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A single parS sequence from the cluster of four sites closest to oriC is necessary and sufficient for proper chromosome segregation in Pseudomonas aeruginosaConvenient broad-host-range unstable vectors for studying stabilization cassettes in diverse bacteria.Increased ParB level affects expression of stress response, adaptation and virulence operons and potentiates repression of promoters adjacent to the high affinity binding sites parS3 and parS4 in Pseudomonas aeruginosa.Functional dissection of the ParB homologue (KorB) from IncP-1 plasmid RK2ParB of Pseudomonas aeruginosa: interactions with its partner ParA and its target parS and specific effects on bacterial growth.Dissection of the region of Pseudomonas aeruginosa ParA that is important for dimerization and interactions with its partner ParBTranscriptional profiling of ParA and ParB mutants in actively dividing cells of an opportunistic human pathogen Pseudomonas aeruginosa.ParB deficiency in Pseudomonas aeruginosa destabilizes the partner protein ParA and affects a variety of physiological parameters.Deletion of the parA (soj) homologue in Pseudomonas aeruginosa causes ParB instability and affects growth rate, chromosome segregation, and motilityIdentification of C-terminal hydrophobic residues important for dimerization and all known functions of ParB of Pseudomonas aeruginosaCorrection: A Single parS Sequence from the Cluster of Four Sites Closest to oriC Is Necessary and Sufficient for Proper Chromosome Segregation in Pseudomonas aeruginosa.Characterization of the replicator region of megaplasmid pTAV3 of Paracoccus versutus and search for plasmid-encoded traits.Concerted action of NIC relaxase and auxiliary protein MobC in RA3 plasmid conjugation.Novel broad-host-range vehicles for cloning and shuffling of gene cassettes.Pseudomonas aeruginosa partitioning protein ParB acts as a nucleoid-associated protein binding to multiple copies of a parS-related motif.
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