A predictive model that describes the effect of prolonged heating at 70 to90 degrees C and subsequent incubation at refrigeration temperatures on growth from spores and toxigenesis by nonproteolytic Clostridium botulinum inthe presence of lysozyme

Citation
Ps. Fernandez et Mw. Peck, A predictive model that describes the effect of prolonged heating at 70 to90 degrees C and subsequent incubation at refrigeration temperatures on growth from spores and toxigenesis by nonproteolytic Clostridium botulinum inthe presence of lysozyme, APPL ENVIR, 65(8), 1999, pp. 3449-3457
Citations number
39
Categorie Soggetti
Biology,Microbiology
Journal title
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
ISSN journal
00992240 → ACNP
Volume
65
Issue
8
Year of publication
1999
Pages
3449 - 3457
Database
ISI
SICI code
0099-2240(199908)65:8<3449:APMTDT>2.0.ZU;2-U
Abstract
Refrigerated processed foods of extended durability such as cook-chill and sous-vide foods rely on a minimal heat treatment at 70 to 95 degrees C and then storage at a refrigeration temperature for safety and preservation. Th ese foods are not sterile and are intended to have an extended shelf life, often up to 42 days. The principal microbiological hazard in foods of this type is growth of and toxin production by nonproteolytic Clostridium botuli num. Lysozyme has been shown to increase the measured heat resistance of no nproteolytic C. botulinum spores. However, the heat treatment guidelines fo r prevention of risk of botulism in these products have not taken into cons ideration the effect of lysozyme, which can be present in many foods. In or der to assess the botulism hazard, the effect of heat treatments at 70, 75, 80, 85, and 90 degrees C combined with refrigerated storage for up to 90 d ays on growth from 10(6) spores of nonproteolytic C. botulinum (types B, E, and F) in an anaerobic meat medium containing 2,400 U of lysozyme per mi ( 50 mu g per ml) was studied. Provided that the storage temperature was no h igher than 8 degrees C, the following heat treatments each prevented growth and toxin production during 90 days; 70 degrees C for greater than or equa l to ,545 min, 75 degrees C for greater than or equal to 463 min, 80 degree s C for greater than or equal to 230 min, 85 degrees C for greater than or equal to 84 min, and 90 degrees C for greater than or equal to 33.5 min. A factorial experimental design allowed development of a predictive model tha t described the incubation time required before the first sample showed gro wth, as a function of heating temperature (70 to 90 degrees C), period of h eat treatment (up to 2,545 min), and incubation temperature (5 to 25 degree s C), Predictions from the model provided a valid description of the data u sed to generate the model and agreed with observations made previously.