Parallel pathways for oxidation of 14‐membered polyketide macrolactones in Saccharopolyspora erythraea

Summary The glycosyltransferases OleG1 and OleG2 and the cytochrome P450 oxidase OleP from the oleandomycin biosynthetic gene cluster of Streptomyces antibioticus have been expressed, either separately or from artificial gene cassettes, in strains of Saccharopolyspora erythraea blocked in erythromycin biosynthesis, to investigate their potential for the production of diverse novel macrolides from erythronolide precursors. OleP was found to oxidize 6‐deoxyerythronolide B, but not erythronolide B. However, OleP did oxidize derivatives of erythronolide B in which a neutral sugar is attached at C‐3. The oxidized products 3‐ O ‐mycarosyl‐8a‐hydroxyerythronolide B, 3‐ O ‐mycarosyl‐8,8a‐epoxyerythronolide B, 6‐deoxy‐8‐hydroxyerythronolide B and the olefin 6‐deoxy‐8,8a‐dehydroerythronolide B were all isolated and their structures determined. When oleP and the mycarosyltransferase eryBV were co‐expressed in a gene cassette, 3‐ O ‐mycarosyl‐6‐deoxy‐8,8a‐dihydroxyerythronolide B was directly obtained. When oleG2 was co‐expressed in a gene cassette together with oleP , 6‐deoxyerythronolide B was converted into a mixture of 3‐ O ‐rhamnosyl‐6‐deoxy‐8,8a‐dehydroerythronolide B and 3‐ O ‐rhamnosyl‐6‐deoxy‐8,8a‐dihydroxyerythronolide B, confirming previous reports that OleG2 can transfer rhamnose, and confirming that oxidation by OleP and attachment of the neutral sugar to the aglycone can occur in either order. Similarly, four different 3‐ O ‐mycarosylerythronolides were found to be substrates for the desosaminyltransferase OleG1. These results provide additional insight into the nature of the intermediates in OleP‐mediated oxidation, and suggest that oleandomycin biosynthesis might follow parallel pathways in which epoxidation either precedes or follows attachment of the neutral sugar.