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Evaluation of growtho growth modelling approaches on a non-abrupt growtho growth interface of Listeria monocytogenes

机译:单核细胞增生李斯特菌的非突然生长/不生长界面上的生长/不生长建模方法评估

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To minimise and estimate food poisoning risks, it is necessary that the growth ability of pathogenic microorganisms in food products can be predicted. Growtho growth models are being developed that predict the interface between environmental conditions that allow growth and conditions that do not. In this paper, the differences and limitations of existing growtho growth model types are illustrated for a case study describing the growth probability of Listeria monocytogenes under conditions typical for mayonnaise based salads. A data set embeds the effects of pH (5.0-6.0), water activity (0.960-0.990) and acetic acid percentage (0-0.8% (w/w)), narrow intervals between the factor levels and many replicates (usually 20). Thus information was gained not only about presence/absence of growth, but also about probability of growth. Among three existing groups of growtho growth models considered: (i) probabilistic models, (ii) a deterministic approach separating growtho growth/uncertainty regions, and (iii) deterministic approaches, only the probabilistic models fully describe the data, since they reflect the incremental increase in growth probability present in the experimental growtho growth interface. The second group of models represented by the Minimum Convex Polyhedron (MCP) method, can partially describe this incremental increase if an extension proposed by the authors is used. Models developed by the third method are not able to describe any increments in growth probability between 0 (no probability of growth) or 1 (certain growth). An MCP based on total acid data is not capable of describing non-convexity in the interface, in contrast to an MCP based on undissociated acid data..
机译:为了最大程度地减少和估计食物中毒的风险,必须预测食物中病原微生物的生长能力。正在开发增长/不增长模型,用于预测允许增长的环境条件与不允许增长的条件之间的接口。在本文中,通过案例研究说明了现有生长/无生长模型类型的差异和局限性,该案例描述了在蛋黄酱色拉典型的条件下单核细胞增生李斯特菌的生长可能性。数据集嵌入了以下影响:pH(5.0-6.0),水活度(0.960-0.990)和乙酸百分比(0-0.8%(w / w)),因子水平之间的间隔窄且重复多次(通常为20) 。因此,不仅获得有关增长存在/不存在的信息,而且还获得有关增长概率的信息。在考虑的三个现有增长/无增长模型组中:(i)概率模型,(ii)区分增长/无增长/不确定性区域的确定性方法,以及(iii)确定性方法,只有概率模型可以完全描述数据,因为它们反映了实验性增长/无增长界面中增长概率的增加。如果使用作者提出的扩展,则由最小凸多面体(MCP)方法表示的第二组模型可以部分描述这种增量增加。通过第三种方法开发的模型无法描述0(无增长)或1(某些增长)之间的增长概率增量。与基于未分离酸数据的MCP相比,基于总酸数据的MCP无法描述界面中的非凸性。

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