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dc.contributor.authorDuzgun, Azer Ozad
dc.date.accessioned2021-11-09T19:42:21Z
dc.date.available2021-11-09T19:42:21Z
dc.date.issued2018
dc.identifier.issn1217-8950
dc.identifier.issn1588-2640
dc.identifier.urihttps://doi.org/10.1556/030.65.2018.022
dc.identifier.urihttps://hdl.handle.net/20.500.12440/3351
dc.description.abstractThe aim of this work was investigation of clinically important amino acid substitutions of NDM-1 variants. A bla(NDM-1) gene was cloned into expression vector pET100/D-TOPO. The sequence of NDM-1 variants with substituted amino acids was determined by ClustalW program. A pET100/D-TOPO + bla(NDM-1) was used to generate the alanine mutations at different positions, such as NDM-2 (P28A), NDM-3 (D95A), NDM-4 (M154A), NDM-5 (V88A), NDM-7 (D130A), and NDM-9 (E152A). The mutant variants were transformed into Escherichia con DH5 alpha. Changes in the activities of alanine mutation variants were determined by E-test. All samples had 32 mu g/ml MIC values against ampicillin. The 28 th amino acid mutation sample had the highest MIC value against ceftazidime, whereas decreased MIC value for piperacillin. It was observed that the resistance to imipenem was increased in mutant variants D95A, M154A, D130A, and E152A, comparing with P28A and V88A. It was found that NDM-1 has 0.64 mu g/ml and the 130th amino acid mutation sample has 0.75 mu g/ml meropenem MIC value.en_US
dc.language.isoengen_US
dc.publisherAkademiai Kiado Zrten_US
dc.relation.ispartofActa Microbiologica Et Immunologica Hungaricaen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMBLen_US
dc.subjectmutationen_US
dc.subjectNDM-1en_US
dc.subjectE-testen_US
dc.titleEFFECT OF AMINO ACID SUBSTITUTION IN NEW DELHI METALLO-beta-LACTAMASE ON CARBAPENEM SUSCEPTIBILITYen_US
dc.typearticleen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.description.wospublicationidWOS:000441080000006en_US
dc.description.scopuspublicationid2-s2.0-85051422265en_US
dc.departmentGümüşhane Üniversitesien_US
dc.authoridDUZGUN, AZER OZAD / 0000-0002-6301-611X
dc.authoridDUZGUN, AZER OZAD / 0000-0002-6301-611X
dc.identifier.volume65en_US
dc.identifier.issue3en_US
dc.identifier.startpage325en_US
dc.identifier.doi10.1556/030.65.2018.022
dc.identifier.endpage333en_US
dc.authorwosidDUZGUN, AZER OZAD / ABB-4068-2020
dc.authorwosidDUZGUN, AZER OZAD / A-1612-2018
dc.authorscopusid55840997800
dc.description.pubmedpublicationidPubMed: 29651859en_US


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