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. Author manuscript; available in PMC: 2013 May 1.
Published in final edited form as: DNA Repair (Amst). 2012 Mar 13;11(5):480–487. doi: 10.1016/j.dnarep.2012.02.001

Fig. 1.

Fig. 1

Outline of the genetic system used to obtain mutator mutants of E. coli carrying defects in the nrdAB genes. Plasmid pHABcat is mutagenized (*) in vitro with hydroxylamine and used to transform a strain containing plasmid pHABamp and a chromosomal nrdAB deletion. Replacement of pHABamp by pHABcat then allows scoring for a mutator phenotype based on colony papillation (lacZ reversion). See text and Materials and Methods for details.