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PMID: 2826394 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Genetic organization of the bacterial conjugative transposon Tn916.

Journal of bacteriology ·Vol. 170 ·No. 1 ·1988-01-00 ·Pages 245-9

Senghas E, Jones JM, Yamamoto M, Gawron-Burke C, Clewell DB

Abstract

Tn916, which encodes resistance to tetracycline, is a 16.4-kilobase conjugative transposon originally identified on the chromosome of Streptococcus faecalis DS16. The transposon has been cloned in Escherichia coli on plasmid vectors, where it expresses tetracycline resistance; it can be reintroduced into S. faecalis via protoplast transformation. We have used a lambda::Tn5 bacteriophage delivery system to introduce Tn5 into numerous sites within Tn916. The Tn5 insertions had various effects on the behavior of Tn916. Some insertions eliminated conjugative transposition but not intracellular transposition, and others eliminated an excision step believed to be essential for both types of transposition. A few inserts had no effect on transposon behavior. Functions were mapped to specific regions on the transposon.

MeSH Terms
Bacteriophage lambda Chromosome Mapping Cloning, Molecular Conjugation, Genetic DNA Transposable Elements Enterococcus faecalis/genetics Escherichia coli/genetics Genes, Bacterial Plasmids Tetracycline Resistance/genetics
Chemicals
DNA Transposable Elements
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Senghas E
Department of Oral Biology, School of Dentistry, University of Michigan, Ann Arbor 48109-0402.
Jones J M
Yamamoto M
Gawron-Burke C
Clewell D B
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19 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1988-01-00
Pages
245-9
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC210634
Subset
IM
Grants
NIAID NIH HHS · AI10318 · United States
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