Large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower RUBISCO turnover rates

Diatoms contribute ~40% of primary production in the modern ocean and encompass the largest cell size range of any phytoplankton group. Diatom cell size influences their nutrient uptake, photosynthetic light capture, carbon export efficiency, and growth responses to increasing pCO2. We therefore exa...

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Main Authors: Yaping eWu, Jennifer eJeans, David eSuggett, Zoe eFinkel, Douglas Andrew Campbell
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-12-01
Series:Frontiers in Marine Science
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fmars.2014.00068/full
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author Yaping eWu
Yaping eWu
Jennifer eJeans
David eSuggett
Zoe eFinkel
Douglas Andrew Campbell
author_facet Yaping eWu
Yaping eWu
Jennifer eJeans
David eSuggett
Zoe eFinkel
Douglas Andrew Campbell
author_sort Yaping eWu
collection DOAJ
description Diatoms contribute ~40% of primary production in the modern ocean and encompass the largest cell size range of any phytoplankton group. Diatom cell size influences their nutrient uptake, photosynthetic light capture, carbon export efficiency, and growth responses to increasing pCO2. We therefore examined nitrogen resource allocations to the key protein complexes mediating photosynthesis across six marine centric diatoms, spanning 5 orders of magnitude in cell volume, under past, current and predicted future pCO2 levels, in balanced growth under nitrogen repletion. Membrane bound photosynthetic protein concentrations declined with cell volume in parallel with cellular concentrations of total protein, total nitrogen and chlorophyll. Larger diatom species, however, allocated a greater fraction (by 3.5 fold) of their total cellular nitrogen to the soluble RUBISCO carbon fixation complex than did smaller species. Carbon assimilation per unit of RUBISCO large subunit (C RbcL-1 s-1) decreased with cell volume, from ~8 to ~2 C RbcL-1 s-1 from the smallest to the largest cells. Whilst a higher allocation of cellular nitrogen to RUBISCO in larger cells increases the burden upon their nitrogen metabolism, the higher RUBISCO allocation buffers their lower achieved RUBISCO turnover rate to enable larger diatoms to maintain carbon assimilation rates per total protein comparable to small diatoms. Individual species responded to increased pCO2, but cell size effects outweigh pCO2 responses across the diatom species size range examined. In large diatoms a higher nitrogen cost for RUBISCO exacerbates the higher nitrogen requirements associated with light absorption, so the metabolic cost to maintain photosynthesis is a cell size-dependent trait.
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spelling doaj.art-0e60db3d15d04f1f916274a5c7cb68ab2022-12-22T00:13:18ZengFrontiers Media S.A.Frontiers in Marine Science2296-77452014-12-01110.3389/fmars.2014.00068119338Large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower RUBISCO turnover ratesYaping eWu0Yaping eWu1Jennifer eJeans2David eSuggett3Zoe eFinkel4Douglas Andrew Campbell5Mount Allison UniversityXiamen UniversityMount Allison UniversityUniversity of Technology, SydneyMount Allison UniversityMount Allison UniversityDiatoms contribute ~40% of primary production in the modern ocean and encompass the largest cell size range of any phytoplankton group. Diatom cell size influences their nutrient uptake, photosynthetic light capture, carbon export efficiency, and growth responses to increasing pCO2. We therefore examined nitrogen resource allocations to the key protein complexes mediating photosynthesis across six marine centric diatoms, spanning 5 orders of magnitude in cell volume, under past, current and predicted future pCO2 levels, in balanced growth under nitrogen repletion. Membrane bound photosynthetic protein concentrations declined with cell volume in parallel with cellular concentrations of total protein, total nitrogen and chlorophyll. Larger diatom species, however, allocated a greater fraction (by 3.5 fold) of their total cellular nitrogen to the soluble RUBISCO carbon fixation complex than did smaller species. Carbon assimilation per unit of RUBISCO large subunit (C RbcL-1 s-1) decreased with cell volume, from ~8 to ~2 C RbcL-1 s-1 from the smallest to the largest cells. Whilst a higher allocation of cellular nitrogen to RUBISCO in larger cells increases the burden upon their nitrogen metabolism, the higher RUBISCO allocation buffers their lower achieved RUBISCO turnover rate to enable larger diatoms to maintain carbon assimilation rates per total protein comparable to small diatoms. Individual species responded to increased pCO2, but cell size effects outweigh pCO2 responses across the diatom species size range examined. In large diatoms a higher nitrogen cost for RUBISCO exacerbates the higher nitrogen requirements associated with light absorption, so the metabolic cost to maintain photosynthesis is a cell size-dependent trait.http://journal.frontiersin.org/Journal/10.3389/fmars.2014.00068/fullPhotosynthesisResource Allocationnitrogen metabolismocean acidificationdiatomRubisco
spellingShingle Yaping eWu
Yaping eWu
Jennifer eJeans
David eSuggett
Zoe eFinkel
Douglas Andrew Campbell
Large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower RUBISCO turnover rates
Frontiers in Marine Science
Photosynthesis
Resource Allocation
nitrogen metabolism
ocean acidification
diatom
Rubisco
title Large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower RUBISCO turnover rates
title_full Large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower RUBISCO turnover rates
title_fullStr Large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower RUBISCO turnover rates
title_full_unstemmed Large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower RUBISCO turnover rates
title_short Large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower RUBISCO turnover rates
title_sort large centric diatoms allocate more cellular nitrogen to photosynthesis to counter slower rubisco turnover rates
topic Photosynthesis
Resource Allocation
nitrogen metabolism
ocean acidification
diatom
Rubisco
url http://journal.frontiersin.org/Journal/10.3389/fmars.2014.00068/full
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