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Characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria

Protein redox chemistry constitutes a major void in knowledge pertaining to photoautotrophic system regulation and signaling processes. We have employed a chemical biology approach to analyze redox sensitive proteins in live Synechococcus sp. PCC 7002 cells in both light and dark periods, and to und...

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Autores principales: Ansong, Charles, Sadler, Natalie C., Hill, Eric A., Lewis, Michael P., Zink, Erika M., Smith, Richard D., Beliaev, Alexander S., Konopka, Allan E., Wright, Aaron T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080843/
https://www.ncbi.nlm.nih.gov/pubmed/25071738
http://dx.doi.org/10.3389/fmicb.2014.00325
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author Ansong, Charles
Sadler, Natalie C.
Hill, Eric A.
Lewis, Michael P.
Zink, Erika M.
Smith, Richard D.
Beliaev, Alexander S.
Konopka, Allan E.
Wright, Aaron T.
author_facet Ansong, Charles
Sadler, Natalie C.
Hill, Eric A.
Lewis, Michael P.
Zink, Erika M.
Smith, Richard D.
Beliaev, Alexander S.
Konopka, Allan E.
Wright, Aaron T.
author_sort Ansong, Charles
collection PubMed
description Protein redox chemistry constitutes a major void in knowledge pertaining to photoautotrophic system regulation and signaling processes. We have employed a chemical biology approach to analyze redox sensitive proteins in live Synechococcus sp. PCC 7002 cells in both light and dark periods, and to understand how cellular redox balance is disrupted during nutrient perturbation. The present work identified 300 putative redox-sensitive proteins that are involved in the generation of reductant, macromolecule synthesis, and carbon flux through central metabolic pathways, and may be involved in cell signaling and response mechanisms. Furthermore, our research suggests that dynamic redox changes in response to specific nutrient limitations, including carbon and nitrogen limitations, contribute to the regulatory changes driven by a shift from light to dark. Taken together, these results contribute to a high-level understanding of post-translational mechanisms regulating flux distributions and suggest potential metabolic engineering targets for redirecting carbon toward biofuel precursors.
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spelling pubmed-40808432014-07-28 Characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria Ansong, Charles Sadler, Natalie C. Hill, Eric A. Lewis, Michael P. Zink, Erika M. Smith, Richard D. Beliaev, Alexander S. Konopka, Allan E. Wright, Aaron T. Front Microbiol Microbiology Protein redox chemistry constitutes a major void in knowledge pertaining to photoautotrophic system regulation and signaling processes. We have employed a chemical biology approach to analyze redox sensitive proteins in live Synechococcus sp. PCC 7002 cells in both light and dark periods, and to understand how cellular redox balance is disrupted during nutrient perturbation. The present work identified 300 putative redox-sensitive proteins that are involved in the generation of reductant, macromolecule synthesis, and carbon flux through central metabolic pathways, and may be involved in cell signaling and response mechanisms. Furthermore, our research suggests that dynamic redox changes in response to specific nutrient limitations, including carbon and nitrogen limitations, contribute to the regulatory changes driven by a shift from light to dark. Taken together, these results contribute to a high-level understanding of post-translational mechanisms regulating flux distributions and suggest potential metabolic engineering targets for redirecting carbon toward biofuel precursors. Frontiers Media S.A. 2014-07-03 /pmc/articles/PMC4080843/ /pubmed/25071738 http://dx.doi.org/10.3389/fmicb.2014.00325 Text en Copyright © 2014 Ansong, Sadler, Hill, Lewis, Zink, Smith, Beliaev, Konopka and Wright. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Ansong, Charles
Sadler, Natalie C.
Hill, Eric A.
Lewis, Michael P.
Zink, Erika M.
Smith, Richard D.
Beliaev, Alexander S.
Konopka, Allan E.
Wright, Aaron T.
Characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria
title Characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria
title_full Characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria
title_fullStr Characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria
title_full_unstemmed Characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria
title_short Characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria
title_sort characterization of protein redox dynamics induced during light-to-dark transitions and nutrient limitation in cyanobacteria
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080843/
https://www.ncbi.nlm.nih.gov/pubmed/25071738
http://dx.doi.org/10.3389/fmicb.2014.00325
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