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Towards a quantitative assessment of inorganic carbon cycling in photosynthetic microorganisms

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    SYSNO ASEP0510250
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleTowards a quantitative assessment of inorganic carbon cycling in photosynthetic microorganisms
    Author(s) Müller, S. (AT)
    Zavřel, Tomáš (UEK-B) RID, SAI, ORCID
    Červený, Jan (UEK-B) RID, ORCID, SAI
    Source TitleEngineering in Life Sciences. - : Wiley - ISSN 1618-0240
    Roč. 19, č. 10 (2019), s. 1-13
    Number of pages13 s.
    Languageeng - English
    CountryDE - Germany
    Keywordscarbonate chemistry ; computational modeling ; cyanobacteria ; futile cycles ; photosynthesis
    Subject RIVEF - Botanics
    OECD categoryPlant sciences, botany
    R&D ProjectsLO1415 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Research InfrastructureCzeCOS II - 90061 - Ústav výzkumu globální změny AV ČR, v. v. i.
    Method of publishingOpen access
    Institutional supportUEK-B - RVO:86652079
    UT WOS000502733800001
    DOI10.1002/elsc.201900061
    AnnotationPhotosynthetic organisms developed various strategies to mitigate high light stress. For instance, aquatic organisms are able to spend excessive energy by exchanging dissolved carbon dioxide (dCO2) and bicarbonate (HCO3-) with the environment. Simultaneous uptake and excretion of the two carbon species is referred to as inorganic carbon cycling (ICC). Often, ICC is indicated by displacements of the extracellular dCO2 signal from the equilibrium value after changing the light conditions. In this work, we additionally use (i) the extracellular pH signal, which requires non- or weakly-buffered medium, and (ii) a dynamic model of carbonate chemistry in the aquatic environment in order to detect and quantitatively describe ICC. Based on simulations and experiments in precisely controlled photobioreactors, we show that the magnitude of the observed dCO2 displacement crucially depends on extracellular pH level and buffer concentration. Moreover, we find that the dCO2 displacement can also be caused by simultaneous uptake of both dCO2 and HCO3- (no ICC). In a next step, the dynamic model of carbonate chemistry allows for a quantitative assessment of cellular dCO2 , HCO3- , and H+ exchange rates from the measured dCO2 and pH signals. Limitations of the method are discussed.
    WorkplaceGlobal Change Research Institute
    ContactNikola Šviková, svikova.n@czechglobe.cz, Tel.: 511 192 268
    Year of Publishing2020
    Electronic addresshttps://onlinelibrary.wiley.com/doi/full/10.1002/elsc.201900061
Number of the records: 1  

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