A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate

The biosynthetic pathway of preakuammicine, a monoterpene precursor of the anti-cancer agent vinblastine, has remained largely unexplored. Here, the authors provide transcriptomic and biochemical data to identify two enzymes that, in tandem, convert strictosidine to akuammicine, the stable shunt pro...

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Autores principales: Evangelos C. Tatsis, Inês Carqueijeiro, Thomas Dugé de Bernonville, Jakob Franke, Thu-Thuy T. Dang, Audrey Oudin, Arnaud Lanoue, Florent Lafontaine, Anna K. Stavrinides, Marc Clastre, Vincent Courdavault, Sarah E. O’Connor
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/03bb68418f55480082f388e21cdaf80b
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spelling oai:doaj.org-article:03bb68418f55480082f388e21cdaf80b2021-12-02T10:48:10ZA three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate10.1038/s41467-017-00154-x2041-1723https://doaj.org/article/03bb68418f55480082f388e21cdaf80b2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-00154-xhttps://doaj.org/toc/2041-1723The biosynthetic pathway of preakuammicine, a monoterpene precursor of the anti-cancer agent vinblastine, has remained largely unexplored. Here, the authors provide transcriptomic and biochemical data to identify two enzymes that, in tandem, convert strictosidine to akuammicine, the stable shunt product of preakuammicine.Evangelos C. TatsisInês CarqueijeiroThomas Dugé de BernonvilleJakob FrankeThu-Thuy T. DangAudrey OudinArnaud LanoueFlorent LafontaineAnna K. StavrinidesMarc ClastreVincent CourdavaultSarah E. O’ConnorNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Evangelos C. Tatsis
Inês Carqueijeiro
Thomas Dugé de Bernonville
Jakob Franke
Thu-Thuy T. Dang
Audrey Oudin
Arnaud Lanoue
Florent Lafontaine
Anna K. Stavrinides
Marc Clastre
Vincent Courdavault
Sarah E. O’Connor
A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate
description The biosynthetic pathway of preakuammicine, a monoterpene precursor of the anti-cancer agent vinblastine, has remained largely unexplored. Here, the authors provide transcriptomic and biochemical data to identify two enzymes that, in tandem, convert strictosidine to akuammicine, the stable shunt product of preakuammicine.
format article
author Evangelos C. Tatsis
Inês Carqueijeiro
Thomas Dugé de Bernonville
Jakob Franke
Thu-Thuy T. Dang
Audrey Oudin
Arnaud Lanoue
Florent Lafontaine
Anna K. Stavrinides
Marc Clastre
Vincent Courdavault
Sarah E. O’Connor
author_facet Evangelos C. Tatsis
Inês Carqueijeiro
Thomas Dugé de Bernonville
Jakob Franke
Thu-Thuy T. Dang
Audrey Oudin
Arnaud Lanoue
Florent Lafontaine
Anna K. Stavrinides
Marc Clastre
Vincent Courdavault
Sarah E. O’Connor
author_sort Evangelos C. Tatsis
title A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate
title_short A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate
title_full A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate
title_fullStr A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate
title_full_unstemmed A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate
title_sort three enzyme system to generate the strychnos alkaloid scaffold from a central biosynthetic intermediate
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/03bb68418f55480082f388e21cdaf80b
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