The 
 nag genes are an operon in Ralstonia sp. strain U2 that is 
 regulated by NagR, a LysR-type transcriptional regulator.Jones, R.M., Britt-Compton B. 
 & Williams P.A.  J. Bacteriol. (Submitted)
 
 ABSTRACT
 
 In Ralstonia sp. strain U2, the nag catabolic genes which encode 
 the enzymes for the pathway that catabolize naphthalene via the alternative 
 ring-cleavage gentisate pathway are transcribed as an operon under the 
 same promoter. Divergently transcribed to the nag catabolic genes 
 is nagR, which encodes a LysR-type transcriptional regulator. A 
 4 bp frameshift deletion in nagR demonstrated that NagR is required 
 for the expression of the nag operon. The transcriptional start 
 of the nag operon was mapped, and a putative -10, -35 sigma 70-type promoter 
 binding site was identified. Further upstream, a site proximal to the promoter 
 was identified as having bases which have been found to be conserved in 
 the LysR-type activator-binding motif. Transcriptional fusion studies demonstrated 
 that NagR regulates the expression of the nag operon positively in the 
 presence of salicylate, and to a lesser extent in the presence of 2-nitrobenzoate. 
 Mutation of the LysR-type activator-binding motif in the nag promoter-proximal 
 region,  resulted in loss of inducibility of a LacZ reporter gene 
 transcriptionally fused the nagAa, the first gene of the operon. 
 However other mutations within the region produced elevated levels of  
 nag gene expression even in the presence of the inducer salicylate.