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Construction, transfer and properties of a novel temperature‐sensitive integrable plasmid for genomic analysis of Staphyiococcus aureus
Author(s) -
Luchansky J. B.,
Benson A. K.,
Atherly A. G.
Publication year - 1989
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.1989.tb00105.x
Subject(s) - plasmid , biology , replicon , transformation (genetics) , genetics , t dna binary system , transposable element , microbiology and biotechnology , gene , genome , recombinant dna , vector (molecular biology)
Summary As an alternative approach to genetic transfer and analysis, a novel integrable plasmid system was developed that should prove useful for mapping and cloning various genes in Staphylococcus aureus and other Gram‐positive bacteria. The use of a restriction‐deficient recipient strain and an improved protocol for protoplast plasmid transformation facilitated direct cloning of a recombinant plasmid (pPQ126) in S. aureus NCTC 8325‐4. Plasmid pPQ126 (13.6 kb) is a novel, temperature‐sensitive integrable plasmid containing genes encoding resistance to erythromycin and chloramphenicol (from plasmid pTV1 ts ), and resistance to gentamicin (from transposon Tn 4001 ). When introduced into an appropriate recipient strain at the permissive temperature (30°C), pPQ126 replicates autonomously. Integration of pPQ126 is directed into homologous chromosomal target sequences (chromosomal insertions of Tn 551 or Tn4001 ) by growing a population of cells containing autonomous pPQ126 in the presence of gentamicin, erythromycin, and chloramphenicol at 39°C (nonpermissive temperature). Elevated temperature both selects for and maintains pPQ126 as an integrated replicon. Integration of pPQ126 occurs at significantly reduced frequency in a recombination‐deficient host, and does not occur in the absence of host chromosomal homology. Integrated pPQ126 excises from the chromosome under permissive conditions (30°C), and excision results in derivatives of pPQ126 that harbour DNA of chromosomal origin.