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. 2014 Apr 7;111(16):6016–6021. doi: 10.1073/pnas.1320538111

Table 1.

Effect of phage mutations on phage and SaPI titers

Donor strain Titer
Phage SaPI pCN51* Phage SaPI
ϕ11 6.6 × 109
ϕ11 ΔterS <10
ϕ11 SaPIbov1 2 × 107 1 × 107
ϕ11 SaPIbov5 2 × 109 1.3 × 107
ϕ11 SaPIbov5 Δcos 1.6 × 109 1.1 × 107
ϕ11 ΔterS SaPIbov1 <10 1.9 × 107
ϕ11 ΔterS SaPIbov5 <10 <10
ϕ11 ΔterS SaPIbov5 pCN51-terSϕ11 1.8 × 105 2.3 × 105
80α 8 × 1010
80α SaPIbov1 3.4 × 109 1 × 107
80α SaPIbov5 1.5 × 1011 1.2 × 107
ϕ12 8 × 107
ϕ12 Δhnh <10
ϕ12 Δhnh pCN51-hnhϕ12 2.2 × 104
ϕ12 SaPIbov1 1.1 × 109 <10
ϕ12 SaPIbov5 1.1 × 106 1.1 × 106
ϕ12 SaPIbov5 Δcos 1.4 × 107 <10
ϕ12 Δhnh SaPIbov5 <10 <10
ϕ12 Δhnh SaPIbov5 pCN51-hnhϕ12 1.4 × 104 8.1 × 104
ϕSLT 6.2 × 106
ϕSLT Δhnh <10
ϕSLT Δhnh pCN51-hnhϕSLT 3.1 × 104
ϕSLT SaPIbov1 2.7 × 106 <10
ϕSLT SaPIbov5 8.2 × 105 8.7 × 103
ϕSLT SaPIbov5 Δcos 3.3 × 106 <10
ϕSLT Δhnh SaPIbov5 <10 <10
ϕSLT Δhnh SaPIbov5 pCN51-hnhϕSLT 5.7 × 103 1.3 × 103

The means of results from three independent experiments are shown. Variation was within ±5% in all cases. —, the strain has not SaPIs or plasmids, and consequently, the transfer of the SaPIs can not be analyzed.

*

Complemented both the donor and the recipient strains.

PFU/mL induced culture, using RN4220 as the recipient strain.

Number of transductants per milliliter induced culture, using RN4220 as the recipient strain.