The Transcriptional Regulator MphR(A): Characterization and Circuit Engineering

dc.contributor.advisorCropp, T Aen_US
dc.contributor.authorSmolinsky, Adam Randallen_US
dc.contributor.departmentChemistryen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2008-06-20T05:38:52Z
dc.date.available2008-06-20T05:38:52Z
dc.date.issued2008-05-09en_US
dc.description.abstractThe MphR(A) transcriptional repressor protein was incorporated into high-efficiency ex-pression vectors, purified and characterized. Initial screens for crystallography solvents were conducted along with preliminary gel-shift and intrinsic fluorescence quenching ex-periments to obtain the equilibrium dissociation constant for the protein-DNA interac-tions. The constant was found to be 0.5 - 1.9 μM, depending on the method used. The gene was also incorporated into positive feedback circuits to detect macrolide antibiotics using various reporter genes and plasmid constructs. Qualitatively, the circuits showed a change in output upon the addition of MphR to the system.en_US
dc.format.extent1127466 bytes
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/1903/8229
dc.language.isoen_US
dc.subject.pqcontrolledChemistry, Biochemistryen_US
dc.titleThe Transcriptional Regulator MphR(A): Characterization and Circuit Engineeringen_US
dc.typeThesisen_US

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