Elimination of plasmid pKM101 from Salmonella typhimurium by monoammonium salts
Language English Country United States Media print
Document type Journal Article
PubMed
8365694
DOI
10.1007/bf02814373
Knihovny.cz E-resources
- MeSH
- Bromides pharmacology MeSH
- Quaternary Ammonium Compounds pharmacology MeSH
- Plasmids * MeSH
- Salmonella typhimurium drug effects genetics MeSH
- Salts pharmacology MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Bromides MeSH
- Quaternary Ammonium Compounds MeSH
- Salts MeSH
The frequency of elimination of plasmid pKM101 from Salmonella typhimurium TA92 exposed to the action of 1-alkyl-1-ethylpiperidinium bromides and N-alkyl-N-[5-(benzoyloxy)-3-oxapentyl]-N,N-dimethylammonium bromides was non-linear in the homologous series. Change in the length of the alkyl chain markedly affected the elimination properties of the piperidine derivatives but had no effect on the elimination of benzoyl derivatives. Piperidines exhibited a weaker elimination capacity than the benzoyl derivatives. The most potent eliminator was the octylbenzoyl derivative, which causes the elimination of the plasmid in 80-85% cells.
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