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. Author manuscript; available in PMC: 2011 Jan 15.
Published in final edited form as: Arch Biochem Biophys. 2009 Oct 20;493(2):135–142. doi: 10.1016/j.abb.2009.10.006

Fig. 3.

Fig. 3

Loss of recoverable pETBlue plasmid DNA from transformed NovaBlue cells following incubation with HOCl. Conditions: ~1×108 E. coli/mL in 10 mL PBS incubated at 37 °C with the indicated amounts of HOCl for 4 h, after which a 10-fold excess of Na2S2O3 was added to remove remaining oxidant, the plasmid was isolated, resuspended in H2O, and run on 0.8% agarose as described in Experimental Procedures. Lane 1 shows purified pETBlue that had been digested with EcoR1, a restriction enzyme which catalyzes a single double-strand cut in the plasmid. Lane 7 contains the 1 kB DNA ladder. No DNA was recovered from cells exposed to HOCl at higher concentrations ([HOCl] = 250–1000 µM).