Literature DB >> 34541148

Analysis of N-acetylmuramic acid-6-phosphate (MurNAc-6P) Accumulation by HPLC-MS.

Marina Borisova1, Christoph Mayer1.   

Abstract

We describe here in detail a high-performance liquid chromatography-mass spectrometry (HPLC-MS)-based method to determine N-acetylmuramic acid-6-phosphate (MurNAc-6P) in bacterial cell extracts. The method can be applied to both Gram-negative and Gram-positive bacteria, and as an example we use Escherichia coli cells in this study. Wild type and mutant cells are grown for a defined time in a medium of choice and harvested by centrifugation. Then the cells are disintegrated and soluble cell extracts are generated. After removal of proteins by precipitation with acetone, the extracts are analyzed by HPLC-MS. Base peak chromatograms of wild type and mutant cell extracts are used to determine a differential ion spectrum that reveals differences in the MurNAc-6P content of the two samples. Determination of peak areas of extracted chromatograms of MurNAc-6P ((M-H)- = 372.070 m/z in negative ion mode) allows quantifying MurNAc-6P levels, that are used to calculate recycling rates of the MurNAc-content of peptidoglycan.
Copyright © 2017 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Bacteria; Base peak chromatogram (BPC); Cell wall metabolism; Cytosolic metabolites; Extracted ion chromatogram (EIC); LC-MS; MurNAc-6P accumulation; Peptidoglycan recycling

Year:  2017        PMID: 34541148      PMCID: PMC8413491          DOI: 10.21769/BioProtoc.2420

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  6 in total

Review 1.  Peptidoglycan turnover and recycling in Gram-positive bacteria.

Authors:  Jan Reith; Christoph Mayer
Journal:  Appl Microbiol Biotechnol       Date:  2011-07-28       Impact factor: 4.813

2.  Enzymatic synthesis and semi-preparative isolation of N-acetylmuramic acid 6-phosphate.

Authors:  Sandra Unsleber; Marina Borisova; Christoph Mayer
Journal:  Carbohydr Res       Date:  2017-04-06       Impact factor: 2.104

3.  MurQ Etherase is required by Escherichia coli in order to metabolize anhydro-N-acetylmuramic acid obtained either from the environment or from its own cell wall.

Authors:  Tsuyoshi Uehara; Kyoko Suefuji; Tina Jaeger; Christoph Mayer; James T Park
Journal:  J Bacteriol       Date:  2006-02       Impact factor: 3.490

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
Journal:  J Bacteriol       Date:  2010-04-16       Impact factor: 3.490

5.  Scission of the lactyl ether bond of N-acetylmuramic acid by Escherichia coli "etherase".

Authors:  Tina Jaeger; Momo Arsic; Christoph Mayer
Journal:  J Biol Chem       Date:  2005-06-27       Impact factor: 5.157

6.  Peptidoglycan Recycling in Gram-Positive Bacteria Is Crucial for Survival in Stationary Phase.

Authors:  Marina Borisova; Rosmarie Gaupp; Amanda Duckworth; Alexander Schneider; Désirée Dalügge; Maraike Mühleck; Denise Deubel; Sandra Unsleber; Wenqi Yu; Günther Muth; Markus Bischoff; Friedrich Götz; Christoph Mayer
Journal:  MBio       Date:  2016-10-11       Impact factor: 7.867

  6 in total

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