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Volume: 5, Issue: 6, Nov-Dec, 2017
DOI: 10.7324/JABB.2017.50601

Research Article

Chitinolytic efficacy and secretion of cell wall degrading enzymes from Trichoderma spp. in response to phyto-pathological fungi

Dinesh K. Khatri, Durgesh Nandini Tiwari, Himanshu S. Bariya


Chitinolytic activity and major antifungal enzyme secretion form Trichoderma spp. was studied. Soil samples were collected from different environmental niche of North Gujarat Region, India and 12 different species of Trichoderma were obtained and identified. Among 12 isolates, 4 isolates were identified as T. harzianum, 5 isolates were identified as T. virideand remaining 3 isolates were as of T. hamantum. These isolates were identified by using species specific primers amplification by PCR. All identified isolates were screened for chitinase activity using colloidal chitin derived from commercial chitin on the media supplemented with bromocresol purple. According to results of chitinase activity screening assay, T. viride was found to be more potential isolate for chitinase production. From biocontrol assay by using duel culture method, T. viride was found to be more potent antagonist against fungal plant pathogens like A. niger, F. oxysporum and S. rolfsii. T. viridewas selected for further study of biocontrol potential and production of cell wall degrading enzymes. T. viride was inoculated in media containing basal media and mycelia of fungal pathogens for cell wall degrading enzyme production. It was found that T. viride secrete three major cell wall degrading enzymes i.e. chitinase, protease and β- Glucanase. Optimum production of all three enzymes was found at 96 hr incubation. Details of antifungal protein secretion are mentioned in this paper.

Keywords: Trichoderma, Chitinolytic, Chitinase, Protease, Glucanase, Biocontrol.


How to cite this article:

Khatri DK, Tiwari DN, Bariya HS. Chitinolytic efficacy and secretion of cell wall-degrading enzymes from Trichoderma spp. in response to phytopathological fungi. J App Biol Biotech. 2017;5(6):1-8. DOI: 10.7324/JABB.2017.50601.