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[在改良的超级旋转培养器中对生产凝血酶原的基因工程CHO细胞进行连续灌注培养]

[Continuously perfused cultivation of genetically-engineered CHO cells producing prothrombin in a modified Super-Spinner].

作者信息

Chen Z L, Iding K, Lütkemeyer D, Lehmann J

机构信息

Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2001 Jan;17(1):109-12.

PMID:11330179
Abstract

A Super-Spinner was Modified by mounting a stainless steel filter(pore size 75 microns) to the impeller shaft to retain cells while fresh nutrient is perfused. Using Macroporous microcarrier Cytopore 1, continuously perfused cultivation of a recombinant CHO cell line, CHO2DS producing prothrombin was performed with the perfusion of a protein-free medium DF6S. The cell retention rate was more than 90% during the 24 days continuously perfused cultivation. The viable cell density of CHO2DS and prothrombin concentration reached 4.62 x 10(6)(cells.m/L) and 11.3(mg/L) respectively after 9 days culture.

摘要

通过在叶轮轴上安装一个不锈钢过滤器(孔径75微米)来改造一个超级旋转器,以便在灌注新鲜营养物质时留住细胞。使用大孔微载体Cytopore 1,在无蛋白培养基DF6S的灌注下,对生产凝血酶原的重组CHO细胞系CHO2DS进行连续灌注培养。在24天的连续灌注培养过程中,细胞保留率超过90%。培养9天后,CHO2DS的活细胞密度和凝血酶原浓度分别达到4.62×10(6)(细胞/毫升)和11.3(毫克/升)。

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