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Applied and Environmental Microbiology, May 2007, p. 2815-2819, Vol. 73, No. 9
0099-2240/07/$08.00+0 doi:10.1128/AEM.00407-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Area de Microbiología, Instituto Universitario de Biotecnología, Universidad de Oviedo, and Instituto de Productos Lácteos de Asturias, Oviedo, Spain
Received 21 February 2007/ Accepted 22 February 2007
A method for the detection of the SOS response as measured by the liberation of resident prophages from the genomes of their hosts is described. It is based on the use of two converging oligonucleotides that flank the attP attachment site of the phage as primers for real-time PCR. Amplification was observed only after the phage DNA became excised. The system responds to both chemicals and physical conditions. Quantitative data on the concentration and/or potency of the genotoxic condition were obtained. Results can be achieved within 1 day and are less susceptible to possible toxic effects than phage generation or other methods that require DNA synthesis. The use of both gram-positive and gram-negative bacteria widens the range of compounds that can be tested because it eliminates impermeability problems derived from the particular composition of each cell wall type.
Published ahead of print on 2 March 2007.
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