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Behaviour of Listeria monocytogenes under combined chilling processes

Identifieur interne : 00C820 ( Main/Exploration ); précédent : 00C819; suivant : 00C821

Behaviour of Listeria monocytogenes under combined chilling processes

Auteurs : J.-M. Membre [France] ; T. Ross [Australie] ; T. Mcmeekin [Australie]

Source :

RBID : Pascal:99-0264869

Descripteurs français

English descriptors

Abstract

The behaviour of Lisleria monocytogenes under chilling processes was investigated. Growth kinetics were measured at 7 °C in TSBYE culture medium as a function of pH (7.2 and 6.2), pre-incubation temperatures (4 or 7 °C), cooling (0.05 or 0.1°C min-1) and freezing (0 and - 5°C) treatments. Growth curves generated were fitted by Gompertz and Baranyi functions. The Baranyi function gave better parameter estimation values than the Gompertz equation which over-estimated the specific growth rate values. Listeria monocytogenes grew at 7°C without a lag phase, except when the sub-culture was performed at 37°C, whereas the specific growth rate was affected by the chilling processes. In fact, L. monocytogenes grew slightly faster at 7 °C when a 4°C pre-incubation treatment was applied than with a 7 °C pre-incubation treatment. These results suggest that to mimic the processes of contamination in industry, predictive microbiology studies with L. monocytogenes should be performed with organisms cultured at low temperatures.


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Le document en format XML

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<div type="abstract" xml:lang="en">The behaviour of Lisleria monocytogenes under chilling processes was investigated. Growth kinetics were measured at 7 °C in TSBYE culture medium as a function of pH (7.2 and 6.2), pre-incubation temperatures (4 or 7 °C), cooling (0.05 or 0.1°C min
<sup>-1</sup>
) and freezing (0 and - 5°C) treatments. Growth curves generated were fitted by Gompertz and Baranyi functions. The Baranyi function gave better parameter estimation values than the Gompertz equation which over-estimated the specific growth rate values. Listeria monocytogenes grew at 7°C without a lag phase, except when the sub-culture was performed at 37°C, whereas the specific growth rate was affected by the chilling processes. In fact, L. monocytogenes grew slightly faster at 7 °C when a 4°C pre-incubation treatment was applied than with a 7 °C pre-incubation treatment. These results suggest that to mimic the processes of contamination in industry, predictive microbiology studies with L. monocytogenes should be performed with organisms cultured at low temperatures.</div>
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