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    张兴群, 王粱华, 焦炳华, 袁勤生. 高密度培养大肠杆菌TB1/pMAL-hOCIFm的优化条件[J]. 华东理工大学学报(自然科学版), 2005, (1): 72-75.
    引用本文: 张兴群, 王粱华, 焦炳华, 袁勤生. 高密度培养大肠杆菌TB1/pMAL-hOCIFm的优化条件[J]. 华东理工大学学报(自然科学版), 2005, (1): 72-75.
    High Cell-Density Culture of E.coli TB1/pMAL-hOCIFm[J]. Journal of East China University of Science and Technology, 2005, (1): 72-75.
    Citation: High Cell-Density Culture of E.coli TB1/pMAL-hOCIFm[J]. Journal of East China University of Science and Technology, 2005, (1): 72-75.

    高密度培养大肠杆菌TB1/pMAL-hOCIFm的优化条件

    High Cell-Density Culture of E.coli TB1/pMAL-hOCIFm

    • 摘要: 利用Bioengeering 3.7L自控式发酵罐,以分批培养和补料分批培养相结合的培养技术,高密度培养重组大肠杆菌TB1/pMAL-hOCIFm,生产重组人破骨细胞形成抑制因子成熟肽(recombinant human osteoclastogenesis inhibitory factor mature peptide,rhOCIFm)。通过对碳、氮源补加方式以及溶解氧等参数的控制,使工程菌E.coliTB1/pMAL-hOCIFm的发酵菌体OD600达到57.8,rhOCIFm与MBP融合蛋白(hOCIFm-MBP)的含量达到3.2g/L。本研究为工业化生产rhOCIFm奠定了基础。

       

      Abstract: Batch and fed-batch culture process of E.coli TB1/pMAL-hOCIFm were carried out to produce recombinant human osteoclastogenesis inhibitory factor mature peptide (rhOCIFm) in 3.7 L Bioengineering autocontrol fermentor. High cell-density and high expression were achieved by the control of carbon/nitrogen source and dissolved oxygen. The final cell density and concentration of rhOCIFm-MBP (fusion) protein were 57.8 OD_(600) and 3.2 g/L respectively. The purity of rhOCIFm-MBP fusin protein was more than 70% after treated with affinity chromatography on amylose resin. This study provides a basic work for the production of rhOCIFm in industrial scale.

       

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