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When is simple good enough: a comparison of the Gompertz,Baranyi, and three-phase linear models for fitting bacterial growth curves
Affiliation:1. Agriculture and Agri-Food Canada, 6000 C&E Trail, Lacombe, Alberta T4L 1W1, Canada;2. Department of Agricultural, Food and Nutritional Science, University of Alberta, 3-18G Agriculture/Forestry Centre, Edmonton, Alberta T6G 2P5, Canada;1. National Research University – Higher School of Economics, Myasnitskaya st., 20, Moscow 101000, Russian Federation;2. Institute of Applied Physics RAS, Ul''yanov st., 46, Nizhny Novgorod 603950, Russian Federation;3. Nizhny Novgorod State Technical University n.a. R.E. Alekseev, Minin st., 24, Nizhny Novgorod 603950, Russian Federation;4. East China Normal University, Shanghai 200241, China;5. Universidade Federal de São Paulo, São Paulo 04021-001, Brazil;1. Laboratory of Environmental Technology, INET, Tsinghua University, Beijing 100084, PR China;2. Beijing Key Laboratory of Radioactive Waste Treatment, Tsinghua University, Beijing 100084, PR China
Abstract:The use of primary mathematical models with curve fitting software is dramatically changing quantitative food microbiology. The two most widely used primary growth models are the Baranyi and Gompertz models. A three-phase linear model was developed to determine how well growth curves could be described using a simpler model. The model divides bacterial growth curves into three phases: the lag and stationary phases where the specific growth rate is zero (gm=0), and the exponential phase where the logarithm of the bacterial population increases linearly with time (gm=constant). The model has four parameters: No(Log8of initial population density), NMAX(Log8of final population density), tLAG(time when lag phase ends), and tMAX(time when exponential phase ends). A comparison of the linear model was made against the Baranyi and Gompertz models, using established growth data forEscherichia coli0157:H7. The growth curves predicted by the three models showed good agreement. The linear model was more ‘robust' than the others, especially when experimental data were minimal. The physiological assumptions underlying the linear model are discussed, with particular emphasis on assuring that the model is consistent with bacterial behavior both as individual cells and as populations. It is proposed that the transitional behavior of bacteria at the end of the lag phase can be explained on the basis of biological variability.
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