COMPOSITIONAL ANALYSIS OF THE MAJOR CAPSULAR POLYSACCHARIDES OF CRYPTOCOCCUS-NEOFORMANS BY HIGH-PERFORMANCE ANION-EXCHANGE CHROMATOGRAPHY WITH PULSED AMPEROMETRIC DETECTION (HPAEC-PAD)

Citation
C. Corradini et al., COMPOSITIONAL ANALYSIS OF THE MAJOR CAPSULAR POLYSACCHARIDES OF CRYPTOCOCCUS-NEOFORMANS BY HIGH-PERFORMANCE ANION-EXCHANGE CHROMATOGRAPHY WITH PULSED AMPEROMETRIC DETECTION (HPAEC-PAD), Journal of liquid chromatography & related technologies, 21(7), 1998, pp. 941-951
Citations number
13
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
ISSN journal
10826076
Volume
21
Issue
7
Year of publication
1998
Pages
941 - 951
Database
ISI
SICI code
1082-6076(1998)21:7<941:CAOTMC>2.0.ZU;2-U
Abstract
Cryptococcus neoformans is a predominantly saprophytic yeast that can cause serious infections, mostly in individuals with acquired immunode ficiency syndrome (AIDS). A prominent virulence factor of Cryptococcus neoformans is its capsule. This is constituted mainly of glucans; the capsular polysaccharide, glucuronoxylomannan (GXM) (composed of manno se, xylose, glucuronic acid), and at least two minor carbohydrate anti gens, galactoxylomannan (GalXM) and mannoproteins (MP). In this paper we present an optimized HPAEC-based method for the rapid and effective determination of the complete carbohydrate constituents of GXM and Ga lXM. Cryptococcus neoformans strain A 9759 serotype A and the acapsula r mutant CAP 67 were grown in a totally dialyzable synthetic medium at 30 degrees C. Culture supernatants were subjected to tangential filtr ation (10,000-M-r-cut-off) to separate high molecular weight cryptococ cal products from medium constituents. The supernatants were dialyzed against phosphate buffer saline (PBS) containing sodium azide (0.02%) and concentrated to a carbohydrate concentration of 1.5 mg/mL. GXM and GalXM were isolated and purified as described in the experimental sec tion. For neutral sugar and uronic acid composition analysis, 2.5 mg p olysaccharide fractions were hydrolyzed with 2 M trifluoroacetic acid (TFA, 100 degrees C, 6 h), followed by lyophilization, then the residu es were analyzed by HPAEC coupled with pulsed amperometric detection ( PAD). Separations were carried out using either a CarboPac PA 100 or a CarboPac PA 10 column and matching guard column (all from Dionex, Sun nyvale, CA, USA). Employing PA 100, as well as PA 10 column, baseline separation of the neutral monosaccharides galactose, glucose, xylose, mannose and glucuronic acid were obtained. Monosaccharide and uronic a cid compositions of GXM and GalXM determined by this method were found to be highly accurate.