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Evidence for potassium transport activity of Arabidopsis KEA1-KEA6.
Tsujii, Masaru; Kera, Kota; Hamamoto, Shin; Kuromori, Takashi; Shikanai, Toshiharu; Uozumi, Nobuyuki.
Afiliação
  • Tsujii M; Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University, Aobayama 6-6-07, Sendai, 980-8579, Japan.
  • Kera K; Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University, Aobayama 6-6-07, Sendai, 980-8579, Japan.
  • Hamamoto S; Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University, Aobayama 6-6-07, Sendai, 980-8579, Japan.
  • Kuromori T; RIKEN Center for Sustainable Resource Science, Wako, Saitama, 351-0198, Japan.
  • Shikanai T; Department of Botany, Graduate School of Science, Kyoto University, Kyoto, 606-8502, Japan.
  • Uozumi N; Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University, Aobayama 6-6-07, Sendai, 980-8579, Japan. uozumi@tohoku.ac.jp.
Sci Rep ; 9(1): 10040, 2019 07 11.
Article em En | MEDLINE | ID: mdl-31296940
ABSTRACT
Arabidopsis thaliana contains the putative K+ efflux transporters KEA1-KEA6, similar to KefB and KefC of Escherichia coli. KEA1-KEA3 are involved in the regulation of photosynthetic electron transport and chloroplast development. KEA4-KEA6 mediate pH regulation of the endomembrane network during salinity stress. However, the ion transport activities of KEA1-KEA6 have not been directly characterized. In this study, we used an E. coli expression system to examine KEA activity. KEA1-KEA3 and KEA5 showed bi-directional K+ transport activity, whereas KEA4 and KEA6 functioned as a K+ uptake system. The thylakoid membrane-localized Na+/H+ antiporter NhaS3 from the model cyanobacterium Synechocystis is the closest homolog of KEA3. Changing the putative Na+/H+ selective site of KEA3 (Gln-Asp) to that of NhaS3 (Asp-Asp) did not alter the ion selectivity without loss of K+ transport activity. The first residue in the conserved motif was not a determinant for K+ or Na+ selectivity. Deletion of the possible nucleotide-binding KTN domain from KEA3 lowered K+ transport activity, indicating that the KTN domain was important for this function. The KEA3-G422R mutation discovered in the Arabidopsis dpgr mutant increased K+ transport activity, consistent with the mutant phenotype. These results indicate that Arabidopsis KEA1-KEA6 act as K+ transport systems, and support the interpretation that KEA3 promotes dissipation of ΔpH in the thylakoid membrane.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Potássio / Arabidopsis / Antiportadores de Potássio-Hidrogênio Idioma: En Revista: Sci Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Potássio / Arabidopsis / Antiportadores de Potássio-Hidrogênio Idioma: En Revista: Sci Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Japão