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dc.contributor.advisorBenedik, Michael J
dc.creatorPark, Jason M
dc.date.accessioned2015-02-05T17:22:50Z
dc.date.available2016-08-01T05:30:22Z
dc.date.created2014-08
dc.date.issued2014-05-22
dc.date.submittedAugust 2014
dc.identifier.urihttp://hdl.handle.net/1969.1/153257
dc.description.abstractNitrilases offer an economic and environmentally friendly solution for the production of valuable chemicals, and the degradation of toxic industrial nitrile wastes. A lack of fine structural data has impeded rational engineering of these enzymes to expand their utility. The nitrilases form large spiral shaped oligomers, seen by electron microscopy. These spiral structures are seen in all active nitrilases, and mutations altering this structure influence activity, stability, and substrate specificity. Currently no spiral forming nitrilase has been amenable to crystallization, leaving a significant gap in our understanding of these enzymes. Crystal structures from the larger nitrilase-superfamily reveal a conserved dimer structure and active site. Three regions in nitrilases are hypothesized to associate these dimer building blocks into the spiral oligomer. Two stand out as insertions relative to the crystallized homologs. These regions are hypothesized to associate the basic nitrilase dimer to form the large spiral structure. I investigate this hypothesis in the nitrilase CynD_(pum) by constructing mutations throughout these insertion regions and ascertaining their effect on enzyme activity as well as on oligomerization. A third region that stands out from the nitrilase sequences in comparison to the crystallized superfamily members is the extension of the C-terminus. Mutations to the C-terminus in various nitrilases can alter the proteins stability, activation, and substrate specificity, but how it interacts with other regions of the protein is not understood. In CynD, exchanging the C-terminus between the Bacillus pumilus enzyme and that of Pseudomonas stutzeri (CynD_(stut)) shows a one-way compatibility. When CynD_(pum) is paired with the P. stutzeri C-terminus (CynD_(pum-stut)), the hybrid enzyme is active and more stable than either parent enzyme. Conversely, the reverse hybrid, where the P. stutzeri CynD is paired with the B. pumilus C-terminus (CynD_(stut-pum)) is not active. In this study I exploit the stabilizing effect of the C-terminus from B. pumilus to test whether it participates in spiral formation. Additionally, I identify regions interacting with the C-terminus by looking for suppressing substitutions in CynD_(stut-pum) that restore activity.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.subjectCyanideen
dc.subjectcyanide dihydrataseen
dc.titleRegions Involved in the Oligomerization and Activity of the Spiral Forming Nitrilase Cyanide Dihydrataseen
dc.typeThesisen
thesis.degree.departmentBiologyen
thesis.degree.disciplineMicrobiologyen
thesis.degree.grantorTexas A & M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.levelDoctoralen
dc.contributor.committeeMemberManson, Michael D
dc.contributor.committeeMemberLockless, Steve W
dc.contributor.committeeMemberHu, James C
dc.type.materialtexten
dc.date.updated2015-02-05T17:22:50Z
local.embargo.terms2016-08-01
local.etdauthor.orcid0000-0003-2717-4628


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