Initiation of Chromosomal Replication in Predatory Bacterium .

Front Microbiol

Department of Microbiology, Hirszfeld Institute of Immunology and Experimental Therapy - Polish Academy of SciencesWrocław, Poland; Department of Molecular Microbiology, Faculty of Biotechnology, University of WrocławWrocław, Poland.

Published: November 2016

is a small Gram-negative predatory bacterium that attacks other Gram-negative bacteria, including many animal, human, and plant pathogens. This bacterium exhibits a peculiar biphasic life cycle during which two different types of cells are produced: non-replicating highly motile cells (the free-living phase) and replicating cells (the intracellular-growth phase). The process of chromosomal replication in must therefore be temporally and spatially regulated to ensure that it is coordinated with cell differentiation and cell cycle progression. Recently, has received considerable research interest due to its intriguing life cycle and great potential as a prospective antimicrobial agent. Although, we know that chromosomal replication in bacteria is mainly regulated at the initiation step, no data exists about this process in . We report the first characterization of key elements of initiation of chromosomal replication - DnaA protein and region from the predatory bacterium, . studies using different approaches demonstrate that the (Bd) is specifically bound and unwound by the DnaA protein. Sequence comparison of the DnaA-binding sites enabled us to propose a consensus sequence for the DnaA box [5'-NN(A/T)TCCACA-3']. Surprisingly, analysis revealed that Bd is also bound and unwound by the host DnaA proteins (relatively distantly related from ). We compared the architecture of the DnaA- complexes (orisomes) in homologous ( and DnaA from ) and heterologous (Bd and DnaA from prey, or ) systems. This work provides important new entry points toward improving our understanding of the initiation of chromosomal replication in this predatory bacterium.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124646PMC
http://dx.doi.org/10.3389/fmicb.2016.01898DOI Listing

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