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. 2019 Feb 1;14(2):e0211426. doi: 10.1371/journal.pone.0211426

Fig 4. Complementation of the salt tolerance of ppz1 S. cerevisiae cells by the expression of mutant CaPpz1 proteins.

Fig 4

The phosphatase mutant ppz1 S. cerevisiae strain was transformed either with empty plasmids or with YCplac111 (A) or YEplac181 (B) carrying wild type or mutant CaPPZ1 inserts as in Fig 3. After establishing optimal assay conditions the effect of 50 mM LiCl on the transformants was determined after 19 h of cultivation. The growth of the cells containing empty plasmids was taken as 100%. Mean and standard deviation of 3 independent experiments are shown.