Abstract
Conditions optimal for the transformation of Pseudomonas putida and E. coli with a drug-resistance factor (RP 1) DNA, which specifies resistance to carbenicillin, tetracycline, kanamycin, and neomycin, are described. The transformants retain all the fertility, incompatibility, and drug-resistance characteristics present in the parent. Covalently-closed circular molecules of almost identical contour lengths have been isolated from the parent and the transformants. The frequency of transformation is drastically reduced by treatment of RP 1 DNA with DNase and by denaturation or sonication. Shearing of RP 1 DNA in vitro and their subsequent introduction in P. putida cells, by transformation, produces transformants that exhibit a wide range of drug-resistant phenotypes, including those which are resistant to neomycin but sensitive to kanamycin. Isolation of such neomycin-resistant but kanamycin-sensitive transformants indicates that there might be two separate mechanisms specified by RP 1 for resistance to the two antibiotics.
MeSH Terms
Calcium/pharmacology
Carbenicillin
DNA/metabolism
DNA, Bacterial/metabolism
DNA, Satellite/metabolism
Escherichia coli/metabolism
Extrachromosomal Inheritance
Kanamycin
Neomycin
Penicillin Resistance
Plasmids
Pseudomonas/metabolism
R Factors
Tetracycline
Transformation, Genetic/drug effects
Chemicals
DNA, Bacterial
DNA, Satellite
Kanamycin
DNA
Tetracycline
Carbenicillin
Neomycin
Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chakrabarty A M
Mylroie J R
Friello D A
Vacca J G
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