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. Author manuscript; available in PMC: 2015 Jul 1.
Published in final edited form as: Mol Microbiol. 2014 Jun 15;93(2):276–290. doi: 10.1111/mmi.12658

Table 1.

Bacteriophage plating efficiencya

Bacteriophage
Bacterial strain R17 M13
X90 ΔtolA 0.93 ± 0.12 0.0b
X90 ΔtonB 1.2 ± 0.26 1.0 ± 0.20
X90 ΔtolA ΔtonB 1.1 ± 0.15 0.0b
X90 ΔtraA::cat pTrc 0.0b 0.0b
X90 ΔtraA::cat pTrc::traA 1.2 ± 0.18 1.2 ± 0.15
X90 ΔtraA::cat pTrc::traA(D74G) 0.0b 1.1 ± 0.09
X90 ΔtraA::cat pTrc::traA(G120C) 0.09 ± 0.005c 0.77 ± 0.06c
X90 ΔtrbI::cat 0.1 ± 0.04c 0.1 ± 0.03c
a

The indicated bacterial strains were infected with 10 and 100 plaque forming units (pfu). The number of plaques for each strain was divided by the plaques obtained with wild-type X90 cells. The mean plating efficiency ± SEM is reported (n = 4).

b

No plaques were detected when bacteria were incubated with 103 pfu of phage.

c

Plaques were turbid.