The KtrA and KtrE subunits are required for [Na.sup.+]-dependent [K.sup.+] uptake by KtrB across the plasma membrane in Synechocystis sp. strain PCC 6803

The [Na.sup.+]-dependent [K.sup.+] uptake KtrABE system is essential for the adaptation of Synechocystis to salinity stress and high osmolality. While KtrB forms the [K.sup.+]-translocating pore, the role of the subunits KtrA and KtrE for Ktr function remains elusive. Here, we characterized the role of KtrA and KtrE in Ktr-mediated [K.sup.+] uptake and in modulating [Na.sup.+] dependency. Expression of KtrB alone in a [K.sup.+] uptake-deficient Escherichia coli strain conferred low [K.sup.+] uptake activity that was not stimulated by [Na.sup.+]. Coexpression of both KtrA and KtrE with KtrB increased the [K.sup.+] transport activity in a [Na.sup.+]-dependent manner. KtrA and KtrE were found to be localized to the plasma membrane in Synechocystis. Site-directed mutagenesis was used to analyze the role of single charged residues in KtrB for Ktr function. Replacing negatively charged residues facing the extracellular space with residues of the opposite charge increased the apparent K, for [K.sup.+] in all cases. However, none of the mutations eliminated the [Na.sup.+] dependency of Ktr-mediated [K.sup.+] transport. Mutations of residues on the cytoplasmic side had larger effects on [K.sup.+] uptake activity than those of residues on the extracellular side. Further analysis revealed that replacement of R262, which is well conserved among Ktr/Trk/HKT transporters in the third extracellular loop, by Glu abolished transport activity. The atomic-scale homology model indicated that R262 might interact with E247 and D261. Based on these data, interaction of KtrA and KtrE with KtrB increased the [K.sup.+] uptake rate and conferred [Na.sup.+] dependency. doi: 10.1128/JB.00569-10