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dc.contributor.advisor McCafferty, Dewey G en_US
dc.contributor.author Allen, Catherine Leigh en_US
dc.date.accessioned 2012-05-29T16:42:43Z
dc.date.issued 2011 en_US
dc.identifier.uri http://hdl.handle.net/10161/5667
dc.description Dissertation en_US
dc.description.abstract <p>Bacteria recycle pre-existing peptidoglycan in order to minimize the de novo synthesis of peptidoglycan precursors. The recycling pathway is under study for its chemotherapeutic target potential. Anhydromuramic acid kinase (AnmK) is part of this recycling pathway and catalyzes the dual hydrolysis/phosphorylation of anhMurNAc to MurNAc-6-P. This enzyme has been discovered and introduced, but only minimally characterized. Therefore, the overarching goal of this work was to clone, express and purify AnmK to homogeneity; perform further kinetic characterization; solve the open, closed and transition state mimic-bound conformations of AnmK by x-ray crystallography; and develop a putative mechanism based on the accumulated research findings and <super>18</super>O-labeling studies.</p><p>The anmK gene was successfully cloned as a hexahistidine fusion protein and overexpression was optimized. After exhaustive trials, a final purification scheme was designed to yield homogeneous AnmK in three chromatographic steps and in less than 36 hours. Additionally, the synthesis of both anhMurNAc and a pseudosubstrate (anhGlcNAc) were carried out in 35% and 77% overall yield, respectively. The synthesis of these compounds allowed for both kinetic characterization and structural studies. </p><p>To this end, the structure of de novo AnmK was solved using SAD and high-resolution (1.9 &Aring;) data. Also, an ATP analog (ANP) and anhMurNAc substrate-bound, closed conformation structure (1.95 &Aring;) was solved. These structures elucidated an 11&deg; domain closure of the enzyme upon substrate binding and also revealed the active site geometry to be used to determine potential molecular determinants of specificity. </p><p>Insights into the kinetic mechanism of AnmK were then gathered using multiple techniques. First, the structure of AnmK (2.5 &Aring;) was solved the with a known transition state analog, the MgADP-vanadate complex. Following this structure, which sheds light on the potential importance of a residue other than the catalytic base (Asp187), isotopic labeling was performed with H<sub>2</sub><super>18</super>O. Using NMR and MS, the regiochemical selectivity of AnmK hydrolysis to impart the solvent derived oxygen at C1 was established. Additionally, this was carried out with stereochemical preference to create the &alpha;-anomer of the carbohydrate product. This regiochemistry and stereospecificity drove the design of our putative concomitant hydrolysis/phosphorylation mechanism but we are not able to rule out the formation of a transient phosphoenzyme intermediate.</p><p>This research can be applied to the immediate goal of understanding the function of a single, novel enzyme with unique chemistry and the clarification of the AnmK mechanism will facilitate future investigation into enzymes with dual hydrolase/kinase functionality. Furthermore, this research contributes to understanding of the complex bacterial peptidoglycan layer in order to harness new ideas for developing antibiotics.</p> en_US
dc.subject Chemistry en_US
dc.subject Biochemistry en_US
dc.subject anhMurNAc en_US
dc.subject AnmK en_US
dc.subject Murein recycling en_US
dc.subject Peptidoglycan en_US
dc.subject Structural biology en_US
dc.title Insights into the Structure and Mechanism of Anhydromuramic Acid Kinase (AnmK): A Novel Peptidoglycan Recycling Enzyme with Dual Hydrolase and Kinase Functionality en_US
dc.type Dissertation en_US
dc.department Chemistry en_US
duke.embargo.months 24 en_US
duke.embargo.release 2014-05-19

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