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dc.creatorIlić-Tomić, Tatjana
dc.creatorMorić, Ivana
dc.creatorConn, Graeme L.
dc.creatorVasiljević, Branka
dc.date.accessioned2022-11-15T13:50:15Z
dc.date.available2022-11-15T13:50:15Z
dc.date.issued2008
dc.identifier.issn0923-2508
dc.identifier.urihttps://imagine.imgge.bg.ac.rs/handle/123456789/324
dc.description.abstractThe aminoglycoside resistance genes sgm from Micromonospora zionensis and kgmB from Streptomyces tenebrarius were cloned into a yeast expression vector to test whether the encoded prokaryotic methylases can modify the 18S rRNA A-site and thus confer resistance to G-418. Despite the detectable presence of mRNAs in yeast cells, neither G-418-resistant yeast transformants nor positive western blot signals were obtained. Neither methylase was capable of methylating 40S subunits despite very high conservation of the antibiotic rRNA binding sites. However, the results provide novel insight into the action of Sgm by showing that it methylates the same site as KgmB, i.e. G1405 in 16S rRNA.en
dc.publisherElsevier Science Bv, Amsterdam
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/143056/RS//
dc.relationThe Wellcome Trust [078374]
dc.rightsopenAccess
dc.sourceResearch in Microbiology
dc.subjectSite of actionen
dc.subjectG1405en
dc.subjectExpression in yeasten
dc.subjectAminoglycoside resistanceen
dc.subject16S rRNA methylasesen
dc.titleAminoglycoside resistance genes sgm and kgmB protect bacterial but not yeast small ribosomal subunits in vitro despite high conservation of the rRNA A-siteen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage662
dc.citation.issue9-10
dc.citation.other159(9-10): 658-662
dc.citation.rankM23
dc.citation.spage658
dc.citation.volume159
dc.identifier.doi10.1016/j.resmic.2008.09.006
dc.identifier.fulltexthttps://imagine.imgge.bg.ac.rs/bitstream/id/290/321.pdf
dc.identifier.pmid18930134
dc.identifier.scopus2-s2.0-57049159208
dc.identifier.wos000262129900010
dc.type.versionpublishedVersion


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