Literature DB >> 3280547

Division behavior and shape changes in isogenic ftsZ, ftsQ, ftsA, pbpB, and ftsE cell division mutants of Escherichia coli during temperature shift experiments.

P E Taschner1, P G Huls, E Pas, C L Woldringh.   

Abstract

Isogenic ftsZ, ftsQ, ftsA, pbpB, and ftsE cell division mutants of Escherichia coli were compared with their parent strain in temperature shift experiments. To improve detection of phenotypic differences in division behavior and cell shape, the strains were grown in glucose-minimal medium with a decreased osmolality (about 100 mosM). Already at the premissive temperature, all mutants, particularly the pbpB and ftsQ mutants, showed an increased average cell length and cell mass. The pbpB and ftsQ mutants also exhibited a prolonged duration of the constriction period. All strains, except ftsZ, continued to initiate new constrictions at 42 degrees C, suggesting the involvement of FtsZ in an early step of the constriction process. The new constrictions were blunt in ftsQ and more pronounced in ftsA and pbpB filaments, which also had elongated median constrictions. Whereas the latter strains showed a slow recovery of cell division after a shift back to the permissive temperature, ftsZ and ftsQ filaments recovered quickly. Recovery of filaments occurred in all strains by the separation of newborn cells with an average length of two times LO, the length of newborn cells at the permissive temperature. The increased size of the newborn cells could indicate that the cell division machinery recovers too slowly to create normal-sized cells. Our results indicate a phenotypic resemblance between ftsA and pbpB mutants and suggest that the cell division gene products function in the order FtsZ-FtsQ-FtsA, PBP3. The ftsE mutant continued to constrict and divide at 42 degrees C, forming short filaments, which recovered quickly after a shift back to the permissive temperature. After prolonged growth at 42 degree C, chains of cells, which eventually swelled up, were formed. Although the ftsE mutant produced filaments in broth medium at the restrictive temperature, it cannot be considered a cell division mutant under the presently applied conditions.

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Year:  1988        PMID: 3280547      PMCID: PMC210998          DOI: 10.1128/jb.170.4.1533-1540.1988

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


  43 in total

1.  Role of the ftsA gene product in control of Escherichia coli cell division.

Authors:  W D Donachie; K J Begg; J F Lutkenhaus; G P Salmond; E Martinez-Salas; M Vincente
Journal:  J Bacteriol       Date:  1979-11       Impact factor: 3.490

2.  A genetic map of several mutations affecting the mucopeptide layer of Escherichia coli.

Authors:  H J Wijsman
Journal:  Genet Res       Date:  1972-08       Impact factor: 1.588

3.  Growth of the bacterial cell.

Authors:  W D Donachie; K J Begg
Journal:  Nature       Date:  1970-09-19       Impact factor: 49.962

4.  Changes in cell diameter during the division cycle of Escherichia coli.

Authors:  F J Trueba; C L Woldringh
Journal:  J Bacteriol       Date:  1980-06       Impact factor: 3.490

5.  Identification of new genes in a cell envelope-cell division gene cluster of Escherichia coli: cell division gene ftsQ.

Authors:  K J Begg; G F Hatfull; W D Donachie
Journal:  J Bacteriol       Date:  1980-10       Impact factor: 3.490

6.  Organization of genes in the ftsA-envA region of the Escherichia coli genetic map and identification of a new fts locus (ftsZ).

Authors:  J F Lutkenhaus; H Wolf-Watz; W D Donachie
Journal:  J Bacteriol       Date:  1980-05       Impact factor: 3.490

Review 7.  Procaryotic cell division with respect to wall and membranes.

Authors:  M L Higgins; G D Shockman
Journal:  CRC Crit Rev Microbiol       Date:  1971-05

8.  A mutant of Escherichia coli defective in DNA polymerase II activity.

Authors:  Y Hirota; M Gefter; L Mindich
Journal:  Proc Natl Acad Sci U S A       Date:  1972-11       Impact factor: 11.205

9.  DNA-damaging agents stimulate gene expression at specific loci in Escherichia coli.

Authors:  C J Kenyon; G C Walker
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

10.  The contractile ring. II. Determining its brief existence, volumetric changes, and vital role in cleaving Arbacia eggs.

Authors:  T E Schroeder
Journal:  J Cell Biol       Date:  1972-05       Impact factor: 10.539

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  71 in total

1.  Timing of FtsZ assembly in Escherichia coli.

Authors:  T Den Blaauwen; N Buddelmeijer; M E Aarsman; C M Hameete; N Nanninga
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

2.  Escherichia coli minicell membranes are enriched in cardiolipin.

Authors:  C M Koppelman; T Den Blaauwen; M C Duursma; R M Heeren; N Nanninga
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

3.  New insights into the developmental history of the bacterial cell division site.

Authors:  Lawrence Rothfield
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

4.  Differential effect of mutational impairment of penicillin-binding proteins 1A and 1B on Escherichia coli strains harboring thermosensitive mutations in the cell division genes ftsA, ftsQ, ftsZ, and pbpB.

Authors:  F García del Portillo; M A de Pedro
Journal:  J Bacteriol       Date:  1990-10       Impact factor: 3.490

5.  Inhibition of cell division in hupA hupB mutant bacteria lacking HU protein.

Authors:  A M Dri; J Rouviere-Yaniv; P L Moreau
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

6.  The FtsQ protein of Escherichia coli: membrane topology, abundance, and cell division phenotypes due to overproduction and insertion mutations.

Authors:  M J Carson; J Barondess; J Beckwith
Journal:  J Bacteriol       Date:  1991-04       Impact factor: 3.490

7.  Defining the rate-limiting processes of bacterial cytokinesis.

Authors:  Carla Coltharp; Jackson Buss; Trevor M Plumer; Jie Xiao
Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-01       Impact factor: 11.205

8.  Functional analysis of the cell division protein FtsW of Escherichia coli.

Authors:  Soumya Pastoret; Claudine Fraipont; Tanneke den Blaauwen; Benoît Wolf; Mirjam E G Aarsman; André Piette; Annick Thomas; Robert Brasseur; Martine Nguyen-Distèche
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

Review 9.  Roles of FtsEX in cell division.

Authors:  Sebastien Pichoff; Shishen Du; Joe Lutkenhaus
Journal:  Res Microbiol       Date:  2019-08-01       Impact factor: 3.992

10.  Isolation and characterization of the Escherichia coli htrB gene, whose product is essential for bacterial viability above 33 degrees C in rich media.

Authors:  M Karow; O Fayet; A Cegielska; T Ziegelhoffer; C Georgopoulos
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

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