Abstract
In Escherichia coli hosts, hydrogen peroxide is one of the factors that may cause induction of λ prophage. Here, we demonstrate that H 2 O 2 -mediated λ prophage induction is significantly enhanced in the oxyR mutant host. The mRNA levels for cI gene expression were increased in a λ lysogen in the presence of H 2 O 2 . On the other hand, stimulation of the p M promoter by cI857 overproduced from a multicopy plasmid was decreased in the ΔoxyR mutant in the presence of H 2 O 2 but not under normal growth conditions. The purified OxyR protein did bind specifically to the p M promoter region. This binding impaired efficiency of interaction of the cI protein with the OR3 site, while stimulating such a binding to OR2 and OR1 sites, in the regulatory region of the p M promoter. We propose that changes in cI gene expression, perhaps in combination with moderately induced SOS response, may be responsible for enhanced λ prophage induction by hydrogen peroxide in the oxyR mutant. Therefore, OxyR seems to be a factor stimulating λ prophage maintenance under conditions of oxidative stress. This proposal is discussed in the light of efficiency of induction of lambdoid prophages bearing genes coding for Shiga toxins. © 2010 The Author(s).
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Glinkowska, M., Łoś, J. M., Szambowska, A., Czyż, A., Całkiewicz, J., Herman-Antosiewicz, A., … Łoś, M. (2010). Influence of the Escherichia coli oxyR gene function on λ prophage maintenance. Archives of Microbiology, 192(8), 673–683. https://doi.org/10.1007/s00203-010-0596-2
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