Literature DB >> 3902797

Cell cycle parameters of Proteus mirabilis: interdependence of the biosynthetic cell cycle and the interdivision cycle.

J Gmeiner, E Sarnow, K Milde.   

Abstract

We investigated the time periods of DNA replication, lateral cell wall extension, and septum formation within the cell cycle of Proteus mirabilis. Cells were cultivated under three different conditions, yielding interdivision times of approximately 55, 57, and 160 min, respectively. Synchrony was achieved by sucrose density gradient centrifugation. The time periods were estimated by division inhibition studies with cephalexin, mecillinam, and nalidixic acid. In addition, DNA replication was measured by thymidine incorporation, and murein biosynthesis was measured by incorporation of N-acetylglucosamine into sodium dodecyl sulfate-insoluble murein sacculi. At interdivision times of 55 to 57 min murein biosynthesis for reproduction of a unit cell lasted longer than the interdivision time itself, whereas DNA replication finished within 40 min. Surprisingly, inhibition of DNA replication by nalidixic acid did not inhibit the subsequent cell division but rather the one after that. Because P. mirabilis fails to express several reactions of the recA-dependent SOS functions known from Escherichia coli, the drug allowed us to determine which DNA replication period actually governed which cell division. Taken together, the results indicate that at an interdivision time of 55 to 57 min, the biosynthetic cell cycle of P. mirabilis lasts approximately 120 min. To achieve the observed interdivision time, it is necessary that two subsequent biosynthetic cell cycles be tightly interlocked. The implications of these findings for the regulation of the cell cycle are discussed.

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Year:  1985        PMID: 3902797      PMCID: PMC214314          DOI: 10.1128/jb.164.2.741-748.1985

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  17 in total

1.  Penicillin-binding proteins and cell shape in E. coli.

Authors:  B G Spratt; A B Pardee
Journal:  Nature       Date:  1975-04-10       Impact factor: 49.962

2.  Inhibition of an early event in the cell division cycle of Escherichia coli by FL1060, an amidinopenicillanic acid.

Authors:  R James; J Y Haga; A B Pardee
Journal:  J Bacteriol       Date:  1975-06       Impact factor: 3.490

3.  Characterization of a conditional mutant with altered envelope showing pH-dependent morphology and temperature-dependent division.

Authors:  G Satta; R Fontana
Journal:  J Gen Microbiol       Date:  1974-01

4.  [Incorporation of thymine and thymidine into DNA of Proteus mirabilis].

Authors:  K Störl; H Venner
Journal:  Z Allg Mikrobiol       Date:  1972

5.  Regulation of polar cap formation in the life cycle of Escherichia coli.

Authors:  B Hoffmann; W Messer; U Schwarz
Journal:  J Supramol Struct       Date:  1972

6.  Model for regulation of Escherichia coli DNA repair functions.

Authors:  L J Gudas; A B Pardee
Journal:  Proc Natl Acad Sci U S A       Date:  1975-06       Impact factor: 11.205

7.  DNA repair in Proteus mirabilis. III.Survival, dimer excision, and UV reactivation in comparison with Escherichia coli K12.

Authors:  J Hofemeister; H Böhme
Journal:  Mol Gen Genet       Date:  1975-11-24

8.  Methionine synthesis in Proteus mirabilis.

Authors:  W O Grabow; J A Smit
Journal:  J Gen Microbiol       Date:  1967-01

9.  Model for the structure of the shape-maintaining layer of the Escherichia coli cell envelope.

Authors:  V Braun; H Gnirke; U Henning; K Rehn
Journal:  J Bacteriol       Date:  1973-06       Impact factor: 3.490

10.  Two pathways of division inhibition in UV-irradiated E. coli.

Authors:  P Burton; I B Holland
Journal:  Mol Gen Genet       Date:  1983
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  2 in total

1.  Proteus mirabilis mutants defective in swarmer cell differentiation and multicellular behavior.

Authors:  R Belas; D Erskine; D Flaherty
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

2.  Rate and topography of peptidoglycan synthesis during cell division in Escherichia coli: concept of a leading edge.

Authors:  F B Wientjes; N Nanninga
Journal:  J Bacteriol       Date:  1989-06       Impact factor: 3.490

  2 in total

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