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机构地区:[1]河南城建学院生命科学与工程学院,平顶山467036 [2]平顶山市第一高级中学数学教研组,平顶山467000
出 处:《生物技术通报》2013年第12期167-172,共6页Biotechnology Bulletin
基 金:河南省科技攻关重点项目(092102310069)
摘 要:优化降解有机氮细菌N24的种子培养基来提高发酵液对数期末期的细菌浓度。首先用Plackett-Burman设计对影响降解有机氮细菌N24菌体浓度的因素进行评估并筛选出具有显著效应的3个因素蛋白胨、K2HPO4和FeSO4·7H2O,接着用最陡爬坡试验法逼近以上3个因素的最大响应区域后,采用Box-Behnken设计以及响应面分析法确定3个因素的最优水平。优化后的种子培养基:蛋白胨6.55 g,K2HPO40.66 g,FeSO4·7H2O 0.024 g,NaC1 0.3g,MgSO4·7H2O 0.6 g,蒸馏水1 000 mL,初始pH值7.2。优化后发酵液对数期末期细菌浓度达到2.4440×1010CFU/mL,比优化前6.2467×109CFU/mL提高了2.91倍。Plackett-Burman设计和响应面相结合的试验方法优化了菌株N24的种子培养基,可大大提高菌株N24的细菌浓度,有望用于大规模生产。The seed culture medium was optimized to improve the cell density of strain N24. Firstly, Plackett-Burman design was used to investigate the effects of different factors on cell density in the seed culture medium, three statistically significant factors are:peptone, K4HPO2 and FeSO4 ?7H2O, and then a steepest ascent procedure were employed to define optimal response region for these three factors. Finally, Box-Behnken design and RSM were employed to define the optimal level of these three factors. The optimal seed culture medium is:peptone 6.55 g, K2HPO4 0.66 g, FeSO24·7H2 2O 0.024 g, NaC1 0.3g, MgSO 4·7H2O 0.6 g, distilled water 1 000 mL, initial pH value 7.2. The bacteria concentration reached 2.4440×1010 CFU/mL at the telophase of logarithmic phase after optimization, which increased 291% than before. The cell density of strain N24 can be increased by the optimized seed culture medium through Plackett-Burman design combined with response surface analysis, which can be used industrially.
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