Control of potassium homeostasis is an essential function of the second messenger cyclic di-AMP in <i>Bacillus subtilis</i>

Abstract

The second messenger cyclic di-adenosine monophosphate (c-di-AMP) is essential in the Gram-positive model organism <i>Bacillus subtilis</i> and in related pathogenic bacteria. It controls the activity of the conserved <i>ydaO</i> riboswitch and of several proteins involved in potassium (K⁺) uptake. We found that the YdaO protein was conserved among several different bacteria and provide evidence that YdaO functions as a K⁺ transporter. Thus, we renamed the gene and protein KimA (K⁺ importer A). Reporter activity assays indicated that expression beyond the c-di-AMP-responsive riboswitch of the <i>kimA</i> upstream regulatory region occurred only in bacteria grown in medium containing low K⁺ concentrations. Furthermore, mass spectrometry analysis indicated that c-di-AMP accumulated in bacteria grown in the presence of high K⁺ concentrations but not in low concentrations. A bacterial strain lacking all genes encoding c-di-AMP-synthesizing enzymes was viable when grown in medium containing low K⁺ concentrations, but not at higher K⁺ concentrations unless it acquired suppressor mutations in the gene encoding the cation exporter NhaK. Thus, our results indicated that the control of potassium homeostasis is an essential function of c-di-AMP.