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dc.contributor.authorNabachwa, Rita
dc.date.accessioned2014-10-28T11:34:19Z
dc.date.available2014-10-28T11:34:19Z
dc.date.issued2011-07
dc.identifier.citationNabachwa, R. (2011). Phytogenetic analysis by 16s rRNA gene sequence of a protease-secreting thermophilic bacterial isolate KITNT-3 from Kiteezi landfill (Unpublished master's thesis). Makerere University, Kampala, Ugandaen_US
dc.identifier.urihttp://hdl.handle.net/10570/4049
dc.descriptionA Thesis submitted to the School of Graduate Studies in partial fulfillment of the requirements for the award of the Degree of Master of Science in Chemistry of Makerere Universityen_US
dc.description.abstractA thermophilic protease-secreting bacterial isolate KITNT-3 from Kiteezi landfill was characterized phylogenetically by determining its relationship with other existing known bacterial strains. Genomic DNA was isolated from the cells and the 16S rRNA gene amplified using universal primers. The amplified PCR product was purified using an elaborate ethanol/EDTA precipitation method and subjected to sequence analysis using an ABI 3130XL genetic analyzer. In order to determine the phylogenetic position of the isolate, the partial 16S rRNA gene sequence was compared with other known 16S rRNA gene sequences of related taxa from the GenBank. A phylogenetic tree was constructed using the MEGA v4 program. The analysis showed that the isolate clusters with members of the genus Bacillus and was closest to Bacillus thuringiensis strain T13001 (ACNC01000278), sharing 99.8 % nucleotide sequence similarity. The crude enzyme was obtained from the culture filtrate of the isolate after an overnight incubation at 550C in a shaking incubator at 80 rpm and the extract was characterized for its caseinolytic activity. The morphological and growth characteristics showed that isolate KITNT-3 is an aerobic, Gram-positive, endospore-forming, thermophile with rod-shaped cells measuring 3.2 µm in length and 0.8 µm in width respectively. The crude enzyme was found to exhibit a specific caseinolytic activity of 0.0065 µmoles tyrosine equivalents/min/mg protein at optimal assay conditions of pH 6 and temperature of 550C. Further purification and characterization of the crude enzyme solution is deemed necessary for a comprehensive enzyme classification.en_US
dc.language.isoenen_US
dc.publisherMakerere Universityen_US
dc.subjectBacterial isolate KITNT-3en_US
dc.subjectProtease-secreting thermophyleen_US
dc.subject16s rRNA geneen_US
dc.subjectSequenceen_US
dc.subjectPhytogenetic analysisen_US
dc.subjectKiteezi landfill, Kampala, Ugandaen_US
dc.titlePhytogenetic analysis by 16s rRNA gene sequence of a protease-secreting thermophilic bacterial isolate KITNT-3 from Kiteezi landfillen_US
dc.typeThesisen_US


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