A major part of Trichoderma antifungal system consists of a number of genes encoding for an astonishing variety of secreted lytic enzymes including; e.g. chitinase, cellulases and β-1,3-glucanases. The present work aimed to apply the mutagenesis technique in genetically breeding program of the bioagent Trichoderma viride to enhance three effective hydrolytic enzymes in their biocontrol abilities against two of the important plant fungal pathogens; Sclerotia rolfesii and Sclerotinia sclerotiorum the causal fungi of rot-root and white-rot diseases, respectively. Subjecting the spores of the wild type (T. viride) to the first UV-exposure time induced highly decrease in survival reached to 99.85%. Also, subjecting the spores of the two selected mutants (TvM1-UV1 and TvM9-UV1) to the second UV-exposure time induced highly decrease in their survival reached to 99.81 and 99.52%, respectively. The first and the second UV-treatments induced mutants with high growth and better sporulation measurements as well as superiority in biological control activities against some rot pathogens formed sclerotia than their parental wild type, Trichoderma viride. Four UV-induced mutants (TvM1-UV1, TvM9-UV1, TvM1-UV2 and TvM9-UV2) that obtained after UV-exposure of the parental wild type, Trichoderma viride were in vitro assessed for their biological control activities (Dual culture, filtrate inhibition, inhibition of sclerotia viability and inhibition of Polygalacuronase (PG) and Pectin methyl esterase (PME) activities against both pathogens. Through in vitro inhibitory activity by culture filtrates of the selected mutants (TvM1-UV1, TvM9-UV1, TvM1-UV2 and TvM9-UV2) and their parental wild type, T. viride, the growth rates, sclerotia viability as well as PG and PME activities were decreased the pathogens compared with the wild type. The filtrate inhibition activities of the selected mutants were considerably increased than that of their parental wild type. The pathogen S. sclerotiorum was more senstive to the inhibition effects of the culture filtrates of the tested T. viride mutants than the other pathogen S. rolfsii. Spectrophotometer was used to assay the hydrolytic enzymes; chitinase, β-1,3-glacturoranase and cellulases activities from the selected mutants (TvM1-UV1, TvM9-UV1, TvM1-UV2 and TvM9-UV2) and their parental wild type, T. viride. The selected mutants showed higher hydrolytic enzyme activities than their parental wild type. The greatest enzyme production by the tested T. viride mutants was cellulases followed by β-1,3-glucanase then chitinase. Total protein extraction and banding patterns SDS-polyacrylamid gel electrophoresis of mutants showed fold increased in bands numbers compared with wild type. In biological control experiments against rot-root and white-rot diseases caused by S. rolfesii and S. sclerotiorum, respectively in bean plants under artificial and natural infested soil, complete control of the disease was achieved, in which even the higher producer-hydrolytic enzymes of T. viride mutants treatment fa...