Analysis of Frameshifting Frequencies Due to Homopolymeric Nucleotide Tracts in Neisseria gonorrhoeae

dc.contributor.advisorStein, Daniel Cen_US
dc.contributor.authorHolder, Robert Christopheren_US
dc.contributor.departmentCell Biology & Molecular Geneticsen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2006-06-14T05:34:42Z
dc.date.available2006-06-14T05:34:42Z
dc.date.issued2006-03-10en_US
dc.description.abstractOrganisms that are sensitive to the antimicrobial agent nitrofurantoin express nitroreductases, which reduce nitrofuran containing compounds to highly reactive and damaging intermediates. A single nitroreductase, nfsB, was identified in N. gonorrhoeae FA1090. The sequence of nfsB was modified to contain polyguanine tracts of varying lengths. Analysis indicated that mutations yielding nitrofurantoin resistance occurred at a higher rate in strains containing modified nfsB genes when compared to wildtype FA1090. The frequency of mutation also increased as polyguanine tract length increased. A polyguanine tract length of 5 residues did not produce elevated mutation frequencies. The use of PCR and polyacrylamide gel electrophoresis proved to be a reliable method for quickly identifying nitrofurantoin resistant mutants that contained nfsB frameshift mutations. When nfsB fragments amplified from nitrofurantoin resistant mutants were electrophoresed, the presence of insertions or deletions in the nfsB coding sequence was easily detected.en_US
dc.format.extent1439401 bytes
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/1903/3375
dc.language.isoen_US
dc.subject.pqcontrolledBiology, Microbiologyen_US
dc.titleAnalysis of Frameshifting Frequencies Due to Homopolymeric Nucleotide Tracts in Neisseria gonorrhoeaeen_US
dc.typeThesisen_US

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