2008
DOI: 10.1590/s0103-84782008000300026
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Qualidade microbiológica de leite UHT caprino: pesquisa de bactérias dos gêneros Staphylococcus, Bacillus e Clostridium

Abstract: RESUMO Com o objetivo de avaliar a qualidade microbiológica do leite UHT caprino, 100 amostras provenientes das regiões Sul e Sudeste do país foram analisadas através do isolamento e da identificação de bactérias do gênero

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Cited by 11 publications
(10 citation statements)
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“…According to Vittori et al (2008), post-processing contamination may be due to deficiency in packaging sterilization or to recontamination by handlers. The emergence of biofilms in milk processing environments contributes towards an increase in the probability of microbial contamination of processed milk products with deteriorating and pathogenic microorganisms (Marchand et al, 2012).…”
Section: Resultsmentioning
confidence: 99%
“…According to Vittori et al (2008), post-processing contamination may be due to deficiency in packaging sterilization or to recontamination by handlers. The emergence of biofilms in milk processing environments contributes towards an increase in the probability of microbial contamination of processed milk products with deteriorating and pathogenic microorganisms (Marchand et al, 2012).…”
Section: Resultsmentioning
confidence: 99%
“…After a serial dilution to 10 -3 , a 20 μL aliquot of each dilution was seeded on nutrient agar with 1.5% NaCl. The plates were incubated at 37 °C for 48 h. 10 Subsequently, the fish scale isolates, as well as the strains of Bacillus spp. from the UFRB (University Federal of the Recôncavo of Bahia) collection that were capable of growth on a crushed scale agar medium [(g.L -1 ): 1 tryptone, 0.5 yeast extract, 1 NaCl, 5 scales, and 15 agar; pH 6.5; 35 °C/48 h)] and milk agar (37 °C/48 h), were selected.…”
Section: Methodsmentioning
confidence: 99%
“…The dilutions were seeded onto Sabouraud agar (Himedia ® ) and malt agar (Himedia ® ), and incubated at 30 ºC for 14 days to evaluate growth and to count the colony forming units (CFU) of filamentous fungi and yeast. The dilutions were subjected to hyperthermia (80 ºC) for 20 minutes followed by water cooling at 5 ºC to activate spores and eliminate vegetative cells, adapting the methods described by Vittori et al (2008). Aliquots were then seeded in 9 cm Petri plates, with nutrient agar (Himedia ® ), and incubated at 30 ºC for up to 72 hours for the CFU counting.…”
Section: Methodsmentioning
confidence: 99%