2008
DOI: 10.1016/j.foodcont.2007.11.001
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An evaluation of Clostridium perfringens media

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Cited by 19 publications
(9 citation statements)
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References 26 publications
(24 reference statements)
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“…All samples were analysed according to the ISO 7937 Standard (1997) to enumerate Clostridium perfringens. As described by Romero et al (2009a), five dilutions per sample were plated on agar tryptose sulphite supplemented with antibiotic D-cycloserine (Byrne et al, 2008) and then incubated at 37ºC in anaerobic jars. In addition, the 10-fold diluted solution was previously heated to 75ºC for 15 min to estimate the concentration of spores in the samples.…”
Section: Evaluation Of Environmental Hygienementioning
confidence: 99%
“…All samples were analysed according to the ISO 7937 Standard (1997) to enumerate Clostridium perfringens. As described by Romero et al (2009a), five dilutions per sample were plated on agar tryptose sulphite supplemented with antibiotic D-cycloserine (Byrne et al, 2008) and then incubated at 37ºC in anaerobic jars. In addition, the 10-fold diluted solution was previously heated to 75ºC for 15 min to estimate the concentration of spores in the samples.…”
Section: Evaluation Of Environmental Hygienementioning
confidence: 99%
“…Recently, Byrne et al (2008) conducted an evaluation study on cultural agar media for C. perfringens vegetative cells and spores and also found that Reinforced Clostridial Agar (RCA), similar to DRCM, was a significantly better medium for recovering thermally treated and untreated C. perfringens spores compared with TSC and six other agar media.…”
Section: Resultsmentioning
confidence: 99%
“…The TSC method is widely used in food analysis (Byrne et al 2008). Its use for the examination of water, in conjunction with the membrane filtration technique, was proposed and evaluated by Sartory (1986) and Sartory et al (1998).…”
Section: Introductionmentioning
confidence: 99%
“…All dilutions (5 dilutions per sample) were plated to determine the populations of the suspensions. The cultural medium used was agar tryptose sulfite added with antibiotic D-cycloserine (Byrne et al, 2008). Agar plates were incubated at 37°C in anaerobic jars with C02-generating envelopes for 18 h. The C. perfringens cells reduced sulfite to sulfide and, in the presence of iron, black colonies developed.…”
Section: Chemical Analysis and Clostridium Perfringens Enumerationmentioning
confidence: 99%