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oai:www.ideals.illinois.edu:2142/122200 2024-03-02 col_2142_5131 col_2142_16338 com_2142_5130 com_2142_16337 com_2142_14793 com_2142_8903

Mitchell, Douglas Alan Mitchell, Douglas Alan Kehl-Fie, Thomas Everett Metcalf, William W Nair, Satish K 2023-12 application/pdf en text Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2025-12-01 The student, Sangeetha Ramesh, accepted the attached license on 2023-09-10 at 15:46. The student, Sangeetha Ramesh, submitted this Dissertation for approval on 2023-09-10 at 15:59. This Dissertation was approved for publication on 2023-09-14 at 16:32. DSpace SAF Submission Ingestion Package generated from Vireo submission #19825 on 2024-03-01 at 13:47:47 Bioinformatics-guided discovery and characterization of graspetides Ramesh, Sangeetha Natural Products Genome Mining Ripps Atp-grasp Ligases Graspetides Rodeo 2023-09-14 Natural products are molecules of biotic origin predominantly comprising secondary metabolites that make organisms unique. They frequently confer a selective advantage to the producer over other organisms under challenging life conditions. Ribosomally synthesized and post-translationally modified peptides (RiPPs) are a diverse family of natural products featuring chemical modifications installed by enzymes on a peptide scaffold. Owing to increased access to genomic data and the availability of genome mining tools to parse this treasure trove of information, the RiPP research field has garnered a lot of traction these past few decades. Chapter-1 and Appendix A of this dissertation discusses new developments in the field of RiPP discovery, enzymology, engineering, and genome mining. Microviridins are serine protease inhibitory RiPPs comprising a cage-like tricyclic structure resulting from two macrolactones and a macrolactam installed by dedicated members of the ATP-grasp ligase enzyme family. Recent discovery of non-microviridin RiPPs, plesiocin and thuringinin, also featuring ATP-grasp ligase-mediated modifications suggested a much broader use of ATP-grasp ligases in RiPP biosynthesis beyond microviridins. This led us to reclassify microviridins, plesiocin, and thuringinin as members of the graspetide RiPP class after the enzymes that install the class-defining modifications (Chapter-1). Chapter-1 summarizes the current state of knowledge about graspetides and the class-defining ATP-grasp ligases. While several recent genome mining studies have expanded the sequence space of the graspetide class, their true biosynthetic diversity remained hidden owing to the lack of a genome mining tool to systematically parse the available genomic information. To address this issue, chapter-2 reports an update to Raid ORF Description and Evaluation Online (RODEO) for the automated detection of graspetides. RODEO-mediated genome mining identified 3,923 high-confidence graspetide biosynthetic gene clusters. Sequence and co-occurrence analyses doubled the number of graspetide groups, from 12 to 24, defined on core consensus sequence and putative secondary modification. Furthermore, we characterized thatisin and iso-thatisin, two graspetides related by conformational stereoisomerism from Lysobacter antibioticus. Derived from a newly identified graspetide group, thatisin and iso-thatisin feature two interlocking macrolactones with identical ring connectivity, as determined by a combination of tandem mass spectrometry (MS/MS), methanolytic, and mutational analyses. NMR spectroscopy of thatisin revealed a cis conformation for a key proline residue, while molecular dynamics simulations, solvent-accessible surface area calculations, and partial methanolytic analysis coupled with MS/MS support a trans conformation for iso-thatisin at the same position. Chapter-3 describes the characterization of a group-21 graspetide from Micromonospora rosaria that was newly identified in chapter-2. Group-21 graspetides display a novel tricylic structure as demonstrated through a combination of MS/MS, methanolysis, mutational and NMR spectroscopic analyses. Intriguingly, they also represent the first example of a graspetide that requires both a graspetide synthetase and a putative peptidyl prolyl isomerase (PPIase)/chaperone to observe the macrolactone modifications. Chapter-3 also delves into the initial characterization of the role of the PPIase/chaperone in graspetide biosynthesis. Overall, this dissertation provides a comprehensive overview of the graspetide biosynthetic landscape, and the improved RODEO algorithm will accelerate future graspetide discoveries as exemplified in Appendix B by enabling open-access analysis of existing and emerging genomes. Text eng https://hdl.handle.net/2142/122200 Copyright 2023 Sangeetha Ramesh Ph.D. Dissertation Microbiology University of Illinois at Urbana-Champaign Microbiology