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. Author manuscript; available in PMC: 2011 Jul 1.
Published in final edited form as: Mol Microbiol. 2010 May 24;77(1):74–89. doi: 10.1111/j.1365-2958.2010.07223.x

Fig. 1.

Fig. 1

Phenotypic characterization of the ΔdipM mutant. (A) Growth rates (in doublings/h) of wild-type and ΔdipM (CJW3137) CB15N strains grown at 30°C in liquid cultures containing M2G minimal medium, M2G medium supplemented with 15% of rich PYE medium, or PYE medium. Average values and standard deviations for three experiments are shown. (B) Phase contrast images of ΔdipM cells grown at 22°C in different media. ΔdipM cells from overnight M2G cultures at 30°C were used to inoculate culture tubes containing M2G medium, PYE medium or M2G supplemented with 10 or 15% of PYE medium, which were then incubated at 22°C for an additional 24 h prior to imaging. At the time of imaging, the cultures were at an OD660 ≤ 0.5. (C) Scanning EM images of ΔdipM mutant cells grown at 30°C in liquid M2G medium. White and black arrows indicate constriction sites and bulged poles, respectively. For comparison, the inset shows scanning EM images of a wild-type predivisional cell grown under the same conditions.