Regulation of amino-acid metabolism controls flux to lipid accumulation in Yarrowia lipolytica

Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its metabolism. Here we performed the first integrated data analysis of Y. lipolytica grown in carbon and nitrogen limited chemostat cu...

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Published inNPJ systems biology and applications Vol. 2; no. 1; p. 16005
Main Authors Kerkhoven, Eduard J, Pomraning, Kyle R, Baker, Scott E, Nielsen, Jens
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.01.2016
Nature Publishing Group
Springer Nature
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Abstract Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its metabolism. Here we performed the first integrated data analysis of Y. lipolytica grown in carbon and nitrogen limited chemostat cultures. We first reconstructed a genome-scale metabolic model and used this for integrative analysis of multilevel omics data. Metabolite profiling and lipidomics was used to quantify the cellular physiology, while regulatory changes were measured using RNAseq. Analysis of the data showed that lipid accumulation in Y. lipolytica does not involve transcriptional regulation of lipid metabolism but is associated with regulation of amino-acid biosynthesis, resulting in redirection of carbon flux during nitrogen limitation from amino acids to lipids. Lipid accumulation in Y. lipolytica at nitrogen limitation is similar to the overflow metabolism observed in many other microorganisms, e.g. ethanol production by Sacchromyces cerevisiae at nitrogen limitation. Biofuels: Yeast produces fatty oils in absence of nitrogen When nitrogen is in short supply, the yeast Yarrowia lipolytica redirects its energy production from protein building blocks to fatty lipids. Scientists hope to use Y. lipolytica as a microbial factory to produce fat-based biofuels, and these findings could help them create cells with greater lipid yields. A team led by Eduard Kerkhoven from Chalmers University of Technology in Göteborg, Sweden, constructed a comprehensive metabolic model of Y. lipolytica grown in a bioreactor under different nutrient conditions. At low nitrogen levels, the researchers observed lipid accumulation in the cell, although the regulation of fat metabolism was unchanged. What did change was amino acid synthesis, which was tamped down, leading to an overflow in fat production–in the same way that baker’s yeast, Saccharomyces cerevisiae , produces ethanol when nitrogen is limited.
AbstractList is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its metabolism. Here we performed the first integrated data analysis of grown in carbon and nitrogen limited chemostat cultures. We first reconstructed a genome-scale metabolic model and used this for integrative analysis of multilevel omics data. Metabolite profiling and lipidomics was used to quantify the cellular physiology, while regulatory changes were measured using RNAseq. Analysis of the data showed that lipid accumulation in does not involve transcriptional regulation of lipid metabolism but is associated with regulation of amino-acid biosynthesis, resulting in redirection of carbon flux during nitrogen limitation from amino acids to lipids. Lipid accumulation in at nitrogen limitation is similar to the overflow metabolism observed in many other microorganisms, e.g. ethanol production by at nitrogen limitation.
Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its metabolism. Here we performed the first integrated data analysis of Y. lipolytica grown in carbon and nitrogen limited chemostat cultures. We first reconstructed a genome-scale metabolic model and used this for integrative analysis of multilevel omics data. Metabolite profiling and lipidomics was used to quantify the cellular physiology, while regulatory changes were measured using RNAseq. Analysis of the data showed that lipid accumulation in Y. lipolytica does not involve transcriptional regulation of lipid metabolism but is associated with regulation of amino-acid biosynthesis, resulting in redirection of carbon flux during nitrogen limitation from amino acids to lipids. Lipid accumulation in Y. lipolytica at nitrogen limitation is similar to the overflow metabolism observed in many other microorganisms, e.g. ethanol production by Sacchromyces cerevisiae at nitrogen limitation.
Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its metabolism. Here we performed the first integrated data analysis of Y. lipolytica grown in carbon and nitrogen limited chemostat cultures. We first reconstructed a genome-scale metabolic model and used this for integrative analysis of multilevel omics data. Metabolite profiling and lipidomics was used to quantify the cellular physiology, while regulatory changes were measured using RNAseq. Analysis of the data showed that lipid accumulation in Y. lipolytica does not involve transcriptional regulation of lipid metabolism but is associated with regulation of amino-acid biosynthesis, resulting in redirection of carbon flux during nitrogen limitation from amino acids to lipids. Lipid accumulation in Y. lipolytica at nitrogen limitation is similar to the overflow metabolism observed in many other microorganisms, e.g. ethanol production by Sacchromyces cerevisiae at nitrogen limitation.
Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its metabolism. Here we performed the first integrated data analysis of Y. lipolytica grown in carbon and nitrogen limited chemostat cultures. We first reconstructed a genome-scale metabolic model and used this for integrative analysis of multilevel omics data. Metabolite profiling and lipidomics was used to quantify the cellular physiology, while regulatory changes were measured using RNAseq. Analysis of the data showed that lipid accumulation in Y. lipolytica does not involve transcriptional regulation of lipid metabolism but is associated with regulation of amino-acid biosynthesis, resulting in redirection of carbon flux during nitrogen limitation from amino acids to lipids. Lipid accumulation in Y. lipolytica at nitrogen limitation is similar to the overflow metabolism observed in many other microorganisms, e.g. ethanol production by Sacchromyces cerevisiae at nitrogen limitation.Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its metabolism. Here we performed the first integrated data analysis of Y. lipolytica grown in carbon and nitrogen limited chemostat cultures. We first reconstructed a genome-scale metabolic model and used this for integrative analysis of multilevel omics data. Metabolite profiling and lipidomics was used to quantify the cellular physiology, while regulatory changes were measured using RNAseq. Analysis of the data showed that lipid accumulation in Y. lipolytica does not involve transcriptional regulation of lipid metabolism but is associated with regulation of amino-acid biosynthesis, resulting in redirection of carbon flux during nitrogen limitation from amino acids to lipids. Lipid accumulation in Y. lipolytica at nitrogen limitation is similar to the overflow metabolism observed in many other microorganisms, e.g. ethanol production by Sacchromyces cerevisiae at nitrogen limitation.
Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its metabolism. Here we performed the first integrated data analysis of Y. lipolytica grown in carbon and nitrogen limited chemostat cultures. We first reconstructed a genome-scale metabolic model and used this for integrative analysis of multilevel omics data. Metabolite profiling and lipidomics was used to quantify the cellular physiology, while regulatory changes were measured using RNAseq. Analysis of the data showed that lipid accumulation in Y. lipolytica does not involve transcriptional regulation of lipid metabolism but is associated with regulation of amino-acid biosynthesis, resulting in redirection of carbon flux during nitrogen limitation from amino acids to lipids. Lipid accumulation in Y. lipolytica at nitrogen limitation is similar to the overflow metabolism observed in many other microorganisms, e.g. ethanol production by Sacchromyces cerevisiae at nitrogen limitation. Biofuels: Yeast produces fatty oils in absence of nitrogen When nitrogen is in short supply, the yeast Yarrowia lipolytica redirects its energy production from protein building blocks to fatty lipids. Scientists hope to use Y. lipolytica as a microbial factory to produce fat-based biofuels, and these findings could help them create cells with greater lipid yields. A team led by Eduard Kerkhoven from Chalmers University of Technology in Göteborg, Sweden, constructed a comprehensive metabolic model of Y. lipolytica grown in a bioreactor under different nutrient conditions. At low nitrogen levels, the researchers observed lipid accumulation in the cell, although the regulation of fat metabolism was unchanged. What did change was amino acid synthesis, which was tamped down, leading to an overflow in fat production–in the same way that baker’s yeast, Saccharomyces cerevisiae , produces ethanol when nitrogen is limited.
ArticleNumber 16005
Author Nielsen, Jens
Kerkhoven, Eduard J
Pomraning, Kyle R
Baker, Scott E
Author_xml – sequence: 1
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  orcidid: 0000-0002-3593-5792
  surname: Kerkhoven
  fullname: Kerkhoven, Eduard J
  organization: Department of Biology and Biological Engineering, Systems and Synthetic Biology, Chalmers University of Technology
– sequence: 2
  givenname: Kyle R
  surname: Pomraning
  fullname: Pomraning, Kyle R
  organization: Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory
– sequence: 3
  givenname: Scott E
  surname: Baker
  fullname: Baker, Scott E
  organization: Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory
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  givenname: Jens
  orcidid: 0000-0002-9955-6003
  surname: Nielsen
  fullname: Nielsen, Jens
  email: nielsenj@chalmers.se
  organization: Department of Biology and Biological Engineering, Systems and Synthetic Biology, Chalmers University of Technology, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28725468$$D View this record in MEDLINE/PubMed
https://www.osti.gov/servlets/purl/1624016$$D View this record in Osti.gov
https://research.chalmers.se/publication/505139$$DView record from Swedish Publication Index
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ContentType Journal Article
Copyright The Author(s) 2016
Copyright Nature Publishing Group Mar 2016
Copyright © 2016 The Systems Biology Institute/Macmillan Publishers Limited 2016 The Systems Biology Institute/Macmillan Publishers Limited
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Technical Univ. of Denmark, Hørsholm (Denmark)
Chalmers Univ. of Technology, Göteborg (Sweden)
Pacific Northwest National Laboratory (PNNL), Richland, WA (United States)
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Snippet Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on...
is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on regulation of its...
Yarrowia lipolytica is a promising microbial cell factory for the production of lipids to be used as fuels and chemicals, but there are few studies on...
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BASIC BIOLOGICAL SCIENCES
Bioinformatics
biotechnology
chemostat
Computational Biology/Bioinformatics
Computer Appl. in Life Sciences
Life Sciences
lipid
metabolic engineering
microbiology
systems analysis
Systems Biology
Yarrowia lipolytica
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Title Regulation of amino-acid metabolism controls flux to lipid accumulation in Yarrowia lipolytica
URI https://link.springer.com/article/10.1038/npjsba.2016.5
https://www.ncbi.nlm.nih.gov/pubmed/28725468
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Volume 2
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