Separation of different physical forms of plasmid DNA using a combination of low electric field strength and flow in porous media: Effect of different field gradients and porosity of the media

Citation
Kd. Cole et al., Separation of different physical forms of plasmid DNA using a combination of low electric field strength and flow in porous media: Effect of different field gradients and porosity of the media, ELECTROPHOR, 21(5), 2000, pp. 1010-1017
Citations number
27
Categorie Soggetti
Chemistry & Analysis
Journal title
ELECTROPHORESIS
ISSN journal
01730835 → ACNP
Volume
21
Issue
5
Year of publication
2000
Pages
1010 - 1017
Database
ISI
SICI code
0173-0835(200003)21:5<1010:SODPFO>2.0.ZU;2-J
Abstract
The retention of different physical forms of DNA by an electric field in a chromatography system was studied. We were able to effectively separate the supercoiled and the open circular forms of plasmid DNA using this type of electrochromatography system. Chromatography columns were packed with porou s beads, and an axial electric field was applied so that convective buffer flow opposed the direction of electrophoresis of the DNA. A model system co mposed of approximately equal amounts of the supercoiled and open circular forms of the plasmid pBR 322 (4322 base pairs) was used to test the separat ion. Chromatography beads (agarose-based) with different porosities were us ed to determine the effect of the stationary phase on the separation. The p orous media did not have a major effect on the separation, but the best sep arations were obtained using porous chromatography media made with the high est agarose concentration (10% agarose). Selective elution of plasmid DNA w ith different forms was obtained by either increasing the flow rates or dec reasing the electric field strength (by steps or a gradient). in all the se parations, the more compact supercoiled form of the plasmid was retained le ss strongly than either the open circular form (nicked) or the linear form. High molecular weight host genomic DNA was more strongly retained than the plasmid DNA. Increasing the ionic strength of the buffer improved resoluti on and capacity. The capacity of the separation was determined by injecting increasing amounts of plasmid DNA. Satisfactory separation was obtained at sample loading of up to 360 mu g of total DNA on a column with dimensions of 2.5 by II cm (bed volume of 54 mt). The retention of DNA depends upon a counter-current flow of electrophoresis and convective flow and could be re garded as a type of field flow fractionation. The retention of the DNA by t he electric field and flow is discussed in relation to the diffusion coeffi cients of the DNA.