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. 2012 Mar 28;13(8):923–934. doi: 10.1111/j.1364-3703.2012.00800.x

Table 3.

The expression of nlxA and other lipopolysaccharide (LPS) biosynthesis genes was induced on semi‐solid agar plates.

Target gene Locus tag Annotated function Primer sequence (5' to 3') Fold change ± SE* P value (Student's t‐test)
nlxA NA F: AGCCATGCAAACATCGTGTCGTTG 2.611095 ± 0.705173 0.0304023
R: AAACGTAGGCATCGTCTAAGGCCA
NA XAC3588 Integral membrane protein F: TCGGAATTTCTACTGCAGACGCCA 2.694485 ± 0.200239 0.0005489
R: CGAATTCTGCAGCAAGCATGGACA
NA XAC3590 Oxidoreductase F: TCCTTCGGGCTTTCTGCAGTATCA 3.367230 ± 0.324939 0.001889
R: TGTTGCCGAATTCCTTCAACACGG
wxacO XAC3596 Putative transmembrane protein F: TCTTTATGCGCTCTTGGCCGTAGT 5.199567 ± 0.647125 0.0128718
R: ACATCGGTCATCTGGCGGACATAA
rfbC XAC3598 Truncated O‐antigen biosynthesis protein F: ATCCATCACCAGCACCTGTTCGTA 2.772365 ± 0.842772 0.0052181
R: GAATCCGCCAATGGCATCGAAGTT
wzm XAC3601 ABC transporter permease F: TTGAAATGGTCCCGATGCTGCTTG 2.393728 ± 0.488077 0.0213009
R: AAAGCAGAACGCTGCTCAGAATGC

F, forward primer; R, reverse primer.

*

The wild‐type was cultured in nutrient broth (NB) for 20 h or on a semi‐solid plate for 24 h; the fold change was calculated using gene expression of the wild‐type after culture in NB for 20 h as calibrator according to the formula 2–ΔΔ CT (Livak and Schmittgen, 2001). SE, standard error.

Target genes and the corresponding ID are listed. NA denotes a gene name or ID that has not yet been assigned.