Antirestriction Activity of ArdA Encoded by the IncI1 Transmissive Plasmid R64

2004 ◽  
Vol 38 (5) ◽  
pp. 765-769 ◽  
Author(s):  
G. B. Zavilgelsky ◽  
T. A. Letutchaja ◽  
S. M. Rastorguev
Keyword(s):  
1998 ◽  
Vol 180 (20) ◽  
pp. 5285-5290 ◽  
Author(s):  
Richard van Kranenburg ◽  
Willem M. de Vos

ABSTRACT We characterized the regions involved in replication and mobilization of the 40-kb plasmid pNZ4000, encoding exopolysaccharide (EPS) production in Lactococcus lactis NIZO B40. The plasmid contains four highly conserved replication regions with homologous rep genes (repB1, repB2,repB3, and repB4) that belong to the lactococcal theta replicon family. Subcloning of each replicon individually showed that all are functional and compatible in L. lactis. Plasmid pNZ4000 and genetically labeled derivatives could be transferred to different L. lactis strains by conjugation, and pNZ4000 was shown to be a mobilization plasmid. Two regions involved in mobilization were identified near two of the replicons; both included an oriT sequence rich in inverted repeats. Conjugative mobilization of the nonmobilizable plasmid pNZ124 was promoted by either one of these oriT sequences, demonstrating their functionality. One oriT sequence was followed by a mobA gene, coding for atrans-acting protein, which increased the frequency of conjugative transfer 100-fold. The predicted MobA protein and theoriT sequences show protein and nucleotide similarity, respectively, with the relaxase and with the inverted repeat andnic site of the oriT from the Escherichia coli plasmid R64. The presence on pNZ4000 of four functional replicons, two oriT sequences, and several insertion sequence-like elements strongly suggests that this EPS plasmid is a naturally occurring cointegrate.


1988 ◽  
Vol 170 (9) ◽  
pp. 4385-4387 ◽  
Author(s):  
T Komano ◽  
A Toyoshima ◽  
K Morita ◽  
T Nisioka

2007 ◽  
Vol 190 (4) ◽  
pp. 1202-1208 ◽  
Author(s):  
Eriko Shimoda ◽  
Tatsuya Muto ◽  
Takayuki Horiuchi ◽  
Nobuhisa Furuya ◽  
Teruya Komano

ABSTRACT The type IV pili of plasmid R64 belonging to the type IVB group are required only for liquid mating. They consist of the major and minor components PilS pilin and PilV adhesin, respectively. PilS pilin is first synthesized as a 22-kDa prepilin from the pilS gene and is then processed to a 19-kDa mature pilin by PilU prepilin peptidase. In a previous genetic analysis, we identified four classes of the pilS mutants (T. Horiuchi and T. Komano, J. Bacteriol. 180:4613-4620, 1998). The products of the class I pilS mutants were not processed by prepilin peptidase; the products of the class II mutants were not secreted; in the class III mutants type IV pili with reduced activities in liquid mating were produced; and in the class IV mutants type IV pili with normal activities were produced. Here, we describe a novel class, class V, of pilS mutants. Mutations in the pilS gene at Gly-56 or Tyr-57 produced type IV pili lacking PilV adhesin, which were inactive in liquid mating. Residues 56 and 57 of PilS pilin are suggested to function as an interface of PilS-PilV interactions.


2003 ◽  
Vol 185 (13) ◽  
pp. 3871-3877 ◽  
Author(s):  
Nobuhisa Furuya ◽  
Teruya Komano

ABSTRACT The origin of transfer (oriT) of a bacterial plasmid plays a key role in both the initiation and termination of conjugative DNA transfer. We have previously shown that a conjugation-dependent recombination between the tandem R64 oriT sequences cloned into pHSG398 occurred, resulting in the deletion of the intervening sequence during DNA transfer. In this study, we tandemly cloned two oriT sequences of IncI1 plasmid R64 into pUC18. Specific recombination between the two oriT sequences in pUC18 was observed within Escherichia coli cells harboring mini-R64. This recombination was found to be independent of both the recA gene and conjugative DNA transfer. The R64 genes nikA and nikB, required for conjugal DNA processing, were essential for this recombination. Although a fully active 92-bp oriT sequence was required at one site for the recombination, the 44-bp oriT core sequence was sufficient at the other site. Furthermore, when two oriT sequences were tandemly cloned into the single-stranded phage vector M13 and propagated within E. coli cells, recombination between the two oriT sequences was observed, depending on the nikB gene. These results suggest that the R64 relaxase protein NikB can execute cleavage and rejoining of single-stranded oriT DNA within E. coli cells, whereas such a reaction in double-stranded oriT DNA requires collaboration of the two relaxosome proteins, NikA and NikB.


1986 ◽  
Vol 165 (1) ◽  
pp. 94-100 ◽  
Author(s):  
T Komano ◽  
A Kubo ◽  
T Kayanuma ◽  
T Furuichi ◽  
T Nisioka

2006 ◽  
Vol 281 (30) ◽  
pp. 20772-20779 ◽  
Author(s):  
Atsuko Gyohda ◽  
Shujuan Zhu ◽  
Nobuhisa Furuya ◽  
Teruya Komano
Keyword(s):  

1997 ◽  
Vol 179 (11) ◽  
pp. 3594-3603 ◽  
Author(s):  
S R Kim ◽  
T Komano
Keyword(s):  
Type Iv ◽  

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