首页> 外文期刊>Biotechnology and Bioengineering >High cell density fed batch and perfusion processes for stable non-viral expression of secreted alkaline phosphatase (SEAP) using insect cells: Comparison to a batch Sf-9-BEV system
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High cell density fed batch and perfusion processes for stable non-viral expression of secreted alkaline phosphatase (SEAP) using insect cells: Comparison to a batch Sf-9-BEV system

机译:高细胞密度补料分批处理和灌注过程,可使用昆虫细胞稳定地进行非病毒分泌的碱性磷酸酶(SEAP)表达:与批处理Sf-9-BEV系统的比较

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摘要

The development of insect cells expressing recombinant proteins in a stable continuous manner is an attractive alternative to the BEV system for recombinant protein production. High cell density fed batch and continuous perfusion processes can be designed to maximize the productivity of stably transformed cells. A cell line (Sf-9SEAP) expressing high levels of the reporter protein SEAP stably was obtained by lipid-mediated transfection of Sf-9 insect cells and further selection and screening. The expression of the Sf-9SEAP cells was compared with the BEVS system. It was observed that, the yield obtained in BEVS was similar to the batch Sf-9SEAP at 8 and 7 IU/mL, respectively. The productivity of this foreign gene product with the stable cells was enhanced by bioprocess intensification employing the fed-batch and perfusion modes of culture to increase the cell density in culture. The fed batch process yielded a maximum cell density of 28 x 10(6) cells/mL and 12 IU/mL of SEAP. Further improvements in the productivity could be made using the perfusion process, which demonstrated a stable production rate for extended periods of time. The process was maintained for 43 days, with a steady-state cell density of 17-20 x 10(6) cells/mL and 7 IU/mL SEAP. The total yield obtained in the perfusion process (394 IU) was approximately 22 and 8 times higher than that obtained in a batch (17.6 IU) and fed batch (46.1 IU) process, respectively.
机译:以稳定的连续方式表达重组蛋白的昆虫细胞的开发是BEV系统用于重组蛋白生产的一种有吸引力的替代方法。可以设计高细胞密度分批补料和连续灌注过程,以最大化稳定转化细胞的生产力。通过脂质介导的Sf-9昆虫细胞转染以及进一步的选择和筛选,获得了稳定表达高水平报道蛋白SEAP的细胞系(Sf-9SEAP)。将Sf-9SEAP细胞的表达与BEVS系统进行比较。观察到,BEVS中得到的产率分别类似于批次Sf-9SEAP,分别为8 IU / mL和7 IU / mL。通过使用补料分批和灌注培养模式以增加培养中的细胞密度的生物过程强化来提高具有稳定细胞的该外源基因产物的生产率。分批补料过程产生的最大细胞密度为28 x 10(6)个细胞/ mL和12 IU / mL的SEAP。使用灌注过程可以进一步提高生产率,这证明了长时间稳定的生产率。该过程维持43天,稳态细胞密度为17-20 x 10(6)细胞/ mL,SEAP为7 IU / mL。灌注过程(394 IU)获得的总产量分别比分批(17.6 IU)和补料分批(46.1 IU)的分别高约22倍和8倍。

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