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dc.contributor.authorMoreno, Soledad
dc.contributor.authorErtesvåg, Helga
dc.contributor.authorValla, Svein
dc.contributor.authorNunez, C
dc.contributor.authorEspín, Guadalupe
dc.contributor.authorCocotl-Yanez, Miguel
dc.date.accessioned2019-01-05T14:08:41Z
dc.date.available2019-01-05T14:08:41Z
dc.date.created2018-12-05T13:40:16Z
dc.date.issued2018
dc.identifier.issn0378-1097
dc.identifier.urihttp://hdl.handle.net/11250/2579336
dc.description.abstractAzotobacter vinelandii produces differentiated cells, called cysts, surrounded by two alginate layers, which are necessary for their desiccation resistance. This alginate contains variable proportions of guluronate residues, resulting from the activity of seven extracytoplasmic epimerases, AlgE1–7. These enzymes are exported by a system secretion encoded by the eexDEF operon; mutants lacking the AlgE1-7 epimerases, the EexDEF or the RpoS sigma factor produce alginate, but are unable to form desiccation resistant cysts. Herein, we found that RpoS was required for full transcription of the algE1-7 and eexDEF genes. We found that the AlgE1-7 protein levels were diminished in the rpoS mutant strain. In addition, the alginate produced in the absence of RpoS was more viscous in the presence of proteases, a phenotype similar to that of the eexD mutant. Primer extension analysis located two promoters for the eexDEF operon, one of them was RpoS-dependent. Thus, during encysting conditions, RpoS coordinates the expression of both the AlgE1-7 epimerases and the EexDEF protein complex responsible for their transport.nb_NO
dc.language.isoengnb_NO
dc.publisherOxford University Pressnb_NO
dc.relation.urihttps://doi.org/10.1093/femsle/fny210
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleRpoS controls the expression and the transport of the AlgE1-7 epimerases in Azotobacter vinelandiinb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.volume365nb_NO
dc.source.journalFEMS Microbiology Lettersnb_NO
dc.source.issue19nb_NO
dc.identifier.doi10.1093/femsle/fny210
dc.identifier.cristin1639483
dc.relation.projectNorges forskningsråd: 221576nb_NO
dc.description.localcode© FEMS 2018. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/)nb_NO
cristin.unitcode194,66,15,0
cristin.unitnameInstitutt for bioteknologi og matvitenskap
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal