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. 2007 Nov 9;190(5):1792–1811. doi: 10.1128/JB.01322-07

TABLE 6.

Effects of RelA′ production on doubling times, FtsZ levels, and cell sizesa

Strain Genotype IPTG concn (μM) Tdb (min) [FtsZ]c,f Long axisd,f (μm) Short axisd,f (μm) Vold,e,f (μm3)
TB28/pJF118EH wt/vector 0 61 ND ND ND ND
TB28/pJF118EH wt/vector 50 59 1.0 4.1 (0.9) 1.1 (0.1) 3.45 (1.1)
TB28/pYT11 wt/Ptac::relA 0 62 ND ND ND ND
TB28/pYT11 wt/Ptac::relA 50 103 1.3 (0.0) 1.9 (0.4) 0.9 (0.1) 1.0 (0.3)
FB30/pFB174/pJF118EH ΔmreBCD/PBAD::mreBCD/vector 50 76 1.1 (0.1) 4.0 (0.1) 3.0 (0.6) 20.2 (10.9)
FB30/pFB174/pYT11 ΔmreBCD/PBAD::mreBCD/Ptac::relA 0 68 ND ND ND ND
FB30/pFB174/pYT11 ΔmreBCD/PBAD::mreBCD/Ptac::relA 50 108 1.6 (0.1) 2.3 (0.6) 1.7 (0.3) 3.9 (2.6)
a

Cells were first grown to density in M9-maltose plus 0.5% arabinose. They were then diluted in LB lacking arabinose and containing IPTG as indicated and incubated at 30°C.

b

Td as determined by OD600 measurements.

c

At an OD600 of 0.5, relative FtsZ levels were measured by quantitative Western analyses. Values were normalized to that for TB28/pJF118EH with 50 μM IPTG.

d

Average values for 100 cells at an OD600 of 0.5.

e

TB28 and FB30 cells were considered perfect capsules and prolate spheroids, respectively.

f

Standard deviations are shown in parentheses. ND, not determined.