Improvement of Bacillus clausii cell HH1 density via culture medium optimization and pH-stat fed batch fermentation

T. Pham, T. Nguyen, K. To
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Abstract

In this study, the culture medium and fermentation modes were studied aiming to improve the cell density of Bacillus clausii. Firstly, the factorial design method using Minimum Run Resolution IV design was used to evaluate the relative importance of culture medium components to the growth of Bacillus clausii. The results showed that three components peptone, yeast extract and malt extract were the components significantly affecting the bacterial biomass. Then, the optimization of these three ingredient concentrations using a response surface methodology with the Box-Behnken design resulted that the maximal biomass had been achieved using the medium containing 7.64 g/L peptone, 10 g/L yeast extract and 6.36 g/L malt extract. Finally, the pH-stat fed batch fermentation was conducted in a 2-liter bioreactor where the 9X concentrated optimal culture medium was feed into the bioreactor based on the pH signal. As a result, the microbial cell density increased by 2.9-fold compared to that achieved through batch fermentation.
通过培养基优化和ph值分批发酵提高克氏芽孢杆菌细胞h1密度
为了提高克氏芽孢杆菌的细胞密度,对培养基和发酵方式进行了研究。首先,采用最小运行分辨率IV设计的因子设计方法,评价培养基组分对克氏芽孢杆菌生长的相对重要性。结果表明,蛋白胨、酵母浸出物和麦芽浸出物是影响细菌生物量的主要成分。然后,采用Box-Behnken设计的响应面法对这三种成分的浓度进行优化,结果表明,在含有7.64 g/L蛋白胨、10 g/L酵母提取物和6.36 g/L麦芽提取物的培养基中,生物量达到最大。最后,在2升生物反应器中进行pH-stat分批发酵,根据pH信号向生物反应器中加入9X浓度的最优培养基。结果,与批量发酵相比,微生物细胞密度增加了2.9倍。
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