1. Fresh conidia of the WT and mutant strains were harvested from cultures grown on mCDB plates at 28° C for 12 days and afterwards filtered using sterile Mira cloth.
2. 1 ul of conidia suspension containing 5000 conidia of the WT or mutant strains were inoculated on mCDB plates previously supplemented with 0.8 M NACl and 1 M KCl for osmotic stress assay.
3. For oxidative and cell wall perturbing stress, same procedure in step (2) was repeated.
4. All cultures were incubated at 28° C for 4 days.
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