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首页> 外文期刊>Biochemical Engineering Journal >Modelling the stress inducing biphasic growth and pediocin production by Pediococcus acidilactici NRRL B-5627 in re-alkalized fed-batch cultures
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Modelling the stress inducing biphasic growth and pediocin production by Pediococcus acidilactici NRRL B-5627 in re-alkalized fed-batch cultures

机译:在重碱化分批补料分批培养中模拟乳酸小球菌NRRL B-56​​27诱导胁迫诱导两相生长和pediocin产生的过程

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摘要

Five re-alkalized fed-batch cultures of Pediococcus acidilactici NRRL B-5627 were carried out in culture media prepared with mussel processing wastes (MPWs) and whey under different fermentation conditions. The shift from homolactic to mixed acid product formation and the biphasic kinetics observed for cell growth, nitrogen consumption and pediocin production were the most noteworthy observations of these cultures. For a better understanding of the culture dynamics and for a suitable description of the bacteriocin production system, an unstructured mathematical model based on the two phases of nitrogen consumption was developed. The model was expressed in terms of biomass, product accumulation and substrate utilization. Excellent agreements between model predictions and experimental data were achieved in the five re-alkalized fed-batch cultures and a reasonable description for each parameter in each growth phase was provided by the model. Using published experimental data by other researchers, model agreement was also found for the growth of Ped. acidilactici NRRL B-5627 in a repeatedly re-alkalized culture in a synthetic culture medium. The developed model appears to be useful for the design, scale-up, control and optimization of the production of potentially probiotic cultures and bacteriocins.
机译:在贻贝加工废料(MPW)和乳清制备的培养基中,在不同的发酵条件下,进行了五个乳酸化乳酸球菌NRRL B-56​​27的补料分批培养。从高纯酸向混合酸产物的转变以及细胞生长,氮消耗和pediocin产生的双相动力学是这些培养物中最值得注意的观察结果。为了更好地了解培养动力学并适当描述细菌素生产系统,开发了基于氮消耗两个阶段的非结构化数学模型。该模型以生物量,产物积累和底物利用率表示。在五种重新碱化的分批补料培养物中,模型预测与实验数据之间达到了极好的一致性,并且模型为每个生长阶段的每个参数提供了合理的描述。利用其他研究人员发表的实验数据,还发现了Ped生长的模型一致性。在合成培养基中反复碱化的酸性乳酸NRRL B-56​​27。所开发的模型对于潜在的益生菌培养物和细菌素的生产的设计,放大,控制和优化似乎是有用的。

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