dc.contributorLund Univ
dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T14:02:37Z
dc.date.available2014-05-20T14:02:37Z
dc.date.created2014-05-20T14:02:37Z
dc.date.issued2012-04-13
dc.identifierJournal of Chromatography A. Amsterdam: Elsevier B.V., v. 1233, p. 30-35, 2012.
dc.identifier0021-9673
dc.identifierhttp://hdl.handle.net/11449/22077
dc.identifier10.1016/j.chroma.2012.02.028
dc.identifierWOS:000302663000005
dc.identifier5731856650217859
dc.description.abstractPhase diagrams of poly(ethylene glycol)/polyacrylate/Na2SO4 systems have been investigated with respect to polymer size and pH. Plasmid DNA from Escherichia coil 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. coil 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.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationJournal of Chromatography A
dc.relation3.716
dc.relation1,378
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectPlasmid DNA
dc.subjectPartitioning
dc.subjectAqueous two-phase systems
dc.subjectPolyethylene glycol
dc.subjectPolyacrylate
dc.titlePlasmid DNA partitioning and separation using poly(ethylene glycol)/poly(acrylate)/salt aqueous two-phase systems
dc.typeArtículos de revistas


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