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Quantitative Proteomic and Microcystin Production Response of Microcystis aeruginosa to Phosphorus Depletion

Microcystis blooms are the most widely distributed and frequently occurring cyanobacterial blooms in freshwater. Reducing phosphorus is suggested to be effective in mitigating cyanobacterial blooms, while the underlying molecular mechanisms are yet to be elucidated. In the present study, isobaric ta...

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Autores principales: Wei, Nian, Song, Lirong, Gan, Nanqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227402/
https://www.ncbi.nlm.nih.gov/pubmed/34072711
http://dx.doi.org/10.3390/microorganisms9061183
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author Wei, Nian
Song, Lirong
Gan, Nanqin
author_facet Wei, Nian
Song, Lirong
Gan, Nanqin
author_sort Wei, Nian
collection PubMed
description Microcystis blooms are the most widely distributed and frequently occurring cyanobacterial blooms in freshwater. Reducing phosphorus is suggested to be effective in mitigating cyanobacterial blooms, while the underlying molecular mechanisms are yet to be elucidated. In the present study, isobaric tags for relative and absolute quantitation (iTRAQ)-based quantitative proteomics was employed to study the effects of phosphorus depletion on Microcystis aeruginosa FACHB-905. The production of microcystins (MCs), a severe hazard of Microcystis blooms, was also analyzed. In total, 230 proteins were found to be differentially abundant, with 136 downregulated proteins. The results revealed that, upon phosphorus limitation stress, Microcystis aeruginosa FACHB-905 raised the availability of phosphorus primarily by upregulating the expression of orthophosphate transport system proteins, with no alkaline phosphatase producing ability. Phosphorus depletion remarkably inhibited cell growth and the primary metabolic processes of Microcystis, including transcription, translation and photosynthesis, with structures of photosystems remaining intact. Moreover, expression of nitrogen assimilation proteins was downregulated, while proteins involved in carbon catabolism were significantly upregulated, which was considered beneficial for the intracellular balance among carbon, nitrogen and phosphorus. The expression of MC synthetase was not significantly different upon phosphorus depletion, while MC content was significantly suppressed. It is assumed that phosphorus depletion indirectly regulates the production of MC by the inhibition of metabolic processes and energy production. These results contribute to further understanding of the influence mechanisms of phosphorus depletion on both biological processes and MC production in Microcystis cells.
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spelling pubmed-82274022021-06-26 Quantitative Proteomic and Microcystin Production Response of Microcystis aeruginosa to Phosphorus Depletion Wei, Nian Song, Lirong Gan, Nanqin Microorganisms Article Microcystis blooms are the most widely distributed and frequently occurring cyanobacterial blooms in freshwater. Reducing phosphorus is suggested to be effective in mitigating cyanobacterial blooms, while the underlying molecular mechanisms are yet to be elucidated. In the present study, isobaric tags for relative and absolute quantitation (iTRAQ)-based quantitative proteomics was employed to study the effects of phosphorus depletion on Microcystis aeruginosa FACHB-905. The production of microcystins (MCs), a severe hazard of Microcystis blooms, was also analyzed. In total, 230 proteins were found to be differentially abundant, with 136 downregulated proteins. The results revealed that, upon phosphorus limitation stress, Microcystis aeruginosa FACHB-905 raised the availability of phosphorus primarily by upregulating the expression of orthophosphate transport system proteins, with no alkaline phosphatase producing ability. Phosphorus depletion remarkably inhibited cell growth and the primary metabolic processes of Microcystis, including transcription, translation and photosynthesis, with structures of photosystems remaining intact. Moreover, expression of nitrogen assimilation proteins was downregulated, while proteins involved in carbon catabolism were significantly upregulated, which was considered beneficial for the intracellular balance among carbon, nitrogen and phosphorus. The expression of MC synthetase was not significantly different upon phosphorus depletion, while MC content was significantly suppressed. It is assumed that phosphorus depletion indirectly regulates the production of MC by the inhibition of metabolic processes and energy production. These results contribute to further understanding of the influence mechanisms of phosphorus depletion on both biological processes and MC production in Microcystis cells. MDPI 2021-05-31 /pmc/articles/PMC8227402/ /pubmed/34072711 http://dx.doi.org/10.3390/microorganisms9061183 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wei, Nian
Song, Lirong
Gan, Nanqin
Quantitative Proteomic and Microcystin Production Response of Microcystis aeruginosa to Phosphorus Depletion
title Quantitative Proteomic and Microcystin Production Response of Microcystis aeruginosa to Phosphorus Depletion
title_full Quantitative Proteomic and Microcystin Production Response of Microcystis aeruginosa to Phosphorus Depletion
title_fullStr Quantitative Proteomic and Microcystin Production Response of Microcystis aeruginosa to Phosphorus Depletion
title_full_unstemmed Quantitative Proteomic and Microcystin Production Response of Microcystis aeruginosa to Phosphorus Depletion
title_short Quantitative Proteomic and Microcystin Production Response of Microcystis aeruginosa to Phosphorus Depletion
title_sort quantitative proteomic and microcystin production response of microcystis aeruginosa to phosphorus depletion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227402/
https://www.ncbi.nlm.nih.gov/pubmed/34072711
http://dx.doi.org/10.3390/microorganisms9061183
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