The possibilities of using plasmid ORF clone library for ybeY gene compensation studies in Escherichia coli

dc.contributor.advisorMaiväli, Ülo, juhendaja
dc.contributor.advisorSarigül, Ismail, juhendaja
dc.contributor.authorŽukova, Amata
dc.contributor.otherTartu Ülikool. Loodus- ja täppisteaduste valdkondet
dc.contributor.otherTartu Ülikool. Molekulaar- ja rakubioloogia instituutet
dc.date.accessioned2020-06-18T08:55:32Z
dc.date.available2020-06-18T08:55:32Z
dc.date.issued2020
dc.description.abstractThe YbeY, encoded by the highly conserved ybeY gene, is a multi-functional protein in Escherichia coli. The processing of the 3′ terminus of 16S rRNA is its most important function, which has a direct effect on the biogenesis of ribosomes. The deletion of ybeY leads to phenotypic and translational defects. YbeY has an extensive network of interactions with other proteins, many of which are still not fully understood. ORF library can be used as a powerful biological tool to detect interactions between proteins. Two different selection strategies were applied using two pooled Gateway® entry clone libraries. Fully pooled library containing all genes represented in the library, and partially pooled library with the lack of some library genes, were electroporated into ybeY null mutants. According to the specificity of each pooled library, the growth selections and PCR methods for genes detecting were different. Results have shown that cultures growth improves during selection. Several genes, whose amount prevails over others in the last selection cycles, were sequenced.et
dc.identifier.urihttp://hdl.handle.net/10062/68040
dc.publisherTartu Ülikoolet
dc.rightsopenAccesset
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectYbeYet
dc.subjectORF libraryet
dc.subjectselectionet
dc.subjectGateway® entry clone libraryet
dc.subject.otherbakalaureusetöödet
dc.titleThe possibilities of using plasmid ORF clone library for ybeY gene compensation studies in Escherichia coliet
dc.typeThesiset

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