Genome-scale model of Rhodotorula toruloides metabolism.


Journal

Biotechnology and bioengineering
ISSN: 1097-0290
Titre abrégé: Biotechnol Bioeng
Pays: United States
ID NLM: 7502021

Informations de publication

Date de publication:
12 2019
Historique:
received: 01 04 2019
revised: 08 08 2019
accepted: 05 09 2019
pubmed: 11 9 2019
medline: 17 9 2020
entrez: 11 9 2019
Statut: ppublish

Résumé

The basidiomycete red yeast Rhodotorula toruloides is a promising platform organism for production of biooils. We present rhto-GEM, the first genome-scale model (GEM) of R. toruloides metabolism, that was largely reconstructed using RAVEN toolbox. The model includes 852 genes, 2,731 reactions, and 2,277 metabolites, while lipid metabolism is described using the SLIMEr formalism allowing direct integration of lipid class and acyl chain experimental distribution data. The simulation results confirmed that the R. toruloides model provides valid growth predictions on glucose, xylose, and glycerol, while prediction of genetic engineering targets to increase production of linolenic acid, triacylglycerols, and carotenoids identified genes-some of which have previously been engineered to successfully increase production. This renders rtho-GEM valuable for future studies to improve the production of other oleochemicals of industrial relevance including value-added fatty acids and carotenoids, in addition to facilitate system-wide omics-data analysis in R. toruloides. Expanding the portfolio of GEMs for lipid-accumulating fungi contributes to both understanding of metabolic mechanisms of the oleaginous phenotype but also uncover particularities of the lipid production machinery in R. toruloides.

Identifiants

pubmed: 31502665
doi: 10.1002/bit.27162
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3396-3408

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Ievgeniia A Tiukova (IA)

Systems and Synthetic Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Department of Molecular Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.

Sylvain Prigent (S)

UMR 1332 BFP, Univ Bordeaux, Villenave d'Ornon, France.

Jens Nielsen (J)

Systems and Synthetic Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.

Mats Sandgren (M)

Department of Molecular Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.

Eduard J Kerkhoven (EJ)

Systems and Synthetic Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.

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