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Evidence for potassium transport activity of Arabidopsis KEA1-KEA6

机译:拟南芥KEA1-KEA6钾转运活性的证据

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摘要

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.
机译:拟南芥含有推定的K + 外排转运蛋白KEA1-KEA6,类似于大肠杆菌的KefB和KefC。 KEA1-KEA3参与光合作用电子运输和叶绿体发育的调节。在盐分胁迫期间,KEA4-KEA6介导内膜网络的pH调节。然而,尚未直接表征KEA1-KEA6的离子迁移活性。在这项研究中,我们使用了大肠杆菌表达系统来检查KEA活性。 KEA1-KEA3和KEA5表现出双向的K + 转运活性,而KEA4和KEA6充当K + 吸收系统。来自蓝藻集胞藻模型的类囊体膜定位的Na + / H + 反向转运蛋白NhaS3是KEA3的最接近同源物。将假定的KEA3(Gln-Asp)的Na + / H + 选择性位点更改为NhaS3(Asp-Asp)的位点不会改变离子选择性而不会损失K + 传输活动。保守基序中的第一个残基不是K + 或Na + 选择性的决定因素。从KEA3中删除可能的核苷酸结合KTN结构域降低了K + 转运活性,表明KTN结构域对该功能很重要。在拟南芥dpgr突变体中发现的KEA3-G422R突变增加了K + 转运活性,与突变体表型一致。这些结果表明拟南芥KEA1-KEA6充当K + 转运系统,并支持KEA3促进类囊体膜中ΔpH耗散的解释。

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