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. 2010 Jan 14;192(6):1573–1585. doi: 10.1128/JB.01394-09

FIG. 6.

FIG. 6.

Effect of replacement of guanine at the transcription initiation base (+1) of the pdhABCD operon with adenine on the negative stringent control of this operon. (A) The guanine at the transcription initiation site (+1) of the pdhABCD promoter (nucleotides −47 to 167) was replaced by adenine. The −35 and −10 regions of the pdhABCD promoter are underlined. (B) The mutant pdhABCD promoter was placed upstream of lacZ in the relA+ and codY+ backgrounds. lacZ expression in the resulting strains (FU1019 [wild type] and FU1044 [mutant]) was monitored upon lysine starvation and decoyinine treatment, as described in Materials and Methods. OD600 values (small symbols) and LacZ activities (large symbols) are indicated by circles for FU1019 and by squares for FU1044; filled and open symbols indicate results obtained with and without lysine starvation and decoyinine treatment, respectively. The arrows indicate the onset of these stresses.