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The Terpene Mini-Path, a New Promising Alternative for Terpenoids Bio-Production

Terpenoids constitute the largest class of natural compounds and are extremely valuable from an economic point of view due to their extended physicochemical properties and biological activities. Due to recent environmental concerns, terpene extraction from natural sources is no longer considered as...

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Detalles Bibliográficos
Autores principales: Couillaud, Julie, Leydet, Létitia, Duquesne, Katia, Iacazio, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701039/
https://www.ncbi.nlm.nih.gov/pubmed/34946923
http://dx.doi.org/10.3390/genes12121974
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author Couillaud, Julie
Leydet, Létitia
Duquesne, Katia
Iacazio, Gilles
author_facet Couillaud, Julie
Leydet, Létitia
Duquesne, Katia
Iacazio, Gilles
author_sort Couillaud, Julie
collection PubMed
description Terpenoids constitute the largest class of natural compounds and are extremely valuable from an economic point of view due to their extended physicochemical properties and biological activities. Due to recent environmental concerns, terpene extraction from natural sources is no longer considered as a viable option, and neither is the chemical synthesis to access such chemicals due to their sophisticated structural characteristics. An alternative to produce terpenoids is the use of biotechnological tools involving, for example, the construction of enzymatic cascades (cell-free synthesis) or a microbial bio-production thanks to metabolic engineering techniques. Despite outstanding successes, these approaches have been hampered by the length of the two natural biosynthetic routes (the mevalonate and the methyl erythritol phosphate pathways), leading to dimethylallyl diphosphate (DMAPP) and isopentenyl diphosphate (IPP), the two common universal precursors of all terpenoids. Recently, we, and others, developed what we called the terpene mini-path, a robust two enzyme access to DMAPP and IPP starting from their corresponding two alcohols, dimethylallyl alcohol and isopentenol. The aim here is to present the potential of this artificial bio-access to terpenoids, either in vitro or in vivo, through a review of the publications appearing since 2016 on this very new and fascinating field of investigation.
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spelling pubmed-87010392021-12-24 The Terpene Mini-Path, a New Promising Alternative for Terpenoids Bio-Production Couillaud, Julie Leydet, Létitia Duquesne, Katia Iacazio, Gilles Genes (Basel) Review Terpenoids constitute the largest class of natural compounds and are extremely valuable from an economic point of view due to their extended physicochemical properties and biological activities. Due to recent environmental concerns, terpene extraction from natural sources is no longer considered as a viable option, and neither is the chemical synthesis to access such chemicals due to their sophisticated structural characteristics. An alternative to produce terpenoids is the use of biotechnological tools involving, for example, the construction of enzymatic cascades (cell-free synthesis) or a microbial bio-production thanks to metabolic engineering techniques. Despite outstanding successes, these approaches have been hampered by the length of the two natural biosynthetic routes (the mevalonate and the methyl erythritol phosphate pathways), leading to dimethylallyl diphosphate (DMAPP) and isopentenyl diphosphate (IPP), the two common universal precursors of all terpenoids. Recently, we, and others, developed what we called the terpene mini-path, a robust two enzyme access to DMAPP and IPP starting from their corresponding two alcohols, dimethylallyl alcohol and isopentenol. The aim here is to present the potential of this artificial bio-access to terpenoids, either in vitro or in vivo, through a review of the publications appearing since 2016 on this very new and fascinating field of investigation. MDPI 2021-12-10 /pmc/articles/PMC8701039/ /pubmed/34946923 http://dx.doi.org/10.3390/genes12121974 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Couillaud, Julie
Leydet, Létitia
Duquesne, Katia
Iacazio, Gilles
The Terpene Mini-Path, a New Promising Alternative for Terpenoids Bio-Production
title The Terpene Mini-Path, a New Promising Alternative for Terpenoids Bio-Production
title_full The Terpene Mini-Path, a New Promising Alternative for Terpenoids Bio-Production
title_fullStr The Terpene Mini-Path, a New Promising Alternative for Terpenoids Bio-Production
title_full_unstemmed The Terpene Mini-Path, a New Promising Alternative for Terpenoids Bio-Production
title_short The Terpene Mini-Path, a New Promising Alternative for Terpenoids Bio-Production
title_sort terpene mini-path, a new promising alternative for terpenoids bio-production
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701039/
https://www.ncbi.nlm.nih.gov/pubmed/34946923
http://dx.doi.org/10.3390/genes12121974
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