Affiliation:
1. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA
Abstract
ABSTRACT
Bacillus anthracis
pXO1 minireplicon (MR) plasmid consisting of open reading frames (ORFs) GBAA_pXO1_0020 to GBAA_pXO1_0023 is not stably maintained in
B. anthracis
, whereas the full-size parent pXO1 plasmid (having 181,677 bp and 217 ORFs) is extremely stable under the same growth conditions. Two genetic tools developed for DNA manipulation in
B. anthracis
(Cre-
loxP
and Flp-
FRT
systems) were used to identify pXO1 regions important for plasmid stability. We localized a large segment of pXO1 that enables stable plasmid maintenance during vegetative growth. Further genetic analysis identified three genes that are necessary for pXO1 maintenance:
amsP
(GBAA_pXO1_0069),
minP
(GBAA_pXO1_0082), and
sojP
(GBAA_pXO1_0084). Analysis of conserved domains in the corresponding proteins indicated that only AmsP (activator of maintenance system of pXO1) is predicted to bind DNA, due to its strong helix-turn-helix domain. Two conserved domains were found in the MinP protein (Min protein from pXO1): an N-terminal domain having some similarity to the
B. anthracis
septum site-determining protein MinD and a C-terminal domain that resembles a baculovirus single-stranded-DNA-binding protein. The SojP protein (Soj from pXO1) contains putative Walker box motifs and belongs to the ParA family of ATPases. No sequences encoding other components of type I plasmid partition systems, namely,
cis
-acting centromere
parS
and its binding ParB protein, were identified within the pXO1 genome. A model describing the role of the MinP protein in pXO1 distribution between daughter cells is proposed.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
7 articles.
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