Production of Putative Diterpene Carboxylic Acid Intermediates of Triptolide in Yeast

• Published in: Molecules (Basel, Switzerland) Switzerland), 2017-06, Vol.22 (6), p.981
• Main Authors: Forman, Victor, Callari, Roberta, Folly, Christophe, Heider, Harald, Hamberger, Björn
• Format: Article
• Language: English
• Subjects: Abietanes - biosynthesis; Abietanes - genetics; Acids; Alkenes; Baking yeast; BASIC BIOLOGICAL SCIENCES; Biosynthetic Pathways - genetics; Carboxylic acids; Cytochrome P-450 Enzyme System - genetics; Cytochrome P450; Cytochromes P450; dehydroabietadiene; Dehydroabietic acid; Diterpenes - chemistry; Diterpenes - therapeutic use; Enantiomers; Epoxy Compounds - chemistry; Epoxy Compounds - therapeutic use; Glucose - chemistry; Glucose - metabolism; In vivo methods and tests; Indigenous plants; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Intermediates; medicinal diterpenes; Metabolic Engineering; miltiradiene; miltiradienic acid; NADP; Nicotiana - enzymology; Nicotiana - genetics; Nicotiana benthamiana; Phenanthrenes - chemistry; Phenanthrenes - therapeutic use; Phylogeny; Picea - enzymology; Picea - genetics; Picea sitchensis; Reductases; Saccharomyces cerevisiae; Saccharomyces cerevisiae - enzymology; Saccharomyces cerevisiae - genetics; Tripterygium - enzymology; Tripterygium - genetics; Tripterygium wilfordii; Triptolide; Yeast
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules22060981

The development of medical applications exploiting the broad bioactivities of the diterpene therapeutic triptolide from is limited by low extraction yields from the native plant. Furthermore, the extraordinarily high structural complexity prevents an economically attractive enantioselective total synthesis. An alternative production route of triptolide through engineered (yeast) could provide a sustainable source of triptolide. A potential intermediate in the unknown biosynthetic route to triptolide is the diterpene dehydroabietic acid. Here, we report a biosynthetic route to dehydroabietic acid by transient expression of enzymes from and Sitka spruce ( ) in . The combination of diterpene synthases TPS9, TPS27, and cytochromes P450 CYP720B4 yielded dehydroabietic acid and a novel analog, tentatively identified as 'miltiradienic acid'. This biosynthetic pathway was reassembled in a yeast strain engineered for increased yields of the pathway intermediates, the diterpene olefins miltiradiene and dehydroabietadiene. Introduction in that strain of CYP720B4 in combination with two alternative NADPH-dependent cytochrome P450 reductases resulted in scalable in vivo production of dehydroabietic acid and its analog from glucose. Approaching future elucidation of the remaining biosynthetic steps to triptolide, our findings may provide an independent platform for testing of additional recombinant candidate genes, and ultimately pave the way to biotechnological production of the high value diterpenoid therapeutic.