The organization of the components of the cell wall from Candida albic
ans was studied by means of sequential treatment with hot SDS, anhydro
us ethylenediamine (EDA) and lytic enzymes. followed by chemical and m
icroscopic analyses of the different separated fractions. The EDA-inso
luble fraction retained the original morphology of the wall, which was
destroyed by beta-glucanase, but not by chitinase treatments. Stainin
g with fluorescent lectins revealed distinct distributions of mannopro
teins, glucans and chitin in the wall. Amino acid analysis of SDS-extr
acted walls, and the EDA-soluble and -resistant fractions gave similar
results, with seven amino acids making up about 70% of the total prot
ein weight. Treatment of the EDA-insoluble fraction with Zymolyase or
chitinase released fragments of variable size whose susceptibility to
these and other hydrolases suggests that they are made of glucan, chit
in and mannan oligomers associated with proteins. Treatment of the Zym
olyase-insoluble residue with chitinase released a series of low-molec
ular-mass oligomers made of neutral sugars, GlcNAc and amino acids, ma
inly lysine. It is suggested that they represent fragments of the core
making up the scaffold of the cell wall of the fungus.