1. FtsK‐independent dif recombination in the presence of HinXerC.
FtsK‐independent dif recombination in the presence of HinXerC. Strains AB1157 (Xer+ FtsK+), DS8029 (XerC−) and GR51 (XerC− FtsKc−) were transformed with either pLMN132 (HinXerC+) or pSDC107 (EcoXerC+), followed by the dif reporter plasmid pSDC124. S, reporter plasmid substrate; RP, replicative resolved product. The arrow indicates the presence of an Xer‐dependent multimeric species containing three dif sites.
Gavin D. Recchia et al. EMBO J. 1999;18:
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