Use of the lambda Red recombinase system to rapidly generate mutants in Pseudomonas aeruginosa

BMC Molecular Biology

Volumn 9, Issue , 2008, Pages

  Lesic, Biliana ^a,b,c   Rahme, Laurence G ^a,b,c  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b Shriners Burns Institute   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; RECOMBINASE; BACTERIAL DNA; PYOCYANINE;

ARTICLE; BACTERIAL STRAIN; BACTERIOPHAGE LAMBDA; BACTERIUM MUTANT; CHROMOSOME DELETION; CONTROLLED STUDY; DNA FLANKING REGION; GENE DELETION; GENE DISRUPTION; GENE MUTATION; GENE SEQUENCE; GENE TRANSFER; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PSEUDOMONAS AERUGINOSA; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; TRANSPOSON; BIOSYNTHESIS; ELECTROPORATION; ENZYMOLOGY; GENETIC ENGINEERING; GENETICS; METABOLISM; METHODOLOGY; MUTAGENESIS; MUTATION; PLASMID; REPRODUCIBILITY; SOUTHERN BLOTTING;

ENTEROBACTERIA PHAGE LAMBDA; FUNGI; PSEUDOMONAS AERUGINOSA;

BACTERIOPHAGE LAMBDA; BLOTTING, SOUTHERN; DNA, BACTERIAL; ELECTROPORATION; GENETIC ENGINEERING; MUTAGENESIS; MUTATION; PLASMIDS; POLYMERASE CHAIN REACTION; PSEUDOMONAS AERUGINOSA; PYOCYANINE; RECOMBINASES; REPRODUCIBILITY OF RESULTS; SEQUENCE DELETION;

EID: 41549105328     PISSN: None     EISSN: 14712199     Source Type: Journal    
DOI: 10.1186/1471-2199-9-20     Document Type: Article

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