Characterization of Sphingolipids from Mycopathogens: Factors Correlating with Expression of 2-Hydroxy Fatty Acyl (E)-Δ3-Unsaturation in Cerebrosides of Paracoccidioides brasiliensis and Aspergillus fumigatus
- 11 May 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 38 (22) , 7294-7306
- https://doi.org/10.1021/bi982898z
Abstract
Significant differences exist between mammals and fungi with respect to glycosphingolipid (GSL) structure and biosynthesis. Thus, these compounds, as well as the cellular machinery regulating their expression, have considerable potential as targets for the diagnosis and treatment of fungal diseases. In this study, the major neutral GSL components extracted from both yeast and mycelium forms of the thermally dimorphic mycopathogen Paracoccidioides brasiliensis were purified and characterized by 1H and 13C NMR spectroscopy, ESI-MS and ESI-MS/CID-MS, and GC-MS. The major GSLs of both forms were identified as β-glucopyranosylceramides (GlcCer) having (4E,8E)-9-methyl-4,8-sphingadienine as long chain base in combination with either N-2‘-hydroxyoctadecanoate or N-2‘-hydroxy-(E)-3‘-octadecenoate. The mycelium form GlcCer had both fatty acids in a ∼1:1 ratio, while that of the yeast form had on average only ∼15% of the (E)-Δ3-unsaturated fatty acid. Cerebrosides from two strains of Aspergillus fumigatus (237 and ATCC 9197) expressing both GalCer and GlcCer were also purified and characterized by similar methods. The GalCer fractions were found to have ∼70% and ∼90% N-2‘-hydroxy-(E)-3‘-octadecenoate, respectively, in the two strains. In contrast, the GlcCer fractions had N-2‘-hydroxy-(E)-3‘-octadecenoate at only ∼20 and ∼50%, respectively. The remainder in all cases was the saturated 2-OH fatty acid, which has not been previously reported in cerebrosides from A. fumigatus. The availability of detailed structures of both glycosylinositol phosphorylceramides [Levery, S. B., Toledo, M. S., Straus, A. H., and Takahashi, H. K. (1998) Biochemistry37, 8764−8775] and cerebrosides from P. brasiliensis revealed parallel quantitative differences in expression between yeast and mycelium forms, as well as a striking general partitioning of ceramide structure between the two classes of GSLs. These results are discussed with respect to possible functional roles for fungal sphingolipids, particularly as they relate to the morphological transitions exhibited by P. brasiliensis.Keywords
This publication has 17 references indexed in Scilit:
- A Mushroom Fruiting Body-Inducing Substance Inhibits Activities of Replicative DNA PolymerasesBiochemical and Biophysical Research Communications, 1998
- SPHINGOLIPID FUNCTIONS INSACCHAROMYCES CEREVISIAE: Comparison to MammalsAnnual Review of Biochemistry, 1998
- Immunochemical and subcellular localization of the 43 kDa glycoprotein antigen ofParacoccidioides brasiliensiswith monoclonal antibodiesMedical Mycology, 1996
- Glycolipids fromParacoccidioides brasiliensis. Isolation of a galactofuranose-containing glycolipid reactive with sera of patients with paracoccidioidomycosisMedical Mycology, 1995
- Structural determination of , 8-sphingadienine from species of AspergillusChemistry and Physics of Lipids, 1994
- Isolation and structure determination of Pachybasium cerebrosides which potentiate the antifungal activity of aculeacin.The Journal of Antibiotics, 1988
- Cerebroside of the dimorphic human pathogen, Candida albicansChemistry and Physics of Lipids, 1987
- Isolation ofN-2?-Hydroxyhexadecanoyl-1-O-?-d-glucopyranosyl-9-methyl-4,8-d-erythro-sphingadienine from fruiting bodies of twoBasidiomycetes fungiGlycoconjugate Journal, 1986
- Natural abundance nitrogen-15 NMR by enhanced heteronuclear spectroscopyChemical Physics Letters, 1980
- Notizen: Sphingolipide und Glykolipide von Pilzen und höheren Pflanzen.Zeitschrift für Naturforschung B, 1969