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Localization and characterization θ carbonic anhydrases in Thalassiosira pseudonana.
Nawaly, Hermanus; Tanaka, Atsuko; Toyoshima, Yui; Tsuji, Yoshinori; Matsuda, Yusuke.
Afiliación
  • Nawaly H; Department of Bioscience, School of Biological and Environmental Sciences, Kwansei Gakuin University, 1 Gakuen Uegahara, Sanda, Hyogo, 669-1330, Japan.
  • Tanaka A; Department of Chemistry, Biology and Marine Science, Faculty of Science, University of the Ryukyus, Nishihara, 903-0213, Japan.
  • Toyoshima Y; Department of Bioscience, School of Biological and Environmental Sciences, Kwansei Gakuin University, 1 Gakuen Uegahara, Sanda, Hyogo, 669-1330, Japan.
  • Tsuji Y; Graduate School of Biostudies, Kyoto University, Kyoto, 606-8502, Japan.
  • Matsuda Y; Department of Bioscience, School of Biological and Environmental Sciences, Kwansei Gakuin University, 1 Gakuen Uegahara, Sanda, Hyogo, 669-1330, Japan. yusuke@kwansei.ac.jp.
Photosynth Res ; 156(2): 217-229, 2023 May.
Article en En | MEDLINE | ID: mdl-36862281
ABSTRACT
Carbonic anhydrase (CA) is a crucial component for the operation of CO2-concentrating mechanisms (CCMs) in the majority of aquatic photoautotrophs that maintain the global primary production. In the genome of the centric marine diatom, Thalassiosira pseudonana, there are four putative gene sequences that encode θ-type CA, which was a type of CA recently identified in marine diatoms and green algae. In the present study, specific subcellular locations of four θCAs, TpθCA1, TpθCA2, TpθCA3, and TpθCA4 were determined by expressing GFP-fused proteins of these TpθCAs in T. pseudonana. As a result, C-terminal GFP fusion proteins of TpθCA1, TpθCA2, and TpθCA3 were all localized in the chloroplast; TpθCA2 was at the central chloroplast area, and the other two TpθCAs were throughout the chloroplast. Immunogold-labeling transmission electron microscopy was further performed for the transformants expressing TpθCA1GFP and TpθCA2GFP with anti-GFP-monoclonal antibody. TpθCA1GFP was localized in the free stroma area, including the peripheral pyrenoid area. TpθCA2GFP was clearly located as a lined distribution at the central part of the pyrenoid structure, which was most likely the pyrenoid-penetrating thylakoid. Considering the presence of the sequence encoding the N-terminal thylakoid-targeting domain in the TpθCA2 gene, this localization was likely the lumen of the pyrenoid-penetrating thylakoid. On the other hand, TpθCA4GFP was localized in the cytoplasm. Transcript analysis of these TpθCAs revealed that TpθCA2 and TpθCA3 were upregulated in atmospheric CO2 (0.04% CO2, LC) levels, while TpθCA1 and TpθCA4 were highly induced under 1% CO2 (HC) condition. The genome-editing knockout (KO) of TpθCA1, by CRISPR/Cas9 nickase, gave a silent phenotype in T. pseudonana under LC-HC conditions, which was in sharp agreement with the case of the previously reported TpθCA3 KO. In sharp contrast, TpθCA2 KO is so far unsuccessful, suggesting a housekeeping role of TpθCA2. The silent phenotype of KO strains of stromal CAs suggests that TpαCA1, TpθCA1, and TpθCA3 may have functional redundancy, but different transcript regulations in response to CO2 of these stromal CAs suggest in part their independent roles.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Anhidrasas Carbónicas / Diatomeas Idioma: En Revista: Photosynth Res Asunto de la revista: METABOLISMO Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Anhidrasas Carbónicas / Diatomeas Idioma: En Revista: Photosynth Res Asunto de la revista: METABOLISMO Año: 2023 Tipo del documento: Article País de afiliación: Japón