Table 2.
Strain | Relevant genotypeb | Frequency (%) of the following developmental fate after asymmetric divisionc: |
Total organisms scored | ||
---|---|---|---|---|---|
Monospore (no MC growth) | Abortively disporic (no MC growth) | Escape (MC growth) | |||
SL14826 | spoIIRdelay | 64 | 13 | 22 | 90 |
SL14130 | spoIIRdelay | 60 | 13 | 27 | 126 |
SL14315 | spo+ | 100 | 0 | 0 | 64 |
SL14240 | spoIIR | 0 | 37 | 63 | 103 |
SL15261 | spoIIGB | 0 | 34 | 66 | 88 |
Bacteria were grown on top of a thin layer of agarose in such a way that single cells grew into sporulating microcolonies, which were monitored by time lapse microscopy (50). Fluorescence images were acquired at periodic intervals for FM4-64 (membrane staining) and GFP (origin location and/or σE activity [see the text]). Cell fates were recorded for all organisms that underwent asymmetric division.
All strains contained the Spo0J-GFP fusion for the visualization of chromosome origins. Strain SL14826 contained thrC::PspoIID-gfp for the visualization of σE activity.
MC, mother cell.