Skip to main content
. 2010 Jun 11;192(16):4153–4163. doi: 10.1128/JB.00226-10

FIG. 1.

FIG. 1.

IS256 transposase binding to IS termini. (A) Genetic organization of IS256. The transposase gene (tnp) is flanked by NCRs that harbor imperfect IRs (IRL and IRR) at the ends of the element. The nucleotide sequence of the IRs is indicated by uppercase boldface letters, with nucleotide numbering referring to GenBank accession no. M18086. Insertion of IS256 into the S. epidermidis icaC gene on plasmid pIL2 (27) is shown, and black boxes mark the 8-bp target site duplications (TSDs) generated upon transposition of the element. Black bars at the top indicate localizations of DNA fragments used in the EMSAs presented in panels B to D. (B to D) EMSAs of purified IS256 transposase protein (CBP-Tnp) with various IS256-specific DNA fragments. A 15.5 nM concentration of an IS terminus (left)-carrying DNA fragment (B) or an IS terminus (right)-carrying DNA-fragment (C), as well as an interal IS256 fragment (D), were used with increasing amounts of protein. All experiments were performed in the presence of unspecific competitor [50 μg of poly(dI-dC) ml−1]. Molar ratios between DNA and protein comprised a range of 1:3 (50 nM CBP-Tnp) to 1:52 (800 nM CBP-Tnp).