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Updated: Aug 28, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
ent-Kaurene, ent-kauran-16-ol, and shunted diterpenoids from an engineered strain of Aspergillus oryzae
Ahmed Arafa1,2,3, Yuechen Jiang1, Jennifer Gerke1
1Institute for Organic Chemistry and BMWZ, Leibniz University Hannover Schneiderberg 38 30167 Hannover Germany russell.cox@oci.uni-hannover.de.
Abstract:
Aspergillus oryzae was engineered to produce high levels of geranylgeranyldiphosphate (GGPP) and ent-kaurene, via ent-copalyl diphosphate, as precursors for future metabolic engineering projects via the expression of ggs2 and cps/ks genes from Gibberella fujikuroi under the control of strong constitutive promoters. GGPP was shunted to three new metabolites that were fully identified by NMR and HRMS. ent-Copalyl diphosphate was shunted to a further seven new compounds that were also identified by NMR and HRMS. The titre of ent-kaurene was significantly increased by heterologous expression of a truncated hydroxymethylglutaryl CoA reductase gene from Avena strigosa (AstHMGR), while replacement of the dual terpene cyclase encoding gene cps/ks with the individual cyclase genes, ptmT2 from Streptomyces platensis and Bjks from Bradyrhizobium japonicum, resulted mainly in accumulation of ent-copalyl diphosphate-derived shunt products. Finally, ent-kauran-16-ol was biosynthesised by coexpression of ggs2 with the bacterial cyclases ptmT2 and ptmT3.
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