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PMID: 2857162 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Conjugal transfer system of the IncN plasmid pKM101.

Journal of bacteriology ·Vol. 161 ·No. 1 ·1985-01-00 ·Pages 402-10

Winans SC, Walker GC

Abstract

The conjugal transfer system of the broad-host range IncN plasmid pKM101 was analyzed genetically. Its organization differed significantly from that of the F plasmid. The tra genes are located in three regions, each between 3 and 4 kilobases in length. All of the genes in the first two regions are required for sensitivity to "donor-specific" phage which bind to the plasmid-mediated sex pilus, and these genes therefore are involved in the synthesis, and possibly retraction, of the sex pilus. The plasmid's origin of transfer was localized to a 1.2-kilobase region at an extreme end of the transfer region. Using two different methods, we have identified 11 complementation groups required for transfer. One of these, traC, is of special interest in that mutations at this locus can be partially suppressed if, prior to mating, cells carrying a traC mutant plasmid are incubated with cells which elaborate sex pili but are unable to transfer their plasmids. One possible explanation for this is that pilus-elaborating cells can donate traC gene product to a traC mutant in a form that can be reused.

MeSH Terms
Bacteriophages/genetics Conjugation, Genetic DNA, Bacterial/genetics Escherichia coli/genetics Fimbriae, Bacterial Mutation Plasmids Suppression, Genetic Transformation, Bacterial
Chemicals
DNA, Bacterial
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Winans S C
Walker G C
References (30)
30 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1985-01-00
Pages
402-10
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC214885
Subset
IM
Grants
NCI NIH HHS · 1-RO1-CA21615 · United States
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