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dc.contributor.authorSevim, Ali
dc.contributor.authorEryüzlü, Emine
dc.contributor.authorDemirbağ, Zihni
dc.contributor.authorDemir, İsmail
dc.date.accessioned2020-12-19T20:16:51Z
dc.date.available2020-12-19T20:16:51Z
dc.date.issued2012
dc.identifier.citationSevim, A., Eryüzlü, E., Demirbağ, Z., & Demir, I. (2012). A novel cry2Ab gene from the indigenous isolate Bacillus thuringiensis subsp. kurstaki. Journal of microbiology and biotechnology, 22(1), 133–140. https://doi.org/10.4014/jmb.1108.08061en_US
dc.identifier.issn1017-7825
dc.identifier.urihttps://doi.org/10.4014/jmb.1108.08061
dc.identifier.urihttps://hdl.handle.net/11436/4288
dc.description.abstractA novel cry2Ab gene was cloned and sequenced from the indigenous isolate of Bacillus thuringiensis subsp. kurstaki. This gene was designated as cry2Ab25 and its sequence revealed an open reading frame of 1,902 bp encoding a 633 aa protein with calculated molecular mass of 70 kDa and pI value of 8.98. The amino acid sequence of the Cry2Ab25 protein was compared with previously known Cry2Ab toxins, and the phylogenetic relationships among them were determined. The deduced amino acid sequence of the Cry2Ab25 protein showed 99% homology to the known Cry2Ab proteins, except for Cry2Ab10 and Cry2Ab12 with 97% homology, and a variation in one amino acid residue in comparison with all known Cry2Ab proteins. The cry2Ab25 gene was expressed in Escherichia coli BL21(DE3) cells. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) revealed that the Cry2Ab25 protein is about 70 kDa. The toxin expressed in BL21(DE3) exhibited high toxicity against Malacosoma neustria and Rhagoletis cerasi with 73% and 75% mortality after 5 days of treatment, respectively.en_US
dc.language.isoengen_US
dc.publisherKorean Society for Microbiolog and Biotechnologyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCloningen_US
dc.subjectCry2Aben_US
dc.subjectMalacosoma neustriaen_US
dc.subjectRhagoletis cerasien_US
dc.subjectVirulenceen_US
dc.titleA novel cry2Ab gene from the indigenous isolate Bacillus thuringiensis subsp. kurstakien_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Fen - Edebiyat Fakültesi, Biyoloji Bölümüen_US
dc.contributor.institutionauthorSevim, Ali
dc.identifier.doi10.4014/jmb.1108.08061
dc.identifier.volume22en_US
dc.identifier.issue1en_US
dc.identifier.startpage133en_US
dc.identifier.endpage140en_US
dc.relation.journalJournal of Microbiology and Biotechnologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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