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Nitrogen limitation reveals large reserves in metabolic and translational capacities of yeast

Yu, R. (author)
Campbell, Kate, 1987 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Pereira, Rui, 1986 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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Björkeroth, Johan, 1990 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Qi, Qi, 1992 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Vorontsov, Egor, 1988 (author)
Gothenburg University,Göteborgs universitet,Core Facilities, Proteomics,Core Facilities, Proteomics,University of Gothenburg
Sihlbom, Carina, 1973 (author)
Gothenburg University,Göteborgs universitet,Core Facilities, Proteomics,Core Facilities, Proteomics,University of Gothenburg
Nielsen, Jens B, 1962 (author)
Danmarks Tekniske Universitet,Technical University of Denmark,Chalmers tekniska högskola,Chalmers University of Technology,BioInnovation Institute (BII)
Yu, Tao, 1988 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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 (creator_code:org_t)
2020-04-20
2020
English.
In: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 11:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Cells maintain reserves in their metabolic and translational capacities as a strategy to quickly respond to changing environments. Here we quantify these reserves by stepwisereducing nitrogen availability in yeast steady-state chemostat cultures, imposing severe restrictions on total cellular protein and transcript content. Combining multi-omics analysis with metabolic modeling, we find that seven metabolic superpathways maintain >50% metabolic capacity in reserve, with glucose metabolism maintaining >80% reserve capacity. Cells maintain >50% reserve in translational capacity for 2490 out of 3361 expressed genes (74%), with a disproportionately large reserve dedicated to translating metabolic proteins. Finally, ribosome reserves contain up to 30% sub-stoichiometric ribosomal proteins, with activation of reserve translational capacity associated with selective upregulation of 17 ribosomal proteins. Together, our dataset provides a quantitative link between yeast physiology and cellular economics, which could be leveraged in future cell engineering through targeted proteome streamlining. © 2020, The Author(s).

Subject headings

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)
NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Industriell bioteknik -- Annan industriell bioteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Industrial Biotechnology -- Other Industrial Biotechnology (hsv//eng)

Keyword

cell protein
proteome
ribosome protein
transcriptome
bioengineering
cell component
chemostat
crassulacean acid metabolism
glucose
metabolism
nitrogen
protein
proteomics
yeast
Article
biomass production
cell engineering
data processing
fungal cell culture
gene expression
glucose metabolism
high performance liquid chromatography
liquid chromatography-mass spectrometry
metabolic capacity
metabolic flux analysis
metabolomics
multiomics
nitrogen availability
nitrogen limitation
nitrogen metabolism
nonhuman
nutrient limitation
protein analysis
protein expression
quantitative analysis
RNA analysis
RNA extraction
RNA translation
Saccharomyces cerevisiae
steady state
transcriptome sequencing
transcriptomics
upregulation

Publication and Content Type

ref (subject category)
art (subject category)

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