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