Isolation and composition of inositolphosphorylceramide-type sphingolipids of hyphal forms of Candida albicans

被引:50
作者
Wells, GB [1 ]
Dickson, RC [1 ]
Lester, RL [1 ]
机构
[1] UNIV KENTUCKY,COLL MED,DEPT BIOCHEM,LEXINGTON,KY 40536
关键词
D O I
10.1128/jb.178.21.6223-6226.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hyphal forms of the human pathogen Candida albicans have been found to contain substantial quantities of phosphosphingolipids. These lipids were fractionated into three classes by normal-phase high-performance liquid chromatography. The first class contained equimolar amounts of phosphorus, inositol, phytosphingosines, and fatty acids; their composition and chromatographic behavior suggest that these compounds are inositolphosphorylceramides. The second class contained equimolar amounts of phosphorus, mannosylinositol, phytosphingosines, and fatty acids; their composition and chromatographic behavior indicate that these compounds are mannosylinositolphosphorylceramides. The third class of compounds contained phosphorus, mannosylinositol, inositol, phytosphingosines, and fatty acids in a molar ratio of 2:1:1:1:1; their composition and chromatographic behavior indicate that these compounds are mannosyldiinositolphosphorylceramides. Molecular species in each class differ in the composition of long chain bases and fatty acids; the most abundant long chain bases were C-18 and C-20 phytosphingosines, and the most abundant fatty acids were hydroxy and nonhydroxy C-24-26. The array of sphingolipids in C. albicans is similar to that of Saccharomyces cerevisiae. Sphingolipids have been shown to be essential in S. cerevisiae, thus these lipids, which are not present in animals, offer a potentially unique targets for antifungal chemotherapy against C. albicans.
引用
收藏
页码:6223 / 6226
页数:4
相关论文
共 17 条
[1]  
BARTLETT GR, 1959, J BIOL CHEM, V234, P466
[2]  
Bullock W., 1993, ASM News (Washington), V59, P182
[3]   ISOLATION OF MUTANT SACCHAROMYCES-CEREVISIAE STRAINS THAT SURVIVE WITHOUT SPHINGOLIPIDS [J].
DICKSON, RC ;
WELLS, GB ;
SCHMIDT, A ;
LESTER, RL .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (05) :2176-2181
[4]   QUANTITATIVE DENSITOMETRIC THIN-LAYER CHROMATOGRAPHY OF LIPIDS USING COPPER ACETATE REAGENT [J].
FEWSTER, ME ;
BURNS, BJ ;
MEAD, JF .
JOURNAL OF CHROMATOGRAPHY, 1969, 43 (01) :120-+
[5]  
HANSON BA, 1980, J LIPID RES, V21, P309
[6]  
LESTER RL, 1993, ADV LIPID RES, V26, P253
[7]  
LESTER RL, 1993, J BIOL CHEM, V268, P845
[8]   THE DISCOVERY OF AUSTRALIFUNGIN, A NOVEL INHIBITOR OF SPHINGANINE N-ACYLTRANSFERASE FROM SPORORMIELLA-AUSTRALIS - PRODUCING ORGANISM, FERMENTATION, ISOLATION, AND BIOLOGICAL-ACTIVITY [J].
MANDALA, SM ;
THORNTON, RA ;
FROMMER, BR ;
CUROTTO, JE ;
ROZDILSKY, W ;
KURTZ, MB ;
GIACOBBE, RA ;
BILLS, GF ;
CABELLO, MA ;
MARTIN, I ;
PELAEZ, F ;
HARRIS, GH .
JOURNAL OF ANTIBIOTICS, 1995, 48 (05) :349-356
[9]   PHENOTYPES OF SPHINGOLIPID-DEPENDENT STRAINS OF SACCHAROMYCES-CEREVISIAE [J].
PATTON, JL ;
SRINIVASAN, B ;
DICKSON, RC ;
LESTER, RL .
JOURNAL OF BACTERIOLOGY, 1992, 174 (22) :7180-7184
[10]   THE PHOSPHOINOSITOL SPHINGOLIPIDS OF SACCHAROMYCES-CEREVISIAE ARE HIGHLY LOCALIZED IN THE PLASMA-MEMBRANE [J].
PATTON, JL ;
LESTER, RL .
JOURNAL OF BACTERIOLOGY, 1991, 173 (10) :3101-3108