Guerrero-Germán Patricia, Prazeres Duarte M F, Guzmán Roberto, Montesinos-Cisneros Rosa Ma, Tejeda-Mansir Armando
Instituto de Ingeniería, Universidad Autónoma de Baja California, Blvd. Benito Juárez y Calle Normal, Col. Insurgentes Este, 21280, Mexicali, Baja California, Mexico.
Bioprocess Biosyst Eng. 2009 Aug;32(5):615-23. doi: 10.1007/s00449-008-0284-7. Epub 2008 Dec 13.
A new bioprocess using mainly membrane operations to obtain purified plasmid DNA from Escherechia coli ferments was developed. The intermediate recovery and purification of the plasmid DNA in cell lysate was conducted using hollow-fiber tangential filtration and tandem anion-exchange membrane chromatography. The purity of the solutions of plasmid DNA obtained during each process stage was investigated. The results show that more than 97% of RNA in the lysate was removed during the process operations and that the plasmid DNA solution purity increased 28-fold. One of the main characteristics of the developed process is to avoid the use of large quantities of precipitating agents such as salts or alcohols. A better understanding of membrane-based technology for the purification of plasmid DNA from clarified E. coli lysate was developed in this research. The convenience of anion-exchange membranes, configured in ready-to-use devices can further simplify large-scale plasmid purification strategies.
开发了一种主要使用膜操作从大肠杆菌发酵液中获得纯化质粒DNA的新生物工艺。使用中空纤维切向过滤和串联阴离子交换膜色谱法对细胞裂解物中的质粒DNA进行中间回收和纯化。研究了每个工艺阶段获得的质粒DNA溶液的纯度。结果表明,在工艺操作过程中,裂解物中97%以上的RNA被去除,质粒DNA溶液的纯度提高了28倍。所开发工艺的主要特点之一是避免使用大量沉淀剂,如盐或醇。本研究对基于膜的从澄清的大肠杆菌裂解物中纯化质粒DNA的技术有了更好的理解。配置在即用型装置中的阴离子交换膜的便利性可以进一步简化大规模质粒纯化策略。