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dc.contributor.authorChristogianni, A.en
dc.contributor.authorDouka, E.en
dc.contributor.authorKoukkou, A. I.en
dc.contributor.authorHatziloukas, E.en
dc.contributor.authorDrainas, C.en
dc.date.accessioned2015-11-24T16:51:43Z-
dc.date.available2015-11-24T16:51:43Z-
dc.identifier.issn0021-9193-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9775-
dc.rightsDefault Licence-
dc.subjectgreen fluorescent proteinen
dc.subjectrt-pcren
dc.subjectexpressionen
dc.subjectcloningen
dc.subjectbiosynthesisen
dc.subjectpathwayen
dc.subjectgrowthen
dc.subjectbacteriaen
dc.subjectisoprenoidsen
dc.subject5-phosphateen
dc.titleTranscriptional analysis of a gene cluster involved in glucose tolerance in Zymomonas mobilis: Evidence for an osmoregulated promoteren
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1128/Jb.187.15.5179-5188.2005-
heal.identifier.secondary<Go to ISI>://000230716800015-
heal.identifier.secondaryhttp://jb.asm.org/content/187/15/5179.full.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2005-
heal.abstractExponentially growing cells of Zymomonas mobilis normally exhibit a lag period of up to 3 It when they are transferred from a liquid medium containing 2% glucose to a liquid medium containing 10% glucose. A mutant of Z. mobilis (CU1) exhibited a lag period of more than 20 h when it was grown under the same conditions, whereas it failed to grow on a solid medium containing 10% glucose. The glucose-defective phenotype of mutant CU1 was due to a spontaneous insertion in a putative gene (ORF4) identified as part of an operon (glc) which includes three additional putative genes (ORF1, ORF2, and ORF3) with no obvious involvement in the glucose tolerance mechanism. The common promoter controlling glc operon transcription, designated P-glc, was found to be osmoregulated and stimulated by the putative product of OPF4 in an autoregulated fashion, as indicated by expression of the gfp reporter gene. Additionally, reverse transcriptase PCR analysis showed that the gene cluster produces a single mRNA, which verified the operon organization of this transcription unit. Further transcriptional analysis demonstrated that glc operon expression is regulated by the concentration of glucose, which supported the hypothesis that this operon is directly involved in the uncharacterized glucose tolerance mechanism of Z. mobilis.en
heal.publisherAmerican Society for Microbiologyen
heal.journalNameJ Bacteriolen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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