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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,...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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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 |
format | Online Article Text |
id | pubmed-5388535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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