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在固定溶解氧补料分批培养条件下通过大肠杆菌高密度培养生产人重组骨形态发生蛋白-2A

Production of human recombinant bone morphogenetic protein-2A by high density culture of Escherichia coli with stationary dissolved oxygen fed-batch condition.

作者信息

Li M, Chen C, Pu Q, Chen S

机构信息

Shanghai Research Center of Biotechnology, Chinese Academy of Sciences, China.

出版信息

Chin J Biotechnol. 1998;14(3):157-63.

Abstract

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.

摘要

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。

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