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. 2014 May 6;5(3):e00966-14. doi: 10.1128/mBio.00966-14

TABLE 2 .

Activities of the phuR and phuS promoters originating with different clinical isolates of P. aeruginosaa

Strain Promoter Origin of promoter Allele Mean luminescence (± SD) Fold change P value
PAO1 phuR PAO1 WT 365 (±1,018) 1
PAO1 phuR DK2-CF66-2008 M1 34,111 (±3,379) 93 0.00021
PAO1 phuR DK2-CF173-2005 M2 40,726 (±3,422) 112 0.00004
PAO1 phuR DK2-CF173-2002 M3 1,879 (±3,422) 5 0.16
PAO1 phuR DK2-CF240-2002 M4 7,584 (±496) 21 0.00038
PAO1 phuR DK2-CF222-2001 M5 8,968 (±610) 25 0.00023
PAO1 phuR DK2-CF180-2002 M6 6,723 (±701) 18 0.00088
PAO1 phuR DK1-P28F1-1992 M8 13,329 (±1,482) 37 0.00024
PAO1 phuR DK1-P28F1-2009 M9 12,205 (±603) 33 0.00007
PAO1 phuR DK1-CF30-2011 M10 9,563 (±1,586) 26 0.0011
PAO1 phuS PAO1 WT 7,444 (±1,777) 1
PAO1 phuS DK2-CF173-2005 M2 12,030 (±3,191) 1.6 0.01
a

Luminescence production from laboratory reference strain PAO1 (37) with phuR::lux reporter fusions was measured at exponential growth (OD600 = 0.15) in Luria-Bertani (LB) medium and normalized for differences in cell density. Mean luminescence production and standard deviations (SD) were calculated for three biological replicates. Statistical analysis concerning the difference between two means was done using a Student t test, and the P values denote the probability of the mutated alleles having expression equal to that of the wild type (WT).