Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.731420
Title: Elucidating molecular mechanisms of actinobacterial polyketide alkaloid biosynthesis
Author: Ronan, Jade L.
ISNI:       0000 0004 6496 6744
Awarding Body: University of Warwick
Current Institution: University of Warwick
Date of Award: 2017
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Abstract:
Coelimycin P1 is a yellow-pigmented alkaloid with a unique 1,5-oxathiocane ring, produced by Streptomyces coelicolor M145. Recently, it was demonstrated that a type I modular polyketide synthase (PKS) with a C-terminal thioester reductase (TR) domain is involved in its assembly. Due to its unusual biosynthetic origin, unprecedented structure and the antibiotic activity likely associated with coelimycin A, its biosynthesis is of great interest. To investigate the roles of the putative post-PKS tailoring enzymes (CpkG, CpkH, CpkD, ScF, CpkE and CpkI), the recombinant proteins were overproduced in E. coli, purified and incubated with various commercial and synthetic substrates. CpkG was characterised as an (S)-selective ω-transaminase with a broad substrate tolerance, responsible for the incorporation of nitrogen into the six-membered ring of coelimycin P1. Crystal structures of CpkG revealed a rare tri-domain architecture, key active site residues and provided insight into the transamination mechanism. CpkH, CpkD and ScF were all subsequently characterised as flavoproteins. Specifically, CpkH was demonstrated to catalyse an (R)-specific FAD-dependent dehydrogenation, while CpkD was shown to catalyse two FMN-dependent epoxidations. The roles of ScF, CpkE and CpkI in coelimycin biosynthesis remain to be elucidated. Bioinformatics searches identified 22 additional actinobacterial gene clusters, which also encode modular PKSs with a TR domain and a homologue of CpkG. These have been predicted to direct the biosynthesis of both known and novel polyketide alkaloids, suggesting that reductive chain release and transamination constitute a conserved mechanism for the biosynthesis of such metabolites.
Supervisor: Not available Sponsor: Biotechnology and Biological Sciences Research Council ; University of Warwick
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.731420  DOI: Not available
Keywords: QD Chemistry
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