Title | Heterologous production of labdane-type diterpenes in the green alga Chlamydomonas reinhardtii |
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Publication Type | Articolo su Rivista peer-reviewed |
Year of Publication | 2019 |
Authors | Papaefthimiou, D., Diretto Gianfranco, Demurtas Olivia Costantina, Mini P., Ferrante Paola, Giuliano Giovanni, and Kanellis A.K. |
Journal | Phytochemistry |
Volume | 167 |
Pagination | 112082 |
ISSN | 00319422 |
Keywords | 13-diol (sclareol), 15-diol, Alkyl and Aryl Transferases, Chlamydomonas reinhardtii, Chlamydomonas reinhardtii P.A.Dangeard (Chlamydomonadaceae), Chloroplasts, Cistus, Cistus creticus L. (Cistaceae), Copal-8-ol diphosphate synthase, Diterpenes, Ent-13-epi-manoyl oxide, Ent-manoyl oxide, Genetic, Genetic engineering, Heterologous production, Labda-13-ene-8α, Labda-14-ene-8, Labdane diterpenes, microalgae, Plant Proteins, Transformation |
Abstract | Labdane diterpenes (LDs), and especially sclareol, are important feedstocks for the pharmaceutical and cosmetic industries, and therefore several lines of research have led to their heterologous production in non-photosynthetic microbes and higher plants. The potential of microalgae as bioreactors of natural products has been established for a variety of bioactive metabolites, including terpenes. In this work, a codon optimized sequence encoding a key plant labdane-type diterpene (LD) cyclase, copal-8-ol diphosphate synthase from Cistus creticus (CcCLS), was introduced into the chloroplast genome of Chlamydomonas reinhardtii. Of 49 transplastomic algal lines, 12 produced variable amounts of four LD compounds, namely ent-manoyl oxide, sclareol, labda-13-ene-8α,15-diol and ent-13-epi-manoyl oxide. The total LD concentrations measured in the transplastomic lines reached 1.172 ± 0.05 μg/mg cell DW for the highest overall producer, while the highest yield for sclareol was 0.038 ± 0.001 μg/mg cell DW. Thus, transplastomic expression of a key plant labdane diterpene cyclase in the C. reinhardtii chloroplast genome enabled the production of important plant-specific LD compounds. © 2019 |
Notes | cited By 0 |
URL | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85070647525&doi=10.1016%2fj.phytochem.2019.112082&partnerID=40&md5=66fbe11449436d09bf73035b2d2da542 |
DOI | 10.1016/j.phytochem.2019.112082 |
Citation Key | Papaefthimiou2019 |