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Chapter 23 : Chromosomal Replication, Plasmid Replication, and Cell Division

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Chromosomal Replication, Plasmid Replication, and Cell Division, Page 1 of 2

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Abstract:

The study of chromosomal replication and cell division of bacteria has extended beyond , and important insights have emerged recently from studies in other species, especially and . Cell division is coordinated with other cell cycle events such as genomic DNA synthesis that leads to chromosomal replication and partition, increase of cell mass, and cell expansion by cell wall synthesis. This chapter reviews the information about predicted genes related to chromosomal replication, plasmid replication, and cell division in , and a plausible replication machinery of the bacterium is discussed in light of the current understanding of bacterial organization and function of replication and cell division. The DnaA protein is essential for the initiation of chromosomal replication and is highly conserved among different bacteria. Clinical isolates of have been reported to carry plasmids ranging in size from 1.5 to 40 kb. Three cryptic plasmids, pHPK225 (1.5 kb), pHPM180 (3.5 kb), and pHell (2.9 kb), have been completely sequenced. Cell division of gram-negative bacteria proceeds through nucleoid segregation, partitioning of the cytoplasm into two compartments each containing a copy of the cell's genetic information, and invagination of the three layers of the cell envelope between the chromosome. Chromosomal replication and cell division of bacteria are well-organized and coordinately regulated processes operated by a complex genetic machinery. seems to possess almost all the components known to be involved in chromosomal replication and cell division in .

Citation: Takeuchi H, Nakazawa T. 2001. Chromosomal Replication, Plasmid Replication, and Cell Division, p 259-267. In Mobley H, Mendz G, Hazell S (ed), . ASM Press, Washington, DC. doi: 10.1128/9781555818005.ch23

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Figures

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Figure 1

Regions including the putative origin of replication () of 26695 and J99. Numbers at each end of the scale represent the position in nucleotides in the genome. Open boxes without gene names represent hypothetical genes with unknown functions. Genes in this region are (dihydroneopterin), (iron-regulated outer membrane protein aldolase), (selenocysteine synthase), (transcription termination factor), (type II restriction enzyme R and M protein), (type III restriction enzyme R protein), (adenine-specific DNA methyltransferase), (ATP-dependent DNA helicase), and (chromosomal replication initiator protein). JHP1409 is for type II DNA modification enzyme (methyltransferase) ( ). Numbers under the boxes represent HP and JHP numbers of strains 26695 and J99, respectively. Horizontal arrows above the boxes represent the direction of transcription. The DnaA-box sequences with exact matches (•) and a single mismatch (O) are indicated.

Citation: Takeuchi H, Nakazawa T. 2001. Chromosomal Replication, Plasmid Replication, and Cell Division, p 259-267. In Mobley H, Mendz G, Hazell S (ed), . ASM Press, Washington, DC. doi: 10.1128/9781555818005.ch23
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Image of Figure 2
Figure 2

Localization of cell division-related genes on the 26695 genome. Boxes with numbers below represent ORF of strain 26695. Horizontal arrows above the boxes represent the direction of transcription. Boxes are not drawn to scale and are separated when the genes are more than 20 bp apart. Closed boxes represent putative genes involved in cell division listed in Table 2 . Other genes in these regions are (acetohydroxy acid isomeroreductase), (DNA processing chain A), (ribosomal protein L11 methyltransferase), (phosphatidylserine synthase), (pyrroline-5-carboxylate reductase), (translation elongation factor EF-Ts), (flagellar basal-body protein), (flagellar basal-body rod protein), (flagellar basal-body rod protein), and (ferric iron ABC transporter, periplasmic iron-binding protein). Vertical-striped and open boxes represent conserved hypothetical and hypothetical genes, respectively.

Citation: Takeuchi H, Nakazawa T. 2001. Chromosomal Replication, Plasmid Replication, and Cell Division, p 259-267. In Mobley H, Mendz G, Hazell S (ed), . ASM Press, Washington, DC. doi: 10.1128/9781555818005.ch23
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Image of Figure 3
Figure 3

HPK5 (wild type, left) and HPKT510 (-disrupted mutant, right) micrographs. 4′, 6′-diamidino-2-phenylindole (DAP)-stained micrographs (A) and shadowed electron micrographs (B) of HPK5 (wild type) and HPKT510 (-disrupted mutant) from exponential-phase cultures. Cells were grown in brucella broth supplemented with 5% horse serum under a microaerobic condition ( ). Bars indicate 10 μm in A and 1 μm in B.

Citation: Takeuchi H, Nakazawa T. 2001. Chromosomal Replication, Plasmid Replication, and Cell Division, p 259-267. In Mobley H, Mendz G, Hazell S (ed), . ASM Press, Washington, DC. doi: 10.1128/9781555818005.ch23
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Tables

Generic image for table
Table 1

Proteins involved in chromosomal replication of and their homologs recognized in

Citation: Takeuchi H, Nakazawa T. 2001. Chromosomal Replication, Plasmid Replication, and Cell Division, p 259-267. In Mobley H, Mendz G, Hazell S (ed), . ASM Press, Washington, DC. doi: 10.1128/9781555818005.ch23
Generic image for table
Table 2

Proteins involved in cell division of and their homologs identified in strains 26695 and J99

Citation: Takeuchi H, Nakazawa T. 2001. Chromosomal Replication, Plasmid Replication, and Cell Division, p 259-267. In Mobley H, Mendz G, Hazell S (ed), . ASM Press, Washington, DC. doi: 10.1128/9781555818005.ch23

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