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. 2018 Jul 11;8(3):49. doi: 10.3390/biom8030049

Figure 1.

Figure 1

Phenotypes of elp3 and sit4 mutants and their responses to overexpression of tRNAGlnUUG, tRNALysUUU and tRNAGluUUC. (A) BY4741 wild type (WT), elp3 or sit4 mutants were each transformed with empty plasmid pRS425 or pQKE (over-expression of tRNAGlnUUG, tRNALysUUU and tRNAGluUUC) and subjected to drop dilution spot assays involving yeast extract peptone (YP) based media with either glucose, galactose or ethanol as the carbon source. All plates were incubated at 30 °C for 3 days. (B) The same strains as in (A) were subjected to drop dilution spot assays on yeast extract peptone dextrose (YPD) medium (carbon source glucose) cultivated at 39 °C or 40 °C or on YPD medium supplemented with a crude zymocin preparation. (C) Microtiter based measurement of growth inhibition by soraphen A. Relative growth refers to optical density (O.D 600 nm) of microcultures with indicated concentrations of soraphen A as compared to soraphen A free cultures. Measurements were carried out in triplicate and presented as mean with standard deviation.