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. Author manuscript; available in PMC: 2013 Sep 1.
Published in final edited form as: Mol Microbiol. 2012 Jul 18;85(5):916–933. doi: 10.1111/j.1365-2958.2012.08149.x

Table 2.

QS regulator expression in KLH11 null mutants

β-Galactosidase Sp. Act.1
KLH11 Extracts
Synthetic AHLs
Mutants2 Relevant
Genotype
No Extract 2.5% No AHL + AHL3
EC2 ssaI-lacZ, null 6 (1.7) 95 (10.6) 6.3 (0.7) 213.3 (9.2)
EC3 ssbI-lacZ, null 1 (<1) <1 (<0.1) 1.1 (0.3) 1.1(<0.1)
JZ1 ssaR-lacZ, WT 107.1(0.8) 105.0 (4.4) 93.7 (8.3) 99.3 (2.8)
EC4 ssaR-lacZ, null 23 (3) 19 (1.4) 26.7 (1.3) 28.6 (2.4)
JZ2 ssbR-lacZ, WT 11.6 (2.8) 10.8 (3.1) 12.0 (0.5) 12.6 (0.5)
EC5 ssbR-lacZ, null 15 (<) 10 (4.6) 27.6 (4.5) 26.0 (4.2)
1

Specific activity in Miller Units, averages of assays in triplicate (standard deviation)

2

All strains are derived from EC1, spontaneous RifR mutant. Strains EC2, EC3. JZ1 and JZ2 carry Campbell insertions and lacZ transcriptional fusions;

3

2 μM 3-oxo-c16:1 Δ11 was added for ssaIR and 20 μM 3-OH-C14 was added for ssbIR.