days, with special emphasis on indole production as a chemical spoilage indicator. The total psychrotrophic and indole positive microflora were mainly mesophilic, with indole positive microorganisms being less than 10% of the total microflora after 10 days storage under refrigeration. Bacteria from Enterobacteriaceae and Vibrionaceae families prevailed among the isolated indole positive strains. The use of the Most Probable Number-MPN method, using tryptone broth as culture medium, was the most reliable approach for the quantitative evaluation of the indole positive microflora. The stored samples showed increases in pH, L-tryptophan and total volatile bases (TVB), which were more intensive at 5°C. The psychrotrophic counts and TVB values of samples stored at 0°C were lower than the recommended limits (10 7 CFU/g and 30 mg N/100g, respectively), even after 10 days storage. However, in samples stored at 5°C, these values were reached after 10 and 5 days, respectively. The presence of indole in levels above the limit recommended by FDA/USA (25 µg/100g) was confirmed in only one sample, suggesting that this substance, alone, wouldn't be a good indicator of freshwater prawn quality stored under refrigeration.
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