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Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles

BACKGROUND: Unicellular cyanobacteria of the genus Cyanothece are recognized for their ability to execute nitrogen (N(2))-fixation in the dark and photosynthesis in the light. An understanding of these mechanistic processes in an integrated systems context should provide insights into how Cyanothece...

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Autores principales: Aryal, Uma K, Stöckel, Jana, Krovvidi, Ravi K, Gritsenko, Marina A, Monroe, Matthew E, Moore, Ronald J, Koppenaal, David W, Smith, Richard D, Pakrasi, Himadri B, Jacobs, Jon M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261843/
https://www.ncbi.nlm.nih.gov/pubmed/22133144
http://dx.doi.org/10.1186/1752-0509-5-194
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author Aryal, Uma K
Stöckel, Jana
Krovvidi, Ravi K
Gritsenko, Marina A
Monroe, Matthew E
Moore, Ronald J
Koppenaal, David W
Smith, Richard D
Pakrasi, Himadri B
Jacobs, Jon M
author_facet Aryal, Uma K
Stöckel, Jana
Krovvidi, Ravi K
Gritsenko, Marina A
Monroe, Matthew E
Moore, Ronald J
Koppenaal, David W
Smith, Richard D
Pakrasi, Himadri B
Jacobs, Jon M
author_sort Aryal, Uma K
collection PubMed
description BACKGROUND: Unicellular cyanobacteria of the genus Cyanothece are recognized for their ability to execute nitrogen (N(2))-fixation in the dark and photosynthesis in the light. An understanding of these mechanistic processes in an integrated systems context should provide insights into how Cyanothece might be optimized for specialized environments and/or industrial purposes. Systems-wide dynamic proteomic profiling with mass spectrometry (MS) analysis should reveal fundamental insights into the control and regulation of these functions. RESULTS: To expand upon the current knowledge of protein expression patterns in Cyanothece ATCC51142, we performed quantitative proteomic analysis using partial ("unsaturated") metabolic labeling and high mass accuracy LC-MS analysis. This dynamic proteomic profiling identified 721 actively synthesized proteins with significant temporal changes in expression throughout the light-dark cycles, of which 425 proteins matched with previously characterized cycling transcripts. The remaining 296 proteins contained a cluster of proteins uniquely involved in DNA replication and repair, protein degradation, tRNA synthesis and modification, transport and binding, and regulatory functions. Functional classification of labeled proteins suggested that proteins involved in respiration and glycogen metabolism showed increased expression in the dark cycle together with nitrogenase, suggesting that N(2)-fixation is mediated by higher respiration and glycogen metabolism. Results indicated that Cyanothece ATCC51142 might utilize alternative pathways for carbon (C) and nitrogen (N) acquisition, particularly, aspartic acid and glutamate as substrates of C and N, respectively. Utilization of phosphoketolase (PHK) pathway for the conversion of xylulose-5P to pyruvate and acetyl-P likely constitutes an alternative strategy to compensate higher ATP and NADPH demand. CONCLUSION: This study provides a deeper systems level insight into how Cyanothece ATCC51142 modulates cellular functions to accommodate photosynthesis and N(2)-fixation within the single cell.
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spelling pubmed-32618432012-01-20 Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles Aryal, Uma K Stöckel, Jana Krovvidi, Ravi K Gritsenko, Marina A Monroe, Matthew E Moore, Ronald J Koppenaal, David W Smith, Richard D Pakrasi, Himadri B Jacobs, Jon M BMC Syst Biol Research Article BACKGROUND: Unicellular cyanobacteria of the genus Cyanothece are recognized for their ability to execute nitrogen (N(2))-fixation in the dark and photosynthesis in the light. An understanding of these mechanistic processes in an integrated systems context should provide insights into how Cyanothece might be optimized for specialized environments and/or industrial purposes. Systems-wide dynamic proteomic profiling with mass spectrometry (MS) analysis should reveal fundamental insights into the control and regulation of these functions. RESULTS: To expand upon the current knowledge of protein expression patterns in Cyanothece ATCC51142, we performed quantitative proteomic analysis using partial ("unsaturated") metabolic labeling and high mass accuracy LC-MS analysis. This dynamic proteomic profiling identified 721 actively synthesized proteins with significant temporal changes in expression throughout the light-dark cycles, of which 425 proteins matched with previously characterized cycling transcripts. The remaining 296 proteins contained a cluster of proteins uniquely involved in DNA replication and repair, protein degradation, tRNA synthesis and modification, transport and binding, and regulatory functions. Functional classification of labeled proteins suggested that proteins involved in respiration and glycogen metabolism showed increased expression in the dark cycle together with nitrogenase, suggesting that N(2)-fixation is mediated by higher respiration and glycogen metabolism. Results indicated that Cyanothece ATCC51142 might utilize alternative pathways for carbon (C) and nitrogen (N) acquisition, particularly, aspartic acid and glutamate as substrates of C and N, respectively. Utilization of phosphoketolase (PHK) pathway for the conversion of xylulose-5P to pyruvate and acetyl-P likely constitutes an alternative strategy to compensate higher ATP and NADPH demand. CONCLUSION: This study provides a deeper systems level insight into how Cyanothece ATCC51142 modulates cellular functions to accommodate photosynthesis and N(2)-fixation within the single cell. BioMed Central 2011-12-01 /pmc/articles/PMC3261843/ /pubmed/22133144 http://dx.doi.org/10.1186/1752-0509-5-194 Text en Copyright ©2011 Aryal et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Aryal, Uma K
Stöckel, Jana
Krovvidi, Ravi K
Gritsenko, Marina A
Monroe, Matthew E
Moore, Ronald J
Koppenaal, David W
Smith, Richard D
Pakrasi, Himadri B
Jacobs, Jon M
Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles
title Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles
title_full Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles
title_fullStr Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles
title_full_unstemmed Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles
title_short Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles
title_sort dynamic proteomic profiling of a unicellular cyanobacterium cyanothece atcc51142 across light-dark diurnal cycles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261843/
https://www.ncbi.nlm.nih.gov/pubmed/22133144
http://dx.doi.org/10.1186/1752-0509-5-194
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