STUDY OF THE PROLIFERATIVE ACTIVITY OF SACCHAROMYCES CEREVISIAE IN YEAST BIOTECHNOLOGY AND PHYSICO-CHEMICAL METHODS OF ITS DETERMINATION

I. Bielykh, S. І. Samoilenko, O. N. Bliznjuk, N. Masalitina, A. P. Belinska, O. Varankina, H. F. Chechui, O. V. Zviahintseva
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Abstract

The article discusses the solution of issues related to increasing the efficiency of technological processes and ensuring the release of high-quality finished products, relevant for production based on the use of S. cerevisiae yeast. The paper identifies major reasons for the need to regulate yeast culture metabolism, considers existing practice and proposes methods of changing its metabolic activity. The purpose of the research is to create the classification of the supplements / preparations from different origin to improve yeast vital activity by adjusting its culture medium composition with the use of complex hierarchical faceted method. The proliferative processes taking place in the yeast cell are quite easily regulated. Therefore, knowing the dependence between the specific conditions of the environment and certain aspects of the yeast culture's vital activity, it is possible to purposefully change its growth, development and metabolism. Creating and maintaining certain conditions for the cultivation of yeast allows you to control the course of the fermentation process. The influence of biologically active substances on the proliferative activity of S. cerevisiae cells was investigated. Concentrations were determined and the regulatory effect of succinic and folic acid preparations on the proliferative activity of yeast cells was proven. A comparative analysis of influence of different concentrations of exogenous substances on microorganisms culture growth was carried out. The most optimal concentrations of drugs for activation of yeast cell division were determined: succinic acid/ascorbic acid – 0.0015/0.0002 mg/ml; folic acid – 0.006 mg/ml. Specific growth rate of yeast during cultivation in 20 % sucrose solution with succinic/ascorbic and folic acid preparations was calculated. It was established that the highest specific rate of cell growth was observed in the complex preparation, which included three organic acids. It was established that the specific rate of yeast reproduction in the complex preparation increased by an average of 30–35 % relative to the control sample. Increase in specific growth rate by 20–25 % of yeast was also observed in the medium with folic acid, the addition of succinic/ascorbic acids did not significantly increase specific rate (by approximately 10 %) of the growth of the S. cerevisiae yeast culture. It has been established that biologically active substances have certain concentrations that activate cell division and contribute to their active development and critical limits at which the development and growth of yeast cells are inhibited.
研究酵母生物技术中酿酒酵母的增殖活性及其测定的物理化学方法
文章讨论了如何解决与提高技术流程效率和确保推出高质量成品有关的问题,这些问题与使用酿酒酵母进行生产息息相关。文章指出了需要调节酵母培养物代谢的主要原因,考虑了现有的做法,并提出了改变其代谢活动的方法。研究的目的是对不同来源的补充剂/制剂进行分类,通过使用复杂的分层分面方法调整培养基成分,提高酵母的生命活性。酵母细胞的增殖过程很容易调节。因此,了解特定环境条件与酵母培养物生命活动某些方面之间的关系,就可以有目的地改变其生长、发育和新陈代谢。为培养酵母创造和保持一定的条件,可以控制发酵过程的进程。我们研究了生物活性物质对 S. cerevisiae 细胞增殖活性的影响。测定了琥珀酸和叶酸制剂的浓度,证明了它们对酵母细胞增殖活性的调节作用。对不同浓度的外源物质对微生物培养生长的影响进行了比较分析。确定了激活酵母细胞分裂的最佳药物浓度:琥珀酸/抗坏血酸 - 0.0015/0.0002 mg/ml;叶酸 - 0.006 mg/ml。在 20 % 的蔗糖溶液中用琥珀酸/抗坏血酸和叶酸制剂培养酵母时,计算了酵母的特定生长率。结果表明,在包含三种有机酸的复合制剂中,细胞的特定生长率最高。与对照样本相比,复合制剂中酵母繁殖的特定速率平均提高了 30-35%。在含有叶酸的培养基中,酵母的特定生长率也提高了 20-25%,而琥珀酸/抗坏血酸的添加并没有显著提高 S. cerevisiae 酵母菌培养的特定生长率(约 10%)。已经证实,生物活性物质具有一定的浓度,可以激活细胞分裂,促进细胞的活性发育,同时也具有抑制酵母细胞发育和生长的临界极限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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