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Total biosynthesis of the cyclic AMP booster forskolin from Coleus forskohlii

Forskolin is a unique structurally complex labdane-type diterpenoid used in the treatment of glaucoma and heart failure based on its activity as a cyclic AMP booster. Commercial production of forskolin relies exclusively on extraction from its only known natural source, the plant Coleus forskohlii,...

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Autores principales: Pateraki, Irini, Andersen-Ranberg, Johan, Jensen, Niels Bjerg, Wubshet, Sileshi Gizachew, Heskes, Allison Maree, Forman, Victor, Hallström, Björn, Hamberger, Britta, Motawia, Mohammed Saddik, Olsen, Carl Erik, Staerk, Dan, Hansen, Jørgen, Møller, Birger Lindberg, Hamberger, Björn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388535/
https://www.ncbi.nlm.nih.gov/pubmed/28290983
http://dx.doi.org/10.7554/eLife.23001
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author Pateraki, Irini
Andersen-Ranberg, Johan
Jensen, Niels Bjerg
Wubshet, Sileshi Gizachew
Heskes, Allison Maree
Forman, Victor
Hallström, Björn
Hamberger, Britta
Motawia, Mohammed Saddik
Olsen, Carl Erik
Staerk, Dan
Hansen, Jørgen
Møller, Birger Lindberg
Hamberger, Björn
author_facet Pateraki, Irini
Andersen-Ranberg, Johan
Jensen, Niels Bjerg
Wubshet, Sileshi Gizachew
Heskes, Allison Maree
Forman, Victor
Hallström, Björn
Hamberger, Britta
Motawia, Mohammed Saddik
Olsen, Carl Erik
Staerk, Dan
Hansen, Jørgen
Møller, Birger Lindberg
Hamberger, Björn
author_sort Pateraki, Irini
collection PubMed
description Forskolin is a unique structurally complex labdane-type diterpenoid used in the treatment of glaucoma and heart failure based on its activity as a cyclic AMP booster. Commercial production of forskolin relies exclusively on extraction from its only known natural source, the plant Coleus forskohlii, in which forskolin accumulates in the root cork. Here, we report the discovery of five cytochrome P450s and two acetyltransferases which catalyze a cascade of reactions converting the forskolin precursor 13R-manoyl oxide into forskolin and a diverse array of additional labdane-type diterpenoids. A minimal set of three P450s in combination with a single acetyl transferase was identified that catalyzes the conversion of 13R-manoyl oxide into forskolin as demonstrated by transient expression in Nicotiana benthamiana. The entire pathway for forskolin production from glucose encompassing expression of nine genes was stably integrated into Saccharomyces cerevisiae and afforded forskolin titers of 40 mg/L. DOI: http://dx.doi.org/10.7554/eLife.23001.001
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spelling pubmed-53885352017-04-17 Total biosynthesis of the cyclic AMP booster forskolin from Coleus forskohlii Pateraki, Irini Andersen-Ranberg, Johan Jensen, Niels Bjerg Wubshet, Sileshi Gizachew Heskes, Allison Maree Forman, Victor Hallström, Björn Hamberger, Britta Motawia, Mohammed Saddik Olsen, Carl Erik Staerk, Dan Hansen, Jørgen Møller, Birger Lindberg Hamberger, Björn eLife Biochemistry Forskolin is a unique structurally complex labdane-type diterpenoid used in the treatment of glaucoma and heart failure based on its activity as a cyclic AMP booster. Commercial production of forskolin relies exclusively on extraction from its only known natural source, the plant Coleus forskohlii, in which forskolin accumulates in the root cork. Here, we report the discovery of five cytochrome P450s and two acetyltransferases which catalyze a cascade of reactions converting the forskolin precursor 13R-manoyl oxide into forskolin and a diverse array of additional labdane-type diterpenoids. A minimal set of three P450s in combination with a single acetyl transferase was identified that catalyzes the conversion of 13R-manoyl oxide into forskolin as demonstrated by transient expression in Nicotiana benthamiana. The entire pathway for forskolin production from glucose encompassing expression of nine genes was stably integrated into Saccharomyces cerevisiae and afforded forskolin titers of 40 mg/L. DOI: http://dx.doi.org/10.7554/eLife.23001.001 eLife Sciences Publications, Ltd 2017-03-14 /pmc/articles/PMC5388535/ /pubmed/28290983 http://dx.doi.org/10.7554/eLife.23001 Text en © 2017, Pateraki et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry
Pateraki, Irini
Andersen-Ranberg, Johan
Jensen, Niels Bjerg
Wubshet, Sileshi Gizachew
Heskes, Allison Maree
Forman, Victor
Hallström, Björn
Hamberger, Britta
Motawia, Mohammed Saddik
Olsen, Carl Erik
Staerk, Dan
Hansen, Jørgen
Møller, Birger Lindberg
Hamberger, Björn
Total biosynthesis of the cyclic AMP booster forskolin from Coleus forskohlii
title Total biosynthesis of the cyclic AMP booster forskolin from Coleus forskohlii
title_full Total biosynthesis of the cyclic AMP booster forskolin from Coleus forskohlii
title_fullStr Total biosynthesis of the cyclic AMP booster forskolin from Coleus forskohlii
title_full_unstemmed Total biosynthesis of the cyclic AMP booster forskolin from Coleus forskohlii
title_short Total biosynthesis of the cyclic AMP booster forskolin from Coleus forskohlii
title_sort total biosynthesis of the cyclic amp booster forskolin from coleus forskohlii
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388535/
https://www.ncbi.nlm.nih.gov/pubmed/28290983
http://dx.doi.org/10.7554/eLife.23001
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