Literature DB >> 8468284

Plasmolysis bays in Escherichia coli: are they related to development and positioning of division sites?

E Mulder1, C L Woldringh.   

Abstract

Plasmolysis bays, induced in Escherichia coli by hypertonic treatment, are flanked by zones of adhesion between the plasma membrane and the cell wall. To test the proposition of Cook et al. (W. R. Cook, F. Joseleau-Petit, T. J. MacAlister, and L. I. Rothfield, Proc. Natl. Acad. Sci. USA 84:7144-7148, 1987) that these zones, called periseptal annuli, play a role in determining the division site, we analyzed the positions of these zones by phase-contrast and electron microscopy. In situ treatment of cells grown in agar showed that the youngest cell pole was the most susceptible to plasmolysis, whereas the constriction site was resistant. Lateral bays occurred only at some distance from a polar bay or a resistant constriction site. Orienting cells with their most prominently plasmolyzed polar bay in one direction showed that the lateral bays were always displaced away from the polar bay at about half the distance to the other cell pole. If no poles were plasmolyzed, lateral bays occurred either in the centers of nonconstricting cells or at the 1/4 or 3/4 position of cell length in constricting cells. The asymmetric positions of lateral plasmolysis bays, caused by their abrupt displacement in the presence of polar bays or constriction sites, does not confirm the periseptal annulus model (Cook et al.), which predicts a gradual and symmetric change in the position of lateral bays with increasing cell length. Our analysis indicates that plasmolysis bays have no relation to the development and positioning of the future division site.

Entities:  

Mesh:

Year:  1993        PMID: 8468284      PMCID: PMC204510          DOI: 10.1128/jb.175.8.2241-2247.1993

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


  15 in total

1.  The periseptal annulus: An organelle associated with cell division in Gram-negative bacteria.

Authors:  T J Macalister; B Macdonald; L I Rothfield
Journal:  Proc Natl Acad Sci U S A       Date:  1983-03       Impact factor: 11.205

2.  Biogenesis of the Escherichia coli cell division system.

Authors:  L I Rothfield; W R Cook; P A de Boer
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1991

3.  Biogenesis of cell division sites in ftsA and ftsZ filaments.

Authors:  W R Cook; L I Rothfield
Journal:  Res Microbiol       Date:  1991 Feb-Apr       Impact factor: 3.992

Review 4.  Differentiation of the bacterial cell division site.

Authors:  W R Cook; P A de Boer; L I Rothfield
Journal:  Int Rev Cytol       Date:  1989

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

Authors:  P E Taschner; P G Huls; E Pas; C L Woldringh
Journal:  J Bacteriol       Date:  1988-04       Impact factor: 3.490

7.  Plasmolysis during the division cycle of Escherichia coli.

Authors:  A J Olijhoek; C G Van Eden; F J Trueba; E Pas; N Nanninga
Journal:  J Bacteriol       Date:  1982-10       Impact factor: 3.490

8.  Compartmentalization of the periplasmic space at division sites in gram-negative bacteria.

Authors:  W R Cook; T J MacAlister; L I Rothfield
Journal:  J Bacteriol       Date:  1986-12       Impact factor: 3.490

9.  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

10.  Autoradiographic analysis of diaminopimelic acid incorporation in filamentous cells of Escherichia coli: repression of peptidoglycan synthesis around the nucleoid.

Authors:  E Mulder; C L Woldringh
Journal:  J Bacteriol       Date:  1991-08       Impact factor: 3.490

View more
  5 in total

1.  Constitutive expression of the maltoporin LamB in the absence of OmpR damages the cell envelope.

Authors:  Sylvia A Reimann; Alan J Wolfe
Journal:  J Bacteriol       Date:  2010-12-03       Impact factor: 3.490

2.  Tyrosine phosphorylation-dependent localization of TmaR that controls activity of a major bacterial sugar regulator by polar sequestration.

Authors:  Tamar Szoke; Nitsan Albocher; Sutharsan Govindarajan; Anat Nussbaum-Shochat; Orna Amster-Choder
Journal:  Proc Natl Acad Sci U S A       Date:  2021-01-12       Impact factor: 11.205

3.  Plasmolysis and cell shape depend on solute outer-membrane permeability during hyperosmotic shock in E. coli.

Authors:  Teuta Pilizota; Joshua W Shaevitz
Journal:  Biophys J       Date:  2013-06-18       Impact factor: 4.033

4.  Type II secretion by Aeromonas salmonicida: evidence for two periplasmic pools of proaerolysin.

Authors:  S E Burr; D B Diep; J T Buckley
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

Review 5.  Morphogenesis of Escherichia coli.

Authors:  N Nanninga
Journal:  Microbiol Mol Biol Rev       Date:  1998-03       Impact factor: 11.056

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.