Evidence map›Paper›PMID 26503450›Full record

ArticleBMC systems biology2015

Optimization of lipid production with a genome-scale model of Yarrowia lipolytica.

Martin Kavšček, Govindprasad Bhutada, Tobias Madl, Klaus Natter

Open access · diamondAbstract readValidation Study
In one paragraph

Article in BMC systems biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
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  5. Review
  6. Frontiers in bioengineering and biotechnology · 2025
    Review
  7. Genome-scale model development and genomic sequencing of the oleaginous cladeFrontiers in bioengineering and biotechnology · 2024
    Article
  8. Review
  9. Article
  10. Construction and application of the genome-scale metabolic model ofFrontiers in bioengineering and biotechnology · 2023
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Metabolomics-driven strain improvement: A mini review.Frontiers in molecular biosciences · 2022
    Review
  16. Dissecting carbon metabolism ofComputational and structural biotechnology journal · 2022
    Article
  17. Review
  18. Article
  19. Journal of fungi (Basel, Switzerland) · 2021
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Martin KavščekInstitute of Molecular Biosciences, BioTechMed Graz, University of Graz, Humboldtstrasse 50/II, 8010, Graz, Austria. martin.kavscek@uni-graz.at.
Govindprasad BhutadaInstitute of Molecular Biosciences, BioTechMed Graz, University of Graz, Humboldtstrasse 50/II, 8010, Graz, Austria. govindprasad.bhutada@uni-graz.at.
Tobias MadlInstitute of Molecular Biology and Biochemistry, Medical University of Graz, Graz, Austria. t.madl@tum.de.
Klaus NatterInstitute of Molecular Biosciences, BioTechMed Graz, University of Graz, Humboldtstrasse 50/II, 8010, Graz, Austria. klaus.natter@uni-graz.at.
University of Graz · ATCenter for Integrated Protein Science Munich · DE

Funding

Austrian Science Fund FWF TRP 240
6 · The paper itself

Abstract

backgroundYarrowia lipolytica is a non-conventional yeast that is extensively investigated for its ability to excrete citrate or to accumulate large amounts of storage lipids, which is of great significance for single cell oil production. Both traits are thus of interest for basic research as well as for biotechnological applications but they typically occur simultaneously thus lowering the respective yields. Therefore, engineering of strains with high lipid content relies on novel concepts such as computational simulation to better understand the two competing processes and to eliminate citrate excretion.

resultsUsing a genome-scale model (GSM) of baker's yeast as a scaffold, we reconstructed the metabolic network of Y. lipolytica and optimized it for use in flux balance analysis (FBA), with the aim to simulate growth and lipid production phases of this yeast. We validated our model and found the predictions of the growth behavior of Y. lipolytica in excellent agreement with experimental data. Based on these data, we successfully designed a fed-batch strategy to avoid citrate excretion during the lipid production phase. Further analysis of the network suggested that the oxygen demand of Y. lipolytica is reduced upon induction of lipid synthesis. According to this finding we hypothesized that a reduced aeration rate might induce lipid accumulation. This prediction was indeed confirmed experimentally. In a fermentation combining these two strategies lipid content of the biomass was increased by 80%, and lipid yield was improved more than four-fold, compared to standard conditions.

conclusionsGenome scale network reconstructions provide a powerful tool to predict the effects of genetic modifications and the metabolic response to environmental conditions. The high accuracy and the predictive value of a newly reconstructed GSM of Y. lipolytica to optimize growth conditions for lipid accumulation are demonstrated. Based on these findings, further strategies for engineering Y. lipolytica towards higher efficiency in single cell oil production are discussed.

Indexed as

Genome, FungalBiological Oxygen Demand AnalysisBiomassCitric AcidFermentationGenetic EngineeringLipid MetabolismMetabolic Flux AnalysisMetabolic Networks and PathwaysModels, TheoreticalNADPNitrogenOrganisms, Genetically ModifiedPentose Phosphate PathwayYarrowiaCitric AcidNADPNitrogen

Identifiers

PMID26503450
PMCPMC4623914
OpenAlexW1821513802

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.