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PMID: 2544570 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Mutagenesis of the Tra1 core region of RK2 by using Tn5: identification of plasmid-specific transfer genes.

Journal of bacteriology ·Vol. 171 ·No. 7 ·1989-07-00 ·Pages 4100-3

Guiney DG, Deiss C, Simnad V, Yee L, Pansegrau W, Lanka E

Abstract

The conjugation system of the IncP alpha plasmid RK2/RP4 is encoded by transfer regions designated Tra1, Tra2, and Tra3. The Tra1 core region, cloned on plasmid pDG4 delta 22, consists of the origin of transfer (oriT) and 2.6 kilobases of flanking DNA providing IncP alpha plasmid-specific functions that allow pDG4 delta 22 to be mobilized by the heterologous IncP beta plasmid R751. Tn5 insertions in pDG4 delta 22 define a minimal 2.2-kilobase region required for plasmid-specific transfer of oriT. The Tra1 core contains the traJ and traK genes as well as an 18-kilodalton open reading frame downstream of traJ. The traJ and traK genes were shown to be required for transfer by complementation of inserts within these genes. Genetic evidence for the role of the 18-kilodalton open reading frame in transfer was obtained, although this protein has not been detected in cell lysates. These studies indicate that at least three transfer proteins are involved in plasmid-specific interactions at oriT.

MeSH Terms
Bacterial Proteins/genetics,physiology Base Sequence DNA Transposable Elements Genes, Bacterial Genetic Complementation Test Mutation Plasmids Transfection
Chemicals
Bacterial Proteins DNA Transposable Elements
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Guiney D G
Department of Medicine H811F, UCSD Medical Center, San Diego, California 92103.
Deiss C
Simnad V
Yee L
Pansegrau W
Lanka E
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15 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1989-07-00
Pages
4100-3
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC210173
Subset
IM
Grants
NIGMS NIH HHS · GM 28924 · United States
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