In the present study, the production of ,!?-glucosidase and endoglucanase and the pattern of their corresponding polymorphic forms occurring in the extracellular and cytosolic filtrates of Chaetomium fusisporale (ATCC 64772) has been studied. When C. fusisporale was grown on carboxymethyl cellulose (CMC) as the sole carbon source, the extracellular fractions contained most of these enzymes. The distribution of the enzymes varied with the age of the culture. By the use of electrophoretic techniques the presence of two forms of P-glucosidase, i.e. ,!?-GLU I1 and ,!?-GLU 111 was detected in extracellular and cytosolic filtrates at early stages of growth, while at later stages two more isozymes of B-glucosidase, i.e. D-GLU I and 8-GLU IV, only appeared in the cytosolic filtrates. Similary, endoglucases isozymes EG I and EG I1 were present in both fractions at early stages of growth but at later stages, with the production of perithecia, EG 111 appeared. Thus, EG 111, j-GLU I and /I-GLU IV may indicate that they are correlated with the development of the fungus. In order to differentiate further between the multiple molecular forms of these enzymes two of them have been characterized with respect to temperature, pH, ethylenediamine tetra-acetic acid (EDTA) and metal ions.Isozymes are multiple molecular forms of enzymes which have been found to be important in the study of differential gene actions of an organism. Any marked change occurring in their electrophoretic pattern has been directly related to development changes ( SCANDALIOS 1974, DICKINSON and SULLIVAN 1975, COOPER et al. 1985. In this study, the production of j3-glucosidase and endoglucanase and the pattern of their isozymes in extra-und intracellular filtrates during the development of Chaetomium fusisporale has been investigated. This fungus starts to produce sexual reproductive bodies, the perithecia, after passing through the vegetative phase of life. In order to differenciate further between the isozymes of pglucosidase and endoglucanase some of them have been characterized with respect to temperature, pH, EDTA and metal ions.
Materials and methodsMicroorganism: The strain of Chaetomium fusisporale used in the present study was isolated from local soil. It produces no asexual spores but only perithecia at later stages of growth. The stock cultures were maintained in soil at 4 "C and subcultured on slants containing VOGEL'S glucose medium (VOGEL 1956).Inoculum: The discs (7 mm diameter) cut from the periphery of three day old cultures growing on VOGEL'S medium plates which were incubated at 37 "C were used as inoculum.Enzyme production: 250 ml flasks containing 50 ml of VmeL's medium (SANDHLJ and KALRA 1982) and supplemented with 1 % carboxymethyl cellulose (CMC) were inoculated in each case with five mycelial discs of C. fusisporale. The flasks were incubated at 37 "C as static cultures and always two flasks were analyzed at regular intervals for 20 days. Analytical methods : The enzymes were measured in both extracellular and cytosol fraction. The cul...