The preparation of pharmaceutical grade (1 --> 3)-beta-D-glucans from
Saccharomyces cerevisiae requires that the microparticulate glucans wh
ich are employed as the starting material for drug production be of th
e highest purity. Potential contaminants of the (1 --> 3)P-D-glucan is
olation process are yeast cell wall lipids, which are frequently found
in association with glucans. The lipid content of yeast-derived (1 --
> 3)-beta-D-glucan during various stages of the isolation process by m
ethyl esterification and total ion gas chromatography and mass spectro
metry (GC-MS) was examined. Following sequential alkaline and acid hyd
rolyses, the total lipid content of (1 --> 3)-beta-D-glucan was 100.4
nmol/mg with 9-cis-C 18:1 fatty acid accounting for 45.3 nmol/mg gluca
n (45%). Following ethanol extraction of the (1 --> 3)-beta-D-glucan,
lipid was not detected. Indeed, fatty acid methyl esters were not dete
ctable by total ion CC-MS in all twelve samples investigated. These da
ta demonstrate that the isolation process for yeast-derived (1 --> 3)-
beta-D-glucan effectively reduces contamination by yeast cell wall lip
ids.