Some of the most successful antibiotics in the clinic inhibit bacterial cell wall assembly. However, the continued emergence of multidrug-resistant bacteria is rapidly eroding the efficacy of these drugs - like all other antibiotics - and is a significant threat to human health. New treatment options are urgently needed that hinder bacterial viability, growth, and/or pathogenesis. Wall teichoic acids (WTAs) are integral components of Gram-positive bacterial cell walls and are critical to physiology and pathogenesis. WTA assembly is a bona fide drug target in several pathogens like Staphylococcus aureus. Many whole-cell screens have
been performed to find small molecule inhibitors of this process. These efforts require a deep understanding of WTA assembly to help identify, characterize, and exploit high potential targets and therapeutic strategies. Challenges involved in the isolation of authentic substrates have hampered detailed biochemical study of WTA biosynthesis. Many features of the process remain uncharacterized. In this thesis, I detail a novel chemoenzymatic method to prepare authentic WTA substrates. I show that these materials can be used to study WTA biosynthetic enzymes in vitro and to probe enigmatic features of WTA assembly. With authentic WTA substrates, I reconstituted the final step of B. subtilis WTA synthesis in vitro, which involves ligation of WTAs to peptidoglycan. This process eluded biochemical characterization for decades. I investigated the catalytic requirements and substrate preferences for the LytR-CpsA-Psr family of enzymes that mediate this glycopolymer transfer reaction. Further, I discuss the attractiveness of these enzymes as antibiotic drug targets. Authentic WTA substrates will likely continue to be useful tools in understanding molecular features of WTA assembly and serve to assist drug discovery and development efforts targeting this process. / Thesis / Doctor of Philosophy (PhD)
| Identifer | oai:union.ndltd.org:mcmaster.ca/oai:macsphere.mcmaster.ca:11375/22755 |
| Date | January 2018 |
| Creators | Gale, Robert T |
| Contributors | Brown, Eric, Biochemistry and Biomedical Sciences |
| Source Sets | McMaster University |
| Language | English |
| Detected Language | English |
| Type | Thesis |
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