Contribution of Cf-252-plasma desorption mass spectrometry to structural analysis of lipids A: examples of non-conservatism in lipid A structure

Citation
M. Caroff et al., Contribution of Cf-252-plasma desorption mass spectrometry to structural analysis of lipids A: examples of non-conservatism in lipid A structure, J ENDOTOX R, 5(1-2), 1999, pp. 86-89
Citations number
20
Categorie Soggetti
Immunology
Journal title
JOURNAL OF ENDOTOXIN RESEARCH
ISSN journal
09680519 → ACNP
Volume
5
Issue
1-2
Year of publication
1999
Pages
86 - 89
Database
ISI
SICI code
0968-0519(1999)5:1-2<86:COCDMS>2.0.ZU;2-#
Abstract
The great majority of lipids A studied so far have the enterobacterial lipi d A-type skeleton: a bisphosphorylated glucosamine disaccharide, with fatty acids amidating the 2 amino groups and esterifying the C3 and C3' position s. Differences between these lipids A occur in the nature and localization of the fatty acids. Such differences have been put forward as a possible ta xonomic tool. It is now relatively easy to determine these differences usin g plasma desorption mass spectrometry (PDMS) if one knows the overall compo sition of the pure, native lipids A. We have used this technique to compare the lipids A of 2 or more species of several bacterial genera and found co nsiderable conservatism within genera and sometimes between closely related genera (Salmonella and Escherichia). An exception was Bordetella of which different species varied in the nature and/or the localization of their fat ty acids. B. parapertussis, like B. pertussis, had a single C10OH but at a different location, and quite unusually had a non-hydroxylated fatty acid ( C-16) directly esterifying glucosamine I. On the other hand, 2 strains of B . bronchiseptica had a C12OH in place of the C10OH of B. pertussis, whereas a third strain replaced the C12OH by a C-12, again a primary non-hydroxyla ted fatty acid. PDMS has allowed us to conclude that the combined pattern o f fatty acids in lipids A is not a reliable taxonomic tool.