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. 2013 Jun;195(11):2632–2641. doi: 10.1128/JB.02062-12

Table 1.

Genes that are differentially regulated in the Ng-ntrX mutant compared to the 1291 wild-type strain

Gene type and no.a Product description (gene) ntrX mutant/WT expression ratio by:
Microarray (B statistic)b Enzyme activityc
Downregulated
    NGO1276 Nitrite reductase (aniA) 0.33 (6.91) 0.29
    NGO1275 Nitric oxide reductase (norB) 0.37 (4.09)
    NGO1769 Cytochrome c peroxidase (ccpR) 0.39 (4.19)
    NGO1371 Cytochrome oxidase subunit (ccoP) 0.40 (5.23) 0.46
    NGO1024 Hypothetical protein 0.40 (5.13)
    NGO1064 CstA 0.45 (2.18)
    NGO0718 Putative RpiR family transcriptional regulator 0.50 (4.77)
Upregulated
    NGO0641 Putative type III restriction/modification methylase 2.64 (1.01)
    NGO0640 RmsR 2.62 (3.70)
    NGO1712 Hypothetical protein 2.15 (5.15)
    NGO1889 Hypothetical protein 2.07 (3.67)
a

The “NGO” gene identification numbers refer to the annotation of the Neisseria gonorrhoeae strain FA1090 genome in the Los Alamos database (http://www.stdgen.lanl.gov/stdgen/bacteria/ngon/index.html).

b

The ratio presented is the mean of the ratio of expression of the mutant to that of the wild type (WT) from six replicate spots on three independent microarrays, incorporating a dye swap. Thus, the expression of each gene was measured six times. Only those genes with an expression value above 2-fold (upregulated) or below 0.5-fold (downregulated) and having a B statistic value above 0.0 were considered significant and included in this study. A threshold in the B statistic of 0.0 was adopted because genes with a B score of >0 have a >50% probability of being truly differentially expressed.

c

Enzyme assays were performed as detailed in Materials and Methods, and the results are detailed in Fig. S1 in the supplemental material.