Functional and structural analysis of the angucyclinone ketoreductase SimC7

Schäfer, Martin (2016) Functional and structural analysis of the angucyclinone ketoreductase SimC7. Doctoral thesis, University of East Anglia.

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    Abstract

    The natural product simocyclinone D8 (SD8) is a potent DNA gyrase inhibitor produced by Streptomyces antibioticus Tü6040. The biosynthetic simocyclinone (sim) gene cluster has been sequenced and a hypothetical biosynthetic pathway has been proposed. The tetraene linker in SD8 was suggested to be the product of a modular type I polyketide synthase working in trans with two monofunctional enzymes. SimC7, which belongs to the short-chain dehydrogenase/reductase (SDR) superfamily of proteins, was proposed to supply the dehydratase activity missing from two modules of the polyketide synthase.
    In this study, I report the structure and function of recombinant S. antibioticus SimC7. Because the natural simocyclinone producer is genetically intractable, the ~72-kb sim cluster was isolated on a single phage artificial chromosome (PAC) clone for heterologous production in a Streptomyces coelicolor strain engineered for improved antibiotic production. Deletion of simC7 resulted in production of a novel simocyclinone, 7-oxo-SD8, which carried a normal tetraene linker but was altered in the angucyclinone. I demonstrate that SimC7 is an NAD(P)H-dependent polyketide ketoreductase that catalyses the reduction of the C-7 carbonyl of the angucyclinone and the resulting hydroxyl group is essential for antibiotic activity. SimC7 shares little sequence similarity with characterized ketoreductases, suggesting it might have a distinct catalytic mechanism. To investigate this possibility, I determined the structures of SimC7 alone, in complex with NADP+, and in complex with NADP+ and the substrate 7-oxo-SD8. These structures show that SimC7 is distinct from previously characterized polyketide ketoreductases, lacking the conserved catalytic triad (Ser-Tyr-Lys), including the active site tyrosine that acts as central acid-base catalyst in canonical SDR proteins. Taken together with functional analyses of active site mutants, my data suggest SimC7 catalyses a substrate-assisted, two-step reaction for reduction of the C-7 carbonyl group involving intramolecular transfer of a substrate-derived proton to generate a phenolate intermediate.

    Item Type: Thesis (Doctoral)
    Faculty \ School: Faculty of Science > School of Biological Sciences
    Depositing User: Jackie Webb
    Date Deposited: 09 Nov 2016 09:12
    Last Modified: 09 Nov 2016 09:12
    URI: https://ueaeprints.uea.ac.uk/id/eprint/61276
    DOI:

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