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. 2011 Jun;79(6):2154–2167. doi: 10.1128/IAI.01180-10

Fig. 2.

Fig. 2.

KdpFABC is not a major K+ transporter in S. aureus. (A) Comparison of growth rates of WT, SX8 (kdpDE mutant), and SX13 (kdpFABC mutant) in CDM with different K+ concentrations. (B) Measurement of the internal K contents of the WT and SX13 (kdpFABC mutant) at different K+ concentrations of 0.2 mM, 4 mM, 20 mM, and 100 mM. (C) The regulatory effect of KdpDE on the transcription of kdpFABC in cells grown under different external K+ conditions. The transcript levels of kdpFABC were compared between WT, SX8 (kdpDE mutant), and SX10 (kdpE mutant) cells at different external K+ concentrations of 0.2 mM, 4 mM, and 100 mM. The real-time PCR assay was repeated four times with similar results. Error bars indicate standard deviations.