Literature DB >> 803503

Turnover of the cell wall peptidoglycan of Lactobacillus acidophilus. The presence of a fraction immune to turnover.

L Daneo-Moore, J Coyette, M Sayare, D Boothby, G D Shockman.   

Abstract

Exponentially growing cultures of Lactobacillus acidophilus strain 60AM Gasser were previously shown to lose about one-third of their cell wall peptidoglycan per generation via turnover (Boothby, D., Daneo-Moore, L., Higgins, M. L., Coyette, J., and Shockman, G. D. (1973) J. Biol. Chem. 248, 2161-2169). We now show that 20 to 30% of the [3H]lysine initially present in insoluble peptidoglycan fractions was retained after 4 or more generations of continued exponential growth of cultures in the absence of label. Treatment of peptidoglycan fractions, before and after 6 or 8 generations of chase with lysozyme (EC 3.2.1.17), released soluble products containing [3H]lysine which had electrophoretic mobilities identical with the disaccharide-peptide derivatives obtained from the wall peptidoglycan of this species. Because protein is known to contaminate peptidoglycan residues, the double labeled technique was used to show that one-half or less of the label lysine present after 6 or 8 generations of chase could be attributed to protein contamination. This then left a minimum fraction of 10 to 20% of the peptidoglycan that was immune to turnover. The absence of turnover of peptidoglycan labeled during short pulses has now been quantitated to show that pulses shorter than 12% of a generation (6 to 7 min) did not turn over. This turnover-immune fraction is in reasonably good agreement with the immune fraction of 10 to 20% observed after long periods of chase of extensively labeled peptidoglycan.

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Year:  1975        PMID: 803503

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

Review 1.  Turnover of cell walls in microorganisms.

Authors:  R J Doyle; J Chaloupka; V Vinter
Journal:  Microbiol Rev       Date:  1988-12

2.  Synthesis and turnover of the regularly arranged surface protein of Acinetobacter sp. relative to the other components of the cell envelope.

Authors:  K J Thorne; R C Oliver; A M Glauert
Journal:  J Bacteriol       Date:  1976-07       Impact factor: 3.490

3.  Inhibition of peptidoglycan, ribonucleic acid, and protein synthesis in tolerant strains of Streptococcus mutans.

Authors:  M Mychajlonka; T D McDowell; G D Shockman
Journal:  Antimicrob Agents Chemother       Date:  1980-04       Impact factor: 5.191

4.  Relation between cell wall turnover and cell growth in Bacillus subtilis.

Authors:  L Glaser; B Lindsay
Journal:  J Bacteriol       Date:  1977-05       Impact factor: 3.490

5.  Cell wall turnover in phosphate and potassium limited chemostat cultures of Bacillus subtilis W23.

Authors:  A J Clarke-Sturman; A R Archibald
Journal:  Arch Microbiol       Date:  1982-06       Impact factor: 2.552

6.  Relationship between cellular autolytic activity, peptidoglycan synthesis, septation, and the cell cycle in synchronized populations of Streptococcus faecium.

Authors:  R P Hinks; L Daneo-Moore; G D Shockman
Journal:  J Bacteriol       Date:  1978-06       Impact factor: 3.490

7.  Muropeptide rescue in Bacillus subtilis involves sequential hydrolysis by beta-N-acetylglucosaminidase and N-acetylmuramyl-L-alanine amidase.

Authors:  Silke Litzinger; Amanda Duckworth; Katja Nitzsche; Christian Risinger; Valentin Wittmann; Christoph Mayer
Journal:  J Bacteriol       Date:  2010-04-16       Impact factor: 3.490

8.  Study of cycle of cell wall assembly in Streptococcus faecalis by three-dimensional reconstructions of thin sections of cells.

Authors:  M L Higgins; G D Shockman
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

9.  Conservation of cell wall peptidoglycan by strains of Streptococcus mutans and Streptococcus sanguis.

Authors:  M Mychajlonka; T D McDowell; G D Shockman
Journal:  Infect Immun       Date:  1980-04       Impact factor: 3.441

  9 in total

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