| Literature DB >> 33704752 |
Kenneth G Campellone1, Alyssa M Coulter2.
Abstract
The bacteriophage Lambda (λ) "Red" recombination system has enabled the development of efficient methods for engineering bacterial chromosomes. This system has been particularly important to the field of bacterial pathogenesis, where it has advanced the study of virulence factors from Shiga toxin-producing and enteropathogenic Escherichia coli (STEC and EPEC). Transient plasmid-driven expression of Lambda Red allows homologous recombination between PCR-derived linear DNA substrates and target loci in the STEC/EPEC chromosomes. Red-associated techniques can be used to create individual gene knockouts, generate deletions of large pathogenicity islands, and make markerless allelic exchanges. This chapter describes specific strategies and procedures for performing Lambda Red-mediated genome engineering in STEC.Entities:
Keywords: Allelic exchange; Bacterial genetics; EPEC; Enteropathogenic E. coli; Escherichia coli; Homologous recombination; Lambda Red; Recombineering; STEC; Shiga toxin-producing E. coli
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Year: 2021 PMID: 33704752 DOI: 10.1007/978-1-0716-1339-9_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745