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
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
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.