actinorhodin and tetralol

In the actinorhodin type II polyketide synthase, the first polyketide modification is a regiospecific C9-carbonyl reduction, catalyzed by the ketoreductase (actKR). Our previous studies identified the actKR 94-PGG-96 motif as a determinant of stereospecificity. The molecular basis for reduction regiospecificity is, however, not well understood. In this study, we examined the activities of 20 actKR mutants through a combination of kinetic studies, PKS reconstitution, and structural analyses. Residues have been identified that are necessary for substrate interaction, and these observations have suggested a structural model for this reaction. Polyketides dock at the KR surface and are steered into the enzyme pocket where C7-C12 cyclization is mediated by the KR before C9-ketoreduction can occur. These molecular features can potentially serve as engineering targets for the biosynthesis of novel, reduced polyketides.

Topics: Acyl Carrier Protein; Alcohol Oxidoreductases; Anthraquinones; Bacterial Proteins; Catalytic Domain; Cyclization; Molecular Docking Simulation; Mutagenesis, Site-Directed; Mutation; NADP; Oxidation-Reduction; Polyketides; Stereoisomerism; Substrate Specificity; Tetralones