Boosting the synthesis of pharmaceutically active abietane diterpenes in S. sclarea hairy roots by engineering the GGPPS and CPPS genes

Maria Carmela Vaccaro, Mariaevelina Alfieri, Nunziatina De Tommasi, Tessa Moses, Alain Goossens, Antonietta Leone

Research output: Contribution to journalArticlepeer-review

Abstract

Abietane diterpenoids (ADs), synthesized in the roots of different Salvia species, such as aethiopinone, 1-oxoaethiopinone, salvipisone, and ferruginol, have a variety of known biological activities. We have shown that aethiopinone has promising cytotoxic activity against several human tumor cell lines, including the breast adenocarcinoma MCF7, HeLa, epithelial carcinoma, prostate adenocarcinoma PC3, and human melanoma A375. The low content of these compounds in natural sources, and the limited possibility to synthesize them chemically at low cost, prompted us to optimize the production of abietane diterpenoids by targeting genes ofthe methylerythritol phosphate (MEP) pathway, from which they are derived. Here, we report our current and ongoing efforts to boost the metabolic flux towards this interesting class of compounds in Salvia sclarea hairy roots (HRs). Silencing the gene encoding the ent-copalyldiphosphate synthase gene (entCPPS), acting at the lateral geranylgeranyl pyrophosphate(GGPP) competitive gibberellin route, enhanced the content of aethiopinone and other ADs inS. sclarea HRs, indicating indirectly that the GGPP pool is a metabolic constraint to the accumulation of ADs. This was confirmed by overexpressing the GGPPS gene (geranyl-geranyldiphosphate synthase) which triggered also a significant 8-fold increase of abietane diterpenecontent above the basal constitutive level, with a major boosting effect on aethiopinone accumulation in S. sclarea HRs. A significant accumulation of aethiopinone and other ADcompounds was also achieved by overexpressing the CPPS gene (copalyl diphosphatesynthase) pointing to this biosynthetic step as another potential metabolic target for optimizing the biosynthesis of this class of compounds. However, by co-expressing of GGPPS and CPPS genes, albeit significant, the increase of abietane diterpenoids was less effective than that obtained by overexpressing the two genes individually. Taken together, the results presented here add novel and instrumental knowledge to a rational design of a hairy root based platform to yield reliable amounts of a ethiopinone and other ADs for a deeper understanding of their molecular pharmacological targets and potential future commercialization
Original languageEnglish
Article number924
Number of pages15
JournalFrontiers in plant science
Volume11
DOIs
Publication statusPublished - 18 Jun 2020

Keywords

  • metabolic engineering
  • plant bioactive diterpenes
  • gene co-expression
  • silencing
  • MEP-pathway

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