Cargando…

Harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids

8-Methoxy-γ-humulene, (E)-8-methoxy-β-farnesene, 12-methoxy-β-sesquiphellandrene and 12-methoxyzingiberene can be synthesised in amorphadiene synthase-catalysed reactions from 8- and 12-methoxyfarnesyl diphosphates due to the highly plastic yet tightly controlled carbocationic chemistry of this sesq...

Descripción completa

Detalles Bibliográficos
Autores principales: Demiray, Melodi, Miller, David J, Allemann, Rudolf K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774066/
https://www.ncbi.nlm.nih.gov/pubmed/31598175
http://dx.doi.org/10.3762/bjoc.15.215
_version_ 1783456030767710208
author Demiray, Melodi
Miller, David J
Allemann, Rudolf K
author_facet Demiray, Melodi
Miller, David J
Allemann, Rudolf K
author_sort Demiray, Melodi
collection PubMed
description 8-Methoxy-γ-humulene, (E)-8-methoxy-β-farnesene, 12-methoxy-β-sesquiphellandrene and 12-methoxyzingiberene can be synthesised in amorphadiene synthase-catalysed reactions from 8- and 12-methoxyfarnesyl diphosphates due to the highly plastic yet tightly controlled carbocationic chemistry of this sesquiterpene cyclase.
format Online
Article
Text
id pubmed-6774066
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-67740662019-10-09 Harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids Demiray, Melodi Miller, David J Allemann, Rudolf K Beilstein J Org Chem Full Research Paper 8-Methoxy-γ-humulene, (E)-8-methoxy-β-farnesene, 12-methoxy-β-sesquiphellandrene and 12-methoxyzingiberene can be synthesised in amorphadiene synthase-catalysed reactions from 8- and 12-methoxyfarnesyl diphosphates due to the highly plastic yet tightly controlled carbocationic chemistry of this sesquiterpene cyclase. Beilstein-Institut 2019-09-17 /pmc/articles/PMC6774066/ /pubmed/31598175 http://dx.doi.org/10.3762/bjoc.15.215 Text en Copyright © 2019, Demiray et al. https://creativecommons.org/licenses/by/4.0https://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/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. 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
Demiray, Melodi
Miller, David J
Allemann, Rudolf K
Harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids
title Harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids
title_full Harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids
title_fullStr Harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids
title_full_unstemmed Harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids
title_short Harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids
title_sort harnessing enzyme plasticity for the synthesis of oxygenated sesquiterpenoids
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774066/
https://www.ncbi.nlm.nih.gov/pubmed/31598175
http://dx.doi.org/10.3762/bjoc.15.215
work_keys_str_mv AT demiraymelodi harnessingenzymeplasticityforthesynthesisofoxygenatedsesquiterpenoids
AT millerdavidj harnessingenzymeplasticityforthesynthesisofoxygenatedsesquiterpenoids
AT allemannrudolfk harnessingenzymeplasticityforthesynthesisofoxygenatedsesquiterpenoids