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 in | NPJ systems biology and applications Vol. 2; no. 1; p. 16005 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
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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 givenname: Eduard J 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 – sequence: 4 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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PublicationYear | 2016 |
Publisher | Nature Publishing Group UK Nature Publishing Group Springer Nature |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group – name: Springer Nature |
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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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SubjectTerms | 631/326 631/553/1833 631/553/318 631/61 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 |
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