Novel tnpR-based transposable promoter traps suitable for RIVET studies in different gram-negative bacteria

J Microbiol Methods. 2013 Apr;93(1):9-11. doi: 10.1016/j.mimet.2013.01.017.

Abstract

The preparation of plasmid-borne RIVET libraries can be troublesome when high genomic coverages are needed. We present here the construction and functional validation of a new set of miniTn5 promoter traps to generate tnpR-based RIVET libraries. The ability to generate tnpR transcriptional fusions by transposition will significantly facilitate the setup of RIVET studies in those bacteria where Tn5 transposition is operative.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Transposable Elements
  • Gene Fusion
  • Gene Library
  • Genetics, Microbial / methods*
  • Gram-Negative Bacteria / genetics*
  • Molecular Biology / methods*
  • Promoter Regions, Genetic*

Substances

  • DNA Transposable Elements