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dc.contributor.authorJohansson, Hans-Olof-
dc.contributor.authorMatos, Tiago-
dc.contributor.authorLuz, Juliana S.-
dc.contributor.authorFeitosa, Eloi-
dc.contributor.authorOliveira, Carla C.-
dc.contributor.authorPessoa, Adalberto-
dc.contributor.authorBuelow, Leif-
dc.contributor.authorTjerneld, Folke-
dc.date.accessioned2014-05-20T14:02:37Z-
dc.date.accessioned2016-10-25T17:09:14Z-
dc.date.available2014-05-20T14:02:37Z-
dc.date.available2016-10-25T17:09:14Z-
dc.date.issued2012-04-13-
dc.identifierhttp://dx.doi.org/10.1016/j.chroma.2012.02.028-
dc.identifier.citationJournal of Chromatography A. Amsterdam: Elsevier B.V., v. 1233, p. 30-35, 2012.-
dc.identifier.issn0021-9673-
dc.identifier.urihttp://hdl.handle.net/11449/22077-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/22077-
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.en
dc.format.extent30-35-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectPlasmid DNAen
dc.subjectPartitioningen
dc.subjectAqueous two-phase systemsen
dc.subjectPolyethylene glycolen
dc.subjectPolyacrylateen
dc.titlePlasmid DNA partitioning and separation using poly(ethylene glycol)/poly(acrylate)/salt aqueous two-phase systemsen
dc.typeoutro-
dc.contributor.institutionLund Univ-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationLund Univ, Dept Biochem & Struct Biol, S-22100 Lund, Sweden-
dc.description.affiliationLund Univ, Dept Pure & Appl Biochem, S-22100 Lund, Sweden-
dc.description.affiliationUniv São Paulo, Inst Chem, Dept Biochem, BR-05508000 São Paulo, Brazil-
dc.description.affiliationSão Paulo State Univ, Dept Phys, Sao Jose do Rio Preto, Brazil-
dc.description.affiliationUniv São Paulo, Dept Biochem & Pharmaceut Technol, BR-05508000 São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Dept Phys, Sao Jose do Rio Preto, Brazil-
dc.identifier.doi10.1016/j.chroma.2012.02.028-
dc.identifier.wosWOS:000302663000005-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Chromatography A-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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