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An Escherichia coli strain containing the recA promoter that fused to the luxCDABE operon originationg from Photorhabdus luminescens was shown to respond sensitively to genotoxic stresses. Two different recombinant bacteria, one (DPD1657) harboring a plasmid with the recA promoter that fused to the luxCDABE operon, and the other (DPD1710) containing a chromosomally-integrated recA promoter that fused with lux CDABE, were compared and it was found that the sensitivity of the two strains was significantly different in terms of their boiluminescent level, response time, and the minimum detectable concentration of a chemical causing DNA damaging stress. DPD1710, with a chromosomally-integrated single copy, generally led to lower basal luminescence levels, faster responses, increased response ratios, and an enhanced sensitivity to mutagens, when compared to DPD1657 with a multi-copy plasmid.
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