Diterpenoids constitute a diverse class of metabolites with critical functions in plant development, defense, and ecological adaptation. Major monocot crops, such as maize () and rice (), deploy diverse blends of specialized diterpenoids as core components of biotic and abiotic stress resilience. Here, we describe the genome-wide identification and functional characterization of stress-related diterpene synthases (diTPSs) in the dedicated bioenergy crop switchgrass (). Mining of the allotetraploid switchgrass genome identified an expansive diTPS family of 31 members, and biochemical analysis of 11 diTPSs revealed a modular metabolic network producing a diverse array of diterpenoid metabolites. In addition to -copalyl diphosphate (CPP) and-kaurene synthases predictably involved in gibberellin biosynthesis, we identified -CPP and-labda-13-en-8-ol diphosphate (LPP) synthases as well as two diTPSs forming (+)-labda-8,13-dienyl diphosphate (8,13-CPP) and cis-trans-clerodienyl diphosphate (CT-CLPP) scaffolds not observed previously in plants. Structure-guided mutagenesis of the (+)-8,13-CPP andCT-CLPP synthases revealed residue substitutions in the active sites that altered product outcome, representing potential neofunctionalization events that occurred during diversification of the switchgrass diTPS family. The conversion of -CPP,-LPP, -CPP, and-CT-CLPP by promiscuous diTPSs further yielded distinct labdane-type diterpene olefins and alcohols. Of these metabolites, the formation of 9β-hydroxy--pimar-15-ene and the expression of the corresponding genes were induced in roots and leaves in response to oxidative stress and ultraviolet irradiation, indicating their possible roles in abiotic stress adaptation. Together, these findings expand the known chemical space of diterpenoid metabolism in monocot crops toward systematically investigating and ultimately improving stress resilience traits in crop species.
The diterpene synthase clerodienyl diphosphate synthase 1 (PvCPS1) from the crop plant switchgrass (Panicum virgatum) stereoselectively converts (E,E,E)‐geranylgeranyl diphosphate (GGPP) into the clerodane natural product, cis‐trans‐clerodienyl diphosphate (CLPP, 1). Structure‐guided point mutations of PvCPS1 redirected product stereoselectivity toward the formation of a rare cis‐clerodane diastereomer, cis‐cis‐CLPP (2). Additionally, an alternative cis‐clerodane diastereomer, (5S,8S,9R,10R)‐13Z‐CLPP (3), was produced when treating PvCPS1 and select variants thereof with the cis‐prenyl substrate (Z,Z,Z)‐nerylneryl diphosphate (NNPP). These results support the hypothesis that substrate configuration and minor active‐site alterations impact precatalysis substrate folding in the stereoselective biosynthesis of clerodane diterpenoid scaffolds, and can be employed to provide enzymatic access to a broader range of bioactive clerodane natural products.
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