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Resolution: standard / high Figure 5.
Rim101-mediated metal resistance. (a) Serial dilution assays documenting the cadmium and nickel resistance of rim101Δ and of representative Rim101-related mutants. Wild-type (WT) and mutant strains were
grown in the absence of exogenously supplied metals or in the presence of the indicated
concentrations of cadmium and nickel. (b) Over-expression of Nrg1, but not Smp1 (two transcription factors negatively regulated
by Rim101), enhances tolerance to both cadmium and nickel compared with WT cells.
Scaled down concentrations of cadmium and nickel were utilized for these assays, which
were conducted under selective, synthetic dextrose medium conditions. (c) Increased cadmium/nickel tolerance of a strain disrupted in TAT1, a membrane transporter negatively regulated by Nrg1. (d) Intracellular nickel accumulation by WT, rim101Δ, and tat1Δ cells analyzed by Newport Green staining (see 'Materials and methods' for details);
the percentage of fluorescent cells (average ± standard deviation of three independent
experiments) is expressed relative to WT (100%).
Ruotolo et al. Genome Biology 2008 9:R67 doi:10.1186/gb-2008-9-4-r67 |