Mitochondrial phosphoenolpyruvate carboxylase contributes to carbon fixation in the diatom Phaeodactylum tricornutum at low inorganic carbon concentrations

dc.contributor.authorYu, Guilan
dc.contributor.authorNakajima, Kensuke
dc.contributor.authorGruber, Ansgar
dc.contributor.authorRío Bártulos, Carolina
dc.contributor.authorSchober, Alexander
dc.contributor.authorLepetit, Bernard
dc.contributor.authorYohannes, Elizabeth
dc.contributor.authorMatsuda, Yusuke
dc.contributor.authorKroth, Peter G.
dc.date.accessioned2022-05-30T12:20:24Z
dc.date.available2022-05-30T12:20:24Z
dc.date.issued2022-08
dc.description.abstractPhotosynthetic carbon fixation is often limited by CO2 availability, which led to the evolution of CO2 concentrating mechanisms (CCMs). Some diatoms possess CCMs that employ biochemical fixation of bicarbonate, similar to C4 plants, but it is controversially discussed whether biochemical CCMs are a commonly found in diatoms.
In the diatom Phaeodactylum tricornutum, Phosphoenolpyruvate Carboxylase (PEPC) is present in two isoforms, PEPC1 in the plastids and PEPC2 in the mitochondria. We used real-time quantitative PCR, western blots, and enzymatic assays to examine PEPC expression and PEPC activities, under low and high concentrations of dissolved inorganic carbon (DIC).
We generated and analyzed individual knockout cell lines of PEPC1 and PEPC2, as well as a PEPC1/2 double-knockout strain. While we could not detect an altered phenotype in the PEPC1 knockout strains at ambient, low or high DIC concentrations, PEPC2 and the double-knockout strains grown under ambient air or lower DIC availability, showed reduced growth and photosynthetic affinity to DIC, while behaving similarly as WT cells at high DIC concentrations. These mutants furthermore exhibited significantly lower 13C/12C ratios compared to WT.
Our data implies that in P. tricornutum at least parts of the CCM relies on biochemical bicarbonate fixation catalyzed by the mitochondrial PEPC2.
eng
dc.description.versionpublishedeng
dc.identifier.doi10.1111/nph.18268eng
dc.identifier.pmid35596716eng
dc.identifier.ppn1813114900
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/57699
dc.language.isoengeng
dc.rightsterms-of-use
dc.rights.urihttps://rightsstatements.org/page/InC/1.0/
dc.subject.ddc570eng
dc.titleMitochondrial phosphoenolpyruvate carboxylase contributes to carbon fixation in the diatom Phaeodactylum tricornutum at low inorganic carbon concentrationseng
dc.typeJOURNAL_ARTICLEeng
dspace.entity.typePublication
kops.citation.bibtex
@article{Yu2022-08Mitoc-57699,
  year={2022},
  doi={10.1111/nph.18268},
  title={Mitochondrial phosphoenolpyruvate carboxylase contributes to carbon fixation in the diatom Phaeodactylum tricornutum at low inorganic carbon concentrations},
  number={4},
  volume={235},
  issn={0028-646X},
  journal={The New Phytologist},
  pages={1379--1393},
  author={Yu, Guilan and Nakajima, Kensuke and Gruber, Ansgar and Río Bártulos, Carolina and Schober, Alexander and Lepetit, Bernard and Yohannes, Elizabeth and Matsuda, Yusuke and Kroth, Peter G.}
}
kops.citation.iso690YU, Guilan, Kensuke NAKAJIMA, Ansgar GRUBER, Carolina RÍO BÁRTULOS, Alexander SCHOBER, Bernard LEPETIT, Elizabeth YOHANNES, Yusuke MATSUDA, Peter G. KROTH, 2022. Mitochondrial phosphoenolpyruvate carboxylase contributes to carbon fixation in the diatom Phaeodactylum tricornutum at low inorganic carbon concentrations. In: The New Phytologist. Wiley. 2022, 235(4), pp. 1379-1393. ISSN 0028-646X. eISSN 1469-8137. Available under: doi: 10.1111/nph.18268deu
kops.citation.iso690YU, Guilan, Kensuke NAKAJIMA, Ansgar GRUBER, Carolina RÍO BÁRTULOS, Alexander SCHOBER, Bernard LEPETIT, Elizabeth YOHANNES, Yusuke MATSUDA, Peter G. KROTH, 2022. Mitochondrial phosphoenolpyruvate carboxylase contributes to carbon fixation in the diatom Phaeodactylum tricornutum at low inorganic carbon concentrations. In: The New Phytologist. Wiley. 2022, 235(4), pp. 1379-1393. ISSN 0028-646X. eISSN 1469-8137. Available under: doi: 10.1111/nph.18268eng
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    <dcterms:abstract xml:lang="eng">Photosynthetic carbon fixation is often limited by CO&lt;sub&gt;2&lt;/sub&gt; availability, which led to the evolution of CO&lt;sub&gt;2&lt;/sub&gt; concentrating mechanisms (CCMs). Some diatoms possess CCMs that employ biochemical fixation of bicarbonate, similar to C&lt;sub&gt;4&lt;/sub&gt; plants, but it is controversially discussed whether biochemical CCMs are a commonly found in diatoms.&lt;br /&gt;In the diatom Phaeodactylum tricornutum, Phosphoenolpyruvate Carboxylase (PEPC) is present in two isoforms, PEPC1 in the plastids and PEPC2 in the mitochondria. We used real-time quantitative PCR, western blots, and enzymatic assays to examine PEPC expression and PEPC activities, under low and high concentrations of dissolved inorganic carbon (DIC).&lt;br /&gt;We generated and analyzed individual knockout cell lines of PEPC1 and PEPC2, as well as a PEPC1/2 double-knockout strain. While we could not detect an altered phenotype in the PEPC1 knockout strains at ambient, low or high DIC concentrations, PEPC2 and the double-knockout strains grown under ambient air or lower DIC availability, showed reduced growth and photosynthetic affinity to DIC, while behaving similarly as WT cells at high DIC concentrations. These mutants furthermore exhibited significantly lower &lt;sup&gt;13&lt;/sup&gt;C/&lt;sup&gt;12&lt;/sup&gt;C ratios compared to WT.&lt;br /&gt;Our data implies that in P. tricornutum at least parts of the CCM relies on biochemical bicarbonate fixation catalyzed by the mitochondrial PEPC2.</dcterms:abstract>
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kops.sourcefieldThe New Phytologist. Wiley. 2022, <b>235</b>(4), pp. 1379-1393. ISSN 0028-646X. eISSN 1469-8137. Available under: doi: 10.1111/nph.18268deu
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kops.sourcefield.plainThe New Phytologist. Wiley. 2022, 235(4), pp. 1379-1393. ISSN 0028-646X. eISSN 1469-8137. Available under: doi: 10.1111/nph.18268eng
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