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Biomedical subjects

L N Pasynkova

Publications and source records attributed to L N Pasynkova.

5 recordsLinked to original sources
PubMed1984

[Role of lysogenizing phages in the spread of drug-resistance plasmids in a staphylococcal population].

The frequency of the transduction of plasmids rms5, rms7, pT127, pC194, pS194 and pUB101 by phages belonging to serological group B (80, 52, 52A, 53, 85, phi 11, S2) in two systems was compared. In system 1 phages for transduction were obtained from plasmid-containing lysogenic donors in the process of induction with mitomycin C; in system 2 phages for transduction were obtained by their multiplication in plasmid-containing nonlysogenic donors. In system 1 the transduction of plasmids rms5, rms7, pT127, pS194 by phage 52A was found to occur with a greater (by 3-5 orders) frequency than in system 2 (the frequency of transduction was 10(-2) to 10(-4), and 10(-6) to 10(-8) respectively). A similar situation was observed with plasmids rms5 and rms7 and phage 52; plasmid pT127 and phage 53; but not observed with plasmids rms5 and rms7 and phages 80, phi 11 and S2; plasmids pC194 and pS194 and phage 53; plasmid pUB101 and phages 52A, 80 and phi 11; plasmids pC194, pS194 and pT127 and phage 85.

Anti-Bacterial Agents↗
PubMed1980

[Tn9 integration sites and their effect on transposon properties].

The insertion of transposable deoxyribonucleic acid sequence that specifies chloramphenicol acetyltransferase (Tn9) occurs in the preferential sites of the Escherichia coli K-12 chromosome. It is found that some strains of E. coli K-12 have different preferential sites for the Tn9 insertion, located in various regions of the chromosome. The IS1 element inserted into the galT gene of the N116 strain (insertion mutation galT 116:IS1) serves as a strongly preferential site for the Tn9 insertion in this strain. However, being transferred into the chromosome of the KS836 strain this element loses such preference. It was demonstrated that the transposons (Tn9) inserted into different chromosomal sites are distinguished by such properties as stability, different capability to transposition into genomes of bacteriophages and plasmids, and by the choice of the preferential sites of integration in the course of subsequent insertions.

Acetyltransferases↗