Precision-engineering the Pseudomonas aeruginosa genome with two-step allelic exchange

• Published in: Nature protocols Vol. 10; no. 11; pp. 1820 - 1841
• Main Authors: Hmelo, Laura R, Borlee, Bradley R, Almblad, Henrik, Love, Michelle E, Randall, Trevor E, Tseng, Boo Shan, Lin, Chuyang, Irie, Yasuhiko, Storek, Kelly M, Yang, Jaeun Jane, Siehnel, Richard J, Howell, P Lynne, Singh, Pradeep K, Tolker-Nielsen, Tim, Parsek, Matthew R, Schweizer, Herbert P, Harrison, Joe J
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.11.2015; Nature Publishing Group
• Subjects: 631/114/1564; 631/136; 631/1647/328/2237; 631/80; Alleles; Analysis; Analytical Chemistry; Antibiotic resistance; Antibiotics; Biofilms; Biological Techniques; Chromosomes; Cloning; Computational Biology/Bioinformatics; Conjugation; Crossovers; Deoxyribonucleic acid; DNA; DNA microarrays; Drug resistance; Engineering; Exchanging; Gene mutations; Gene Targeting - methods; Genes; Genetic aspects; Genetic Engineering; Genetic Vectors; Genome editing; Genome, Bacterial; Genomes; Homologous Recombination; Homology; Immunology; Influence; Life Sciences; Microarrays; Microbial mats; Molecular biology; Molecular Biology - methods; Mutants; Mutation; Nucleotides; Organic Chemistry; protocol; Pseudomonas aeruginosa; Pseudomonas aeruginosa - genetics; Sucrose; Suicide; Suicide vectors; Toronto Ontario Canada; Canada; United States > US
• ISSN: 1754-2189; 1750-2799; 1750-2799
• DOI: 10.1038/nprot.2015.115

Here, the authors describe genetically engineering the Pseudomonas genome by two-step allelic exchange. Suicide vector-encoded alleles are used to generate mutations by homologous recombination at the single base pair level. Allelic exchange is an efficient method of bacterial genome engineering. This protocol describes the use of this technique to make gene knockouts and knock-ins, as well as single-nucleotide insertions, deletions and substitutions, in Pseudomonas aeruginosa . Unlike other approaches to allelic exchange, this protocol does not require heterologous recombinases to insert or excise selective markers from the target chromosome. Rather, positive and negative selections are enabled solely by suicide vector–encoded functions and host cell proteins. Here, mutant alleles, which are flanked by regions of homology to the recipient chromosome, are synthesized in vitro and then cloned into allelic exchange vectors using standard procedures. These suicide vectors are then introduced into recipient cells by conjugation. Homologous recombination then results in antibiotic-resistant single-crossover mutants in which the plasmid has integrated site-specifically into the chromosome. Subsequently, unmarked double-crossover mutants are isolated directly using sucrose-mediated counter-selection. This two-step process yields seamless mutations that are precise to a single base pair of DNA. The entire procedure requires ∼2 weeks.