High-Speed Large Scale Chromatographic Purification of Plasmid DNA with a Novel Giant-Pore Stationary Phase |
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Authors: | Lei Wu Guang-chang Pang |
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Affiliation: | (1) Tianjin Key Laboratory of Food and Biotechnology, Tianjin, People’s Republic of China;(2) Department of Biochemical Engineering, School of Biotechnology and Food Science, Tianjin University of Commerce, Tianjin, 300134, People’s Republic of China |
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Abstract: | A rigid spherical giant-pore poly (glycidyl methacrylate-co-ethylene dimethacrylate) matrix has been prepared by radical suspension–polymerization on the basis of a novel porogenic mode using superfine particles of calcium carbonate as a solid porogen. Scanning electron microscopy reveals that the bead has pores as large as 10 μm. The hydrodynamic properties show that this polymeric material has good strength and a low back pressure of 1.0 MPa at a flow velocity of 3,000 cm h−1. After being modified to be an anion-exchange material, high dynamic binding capacity of plasmid DNA of above 1,000 μg plasmid per mL of bed by a column of this material, could be obtained comparing to the 150 μg plasmid per mL of bed with a Q-Sepharose FF column at the same flow rate. Large-scale preparative plasmid separations (2–20 mL) from cell lysate were investigated. A 75% yield and 94.9% purity of SC plasmid DNA were obtained by a 20 mL column of giant-pore beads at a flow rate of 600 cm h−1. |
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Keywords: | Column liquid chromatography Giant-pore polymer bead preparative chromatography Flow-through chromatography Plasmid DNA Gene therapy |
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