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J. Bacteriol., Jul 1996, 3962-3966, Vol 178, No. 13
KD Young
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.
Copyright © 1996, American Society for Microbiology
A simple gel electrophoretic method for analyzing the muropeptide composition of bacterial peptidoglycan [published erratum appears in J Bacteriol 1996 Sep;178(17):5335]
Department of Microbiology and Immunology, School of Medicine, University of North Dakota, Grand Forks, North Dakota 58202-9037, USA. kyoung@mail.med.und.nodak.edu
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