巴氏杆菌连续(恒化器)培养过程数学模型的建立

A. Raevsky
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引用次数: 0

摘要

生产用于特定预防传染病的生物制剂的最重要的技术阶段之一是微生物的培养。抗原的合成恰好发生在疫苗生产的这个技术阶段;免疫修复的有效性取决于它们。在细菌生长的过程中,有必要在提高生物量产量的同时,确保病原体不会改变其生物特性。要做到这一点,有必要创造最佳的培养条件,同时考虑微生物的生理状态。细菌疫苗的制造技术是一个多方面的问题,其关键方向是开发微生物培养的受控工艺。目前,获得用于生产疫苗的微生物菌群是基于周期性培养方法,在此过程中,细胞的特性和培养基的组成发生不可预测的变化。根据许多研究人员的说法,就细菌生物量的积累而言,最有效的是受碳源限制的恒化器培养[1,2]。微生物的连续(恒化器)培养的生产力显著超过分批法的生产力。因此,这是一项非常有前景的研究,旨在组织受控培养的过程,特别是关于微生物生长的连续方法,使您能够创建并长期保持具有恒定且精确定义的生物量浓度、阶段和生长速率以及保护性抗原比例的培养物[3,4]。本工作的目的是建立一个适当的巴斯德菌恒化培养过程的数学模型,以优化其生产抗巴斯德菌疫苗。研究的结果是,建立了多杀性巴氏杆菌连续培养数学模型的结构,确定了其系数,验证了该模型对真实过程的充分性,所获得的过程的数学描述使计算和选择化学静态培养模式——稀释率D和初始葡萄糖浓度S0——成为可能,以获得活巴氏杆菌的最佳浓度、指定的生产力值、底物转化度,等用于制造抗菌疫苗。此外,所获得的数学依赖性使得有可能对在低稀释率下增加巴氏杆菌浓度的代谢机制提出建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a mathematical model of the continuous (chemostat) process of culturing pasteurella
One of the most important technological stages in the production of biological preparations intended for the specific prevention of infectious diseases is the cultivation of microorganisms. The synthesis of antigens occurs precisely at this technological stage of vaccine production; the effectiveness of immunopreparations depends on them. In the process of growing bacteria, it is necessary, simultaneously with an increase in the biomass yield, to ensure that the pathogen does not change its biological properties. To do this, it is necessary to create optimal conditions for cultivation, taking into account the physiological state of microorganisms. The technology of manufacturing bacterial vaccines is a multifaceted problem, the key direction of which is the development of controlled processes for the cultivation of microorganisms. At present, obtaining a bacterial mass of microorganisms for the manufacture of vaccines is based on a periodic method of cultivation, during which the properties of cells and the composition of the culture medium change unpredictably. According to a number of researchers, the most efficient in terms of accumulation of bacterial biomass is chemostat cultivation with limitation by the carbon source [1, 2]. The productivity of continuous (chemostat) cultivation of microorganisms significantly exceeds the productivity of the batch method. Therefore, very promising research aimed at organizing the processes of controlled cultivation and, in particular, on continuous methods of growing microorganisms, allowing you to create and maintain for a long time cultures with a constant and precisely defined biomass concentration, phase and growth rate, as well as the ratio of protective antigens [ 3, 4]. The aim of this work is to build an adequate mathematical model of the process of chemostat cultivation of Pasteurella in the production of anti-Pasteurella vaccine in order to optimize it. As a result of the research, the structure of the mathematical model of continuous cultivation of P. multocida was developed, its coefficients were determined, the adequacy of the model to the real process was verified, the obtained mathematical description of the process makes it possible to calculate and select the modes of chemostatic cultivation - the dilution rate D and the initial glucose concentration S0 - to obtain the optimal concentrations of viable pasteurella, the specified productivity values, the degree of substrate conversion, etc. in the manufacture of antibacterial vaccines. In addition, the obtained mathematical dependences make it possible to make a proposal on the metabolic mechanism for increasing the concentration of pasteurella at low dilution rates.
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Athletic Therapy Today
Athletic Therapy Today 医学-康复医学
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