Nucleotide sequence and replication characteristics of RepFIB, a basic replicon of IncF plasmids

D. Saul*, A. J. Spiers, J. McAnulty, M. G. Gibbs, P. L. Bergquist, D. F. Hill

*Corresponding author for this work

Research output: Contribution to journalArticle

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Abstract

A second autonomous replicon of P307, RepFIB, has been isolated that has significant homology with other replicons in IncFI group plasmids. Eleven homologous repeats of 21 base pairs are present on the sequence and flank an open reading frame capable of coding for a protein of about Mr = 40,000. This protein was identified by maxicell analysis of cloned RepFIB. A series of deletion mutations of RepFIB were inserted into a DNA polymerase I-dependent vector and examined for their replication proficiency in a polA1 strain. These experiments defined a minimal replication region of 1.6 kilobases which includes the three repeats immediately upstream and downstream of the open reading frame. Deletion of a second set of repeats further downstream doubled the copy number of a chimeric plasmid replicating under RepFIB control. It was concluded that these repeats control the copy number of the replicon. Incompatibility tests showed that all three sets of repeats could express incompatibility with a resident RepFIB plasmid.

Original languageEnglish
Pages (from-to)2697-2707
Number of pages11
JournalJournal of Bacteriology
Volume171
Issue number5
DOIs
Publication statusPublished - May 1989
Externally publishedYes

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Replicon
Plasmids
Open Reading Frames
DNA Polymerase I
Sequence Deletion
Base Pairing
Proteins

Cite this

Saul, D. ; Spiers, A. J. ; McAnulty, J. ; Gibbs, M. G. ; Bergquist, P. L. ; Hill, D. F. / Nucleotide sequence and replication characteristics of RepFIB, a basic replicon of IncF plasmids. In: Journal of Bacteriology. 1989 ; Vol. 171, No. 5. pp. 2697-2707.
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abstract = "A second autonomous replicon of P307, RepFIB, has been isolated that has significant homology with other replicons in IncFI group plasmids. Eleven homologous repeats of 21 base pairs are present on the sequence and flank an open reading frame capable of coding for a protein of about Mr = 40,000. This protein was identified by maxicell analysis of cloned RepFIB. A series of deletion mutations of RepFIB were inserted into a DNA polymerase I-dependent vector and examined for their replication proficiency in a polA1 strain. These experiments defined a minimal replication region of 1.6 kilobases which includes the three repeats immediately upstream and downstream of the open reading frame. Deletion of a second set of repeats further downstream doubled the copy number of a chimeric plasmid replicating under RepFIB control. It was concluded that these repeats control the copy number of the replicon. Incompatibility tests showed that all three sets of repeats could express incompatibility with a resident RepFIB plasmid.",
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Nucleotide sequence and replication characteristics of RepFIB, a basic replicon of IncF plasmids. / Saul, D.; Spiers, A. J.; McAnulty, J.; Gibbs, M. G.; Bergquist, P. L.; Hill, D. F.

In: Journal of Bacteriology, Vol. 171, No. 5, 05.1989, p. 2697-2707.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Nucleotide sequence and replication characteristics of RepFIB, a basic replicon of IncF plasmids

AU - Saul, D.

AU - Spiers, A. J.

AU - McAnulty, J.

AU - Gibbs, M. G.

AU - Bergquist, P. L.

AU - Hill, D. F.

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AB - A second autonomous replicon of P307, RepFIB, has been isolated that has significant homology with other replicons in IncFI group plasmids. Eleven homologous repeats of 21 base pairs are present on the sequence and flank an open reading frame capable of coding for a protein of about Mr = 40,000. This protein was identified by maxicell analysis of cloned RepFIB. A series of deletion mutations of RepFIB were inserted into a DNA polymerase I-dependent vector and examined for their replication proficiency in a polA1 strain. These experiments defined a minimal replication region of 1.6 kilobases which includes the three repeats immediately upstream and downstream of the open reading frame. Deletion of a second set of repeats further downstream doubled the copy number of a chimeric plasmid replicating under RepFIB control. It was concluded that these repeats control the copy number of the replicon. Incompatibility tests showed that all three sets of repeats could express incompatibility with a resident RepFIB plasmid.

U2 - 10.1128/jb.171.5.2697-2707.1989

DO - 10.1128/jb.171.5.2697-2707.1989

M3 - Article

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SP - 2697

EP - 2707

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