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. 2002 Feb;184(4):962–970. doi: 10.1128/jb.184.4.962-970.2002

FIG. 5.

FIG. 5.

Northern blot analysis of cpeBA, cpeCDE, and cpcB2A2 expression in WT, the FdBk mutant, and the FdTq1 mutant. (A) Representative autoradiograms of the data presented in panels B to D showing hybridization to the probes listed on the left. RNA was isolated from the WT and the two mutant lines after growth in 15 μmol of RL and GL m−2 s−1. (B) Mean values from four independent experiments of cpeBA RNA, expressed as a percentage of the WT GL value (set to 100%). (C) Mean values from three independent experiments of cpeCDE RNA, expressed as a percentage of the WT GL value (set to 100%). (D) Mean values from four independent experiments of cpcB2A2 RNA, expressed as a percentage of the WT RL value (set to 100%). The numbers in parentheses are the fold induction between RL and GL for each operon in each cell line. Standard errors are shown; P values are provided in the text. Measurements were normalized by using ribosomal values prior to calculation of means.