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Laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity

The bacterial respiratory electron transport system (ETS) is branched to allow condition-specific modulation of energy metabolism. There is a detailed understanding of the structural and biochemical features of respiratory enzymes; however, a holistic examination of the system and its plasticity is...

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Autores principales: Anand, Amitesh, Patel, Arjun, Chen, Ke, Olson, Connor A., Phaneuf, Patrick V., Lamoureux, Cameron, Hefner, Ying, Szubin, Richard, Feist, Adam M., Palsson, Bernhard O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237125/
https://www.ncbi.nlm.nih.gov/pubmed/35760776
http://dx.doi.org/10.1038/s41467-022-30877-5
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author Anand, Amitesh
Patel, Arjun
Chen, Ke
Olson, Connor A.
Phaneuf, Patrick V.
Lamoureux, Cameron
Hefner, Ying
Szubin, Richard
Feist, Adam M.
Palsson, Bernhard O.
author_facet Anand, Amitesh
Patel, Arjun
Chen, Ke
Olson, Connor A.
Phaneuf, Patrick V.
Lamoureux, Cameron
Hefner, Ying
Szubin, Richard
Feist, Adam M.
Palsson, Bernhard O.
author_sort Anand, Amitesh
collection PubMed
description The bacterial respiratory electron transport system (ETS) is branched to allow condition-specific modulation of energy metabolism. There is a detailed understanding of the structural and biochemical features of respiratory enzymes; however, a holistic examination of the system and its plasticity is lacking. Here we generate four strains of Escherichia coli harboring unbranched ETS that pump 1, 2, 3, or 4 proton(s) per electron and characterized them using a combination of synergistic methods (adaptive laboratory evolution, multi-omic analyses, and computation of proteome allocation). We report that: (a) all four ETS variants evolve to a similar optimized growth rate, and (b) the laboratory evolutions generate specific rewiring of major energy-generating pathways, coupled to the ETS, to optimize ATP production capability. We thus define an Aero-Type System (ATS), which is a generalization of the aerobic bioenergetics and is a metabolic systems biology description of respiration and its inherent plasticity.
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spelling pubmed-92371252022-06-29 Laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity Anand, Amitesh Patel, Arjun Chen, Ke Olson, Connor A. Phaneuf, Patrick V. Lamoureux, Cameron Hefner, Ying Szubin, Richard Feist, Adam M. Palsson, Bernhard O. Nat Commun Article The bacterial respiratory electron transport system (ETS) is branched to allow condition-specific modulation of energy metabolism. There is a detailed understanding of the structural and biochemical features of respiratory enzymes; however, a holistic examination of the system and its plasticity is lacking. Here we generate four strains of Escherichia coli harboring unbranched ETS that pump 1, 2, 3, or 4 proton(s) per electron and characterized them using a combination of synergistic methods (adaptive laboratory evolution, multi-omic analyses, and computation of proteome allocation). We report that: (a) all four ETS variants evolve to a similar optimized growth rate, and (b) the laboratory evolutions generate specific rewiring of major energy-generating pathways, coupled to the ETS, to optimize ATP production capability. We thus define an Aero-Type System (ATS), which is a generalization of the aerobic bioenergetics and is a metabolic systems biology description of respiration and its inherent plasticity. Nature Publishing Group UK 2022-06-27 /pmc/articles/PMC9237125/ /pubmed/35760776 http://dx.doi.org/10.1038/s41467-022-30877-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Anand, Amitesh
Patel, Arjun
Chen, Ke
Olson, Connor A.
Phaneuf, Patrick V.
Lamoureux, Cameron
Hefner, Ying
Szubin, Richard
Feist, Adam M.
Palsson, Bernhard O.
Laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity
title Laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity
title_full Laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity
title_fullStr Laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity
title_full_unstemmed Laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity
title_short Laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity
title_sort laboratory evolution of synthetic electron transport system variants reveals a larger metabolic respiratory system and its plasticity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237125/
https://www.ncbi.nlm.nih.gov/pubmed/35760776
http://dx.doi.org/10.1038/s41467-022-30877-5
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