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. 2012 Jan 25;7(1):e30282. doi: 10.1371/journal.pone.0030282

Table 5. Effect of GTP or (p)ppGpp levels in toxin induced PI staining and dormancy.

Conditions of toxin expression Tf % PI stained cellsg CFUs ml−1, h , i
xylR-P XylA+Deca - 3.4±0.2 (530) 2.8 108
xylR-P XylAζY83C No 1.8±0.2 (800) 1.8 108
xylR-P XylAζY83C+Deca No 5.3±0.4 (478) 1.8 108
xylR-P XylAζY83C+Xyla Yes 17±1.3 (937) 1.5 103
xylR-P XylAζY83C+Dec+Xylb Yes 19±1.6 (1041) 5.0 103
xylR-P XylArelA)+Deca - 3.2±0.2 (700) 3.0 108
xylR-P XylAζY83C (ΔrelA) No 4.3±0.5 (800) 2.7 108
xylR-P XylAζY83C (ΔrelA)+Deca No 4.8±0.3 (350) 2.6 108
xylR-P XylAζY83C (ΔrelA)+Xyla Yes 23.9±1.9 (350) 4.6 105
xylR-P XylAζY83C (ΔrelA)+Dec+Xylb Yes 22.7±2.1 (450) 3.0 105

xylR-P XylA or xylR-P XylA ΔrelA or xylR-P XylAζY83C or xylR-P XylAζY83C ΔrelA were grown in MMS7. At ∼5×107 cells/ml−1 0.5% Xyla (to induce ζY83C expression) or 0.5 mg ml−1 Deca (to reduce GTP synthesis) or bothb, Xyl and Dec, were added and the culture was incubated for 120 min.

f

The presence of ζY83C toxin is indicated by yes or no.

g

Number of cells analyzed are shown in parentheses.

h

Due to poor growth of the ΔrelA strains CFUs were measured after two days of incubation.

i

The CFUs were measured after 120 min of toxin induction by plating appropriate dilutions on LB plates. The results are the average of at least three independent experiments and are within a 10% standard error.