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Fluorescence of exponential-phase C. glabrata L5U1 (A) and S. cerevisiae BY4741 (B) cells harboring either the cloning vector pGREG576 (control) or the pGREG576_MTII_CgQDR2 or pGREG576_CgQDR2 plasmid (CgQdr2_GFP) after 5 h of copper- or galactose-induced recombinant protein production, respectively. The results indicate that the CgQdr2-GFP fusion protein localizes to the plasma membranes of both S. cerevisiae and C. glabrata cells.
