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[(2)H(26)]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus

During growth on fully deuterated medium the volatile terpene [(2)H(26)]-1-epi-cubenol was released by the actinomycete Streptomyces griseus. This compound represents the first completely deuterated terpene obtained by fermentation. Despite a few previous reports in the literature the operability of...

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Autores principales: Citron, Christian A, Dickschat, Jeroen S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869315/
https://www.ncbi.nlm.nih.gov/pubmed/24367448
http://dx.doi.org/10.3762/bjoc.9.319
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author Citron, Christian A
Dickschat, Jeroen S
author_facet Citron, Christian A
Dickschat, Jeroen S
author_sort Citron, Christian A
collection PubMed
description During growth on fully deuterated medium the volatile terpene [(2)H(26)]-1-epi-cubenol was released by the actinomycete Streptomyces griseus. This compound represents the first completely deuterated terpene obtained by fermentation. Despite a few previous reports in the literature the operability of this approach to fully deuterated compounds is still surprising, because the strong kinetic isotope effect of deuterium is known to slow down all metabolic processes in living organisms. Potential applications of completely labelled compounds from natural sources in structure elucidation, biosynthetic or pharmacokinetic investigations are discussed.
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spelling pubmed-38693152013-12-23 [(2)H(26)]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus Citron, Christian A Dickschat, Jeroen S Beilstein J Org Chem Full Research Paper During growth on fully deuterated medium the volatile terpene [(2)H(26)]-1-epi-cubenol was released by the actinomycete Streptomyces griseus. This compound represents the first completely deuterated terpene obtained by fermentation. Despite a few previous reports in the literature the operability of this approach to fully deuterated compounds is still surprising, because the strong kinetic isotope effect of deuterium is known to slow down all metabolic processes in living organisms. Potential applications of completely labelled compounds from natural sources in structure elucidation, biosynthetic or pharmacokinetic investigations are discussed. Beilstein-Institut 2013-12-10 /pmc/articles/PMC3869315/ /pubmed/24367448 http://dx.doi.org/10.3762/bjoc.9.319 Text en Copyright © 2013, Citron and Dickschat https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Citron, Christian A
Dickschat, Jeroen S
[(2)H(26)]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus
title [(2)H(26)]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus
title_full [(2)H(26)]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus
title_fullStr [(2)H(26)]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus
title_full_unstemmed [(2)H(26)]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus
title_short [(2)H(26)]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus
title_sort [(2)h(26)]-1-epi-cubenol, a completely deuterated natural product from streptomyces griseus
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869315/
https://www.ncbi.nlm.nih.gov/pubmed/24367448
http://dx.doi.org/10.3762/bjoc.9.319
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