Journal of the American Chemical Society · 2000 · 64 citations · 25 references
PharmacyBiochemistryMolecular BiologyEnzyme MechanismEnzymologyProtein EngineeringCatalytic MechanismsEnzyme-substrate RecognitionPolyketide BiosynthesisProtein DesignSubstrate RecognitionSubstrate SpecificityEnzyme Family SpecificityModular Polyketide BiosynthesisMolecular Recognition FeaturesMolecular Recognition MotifsPolyketide AntibioticsPolyketide Synthase EngineeringSubstrate Binding SpecificitySubstrate Specificity Profiling
6-Deoxyerythronolide B synthase (DEBS), the multifunctional enzyme responsible for the biosynthesis of the macrolide aglycon of the antibiotic erythromycin, is an excellent model system for studying the properties of modular polyketide synthases. In these studies, we analyzed the substrate specificity of selected individual modules of DEBS. Unexpectedly, we observed (i) a high degree of similarity in the specificity of all modules tested, despite the diverse structural features of their natural substrates, and (ii) a distinct preference by all modules for syn diketides over anti diketides. The implications of these results are analyzed from an evolutionary and a protein engineering perspective.
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Robert McDaniel, Arinthip Thamchaipenet, Claes Gustafsson et al. · Proceedings of the National Academy of Sciences · 1999 · 461 citations
Dissecting and Exploiting Intermodular Communication in Polyketide Synthases
Rajesh S. Gokhale, Stuart Y. Tsuji, David E. Cane et al. · Science · 1999 · 325 citations
Engineering Broader Specificity into an Antibiotic-Producing Polyketide Synthase
Andrew F. A. Marsden, Barrie Wilkinson, Jesús Cortés et al. · Science · 1998 · 215 citations
A hybrid modular polyketide synthase obtained by domain swapping
Markiyan Oliynyk, Murray J. B. Brown, Jesús Cortés et al. · Chemistry & Biology · 1996 · 185 citations · Full text