Abstract
A procedure is described that uses an indicator plasmid (pSC201) to identify cells in a bacterial population that have been co-transformed with a second plasmid lacking detectable phenotypic properties. Under appropriate conditions of indirect selection, between 50 and 85% of transformants carrying the indicator plasmid also contain the nonselected plasmid. A temperature-sensitive mutation in the replication functions of the indicator plasmid enables its elimination from doubly transformed bacteria. Using this procedure, we have isolated bacteria that carry only the small cryptic plasmid. P15A, of the Escherichia coli strain 15. This genetic element, which contains only 2,300 nucleotide pairs, is thus capable of functioning as a replicon independently of the two larger plasmids normally associated with it in E. coli 15 strains (Ikeda, Inuzuka, and Tomizawa, 1970).
MeSH Terms
DNA Replication
DNA, Bacterial/analysis,biosynthesis
Escherichia coli/analysis,metabolism
Extrachromosomal Inheritance
Methylnitronitrosoguanidine
Molecular Weight
Mutagens
Mutation
Phenotype
Plasmids
Temperature
Transformation, Genetic
Chemicals
DNA, Bacterial
Mutagens
Methylnitronitrosoguanidine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kretschmer F J
Chang A C
Cohen S N
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24 references, click to expand
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