Li M, Chen C, Pu Q, Chen S
Shanghai Research Center of Biotechnology, Chinese Academy of Sciences, China.
Chin J Biotechnol. 1998;14(3):157-63.
The optimization of cultivation condition in 500 ml shake flasks was carried out to produce recombinant human bone morphogenetic protein-2A (BMP-2A) in recombinant Escherichia coli YK537/pDH-B2m, followed by a 5L fermenter batch and condition-controlled fed-batch culture to obtain BMP-2A. The comparison of these two methods indicated that cultivation by keeping dissolved oxygen at 30%-40% and limiting glucose concentration could obtain BMP-2A 2.78 g/L broth, the final cell density was OD600 53 (dry cell weight 21.2 g/L), and expressed BMP-2A was 25% of the total amount of protein in E.coli. The critical fermentation conditions included: (1) keeping appropriate dissolved oxygen concentration in the process; (2) limiting glucose concentration; (3) taking heat induction at the middle-log phase and maintaining 42 degrees C for 4 hours; (4) controlling specific growth rate around 0.3 h-1 in the duration of growth.
在500毫升摇瓶中对培养条件进行优化,以在重组大肠杆菌YK537/pDH - B2m中生产重组人骨形态发生蛋白 - 2A(BMP - 2A),随后进行5升发酵罐分批培养和条件控制补料分批培养以获得BMP - 2A。这两种方法的比较表明,通过将溶解氧保持在30% - 40%并限制葡萄糖浓度进行培养,可获得2.78克/升发酵液的BMP - 2A,最终细胞密度为OD600 53(干细胞重量21.2克/升),且表达的BMP - 2A占大肠杆菌中蛋白质总量的25%。关键发酵条件包括:(1)在过程中保持适当的溶解氧浓度;(2)限制葡萄糖浓度;(3)在对数中期进行热诱导并在42摄氏度维持4小时;(4)在生长期间将比生长速率控制在约0.3 h-1左右。