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

dc.contributor.authorJohansson, Hans-Olof
dc.contributor.authorMatos, Tiago
dc.contributor.authorLuz, Juliana S.
dc.contributor.authorFeitosa, Eloi [UNESP]
dc.contributor.authorOliveira, Carla C.
dc.contributor.authorPessoa, Adalberto
dc.contributor.authorBuelow, Leif
dc.contributor.authorTjerneld, Folke
dc.contributor.institutionLund Univ
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T14:02:37Z
dc.date.available2014-05-20T14:02:37Z
dc.date.issued2012-04-13
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.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.format.extent30-35
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.doi10.1016/j.chroma.2012.02.028
dc.identifier.issn0021-9673
dc.identifier.lattes5731856650217859
dc.identifier.urihttp://hdl.handle.net/11449/22077
dc.identifier.wosWOS:000302663000005
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofJournal of Chromatography A
dc.relation.ispartofjcr3.716
dc.relation.ispartofsjr1,378
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes5731856650217859
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt
unesp.departmentFísica - IBILCEpt

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