首页> 外文期刊>Microbial Cell Factories >Cultivation of E. coli carrying a plasmid-based Measles vaccine construct (4.2 kbp pcDNA3F) employing medium optimisation and pH-temperature induction techniques
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Cultivation of E. coli carrying a plasmid-based Measles vaccine construct (4.2 kbp pcDNA3F) employing medium optimisation and pH-temperature induction techniques

机译:使用培养基优化和pH温度诱导技术培养携带基于质粒的麻疹疫苗构建体(4.2 kbp pcDNA3F)的大肠杆菌

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Background Plasmid-based measles vaccines offer great promises over the conventional fertilised egg method such as ease of manufacture and mimic wild-type intracellular antigen expression. The increasing number of clinical trials on plasmid-based measles vaccines has triggered the need to make more in less time. Results In this work, we investigated the process variables necessary to improve the volumetric and specific yields of a model plasmid-based measles vaccine (pcDNA3F) harboured in E. coli DH5 α . Results from growth medium optimisation in 500 mL shake flasks by response surface methodology (RSM) generated a maximum volumetric yield of 13.65 mg/L which was 1.75 folds higher than that of the base medium. A controlled fed-batch fermentation employing strategic glycerol feeding and optimised growth conditions resulted in a remarkable pcDNA3F volumetric yield of 110 mg/L and a specific yield of 14 mg/g. In addition, growth pH modification and temperature fluctuation between 35 and 45°C were successfully employed to improve plasmid production. Conclusion Production of a high copy number plasmid DNA containing a foreign gene of interest is often hampered by the low plasmid volumetric yield which results from the over expression of foreign proteins and metabolic repressors. In this work, a simple bioprocess framework was employed and successfully improved the production of pcDNA3F.
机译:背景技术基于质粒的麻疹疫苗比常规的受精卵方法具有广阔的前景,例如易于生产和模拟野生型细胞内抗原表达。基于质粒的麻疹疫苗的临床试验越来越多,这引发了需要在更短的时间内生产更多疫苗的需求。结果在这项工作中,我们研究了改善大肠杆菌DH5α中所含的基于模型质粒的麻疹疫苗(pcDNA3F)的体积和比产量所必需的过程变量。通过响应表面方法(RSM)在500 mL摇瓶中优化生长培养基的结果产生的最大体积产量为13.65 mg / L,比基础培养基高1.75倍。采用策略性甘油进料和优化的生长条件进行的分批补料发酵,可实现110 mg / L的pcDNA3F显着体积产量和14 mg / g的比产量。此外,成功地采用了生长pH调节和35至45°C之间的温度波动来提高质粒产量。结论含有外源目的基因的高拷贝数质粒DNA的生产通常由于外源蛋白质和代谢阻遏物过表达导致的质粒体积低产量而受到阻碍。在这项工作中,采用了一个简单的生物过程框架,成功地提高了pcDNA3F的产量。

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