Maite Colinas, Chloée Tymen, Joshua C. Wood, Anja David, Jens Wurlitzer, Clara Morweiser, Klaus Gase, Ryan M. Alam, Gabriel R. Titchiner, John P. Hamilton, Sarah Heinicke, Ron P. Dirks, Adriana A. Lopes, Lorenzo Caputi, C. Robin Buell, Sarah E. O’Connor
Abstract Iridoids are specialized monoterpenes ancestral to asterid flowering plants 1,2 that play key roles in defence and are also essential precursors for pharmacologically important alkaloids 3,4 . The biosynthesis of all iridoids involves the cyclization of the reactive biosynthetic intermediate 8-oxocitronellyl enol. Here, using a variety of approaches including single-nuclei sequencing, we report the discovery of iridoid cyclases from a phylogenetically broad sample of asterid species that synthesize iridoids. We show that these enzymes catalyse formation of 7 S - cis-trans and 7 R - cis-cis nepetalactol, the two major iridoid stereoisomers found in plants. Our work uncovers a key missing step in the otherwise well-characterized early iridoid biosynthesis pathway in asterids. This discovery unlocks the possibility to generate previously inaccessible iridoid stereoisomers, which will enable metabolic engineering for the sustainable production of valuable iridoid and iridoid-derived compounds.