Topic Introduction

DNA Recombineering Applications

  1. Lionello Bossi1,3
  1. 1Université Paris-Saclay, CEA, CNRS, Institut de Biologie Intégrative de la Cellule (I2BC), 91190 Gif-sur-Yvette, France
  2. 2Departamento de Genética, Facultad de Biología, Universidad de Sevilla, 41080 Sevilla, Spain
  1. 3Correspondence: lionello.bossi{at}i2bc.paris-saclay.fr

Abstract

The ability to manipulate the bacterial genome is an obligatory premise for the study of gene function and regulation in bacterial cells. The λ red recombineering technique allows modification of chromosomal sequences with base-pair precision without the need of intermediate molecular cloning steps. Initially conceived to construct insertion mutants, the technique lends itself to a wide variety of applications including the creation of point mutants, seamless deletions, reporter, and epitope tag fusions and chromosomal rearrangements. Here, we introduce some of the most common implementations of the method.

Footnotes

  • From the Experiments in Bacterial Genetics collection, edited by Lionello Bossi, Andrew Camilli, and Angelika Gründling.

| Table of Contents