Literature DB >> 358938

Pole cap formation in Escherichia coli following induction of the maltose-binding protein.

I Dietzel, V Kolb, W Boos.   

Abstract

After induction with maltose, 30--40% of the total protein in the osmotic shock fluid consist of maltose-binding protein while the induction ratio (maltose versus glycerol grown cells) for the amount of binding protein synthesized as well as for maltose transport is in the order of 10. Induction of maltose transport does not occur during all times of the cell cycle, but only shortly before cell division. Electronmicroscopic analysis of cells grown logarithmically on glycerol or maltose revealed in the latter the formation of large pole caps. These pole caps arise from an enlargement of the periplasmic space. Small cells contain one pole cap, large cells contain two. Pulse label studies with strain BUG-6, a mutant that is temperature sensitive for cell division reveal the following: Growth at the non-permissive temperature prevents maltose-binding protein synthesis and formation of new transport capacity. After shifting to the permissive temperature the cells regain both functions. Simultaneously, the newly formed cells exhibit pole caps. We conclude that the induction of maltose-binding protein is responsible for the formation of pole caps. In addition, beside the presence of inducer, cell cycle events occuring during division are necessary for the synthesis of maltose-binding protein.

Entities:  

Mesh:

Substances:

Year:  1978        PMID: 358938     DOI: 10.1007/bf00415731

Source DB:  PubMed          Journal:  Arch Microbiol        ISSN: 0302-8933            Impact factor:   2.552


  27 in total

1.  On the significance of the retention of ligand by protein.

Authors:  T J Silhavy; S Szmelcman; W Boos; M Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  1975-06       Impact factor: 11.205

2.  Intergration of the receptor for bacteriophage lambda in the outer membrane of Escherichia coli: coupling with cell division.

Authors:  A Ryter; H Shuman; M Schwartz
Journal:  J Bacteriol       Date:  1975-04       Impact factor: 3.490

3.  [Purification and properties of the beta-galactosidase (lactase) of Escherichia coli].

Authors:  M COHN; J MONOD
Journal:  Biochim Biophys Acta       Date:  1951-05

4.  Divergent operons and the genetic structure of the maltose B region in Escherichia coli K12.

Authors:  M Hofnung
Journal:  Genetics       Date:  1974-02       Impact factor: 4.562

5.  Distribution of alkaline phosphatase within the periplasmic space of gram-negative bacteria.

Authors:  T J MacAlister; J W Costerton; L Thompson; J Thompson; J M Ingram
Journal:  J Bacteriol       Date:  1972-09       Impact factor: 3.490

6.  A low-viscosity epoxy resin embedding medium for electron microscopy.

Authors:  A R Spurr
Journal:  J Ultrastruct Res       Date:  1969-01

7.  Further studies on the binding of maltose to the maltose-binding protein of Escherichia coli.

Authors:  M Schwartz; O Kellermann; S Szmelcman; G L Hazelbauer
Journal:  Eur J Biochem       Date:  1976-12

8.  Synthesis of exported proteins by membrane-bound polysomes from Escherichia coli.

Authors:  L L Randall; S J Hardy
Journal:  Eur J Biochem       Date:  1977-05-02

9.  Active transport of maltose in Escherichia coli K12. Involvement of a "periplasmic" maltose binding protein.

Authors:  O Kellermann; S Szmelcman
Journal:  Eur J Biochem       Date:  1974-08-15

10.  Cytochemical localization of certain phosphatases in Escherichia coli.

Authors:  B K Wetzel; S S Spicer; H F Dvorak; L A Heppel
Journal:  J Bacteriol       Date:  1970-10       Impact factor: 3.490

View more
  23 in total

1.  Reversible formation of on-pathway macroscopic aggregates during the folding of maltose binding protein.

Authors:  C Ganesh; F N Zaidi; J B Udgaonkar; R Varadarajan
Journal:  Protein Sci       Date:  2001-08       Impact factor: 6.725

Review 2.  Polarity in action: asymmetric protein localization in bacteria.

Authors:  S R Lybarger; J R Maddock
Journal:  J Bacteriol       Date:  2001-06       Impact factor: 3.490

3.  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

4.  Nucleator function of CsgB for the assembly of adhesive surface organelles in Escherichia coli.

Authors:  Z Bian; S Normark
Journal:  EMBO J       Date:  1997-10-01       Impact factor: 11.598

5.  Lateral diffusion of proteins in the periplasm of Escherichia coli.

Authors:  J M Brass; C F Higgins; M Foley; P A Rugman; J Birmingham; P B Garland
Journal:  J Bacteriol       Date:  1986-03       Impact factor: 3.490

6.  Variation in precursor pool size during the division cycle of Escherichia coli: further evidence for linear cell growth.

Authors:  H E Kubitschek; S R Pai
Journal:  J Bacteriol       Date:  1988-01       Impact factor: 3.490

7.  Temperature-sensitive catabolite activator protein in Escherichia coli BUG6.

Authors:  D Benner; N Müller; W Boos
Journal:  J Bacteriol       Date:  1985-01       Impact factor: 3.490

Review 8.  Structure and mechanism of bacterial periplasmic transport systems.

Authors:  G F Ames
Journal:  J Bioenerg Biomembr       Date:  1988-02       Impact factor: 2.945

9.  Ca2+-induced permeabilization of the Escherichia coli outer membrane: comparison of transformation and reconstitution of binding-protein-dependent transport.

Authors:  B Bukau; J M Brass; W Boos
Journal:  J Bacteriol       Date:  1985-07       Impact factor: 3.490

10.  Reconstitution of maltose chemotaxis in Escherichia coli by addition of maltose-binding protein to calcium-treated cells of maltose regulon mutants.

Authors:  J M Brass; M D Manson
Journal:  J Bacteriol       Date:  1984-03       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.