Literature DB >> 8416911

Turnover and recycling of the murein sacculus in oligopeptide permease-negative strains of Escherichia coli: indirect evidence for an alternative permease system and for a monolayered sacculus.

J T Park1.   

Abstract

Turnover of murein in oligopeptide permease-negative Escherichia coli cells appeared to be minimal or nonexistent. In one strain in which it was possible to measure turnover during the first generation of chase, it was found that the rate of turnover was constant throughout a chase of three generations. This result suggests that an "inside-to-outside" mode of growth of the sacculus does not occur in E. coli. Turnover, though minimal, was significantly higher from cells labeled uniformly than from cells labeled only in the lateral wall, suggesting that a significant portion of the observed turnover is related to cell separation. Actually, turnover only appeared to be minimal in opp mutant strains. Tripeptides were being released by turnover at a rate of about 50% per generation and then were efficiently recycled. This suggests that in addition to opp, a low-affinity uptake system for tripeptide derived from the sacculus may exist.

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Year:  1993        PMID: 8416911      PMCID: PMC196091          DOI: 10.1128/jb.175.1.7-11.1993

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


  18 in total

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Journal:  J Bacteriol       Date:  1982-09       Impact factor: 3.490

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3.  Correlation between degradation and ultrastructure of peptidoglycan during autolysis of Escherichia coli.

Authors:  M Leduc; C Frehel; J van Heijenoort
Journal:  J Bacteriol       Date:  1985-02       Impact factor: 3.490

4.  Analysis of gene control signals by DNA fusion and cloning in Escherichia coli.

Authors:  M J Casadaban; S N Cohen
Journal:  J Mol Biol       Date:  1980-04       Impact factor: 5.469

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

6.  Turnover of the cell wall of Gram-positive bacteria.

Authors:  J Mauck; L Chan; L Glaser
Journal:  J Biol Chem       Date:  1971-03-25       Impact factor: 5.157

7.  Turnover of the cell wall peptidoglycan during growth of Neisseria gonorrhoeae and Escherichia coli. Relative stability of newly synthesized material.

Authors:  D L Greenway; H R Perkins
Journal:  J Gen Microbiol       Date:  1985-02

8.  Escherichia coli K-12 auxotrophs induced by insertion of the transposable element Tn5.

Authors:  K J Shaw; C M Berg
Journal:  Genetics       Date:  1979-07       Impact factor: 4.562

9.  Evidence for multisite growth of Escherichia coli murein involving concomitant endopeptidase and transpeptidase activities.

Authors:  L G Burman; J Reichler; J T Park
Journal:  J Bacteriol       Date:  1983-10       Impact factor: 3.490

10.  Evidence for involvement of penicillin-binding protein 3 in murein synthesis during septation but not during cell elongation.

Authors:  G A Botta; J T Park
Journal:  J Bacteriol       Date:  1981-01       Impact factor: 3.490

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  36 in total

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5.  An extracellular factor regulating expression of the chromosomal aminoglycoside 2'-N-acetyltransferase of Providencia stuartii.

Authors:  P N Rather; M M Parojcic; M R Paradise
Journal:  Antimicrob Agents Chemother       Date:  1997-08       Impact factor: 5.191

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Review 7.  Bacterial cell wall synthesis: new insights from localization studies.

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8.  Z-ring force and cell shape during division in rod-like bacteria.

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9.  Substrate-induced inactivation of the Escherichia coli AmiD N-acetylmuramoyl-L-alanine amidase highlights a new strategy to inhibit this class of enzyme.

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Review 10.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

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