Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by <it>Saccharomyces cerevisiae</it>

<p>Abstract</p> <p>Background</p> <p>Sesquiterpenes are a class of natural products with a diverse range of attractive industrial proprieties. Due to economic difficulties of sesquiterpene production via extraction from plants or chemical synthesis there is interest in...

Full description

Bibliographic Details
Main Authors: Scalcinati Gionata, Partow Siavash, Siewers Verena, Schalk Michel, Daviet Laurent, Nielsen Jens
Format: Article
Language:English
Published: BMC 2012-08-01
Series:Microbial Cell Factories
Subjects:
Online Access:http://www.microbialcellfactories.com/content/11/1/117
_version_ 1818061304523390976
author Scalcinati Gionata
Partow Siavash
Siewers Verena
Schalk Michel
Daviet Laurent
Nielsen Jens
author_facet Scalcinati Gionata
Partow Siavash
Siewers Verena
Schalk Michel
Daviet Laurent
Nielsen Jens
author_sort Scalcinati Gionata
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Sesquiterpenes are a class of natural products with a diverse range of attractive industrial proprieties. Due to economic difficulties of sesquiterpene production via extraction from plants or chemical synthesis there is interest in developing alternative and cost efficient bioprocesses. The hydrocarbon α-santalene is a precursor of sesquiterpenes with relevant commercial applications. Here, we construct an efficient <it>Saccharomyces cerevisiae</it> cell factory for α-santalene production.</p> <p>Results</p> <p>A multistep metabolic engineering strategy targeted to increase precursor and cofactor supply was employed to manipulate the yeast metabolic network in order to redirect carbon toward the desired product. To do so, genetic modifications were introduced acting to optimize the farnesyl diphosphate branch point, modulate the mevalonate pathway, modify the ammonium assimilation pathway and enhance the activity of a transcriptional activator. The approach employed resulted in an overall α-santalene yield of a 0.0052 Cmmol (Cmmol glucose)<sup>-1</sup> corresponding to a 4-fold improvement over the reference strain. This strategy, combined with a specifically developed continuous fermentation process, led to a final α-santalene productivity of 0.036 Cmmol (g biomass)<sup>-1</sup> h<sup>-1</sup>.</p> <p>Conclusions</p> <p>The results reported in this work illustrate how the combination of a metabolic engineering strategy with fermentation technology optimization can be used to obtain significant amounts of the high-value sesquiterpene α-santalene. This represents a starting point toward the construction of a yeast “sesquiterpene factory” and for the development of an economically viable bio-based process that has the potential to replace the current production methods.</p>
first_indexed 2024-12-10T13:46:11Z
format Article
id doaj.art-6f8f819a0fc5458e8919b1b19fff9fc6
institution Directory Open Access Journal
issn 1475-2859
language English
last_indexed 2024-12-10T13:46:11Z
publishDate 2012-08-01
publisher BMC
record_format Article
series Microbial Cell Factories
spelling doaj.art-6f8f819a0fc5458e8919b1b19fff9fc62022-12-22T01:46:26ZengBMCMicrobial Cell Factories1475-28592012-08-0111111710.1186/1475-2859-11-117Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by <it>Saccharomyces cerevisiae</it>Scalcinati GionataPartow SiavashSiewers VerenaSchalk MichelDaviet LaurentNielsen Jens<p>Abstract</p> <p>Background</p> <p>Sesquiterpenes are a class of natural products with a diverse range of attractive industrial proprieties. Due to economic difficulties of sesquiterpene production via extraction from plants or chemical synthesis there is interest in developing alternative and cost efficient bioprocesses. The hydrocarbon α-santalene is a precursor of sesquiterpenes with relevant commercial applications. Here, we construct an efficient <it>Saccharomyces cerevisiae</it> cell factory for α-santalene production.</p> <p>Results</p> <p>A multistep metabolic engineering strategy targeted to increase precursor and cofactor supply was employed to manipulate the yeast metabolic network in order to redirect carbon toward the desired product. To do so, genetic modifications were introduced acting to optimize the farnesyl diphosphate branch point, modulate the mevalonate pathway, modify the ammonium assimilation pathway and enhance the activity of a transcriptional activator. The approach employed resulted in an overall α-santalene yield of a 0.0052 Cmmol (Cmmol glucose)<sup>-1</sup> corresponding to a 4-fold improvement over the reference strain. This strategy, combined with a specifically developed continuous fermentation process, led to a final α-santalene productivity of 0.036 Cmmol (g biomass)<sup>-1</sup> h<sup>-1</sup>.</p> <p>Conclusions</p> <p>The results reported in this work illustrate how the combination of a metabolic engineering strategy with fermentation technology optimization can be used to obtain significant amounts of the high-value sesquiterpene α-santalene. This represents a starting point toward the construction of a yeast “sesquiterpene factory” and for the development of an economically viable bio-based process that has the potential to replace the current production methods.</p>http://www.microbialcellfactories.com/content/11/1/117Metabolic engineeringIsoprenoidsSesquiterpenesContinuous culture<it>Saccharomyces cerevisiae</it>
spellingShingle Scalcinati Gionata
Partow Siavash
Siewers Verena
Schalk Michel
Daviet Laurent
Nielsen Jens
Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by <it>Saccharomyces cerevisiae</it>
Microbial Cell Factories
Metabolic engineering
Isoprenoids
Sesquiterpenes
Continuous culture
<it>Saccharomyces cerevisiae</it>
title Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by <it>Saccharomyces cerevisiae</it>
title_full Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by <it>Saccharomyces cerevisiae</it>
title_fullStr Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by <it>Saccharomyces cerevisiae</it>
title_full_unstemmed Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by <it>Saccharomyces cerevisiae</it>
title_short Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by <it>Saccharomyces cerevisiae</it>
title_sort combined metabolic engineering of precursor and co factor supply to increase α santalene production by it saccharomyces cerevisiae it
topic Metabolic engineering
Isoprenoids
Sesquiterpenes
Continuous culture
<it>Saccharomyces cerevisiae</it>
url http://www.microbialcellfactories.com/content/11/1/117
work_keys_str_mv AT scalcinatigionata combinedmetabolicengineeringofprecursorandcofactorsupplytoincreaseasantaleneproductionbyitsaccharomycescerevisiaeit
AT partowsiavash combinedmetabolicengineeringofprecursorandcofactorsupplytoincreaseasantaleneproductionbyitsaccharomycescerevisiaeit
AT siewersverena combinedmetabolicengineeringofprecursorandcofactorsupplytoincreaseasantaleneproductionbyitsaccharomycescerevisiaeit
AT schalkmichel combinedmetabolicengineeringofprecursorandcofactorsupplytoincreaseasantaleneproductionbyitsaccharomycescerevisiaeit
AT davietlaurent combinedmetabolicengineeringofprecursorandcofactorsupplytoincreaseasantaleneproductionbyitsaccharomycescerevisiaeit
AT nielsenjens combinedmetabolicengineeringofprecursorandcofactorsupplytoincreaseasantaleneproductionbyitsaccharomycescerevisiaeit