This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by de Jonge, B L
Right arrow Articles by Nanninga, N
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by de Jonge, B L
Right arrow Articles by Nanninga, N

 Previous Article  |  Next Article 

J Bacteriol. 1989 November; 171(11): 5783-5794

research-article

Peptidoglycan synthesis during the cell cycle of Escherichia coli: composition and mode of insertion.

B L de Jonge, F B Wientjes, I Jurida, F Driehuis, J T Wouters and N Nanninga

Department of Microbiology, University of Amsterdam, The Netherlands.

ABSTRACT

The composition and the mode of insertion of peptidoglycan synthesized during the cell cycle of Escherichia coli were determined. This was carried out on peptidoglycan that was periodically pulse-labeled in synchronously growing cultures. The chemical composition of the pulse-labeled (newly synthesized) peptidoglycan remained constant throughout the cell cycle, as judged from high-pressure liquid chromatography analysis of the muropeptide composition. The mode of insertion was deduced from the acceptor-donor radioactivity ratio in the bis-disaccharide tetratetra compound. The ratio was low in elongating cells and high in constricting cells. This indicates that during elongation, peptidoglycan was inserted as single strands, whereas during constriction, a multistranded (or sequential single-stranded) insertion occurred. Experiments with an ftsA division mutant suggested that the composition and mode of insertion of newly synthesized peptidoglycan remained the same throughout the constriction process. Our results imply that the changed mode of insertion rather than the chemical structure of the peptidoglycan might be responsible for the transition from cell elongation to polar cap formation.


J Bacteriol. 1989 November; 171(11): 5783-5794




This article has been cited by other articles:

  • Huang, K. C., Mukhopadhyay, R., Wen, B., Gitai, Z., Wingreen, N. S. (2008). Cell shape and cell-wall organization in Gram-negative bacteria. Proc. Natl. Acad. Sci. USA 105: 19282-19287 [Abstract] [Full Text]  
  • Park, J. T., Uehara, T. (2008). How Bacteria Consume Their Own Exoskeletons (Turnover and Recycling of Cell Wall Peptidoglycan). Microbiol. Mol. Biol. Rev. 72: 211-227 [Abstract] [Full Text]  
  • Uehara, T., Park, J. T. (2008). Growth of Escherichia coli: Significance of Peptidoglycan Degradation during Elongation and Septation. J. Bacteriol. 190: 3914-3922 [Abstract] [Full Text]  
  • Carballido-Lopez, R. (2006). The Bacterial Actin-Like Cytoskeleton. Microbiol. Mol. Biol. Rev. 70: 888-909 [Abstract] [Full Text]  
  • Born, P., Breukink, E., Vollmer, W. (2006). In Vitro Synthesis of Cross-linked Murein and Its Attachment to Sacculi by PBP1A from Escherichia coli. J. Biol. Chem. 281: 26985-26993 [Abstract] [Full Text]  
  • Vollmer, W., Holtje, J.-V. (2004). The Architecture of the Murein (Peptidoglycan) in Gram-Negative Bacteria: Vertical Scaffold or Horizontal Layer(s)?. J. Bacteriol. 186: 5978-5987 [Full Text]  
  • Wei, Y., Havasy, T., McPherson, D. C., Popham, D. L. (2003). Rod Shape Determination by the Bacillus subtilis Class B Penicillin-Binding Proteins Encoded by pbpA and pbpH. J. Bacteriol. 185: 4717-4726 [Abstract] [Full Text]  
  • Park, J. T. (2001). Identification of a Dedicated Recycling Pathway for Anhydro-N-Acetylmuramic Acid and N-Acetylglucosamine Derived from Escherichia coli Cell Wall Murein. J. Bacteriol. 183: 3842-3847 [Abstract] [Full Text]  
  • Lybarger, S. R., Maddock, J. R. (2001). Polarity in Action: Asymmetric Protein Localization in Bacteria. J. Bacteriol. 183: 3261-3267 [Full Text]  
  • Kraft, A. R., Prabhu, J., Ursinus, A., Höltje, J.-V. (1999). Interference with Murein Turnover Has No Effect on Growth but Reduces beta -Lactamase Induction in Escherichia coli. J. Bacteriol. 181: 7192-7198 [Abstract] [Full Text]  
  • Schiffer, G., Holtje, J.-V. (1999). Cloning and Characterization of PBP 1C, a Third Member of the Multimodular Class A Penicillin-binding Proteins of Escherichia coli. J. Biol. Chem. 274: 32031-32039 [Abstract] [Full Text]  
  • Nanninga, N. (1998). Morphogenesis of Escherichia coli. Microbiol. Mol. Biol. Rev. 62: 110-129 [Abstract] [Full Text]  
  • Holtje, J.-V. (1998). Growth of the Stress-Bearing and Shape-Maintaining Murein Sacculus of Escherichia coli. Microbiol. Mol. Biol. Rev. 62: 181-203 [Abstract] [Full Text]  
  • Kocks, C, Hellio, R, Gounon, P, Ohayon, H, Cossart, P (1993). Polarized distribution of Listeria monocytogenes surface protein ActA at the site of directional actin assembly. J. Cell Sci. 105: 699-710 [Abstract]