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dc.contributor.authorZwick, Friederike
dc.contributor.authorLale, Rahmi
dc.contributor.authorValla, Svein
dc.date.accessioned2017-11-29T11:36:27Z
dc.date.available2017-11-29T11:36:27Z
dc.date.created2012-11-22T12:45:29Z
dc.date.issued2012
dc.identifier.citationMicrobial Cell Factories. 2012, 11:133.nb_NO
dc.identifier.issn1475-2859
dc.identifier.urihttp://hdl.handle.net/11250/2468515
dc.description.abstractThe XylS/Pm expression system has been used to produce recombinant proteins at industrial levels in Escherichia coli. Activation of transcription from the Pm promoter takes place in the presence of benzoic acid or derivatives of it. Previous mutagenesis studies resulted in identification of several variants of the expression control elements xylS (X), Pm (P) and the 5'-untranslated region (U) that individually gave rise to strongly stimulated expression. The goal of this study was to test if combination of such stimulatory mutations in the same expression vectors would lead to further increase of expression levels.nb_NO
dc.language.isoengnb_NO
dc.publisherBioMed Centralnb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleStrong stimulation of recombinant protein production in Escherichia coli by combining stimulatory control elements in an expression cassettenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.volume11nb_NO
dc.source.journalMicrobial Cell Factoriesnb_NO
dc.source.issue133nb_NO
dc.identifier.doi10.1186/1475-2859-11-133
dc.identifier.cristin964186
dc.relation.projectNorges forskningsråd: 192123nb_NO
dc.description.localcode© Zwick et al.; licensee BioMed Central Ltd. 2012. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.nb_NO
cristin.unitcode194,66,15,0
cristin.unitnameInstitutt for bioteknologi og matvitenskap
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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