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Journal of Bacteriology, February 2001, p. 1058-1068, Vol. 183, No. 3
Department of Microbiology and Immunology,
Temple University School of Medicine, Philadelphia, Pennsylvania
19140,1 and Institute of Cell & Molecular Biology, University of Edinburgh, Edinburgh EH9 3JR,
Scotland2
Received 29 July 2000/Accepted 13 October 2000
Bacteria with circular chromosomes have evolved systems that ensure
multimeric chromosomes, formed by homologous recombination between
sister chromosomes during DNA replication, are resolved to monomers
prior to cell division. The chromosome dimer resolution process in
Escherichia coli is mediated by two tyrosine family site-specific recombinases, XerC and XerD, and requires septal localization of the division protein FtsK. The Xer recombinases act
near the terminus of chromosome replication at a site known as
dif (Ecdif). In Bacillus subtilis
the RipX and CodV site-specific recombinases have been implicated in an
analogous reaction. We present here genetic and biochemical evidence
that a 28-bp sequence of DNA (Bsdif), lying 6°
counterclockwise from the B. subtilis terminus of
replication (172°), is the site at which RipX and CodV catalyze
site-specific recombination reactions required for normal chromosome
partitioning. Bsdif in vivo recombination did not require
the B. subtilis FtsK homologues, SpoIIIE and YtpT. We also
show that the presence or absence of the B. subtilis
SP
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.3.1058-1068.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Identification and Characterization of the
dif Site from Bacillus subtilis
-bacteriophage, and in particular its yopP gene
product, appears to strongly modulate the extent of the partitioning
defects seen in codV strains and, to a lesser extent, those
seen in ripX and dif strains.
*
Corresponding author. Mailing address: Temple
University School of Medicine, 3400 North Broad St., Philadelphia, PA
19140. Phone: (215) 707-7927. Fax: (215) 707-7788. E-mail:
piggotp{at}astro.temple.edu.
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