Thermal death times (F-values) for L. monocytogenes F5069 inoculated into sterile liquid whole egg were determined between 62 and 73°C by a submerged capillary tube procedure. The initial population was 5 × 10 to 2 × 10 CFU/tube (0.05 ml). High populations intentionally were selected to build in a safety factor. At each temperature, F-values were determined to be the shortest heating time which did not permit recovery of L. monocytogenes from six or more replicate tubes. L. monocytogenes were recovered by incubating the entire contents of the capillary tube in brain heart infusion broth at 25°C for 2 weeks. At 62°C, F = 16 min and at 69°C, F = 1.6 min. The z-value was 7.1°C. Minimal pasteurization of egg would not result in product free from L. monocytogenes if initial populations were large. Ultrapasteurization processes may be designed to produce product free from L. monocytogenes and appropriate for prolonged refrigeration.
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http://dx.doi.org/10.4315/0362-028X-53.1.6 | DOI Listing |
Appl Environ Microbiol
March 2009
Department of Food Science, The Pennsylvania State University, University Park, PA 16802, USA.
Changes in barotolerance, thermotolerance, and cellular morphology throughout the life cycle of Listeria monocytogenes were investigated. For part 1 of this analysis, L. monocytogenes ATCC 19115 was grown to log, stationary, death, and long-term-survival phases at 35 degrees C in tryptic soy broth with yeast extract (TSBYE).
View Article and Find Full Text PDFJ Food Prot
August 2002
Department of Nutrition and Food Sciences, University of Vermont, Burlington 05405, USA.
Detection of Listeria in food products is often limited by performance of enrichment media used to support growth of Listeria to detectable levels. In this study, growth curves were generated using healthy and heat-injured Listeria monocytogenes strain F5069 in three nonselective and five selective enrichment broths. Nonselective enrichment media included the current Food and Drug Administration Bacteriological Analytical Manual Listeria enrichment broth base (BAM), Listeria repair broth (LRB), and Trypticase soy broth.
View Article and Find Full Text PDFAppl Environ Microbiol
January 1996
Food Fermentation Laboratory, USDA Agricultural Research Service, North Carolina State University, Raleigh 27695-7624, USA.
A defined medium with glucose as the carbon source was used to quantitatively determine the metabolic end products produced by Listeria monocytogenes under aerobic and anaerobic conditions. Of 10 strains tested, all produced acetoin under aerobic conditions but not anaerobic conditions. Percent carbon recoveries of end products, typified by strain F5069, were as follows: lactate, 28%; acetate, 23%; and acetoin, 26% for aerobic growth and lactate, 79%; acetate, 2%; formate, 5.
View Article and Find Full Text PDFAppl Environ Microbiol
November 1994
Department of Food Science, Pennsylvania State University, University Park 16802.
High pH has been shown to rapidly destroy gram-negative food-borne pathogens; however, the mechanism of destruction has not yet been elucidated. Escherichia coli O157:H7, Salmonella enteritidis ATCC 13706, and Listeria monocytogenes F5069 were suspended in NaHCO3-NaOH buffer solutions at pH 9, 10, 11, or 12 to give a final cell concentration of approximately 5.2 x 10(8) CFU/ml and then held at 37 or 45 degrees C.
View Article and Find Full Text PDFJ Food Prot
August 1992
Department of Animal Sciences, University of Vermont, Burlington, Vermont 05405.
Heat-injured Listeria species were examined for their ability to repair in pasteurized whole and 2% (fat) bovine milk. Listeria monocytogenes F5069 (serotype 4B) and F5027 (serotype 1/2a) and Listeria innocua CWD139 were heated at 55°C. After 20 min, 99% of the surviving population was injured as determined by their inability to grow in the presence of 4% NaCl.
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