Construction and Characterization of a Plasmid Borne Prokaryotic-Eukaryotic Fusion RNA Polymerase Largest Subunit

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dc.contributor.advisorLandick, Robert
dc.contributor.authorRieden, Cynthia L.
dc.date.accessioned2011-08-19T17:21:44Z
dc.date.available2011-08-19T17:21:44Z
dc.date.issued1991
dc.descriptioniv, 33 p.en_US
dc.description.abstractA novel plasmid, pKC91, was created. The plasmid encodes the Escherichia coli RNA polymerase largest subunit β rpoC gene with an altered carboxyl-terminal region. The C-terminal region was modified to include the heptapeptide repeat of Saccharomyces cerevisiae RNA polymerase largest subunit. The repeat has the consensus sequence Tyr-Ser-Pro-Thr-Ser-Pro-Ser, and has been implicated in the processes of DNA binding and RNA chain elongation. The addition of this region was found to have no effect on growth rate or protein expression of transfected cells. It did interfere with functional complementation in rpoC deficient strains. The addition of the heptapeptide repeat disrupts function of the produced RNA polymerase largest subunit, potentially by steric hinderance of the catalytic site, inhibition of the ability to complex with other subunits to form the holoenzyme, or by replacement of a region essential for function.en_US
dc.description.sponsorshipDepartment of Biology. Washington University. St. Louis, Missouri.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/10920/23256
dc.language.isoen_USen_US
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Biology Senior Individualized Projects Collection
dc.relation.ispartofseriesSenior Individualized Projects. Biology;
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.titleConstruction and Characterization of a Plasmid Borne Prokaryotic-Eukaryotic Fusion RNA Polymerase Largest Subuniten_US
dc.typeThesisen_US
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