Cell walls prepared from hyphae and from the outer layers of sclerotia of Sclerotium rolfsii Sacc. grown in the presence or absence of catechol which induces melanin deposition in the hyphal walls or disodiumethylene-diaminetetracetic acid (Na 2EDTA) which prevents melanin formation by the sclerotia, were compared for their susceptibility to β-(1 → 3) glucanase and chitinasc. A bacterial β-(1 → 3) endo-glucanase solubilized 49.5% of insoluble lammarin, 25.2 and 6.3% of the total dry weight of ordinary and melanin-containing hyphal walls respectively, and 5.9 and 10.3% of the total dry weight of ordinary and melanin-free sclerotial walls respectively, after 24 hr of incubation at 37°C. It was found that 2.2, 0.7, 0.8 and 1.3% of the total dry weight were solubilized by chitinase after 2 hr from ordinary hyphal walls, melanin-containing hyphal walls, ordinary slecrotial walls and melanin-free sclerotial walls, respectively. When added to the reaction mixtures, melanin extracted from catechol-grown hyphae and from sclerotial walls of S. rolfsii did not affect the activity of chitinase and glucanase. It was concluded that the susceptibility of various preparations of S. rolfsii walls to glucanase and chitinase is dependent upon both their physical structure and their melanin content.