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. Author manuscript; available in PMC: 2017 May 19.
Published in final edited form as: Fungal Genet Biol. 2017 Jan 16;100:22–32. doi: 10.1016/j.fgb.2017.01.005

Figure 5. Exposure of CATP knockdown strain to hydrogen peroxide.

Figure 5

(A) Quantification of the sensitivity to H2O2 in P. brasiliensis yeast cells. Yeast cells were exposed to increasing concentrations of this compound and the inhibition zone was determined as the area lacking yeast cell growth. (Top) Data presented correspond to the average for three replicate tests, with error bars representing standard deviations. (Bottom) Images of P. brasiliensis growth around H2O2 saturated disks. Saturated filter disks without H2O2 as control, and 0.5 to 8 M H2O2. (B) Determination of the ability of P. brasiliensis yeast cells to degrade H2O2. Extracellular, cell wall and cytoplasmic fractions from PbWT, PbEV and PbCATP-aRNA strains were collected. Relative H2O2 destruction was measured as the decrease in the absorbance at 240 nm. Results are the mean of three individual experiments.