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Evidence for potassium transport activity of Arabidopsis KEA1-KEA6

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 s...

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Autores principales: Tsujii, Masaru, Kera, Kota, Hamamoto, Shin, Kuromori, Takashi, Shikanai, Toshiharu, Uozumi, Nobuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624313/
https://www.ncbi.nlm.nih.gov/pubmed/31296940
http://dx.doi.org/10.1038/s41598-019-46463-7
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author Tsujii, Masaru
Kera, Kota
Hamamoto, Shin
Kuromori, Takashi
Shikanai, Toshiharu
Uozumi, Nobuyuki
author_facet Tsujii, Masaru
Kera, Kota
Hamamoto, Shin
Kuromori, Takashi
Shikanai, Toshiharu
Uozumi, Nobuyuki
author_sort Tsujii, Masaru
collection PubMed
description 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.
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spelling pubmed-66243132019-07-19 Evidence for potassium transport activity of Arabidopsis KEA1-KEA6 Tsujii, Masaru Kera, Kota Hamamoto, Shin Kuromori, Takashi Shikanai, Toshiharu Uozumi, Nobuyuki Sci Rep Article 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. Nature Publishing Group UK 2019-07-11 /pmc/articles/PMC6624313/ /pubmed/31296940 http://dx.doi.org/10.1038/s41598-019-46463-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tsujii, Masaru
Kera, Kota
Hamamoto, Shin
Kuromori, Takashi
Shikanai, Toshiharu
Uozumi, Nobuyuki
Evidence for potassium transport activity of Arabidopsis KEA1-KEA6
title Evidence for potassium transport activity of Arabidopsis KEA1-KEA6
title_full Evidence for potassium transport activity of Arabidopsis KEA1-KEA6
title_fullStr Evidence for potassium transport activity of Arabidopsis KEA1-KEA6
title_full_unstemmed Evidence for potassium transport activity of Arabidopsis KEA1-KEA6
title_short Evidence for potassium transport activity of Arabidopsis KEA1-KEA6
title_sort evidence for potassium transport activity of arabidopsis kea1-kea6
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624313/
https://www.ncbi.nlm.nih.gov/pubmed/31296940
http://dx.doi.org/10.1038/s41598-019-46463-7
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