Literature DB >> 7523361

Nucleoid partitioning and the division plane in Escherichia coli.

C L Woldringh1, A Zaritsky, N B Grover.   

Abstract

Escherichia coli nucleoids were visualized after the DNA of OsO4-fixed but hydrated cells was stained with the fluorochrome DAPI (4',6-diamidino-2-phenylindole dihydrochloride hydrate). In slowly growing cells, the nucleoids are rod shaped and seem to move along the major cell axis, whereas in rapidly growing, wider cells they consist of two- to four-lobed structures that often appear to advance along axes lying perpendicular or oblique to the major axis of the cell. To test the idea that the increase in cell diameter following nutritional shift-up is caused by the increased amount of DNA in the nucleoid, the cells were subjected to DNA synthesis inhibition. In the absence of DNA replication, the nucleoids continued to move in the growing filaments and were pulled apart into small domains along the length of the cell. When these cells were then transferred to a richer medium, their diameters increased, especially in the region enclosing the nucleoid. It thus appears that the nucleoid motive force does not depend on DNA synthesis and that cell diameter is determined not by the amount of DNA per chromosome but rather by the synthetic activity surrounding the nucleoid. Under the non-steady-state but balanced growth conditions induced by thymine limitation, nucleoids become separated into small lobules, often lying in asymmetric configurations along the cell periphery, and oblique and asymmetric division planes occur in more than half of the constricting cells. We suggest that such irregular DNA movement affects both the angle of the division plane and its position.

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Year:  1994        PMID: 7523361      PMCID: PMC196821          DOI: 10.1128/jb.176.19.6030-6038.1994

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


  43 in total

1.  Morphological analysis of nuclear separation and cell division during the life cycle of Escherichia coli.

Authors:  C L Woldringh
Journal:  J Bacteriol       Date:  1976-01       Impact factor: 3.490

2.  On dimensional determination of rod-shaped bacteria.

Authors:  A Zaritsky
Journal:  J Theor Biol       Date:  1975-10       Impact factor: 2.691

3.  Rate maintenance of cell division in Escherichia coli B/r: analysis of a simple nutritional shift-down.

Authors:  A Zaritsky; C E Helmstetter
Journal:  J Bacteriol       Date:  1992-12       Impact factor: 3.490

4.  Isolation and characterization of ftsZ alleles that affect septal morphology.

Authors:  E Bi; J Lutkenhaus
Journal:  J Bacteriol       Date:  1992-08       Impact factor: 3.490

5.  Morphological analysis of the division cycle of two Escherichia coli substrains during slow growth.

Authors:  C L Woldringh; M A de Jong; W van den Berg; L Koppes
Journal:  J Bacteriol       Date:  1977-07       Impact factor: 3.490

6.  Cytological studies of deoxyribonucleic acid replication in Escherichia coli 15T-: replication at slow growth rates and after a shift-up into rich medium.

Authors:  N C Chai; K G Lark
Journal:  J Bacteriol       Date:  1970-10       Impact factor: 3.490

7.  The replicative origin of the E. coli chromosome binds to cell membranes only when hemimethylated.

Authors:  G B Ogden; M J Pratt; M Schaechter
Journal:  Cell       Date:  1988-07-01       Impact factor: 41.582

8.  Toporegulation of bacterial division according to the nucleoid occlusion model.

Authors:  C L Woldringh; E Mulder; P G Huls; N Vischer
Journal:  Res Microbiol       Date:  1991 Feb-Apr       Impact factor: 3.992

9.  Comment on the use of chloramphenicol to study the initiation of deoxyribonucleic acid synthesis.

Authors:  S Cooper; G Weusthoff
Journal:  J Bacteriol       Date:  1971-05       Impact factor: 3.490

10.  Nucleoid partitioning in Escherichia coli during steady-state growth and upon recovery from chloramphenicol treatment.

Authors:  J M van Helvoort; C L Woldringh
Journal:  Mol Microbiol       Date:  1994-08       Impact factor: 3.501

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  16 in total

1.  Chromosome segregation and cell division defects in recBC sbcBC ruvC mutants of Escherichia coli.

Authors:  D Zahradka; K Vlahović; M Petranović; D Petranović
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

2.  On the origin of branches in Escherichia coli.

Authors:  B Gullbrand; T Akerlund; K Nordström
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

3.  Exploring intracellular space: function of the Min system in round-shaped Escherichia coli.

Authors:  Brian D Corbin; Xuan-Chuan Yu; William Margolin
Journal:  EMBO J       Date:  2002-04-15       Impact factor: 11.598

4.  Dysfunctional MreB inhibits chromosome segregation in Escherichia coli.

Authors:  Thomas Kruse; Jakob Møller-Jensen; Anders Løbner-Olesen; Kenn Gerdes
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

5.  Branching of Escherichia coli cells arises from multiple sites of inert peptidoglycan.

Authors:  Miguel A de Pedro; Kevin D Young; Joachim-Volker Höltje; Heinz Schwarz
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

Review 6.  Use of thymine limitation and thymine starvation to study bacterial physiology and cytology.

Authors:  Arieh Zaritsky; Conrad L Woldringh; Monica Einav; Svetlana Alexeeva
Journal:  J Bacteriol       Date:  2006-03       Impact factor: 3.490

7.  Fine-structure evidence for cell membrane partitioning of the nucleoid and cytoplasm during bud formation in Hyphomonas species.

Authors:  P M Zerfas; M Kessel; E J Quintero; R M Weiner
Journal:  J Bacteriol       Date:  1997-01       Impact factor: 3.490

8.  A new slant to the Z ring and bacterial cell branch formation.

Authors:  Veronica L Wells; William Margolin
Journal:  Mol Microbiol       Date:  2012-03-21       Impact factor: 3.501

9.  Escherichia coli low-molecular-weight penicillin-binding proteins help orient septal FtsZ, and their absence leads to asymmetric cell division and branching.

Authors:  Lakshmi-Prasad Potluri; Miguel A de Pedro; Kevin D Young
Journal:  Mol Microbiol       Date:  2012-03-15       Impact factor: 3.501

Review 10.  Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda.

Authors:  A Kuzminov
Journal:  Microbiol Mol Biol Rev       Date:  1999-12       Impact factor: 11.056

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