Prats Clara, López Daniel, Giró Antoni, Ferrer Jordi, Valls Joaquim
Escola Superior d'Agricultura de Barcelona, Departament de Física i Enginyeria Nuclear, Campus del Baix Llobregat, Universitat Politècnica de Catalunya, Av. del Canal Olímpic s/n, 08860 Castelldefels, Barcelona, Spain.
J Theor Biol. 2006 Aug 21;241(4):939-53. doi: 10.1016/j.jtbi.2006.01.029. Epub 2006 Mar 9.
The lag phase has been widely studied for years in an effort to contribute to the improvement of food safety. Many analytical models have been built and tested by several authors. The use of Individual-based Modelling (IbM) allows us to probe deeper into the behaviour of individual cells; it is a bridge between theories and experiments when needed. INDividual DIScrete SIMulation (INDISIM) has been developed and coded by our group as an IbM simulator and used to study bacterial growth, including the microscopic causes of the lag phase. First of all, the evolution of cellular masses, specifically the mean mass and biomass distribution, is shown to be a determining factor in the beginning of the exponential phase. Secondly, whenever there is a need for an enzyme synthesis, its rate has a direct effect on the lag duration. The variability of the lag phase with different factors is also studied. The known decrease of the lag phase with an increase in the temperature is also observed in the simulations. An initial study of the relationship between individual and collective lag phases is presented, as a complement to the studies already published. One important result is the variability of the individual lag times and generation times. It has also been found that the mean of the individual lags is greater than the population lag. This is the first in a series of studies of the lag phase that we are carrying out. Therefore, the present work addresses a generic system by making a simple set of assumptions.
多年来,人们对延迟期进行了广泛研究,以期促进食品安全的改善。多位作者构建并测试了许多分析模型。基于个体的建模(IbM)方法使我们能够更深入地探究单个细胞的行为;在需要时,它是理论与实验之间的桥梁。我们团队开发并编写了个体离散模拟(INDISIM)程序作为一种基于个体的建模模拟器,用于研究细菌生长,包括延迟期的微观成因。首先,细胞质量的演变,特别是平均质量和生物量分布,被证明是指数期开始的一个决定性因素。其次,每当需要进行酶合成时,其合成速率会直接影响延迟持续时间。我们还研究了不同因素下延迟期的变异性。模拟中也观察到了延迟期随温度升高而缩短这一已知现象。作为对已发表研究的补充,我们初步研究了个体延迟期与群体延迟期之间的关系。一个重要结果是个体延迟时间和世代时间的变异性。还发现个体延迟的平均值大于群体延迟。这是我们正在进行的一系列延迟期研究中的第一篇。因此,本研究通过做出一组简单假设来探讨一个通用系统。