Characterization of Pseudomonas Mercury-resistance Transposon Tn502, Which Has a Preferred Insertion Site in RP1
- 1 November 1989
- journal article
- research article
- Published by Microbiology Society in Microbiology
- Vol. 135 (11) , 2909-2915
- https://doi.org/10.1099/00221287-135-11-2909
Abstract
Tn502mer differs in size and restriction map from the well-characterized Tn501mer. It also differs in its preferential and high-frequency insertion into the 6 kb PstI-C region of RP1. The affinity for this region is perpetuated in pVS76, a clone of RP1 PstI-C in pBR322. Restriction mapping of independent pVS76::Tn502 derivatives revealed that Tn502 inserted at the same site (or small region) in PstI-C corresponding to the 35 kb coordinate in RP1. Insertion occurred in both orientations, but one was preferred. When PstI-C was deleted from RP1, acquisition of Tn502 was reduced and the sites of insertion randomized.This publication has 3 references indexed in Scilit:
- The distribution and divergence of DNA sequences related to the Tn21 and Tn501 mer operonsPlasmid, 1988
- Deoxyribonucleic acid sequence of a gene from the Pseudomonas transposon TN501 encoding mercuric reductaseBiochemistry, 1983
- DNA sequences of and complementation by the tnpR genes of Tn21, Tn501 and Tn1721Molecular Genetics and Genomics, 1983