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PMID: 3006104 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

DNA segments of the IncX plasmid R485 determining replication and incompatibility with plasmid R6K.

Plasmid ·Vol. 14 ·No. 3 ·1985-11-00 ·Pages 245-54

Stalker DM, Helinski DR

Abstract

The expression of incompatibility properties between the IncX plasmids R6K and R485 of Escherichia coli was examined. For small autonomously replicating derivatives of both plasmid elements, the requirements for incompatibility expression include a functional R485 replicon and an active R6K beta-origin region. Functional R6K alpha and gamma origins are not directly involved in incompatibility expression between R6K and R485. A trans-acting replication system was constructed for plasmid R485. It consists of a 3.2-(kb) DNA fragment of R485 that specifies a product(s) in trans which supports replication from an R485 origin plasmid. A minimal R485 origin region of 591 bp was derived utilizing this trans-acting replication system and the nucleotide sequence of this origin region determined. The most striking feature of the sequence is the presence of six tandem 22-bp nucleotide sequence direct repeats.

MeSH Terms
Base Sequence DNA Replication DNA Restriction Enzymes DNA, Bacterial/isolation & purification Escherichia coli/genetics Plasmids Species Specificity
Chemicals
DNA, Bacterial DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Stalker D M
Helinski D R
Article Info
Journal
Plasmid
Abbr.
Plasmid
ISSN
0147-619X
Published
1985-11-00
Pages
245-54
Language
English
Region
United States
NLM ID
7802221
Subset
IM
Grants
NIGMS NIH HHS · 1-F32-GM06543 · United States
NIAID NIH HHS · AI-07194 · United States
Databases
GENBANK
M11688
Analysis Services
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