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Biosynthesis of an Anti-Addiction Agent from the Iboga Plant

[Image: see text] (−)-Ibogaine and (−)-voacangine are plant derived psychoactives that show promise as treatments for opioid addiction. However, these compounds are produced by hard to source plants, making these chemicals difficult for broad-scale use. Here we report the complete biosynthesis of (−...

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Autores principales: Farrow, Scott C., Kamileen, Mohamed O., Caputi, Lorenzo, Bussey, Kate, Mundy, Julia E. A., McAtee, Rory C., Stephenson, Corey R. J., O’Connor, Sarah E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706869/
https://www.ncbi.nlm.nih.gov/pubmed/31364847
http://dx.doi.org/10.1021/jacs.9b05999
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author Farrow, Scott C.
Kamileen, Mohamed O.
Caputi, Lorenzo
Bussey, Kate
Mundy, Julia E. A.
McAtee, Rory C.
Stephenson, Corey R. J.
O’Connor, Sarah E.
author_facet Farrow, Scott C.
Kamileen, Mohamed O.
Caputi, Lorenzo
Bussey, Kate
Mundy, Julia E. A.
McAtee, Rory C.
Stephenson, Corey R. J.
O’Connor, Sarah E.
author_sort Farrow, Scott C.
collection PubMed
description [Image: see text] (−)-Ibogaine and (−)-voacangine are plant derived psychoactives that show promise as treatments for opioid addiction. However, these compounds are produced by hard to source plants, making these chemicals difficult for broad-scale use. Here we report the complete biosynthesis of (−)-voacangine, and de-esterified voacangine, which is converted to (−)-ibogaine by heating, enabling biocatalytic production of these compounds. Notably, (−)-ibogaine and (−)-voacangine are of the opposite enantiomeric configuration compared to the other major alkaloids found in this natural product class. Therefore, this discovery provides insight into enantioselective enzymatic formal Diels–Alder reactions.
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spelling pubmed-67068692019-08-26 Biosynthesis of an Anti-Addiction Agent from the Iboga Plant Farrow, Scott C. Kamileen, Mohamed O. Caputi, Lorenzo Bussey, Kate Mundy, Julia E. A. McAtee, Rory C. Stephenson, Corey R. J. O’Connor, Sarah E. J Am Chem Soc [Image: see text] (−)-Ibogaine and (−)-voacangine are plant derived psychoactives that show promise as treatments for opioid addiction. However, these compounds are produced by hard to source plants, making these chemicals difficult for broad-scale use. Here we report the complete biosynthesis of (−)-voacangine, and de-esterified voacangine, which is converted to (−)-ibogaine by heating, enabling biocatalytic production of these compounds. Notably, (−)-ibogaine and (−)-voacangine are of the opposite enantiomeric configuration compared to the other major alkaloids found in this natural product class. Therefore, this discovery provides insight into enantioselective enzymatic formal Diels–Alder reactions. American Chemical Society 2019-07-31 2019-08-21 /pmc/articles/PMC6706869/ /pubmed/31364847 http://dx.doi.org/10.1021/jacs.9b05999 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Farrow, Scott C.
Kamileen, Mohamed O.
Caputi, Lorenzo
Bussey, Kate
Mundy, Julia E. A.
McAtee, Rory C.
Stephenson, Corey R. J.
O’Connor, Sarah E.
Biosynthesis of an Anti-Addiction Agent from the Iboga Plant
title Biosynthesis of an Anti-Addiction Agent from the Iboga Plant
title_full Biosynthesis of an Anti-Addiction Agent from the Iboga Plant
title_fullStr Biosynthesis of an Anti-Addiction Agent from the Iboga Plant
title_full_unstemmed Biosynthesis of an Anti-Addiction Agent from the Iboga Plant
title_short Biosynthesis of an Anti-Addiction Agent from the Iboga Plant
title_sort biosynthesis of an anti-addiction agent from the iboga plant
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706869/
https://www.ncbi.nlm.nih.gov/pubmed/31364847
http://dx.doi.org/10.1021/jacs.9b05999
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