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. 2006 Feb;5(2):313–320. doi: 10.1128/EC.5.2.313-320.2006

FIG. 3.

FIG. 3.

Deletion of AZF1 produces cell wall defects. (A) Wild-type (WT) (BY4741) and azf1Δ (TTL9) mutants were serially diluted and plated in 5-μl drops on YEP-glycerol-lactate media with the indicated cell wall disruptors as described in Materials and Methods. Plates were incubated for 2 days at 30°C. CFW, calcofluor white. (B) WT (BY4741) and azf1Δ (TTL9) mutants were grown to mid-log phase in either YEP-glycerol-lactate (GL) or YEPD (D) medium. Aliquots were resuspended in zymolyase (0.05 U/μl) as described in Materials and Methods, and cell disruption by zymolyase was measured by monitoring the OD600 at the indicated intervals. Error bars represent the standard deviations of this ratio across triplicate experiments.