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一种用于大规模制备质粒DNA的连续热裂解方法。

A continuous thermal lysis procedure for the large-scale preparation of plasmid DNA.

作者信息

Zhu Kaichun, Jin Huali, Ma Yijie, Ren Zhihui, Xiao Chong, He Zhonghuai, Zhang Fuchun, Zhu Qinghong, Wang Bin

机构信息

State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing 100094, China.

出版信息

J Biotechnol. 2005 Aug 22;118(3):257-64. doi: 10.1016/j.jbiotec.2005.05.003.

Abstract

There is an increasing interest and need for the development of scaleable process for the preparation of plasmid DNA for vaccines and gene therapy. In this report, we describe a streamline modified process of plasmid extraction based on boiling lysis in order to simplify the operation and process large volumes of Escherichia coli cultures. The bacteria, harvested using a hollow fiber cartridge after fermentation, were treated with lysozyme at 37 degrees C prior to passing through a heat-exchanger coil. Subsequently, the supernatant was separated from lysed bacteria using a 65 microm nylon filter. The employment of a peristaltic pump and two heating coils at constant temperature without the use of centrifugation enabled the process protocol to be constant and controllable. A relatively low lysis temperature of approximately 70-80 degrees C and a buffer modified for the high-density cultures were also optimized for the process. Prior to thermal lysis, a pre-treatment step with the lysozyme for 20 min at 37 degrees C was one of the crucial steps contributing to the high plasmid quantity and quality from batch to batch. After harvesting 17 L of E. coli cultures (OD600 = 50), the plasmid can be extracted within 45 min with this streamline protocol. The plasmid yields are approximately 100mg/L culture, which makes it attractive and promising for the large-scale preparation of plasmid.

摘要

对于开发用于疫苗和基因治疗的可扩展质粒DNA制备工艺,人们的兴趣和需求日益增加。在本报告中,我们描述了一种基于煮沸裂解的简化改良质粒提取工艺,以简化操作并处理大量大肠杆菌培养物。发酵后使用中空纤维柱收获的细菌,在通过热交换器盘管之前,于37℃用溶菌酶处理。随后,使用65微米尼龙滤器从裂解的细菌中分离出上清液。使用蠕动泵和两个恒温加热盘管且不使用离心,使得工艺方案具有稳定性和可控性。还针对该工艺优化了约70 - 80℃的相对较低裂解温度以及针对高密度培养物改良的缓冲液。在热裂解之前,在37℃用溶菌酶预处理20分钟是实现批次间高质粒产量和质量的关键步骤之一。收获17升大肠杆菌培养物(OD600 = 50)后,使用这种简化方案可在45分钟内提取质粒。质粒产量约为每升培养物100毫克,这使其对于大规模制备质粒具有吸引力且前景广阔。

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