Isolation and Characterization of Bacillus Thuringiensis Strains From Different Grain Habitats

dc.contributor.advisor Güneş, Hatice
dc.contributor.author Apaydın, Özgür
dc.date.accessioned 2014-07-22T13:51:15Z
dc.date.available 2014-07-22T13:51:15Z
dc.date.issued 2004
dc.description Thesis (Master)--Izmir Institute of Technology, Biotechnology, Izmir, 2004 en_US
dc.description Includes bibliographical references (leaves: 46-58) en_US
dc.description Text in English; Abstract: Turkish and English en_US
dc.description vii, 58 leaves en_US
dc.description.abstract Bacillus thuringiensis is a Gram positive, facultative anaerob bacteria that produces proteins toxic against different insect species. This feature makes it the most widely used biological control agent in agriculture. Since B. thuringiensis strains have great genetic diversity, the toxic behaviours of these strains differ from region to region. Native B. thuringiensis strains are isolated from different habitats and characterized to determine their toxic potential all over the world. The aim of this study was to isolate B. thuringiensis strains from different grain habitats in Central Anatolia and Aegean Regions, and to investigate their phenotypic and genotypic characterizations. Total 96 samples containing soil, grain, stored product dust, straw and various residues were collected from wheat farms, grain silos, haylofts and caves in Ereli/Konya, Takale/Karaman, Nikfer/Denizli, and Bozbük/Söke under aseptic conditions. Seven hundred bacteria were isolated from these samples by sodium acetate selection and heat treatment. For phenotypic characterization, 500 of these isolates were grown for 48 h and crystal protein production was observed by phase contrast microscobe during spore formation. One hundred and sixty three of the bacterial colonies were identified as B. thuringiensis. The isolates were divided into 5 different groups based on the shape of the crystals that they produced. Spherical type crystal morphology was mostly observed type among the others. For genotypic characterization, the cry gene content of the isolates were screened by polymerase chain reaction (PCR) analysis. In addition, chromosomal DNA analysis of 34 isolates by Pulsed Field Gel Electrophoresis (PFGE) as well as plasmid DNA profiling for all isolates were also carried out. One hundred and three isolates were positive for 5 different cry genes (cry1, cry2, cry3, cry4, cry9) examined by PCR. Among all cry genes examined, cry1 and cry9 genes were mostly found in the isolates. Morover, plasmid profiling of the isolates indicated that a 15 kb DNA band was present in all the isolates; however, some of them had more than one DNA band at different sizes. Finally, chromosomal DNA profiling by PFGE showed different DNA patterns for isolates containing the same cry gene which suggest a high level of diversity among the B. thuringiensis strains isolated. Further studies related with extensive genetic characterization and toxic activity of each B. thuringiensis strain will give more comprehensive results on biodiversity of B. thuringiensis strains in Anatolia. en_US
dc.identifier.uri https://hdl.handle.net/11147/3294
dc.language.iso en en_US
dc.publisher Izmir Institute of Technology en_US
dc.publisher Izmir Institute of Technology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject.lcc QR82.B3 .A63 2004 en
dc.subject.lcsh Bacillus thuringiensis en
dc.subject.lcsh Bacillus thuringiensis--Genetics en
dc.title Isolation and Characterization of Bacillus Thuringiensis Strains From Different Grain Habitats en_US
dc.type Master Thesis en_US
dspace.entity.type Publication
gdc.author.institutional Apaydın, Özgür
gdc.coar.access open access
gdc.coar.type text::thesis::master thesis
gdc.description.department Thesis (Master)--İzmir Institute of Technology, Bioengineering en_US
gdc.description.publicationcategory Tez en_US
gdc.description.scopusquality N/A
gdc.description.wosquality N/A
relation.isAuthorOfPublication.latestForDiscovery 250fe2cc-7400-4488-8817-8f31a050c083
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4013-8abe-a4dfe192da5e

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