Literature DB >> 8682805

A simple gel electrophoretic method for analyzing the muropeptide composition of bacterial peptidoglycan.

K D Young1.   

Abstract

The muropeptide composition of bacterial peptidoglycan is currently most efficiently determined by reverse-phase high-pressure liquid chromatography (HPLC). Though sensitive, the HPLC procedure is technically demanding and has been applied to a relatively small number of bacterial strains and species. We have found that fluorescence-assisted carbohydrate electrophoresis (FACE) is a simple, rapid method by which reducing muropeptides from multiple peptidoglycan samples can be visualized. Individual reducing muropeptides were covalently labeled with the fluorescent molecule 8-aminonaphthalene-1,3,6-trisulfonic acid, after which they were separated by electrophoresis through a 35% polyacrylamide gel and visualized by exposure to UV light. FACE detected the appropriate numbers of reducing muropeptides in the proper proportions for four bacteria: Escherichia coli, Pseudomonas aeruginosa, Enterobacter cloacae, and Yersinia enterocolitica. As little as 2 to 5 pmol per muropeptide was detected when the intensity of the fluorescent signal was measured with a charge-coupled device camera, at a level of sensitivity between 50 and 250 times higher than that of the classic HPLC technique. Thus, FACE may be used to identify interesting peptidoglycan samples prior to more-extensive analysis by HPLC, or FACE may eventually replace HPLC for some applications.

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Year:  1996        PMID: 8682805      PMCID: PMC232661          DOI: 10.1128/jb.178.13.3962-3966.1996

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


  24 in total

1.  The use of polyacrylamide-gel electrophoresis for the high-resolution separation of reducing saccharides labelled with the fluorophore 8-aminonaphthalene-1,3,6-trisulphonic acid. Detection of picomolar quantities by an imaging system based on a cooled charge-coupled device.

Authors:  P Jackson
Journal:  Biochem J       Date:  1990-09-15       Impact factor: 3.857

2.  Separation and quantification of muropeptides with high-performance liquid chromatography.

Authors:  B Glauner
Journal:  Anal Biochem       Date:  1988-08-01       Impact factor: 3.365

3.  Unusual composition of peptidoglycan in Bordetella pertussis.

Authors:  E Tuomanen; J Schwartz; S Sande; K Light; D Gage
Journal:  J Biol Chem       Date:  1989-07-05       Impact factor: 5.157

4.  Biosynthesis of peptidoglycan in Gaffkya homari: on the target(s) of benzylpenicillin.

Authors:  R K Sinha; F C Neuhaus
Journal:  Antimicrob Agents Chemother       Date:  1991-09       Impact factor: 5.191

5.  Isolation and separation of the glycan strands from murein of Escherichia coli by reversed-phase high-performance liquid chromatography.

Authors:  H Harz; K Burgdorf; J V Höltje
Journal:  Anal Biochem       Date:  1990-10       Impact factor: 3.365

6.  Electrophoretic resolution and fluorescence detection of N-linked glycoprotein oligosaccharides after reductive amination with 8-aminonaphthalene-1,3,6-trisulphonic acid.

Authors:  R J Stack; M T Sullivan
Journal:  Glycobiology       Date:  1992-02       Impact factor: 4.313

7.  The composition of the murein of Escherichia coli.

Authors:  B Glauner; J V Höltje; U Schwarz
Journal:  J Biol Chem       Date:  1988-07-25       Impact factor: 5.157

8.  Analysis of Neisseria gonorrhoeae peptidoglycan by reverse-phase, high-pressure liquid chromatography.

Authors:  T J Dougherty
Journal:  J Bacteriol       Date:  1985-07       Impact factor: 3.490

9.  Structure of the peptide network of pneumococcal peptidoglycan.

Authors:  J F Garcia-Bustos; B T Chait; A Tomasz
Journal:  J Biol Chem       Date:  1987-11-15       Impact factor: 5.157

10.  Volume growth, murein synthesis, and murein cross-linkage during the division cycle of Escherichia coli PA3092.

Authors:  A J Olijhoek; S Klencke; E Pas; N Nanninga; U Schwarz
Journal:  J Bacteriol       Date:  1982-12       Impact factor: 3.490

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Authors:  T L Goins; J E Cutler
Journal:  J Clin Microbiol       Date:  2000-08       Impact factor: 5.948

4.  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
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Authors:  Jonathan P Allen; Melody N Neely
Journal:  Infect Immun       Date:  2012-02-21       Impact factor: 3.441

6.  Comparison of high-performance liquid chromatography and fluorophore-assisted carbohydrate electrophoresis methods for analyzing peptidoglycan composition of Escherichia coli.

Authors:  Shi-Yan Li; Joachim-Volker Höltje; Kevin D Young
Journal:  Anal Biochem       Date:  2004-03-01       Impact factor: 3.365

7.  Bacterial ligands generated in a phagosome are targets of the cytosolic innate immune system.

Authors:  Anat A Herskovits; Victoria Auerbuch; Daniel A Portnoy
Journal:  PLoS Pathog       Date:  2007-03       Impact factor: 6.823

8.  Regulation and Molecular Basis of Environmental Muropeptide Uptake and Utilization in Fastidious Oral Anaerobe Tannerella forsythia.

Authors:  Angela Ruscitto; Kiyonobu Honma; Vamsee M Veeramachineni; Kiyoshi Nishikawa; Graham P Stafford; Ashu Sharma
Journal:  Front Microbiol       Date:  2017-04-12       Impact factor: 5.640

9.  DNA, cell wall and general oxidative damage underlie the tellurite/cefotaxime synergistic effect in Escherichia coli.

Authors:  Roberto C Molina-Quiroz; David E Loyola; Claudia M Muñoz-Villagrán; Raquel Quatrini; Claudio C Vásquez; José M Pérez-Donoso
Journal:  PLoS One       Date:  2013-11-18       Impact factor: 3.240

  9 in total

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