Insights into the Pamamycin Biosynthesis |
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Authors: | Dr. Yuriy Rebets Dr. Elke Brötz Niko Manderscheid Dr. Bogdan Tokovenko Dr. Maksym Myronovskyi Prof. Dr. Peter Metz Dr. Lutz Petzke Dr. Andriy Luzhetskyy |
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Affiliation: | 1. Helmholtz‐Institute for Pharmaceutical Research Saarland, Actinobacteria Metabolic Engineering Group, UdS Campus, C2 3, 66123 Saarbrücken (Germany);2. Fachrichtung Chemie und Lebensmittelchemie, Organische Chemie I, Technische Universit?t Dresden, 01062 Dresden (Germany);3. BASF AG (Germany) |
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Abstract: | Pamamycins are macrodiolides of polyketide origin with antibacterial activities. Their biosynthesis has been proposed to utilize succinate as a building block. However, the mechanism of succinate incorporation into a polyketide was unclear. Here, we report identification of a pamamycin biosynthesis gene cluster by aligning genomes of two pamamycin‐producing strains. This unique cluster contains polyketide synthase (PKS) genes encoding seven discrete ketosynthase (KS) enzymes and one acyl‐carrier protein (ACP)‐encoding gene. A cosmid containing the entire set of genes required for pamamycin biosynthesis was successfully expressed in a heterologous host. Genetic and biochemical studies allowed complete delineation of pamamycin biosynthesis. The pathway proceeds through 3‐oxoadipyl‐CoA, a key intermediate in the primary metabolism of the degradation of aromatic compounds. 3‐Oxoadipyl‐CoA could be used as an extender unit in polyketide assembly to facilitate the incorporation of succinate. |
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Keywords: | biosynthesis polyketide synthase polyketides Streptomyces succinate |
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