Plasmid DNA partitioning and separation using poly(ethylene glycol)/poly(acrylate)/salt aqueous two-phase systems

被引:29
作者
Johansson, Hans-Olof [1 ]
Matos, Tiago [2 ]
Luz, Juliana S. [3 ]
Feitosa, Eloi [4 ]
Oliveira, Carla C. [3 ]
Pessoa, Adalberto, Jr. [5 ]
Buelow, Leif [2 ]
Tjerneld, Folke [1 ]
机构
[1] Lund Univ, Dept Biochem & Struct Biol, S-22100 Lund, Sweden
[2] Lund Univ, Dept Pure & Appl Biochem, S-22100 Lund, Sweden
[3] Univ Sao Paulo, Inst Chem, Dept Biochem, BR-05508000 Sao Paulo, Brazil
[4] Sao Paulo State Univ, Dept Phys, Sao Jose Do Rio Preto, Brazil
[5] Univ Sao Paulo, Dept Biochem & Pharmaceut Technol, BR-05508000 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Plasmid DNA; Partitioning; Aqueous two-phase systems; Poly(ethylene glycol); Polyacrylate; COLI CELL LYSATE; PHASE-SEPARATION; PH; EXTRACTION; PROTEINS; SALT; COMPLEXATION; PURIFICATION; TRANSITION;
D O I
10.1016/j.chroma.2012.02.028
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phase diagrams of poly(ethylene glycol)/polyacrylate/Na2SO4 systems have been investigated with respect to polymer size and pH. Plasmid DNA from Escherichia coli can depending on pH and polymer molecular weight be directed to a poly(ethylene glycol) or to a polyacrylate-rich phase in an aqueous two-phase system formed by these polymers. Bovine serum albumin (BSA) and E. coli homogenate proteins can be directed opposite to the plasmid partitioning in these systems. Two bioseparation processes have been developed where in the final step the pDNA is partitioned to a salt-rich phase giving a total process yield of 60-70%. In one of them the pDNA is partitioned between the polyacrylate and PEG-phases in order to remove proteins. In a more simplified process the plasmid is partitioned to a PEG-phase and back-extracted into a Na2SO4-rich phase. The novel polyacrylate/PEG system allows a strong change of the partitioning between the phases with relatively small changes in composition or pH. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:30 / 35
页数:6
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