Exploration of the biosynthesis of lanthipeptides

Shi, Yanxiang

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Description

Title

Exploration of the biosynthesis of lanthipeptides

Author(s)

Shi, Yanxiang

Issue Date

2014-01-16T18:18:47Z

Director of Research (if dissertation) or Advisor (if thesis)

van der Donk, Wilfred A.

Doctoral Committee Chair(s)

van der Donk, Wilfred A.

Committee Member(s)

• Sweedler, Jonathan V.
• Mitchell, Douglas A.
• Kranz, David M.

Department of Study

Chemistry

Discipline

Chemistry

Degree Granting Institution

University of Illinois at Urbana-Champaign

Degree Name

Ph.D.

Degree Level

Dissertation

Keyword(s)

• Lanthipeptides
• Biosynthesis
• Co-expression

Abstract

Natural products play important roles in the survival of organisms, and provide a large pool of candidates for drug discovery and pharmaceutical investigations. A major class of peptide-based natural products are ribosomally synthesized and post-translationally modified (RiPPs). Lanthipeptides, which possess (methyl)lanthionine structures, are a class of intensively studied RiPPs. Based on the biosynthesis enzymes that introduce the thioether motifs, lanthipeptides are classified into four classes. Class I lanthipeptides utilize two distinct enzymes, a dehydratase and a cyclase, while class II lanthipeptides adopt a bifunctional enzyme. Trifunctional enzymes with independent evolution pathways are employed by class III and class IV lanthipeptides. A major subclass of lanthipeptides possess antimicrobial activity, known as lantibiotics with known modes of action including lipid II binding, pore formation, inhibition of spore outgrowth, and phosphatidylethanolamine (PE) binding. Several lanthipeptides display no antimicrobial activities but have other functions important for bacterial life cycles, such as facilitating aerial hyphae formation during sporulation. In the past, most lanthipeptides were discovered based on their activity mainly through antimicrobial screening campaigns. With the advances in genome sequencing and bioinformatics, a variety of lanthipeptides have been identified by genome mining, presumably with more unexplored functions and molecular targets. Prochlorosins are an unusual group of lanthipeptides, which were discovered through genome mining and have no known antibiotic activities. Further biological function investigations of prochlorosins require pure products in adequate amounts, which was not achievable through natural product isolation or in vitro enzymatic assays. In this thesis, Chapter 2 describes the development of a novel co-expression system to produce prochlorosins by in vivo enzymatic modification in E. coli, providing prochlorosins with high purity and sufficient quantity for subsequent characterizations. Chapter 3 presents an example of utilizing the co-expression methodology to produce antimicrobial lanthipeptides, with additional modifications besides dehydration and cyclization. The precursor peptide of actagardine, one of the only two lantibiotics that have been evaluated in clinical trials thus far, was fully modified in E. coli as presented in Chapter 3. A luciferase-like monooxygenase located in the biosynthetic cluster of actagardine was also reconstituted, both in vitro and in vivo, to introduce a sulfoxide group onto actagardine and its derivatives. Based on the success of in vivo co-expression of lanthipeptides with identified or unidentified activities, Chapter 4 describes efforts towards the incorporation of non-canonical amino acids into lanthipeptides, in order to expand the structural diversity of these natural products, tune their activities, and introduce probes for subsequent functional investigations. The work presented in this thesis provides methods to effectively produce the peptide-based natural products lanthipeptides, in adequate quantities for subsequent investigations including study of substrate peptides and their modification enzymes, peptide structure elucidation, as well as sequence and structure diversification.

Graduation Semester

2013-12

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Copyright and License Information

2013 Yanxiang (Nancy) Shi

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