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Carboxysome Mispositioning Alters Growth, Morphology, and Rubisco Level of the Cyanobacterium Synechococcus elongatus PCC 7942

Cyanobacteria are the prokaryotic group of phytoplankton responsible for a significant fraction of global CO(2) fixation. Like plants, cyanobacteria use the enzyme ribulose 1,5-bisphosphate carboxylase/oxidase (Rubisco) to fix CO(2) into organic carbon molecules via the Calvin-Benson-Bassham cycle....

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Autores principales: Rillema, Rees, Hoang, Y, MacCready, Joshua S., Vecchiarelli, Anthony G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406218/
https://www.ncbi.nlm.nih.gov/pubmed/34340540
http://dx.doi.org/10.1128/mBio.02696-20
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author Rillema, Rees
Hoang, Y
MacCready, Joshua S.
Vecchiarelli, Anthony G.
author_facet Rillema, Rees
Hoang, Y
MacCready, Joshua S.
Vecchiarelli, Anthony G.
author_sort Rillema, Rees
collection PubMed
description Cyanobacteria are the prokaryotic group of phytoplankton responsible for a significant fraction of global CO(2) fixation. Like plants, cyanobacteria use the enzyme ribulose 1,5-bisphosphate carboxylase/oxidase (Rubisco) to fix CO(2) into organic carbon molecules via the Calvin-Benson-Bassham cycle. Unlike plants, cyanobacteria evolved a carbon-concentrating organelle called the carboxysome—a proteinaceous compartment that encapsulates and concentrates Rubisco along with its CO(2) substrate. In the rod-shaped cyanobacterium Synechococcus elongatus PCC 7942, we recently identified the McdAB system responsible for uniformly distributing carboxysomes along the cell length. It remains unknown what role carboxysome positioning plays with respect to cellular physiology. Here, we show that a failure to distribute carboxysomes leads to slower cell growth, cell elongation, asymmetric cell division, and elevated levels of cellular Rubisco. Unexpectedly, we also report that even wild-type S. elongatus undergoes cell elongation and asymmetric cell division when grown at the cool, but environmentally relevant, growth temperature of 20°C or when switched from a high- to ambient-CO(2) environment. The findings suggest that carboxysome positioning by the McdAB system functions to maintain the carbon fixation efficiency of Rubisco by preventing carboxysome aggregation, which is particularly important under growth conditions where rod-shaped cyanobacteria adopt a filamentous morphology.
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spelling pubmed-84062182021-09-09 Carboxysome Mispositioning Alters Growth, Morphology, and Rubisco Level of the Cyanobacterium Synechococcus elongatus PCC 7942 Rillema, Rees Hoang, Y MacCready, Joshua S. Vecchiarelli, Anthony G. mBio Research Article Cyanobacteria are the prokaryotic group of phytoplankton responsible for a significant fraction of global CO(2) fixation. Like plants, cyanobacteria use the enzyme ribulose 1,5-bisphosphate carboxylase/oxidase (Rubisco) to fix CO(2) into organic carbon molecules via the Calvin-Benson-Bassham cycle. Unlike plants, cyanobacteria evolved a carbon-concentrating organelle called the carboxysome—a proteinaceous compartment that encapsulates and concentrates Rubisco along with its CO(2) substrate. In the rod-shaped cyanobacterium Synechococcus elongatus PCC 7942, we recently identified the McdAB system responsible for uniformly distributing carboxysomes along the cell length. It remains unknown what role carboxysome positioning plays with respect to cellular physiology. Here, we show that a failure to distribute carboxysomes leads to slower cell growth, cell elongation, asymmetric cell division, and elevated levels of cellular Rubisco. Unexpectedly, we also report that even wild-type S. elongatus undergoes cell elongation and asymmetric cell division when grown at the cool, but environmentally relevant, growth temperature of 20°C or when switched from a high- to ambient-CO(2) environment. The findings suggest that carboxysome positioning by the McdAB system functions to maintain the carbon fixation efficiency of Rubisco by preventing carboxysome aggregation, which is particularly important under growth conditions where rod-shaped cyanobacteria adopt a filamentous morphology. American Society for Microbiology 2021-08-03 /pmc/articles/PMC8406218/ /pubmed/34340540 http://dx.doi.org/10.1128/mBio.02696-20 Text en Copyright © 2021 Rillema et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Rillema, Rees
Hoang, Y
MacCready, Joshua S.
Vecchiarelli, Anthony G.
Carboxysome Mispositioning Alters Growth, Morphology, and Rubisco Level of the Cyanobacterium Synechococcus elongatus PCC 7942
title Carboxysome Mispositioning Alters Growth, Morphology, and Rubisco Level of the Cyanobacterium Synechococcus elongatus PCC 7942
title_full Carboxysome Mispositioning Alters Growth, Morphology, and Rubisco Level of the Cyanobacterium Synechococcus elongatus PCC 7942
title_fullStr Carboxysome Mispositioning Alters Growth, Morphology, and Rubisco Level of the Cyanobacterium Synechococcus elongatus PCC 7942
title_full_unstemmed Carboxysome Mispositioning Alters Growth, Morphology, and Rubisco Level of the Cyanobacterium Synechococcus elongatus PCC 7942
title_short Carboxysome Mispositioning Alters Growth, Morphology, and Rubisco Level of the Cyanobacterium Synechococcus elongatus PCC 7942
title_sort carboxysome mispositioning alters growth, morphology, and rubisco level of the cyanobacterium synechococcus elongatus pcc 7942
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406218/
https://www.ncbi.nlm.nih.gov/pubmed/34340540
http://dx.doi.org/10.1128/mBio.02696-20
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