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Protein allocation and utilization in the versatile chemolithoautotroph Cupriavidus necator

Bacteria must balance the different needs for substrate assimilation, growth functions, and resilience in order to thrive in their environment. Of all cellular macromolecules, the bacterial proteome is by far the most important resource and its size is limited. Here, we investigated how the highly v...

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Autores principales: Jahn, Michael, Crang, Nick, Janasch, Markus, Hober, Andreas, Forsström, Björn, Kimler, Kyle, Mattausch, Alexander, Chen, Qi, Asplund-Samuelsson, Johannes, Hudson, Elton Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591527/
https://www.ncbi.nlm.nih.gov/pubmed/34723797
http://dx.doi.org/10.7554/eLife.69019
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author Jahn, Michael
Crang, Nick
Janasch, Markus
Hober, Andreas
Forsström, Björn
Kimler, Kyle
Mattausch, Alexander
Chen, Qi
Asplund-Samuelsson, Johannes
Hudson, Elton Paul
author_facet Jahn, Michael
Crang, Nick
Janasch, Markus
Hober, Andreas
Forsström, Björn
Kimler, Kyle
Mattausch, Alexander
Chen, Qi
Asplund-Samuelsson, Johannes
Hudson, Elton Paul
author_sort Jahn, Michael
collection PubMed
description Bacteria must balance the different needs for substrate assimilation, growth functions, and resilience in order to thrive in their environment. Of all cellular macromolecules, the bacterial proteome is by far the most important resource and its size is limited. Here, we investigated how the highly versatile 'knallgas' bacterium Cupriavidus necator reallocates protein resources when grown on different limiting substrates and with different growth rates. We determined protein quantity by mass spectrometry and estimated enzyme utilization by resource balance analysis modeling. We found that C. necator invests a large fraction of its proteome in functions that are hardly utilized. Of the enzymes that are utilized, many are present in excess abundance. One prominent example is the strong expression of CBB cycle genes such as Rubisco during growth on fructose. Modeling and mutant competition experiments suggest that CO(2)-reassimilation through Rubisco does not provide a fitness benefit for heterotrophic growth, but is rather an investment in readiness for autotrophy.
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spelling pubmed-85915272021-11-16 Protein allocation and utilization in the versatile chemolithoautotroph Cupriavidus necator Jahn, Michael Crang, Nick Janasch, Markus Hober, Andreas Forsström, Björn Kimler, Kyle Mattausch, Alexander Chen, Qi Asplund-Samuelsson, Johannes Hudson, Elton Paul eLife Computational and Systems Biology Bacteria must balance the different needs for substrate assimilation, growth functions, and resilience in order to thrive in their environment. Of all cellular macromolecules, the bacterial proteome is by far the most important resource and its size is limited. Here, we investigated how the highly versatile 'knallgas' bacterium Cupriavidus necator reallocates protein resources when grown on different limiting substrates and with different growth rates. We determined protein quantity by mass spectrometry and estimated enzyme utilization by resource balance analysis modeling. We found that C. necator invests a large fraction of its proteome in functions that are hardly utilized. Of the enzymes that are utilized, many are present in excess abundance. One prominent example is the strong expression of CBB cycle genes such as Rubisco during growth on fructose. Modeling and mutant competition experiments suggest that CO(2)-reassimilation through Rubisco does not provide a fitness benefit for heterotrophic growth, but is rather an investment in readiness for autotrophy. eLife Sciences Publications, Ltd 2021-11-01 /pmc/articles/PMC8591527/ /pubmed/34723797 http://dx.doi.org/10.7554/eLife.69019 Text en © 2021, Jahn et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Jahn, Michael
Crang, Nick
Janasch, Markus
Hober, Andreas
Forsström, Björn
Kimler, Kyle
Mattausch, Alexander
Chen, Qi
Asplund-Samuelsson, Johannes
Hudson, Elton Paul
Protein allocation and utilization in the versatile chemolithoautotroph Cupriavidus necator
title Protein allocation and utilization in the versatile chemolithoautotroph Cupriavidus necator
title_full Protein allocation and utilization in the versatile chemolithoautotroph Cupriavidus necator
title_fullStr Protein allocation and utilization in the versatile chemolithoautotroph Cupriavidus necator
title_full_unstemmed Protein allocation and utilization in the versatile chemolithoautotroph Cupriavidus necator
title_short Protein allocation and utilization in the versatile chemolithoautotroph Cupriavidus necator
title_sort protein allocation and utilization in the versatile chemolithoautotroph cupriavidus necator
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591527/
https://www.ncbi.nlm.nih.gov/pubmed/34723797
http://dx.doi.org/10.7554/eLife.69019
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