Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Screening of Trichoderma Isolates for Chitinolytic Activity Using Glycol Chitin Plate Assay


Affiliations
1 Central Food Technological Institute, Mysore (Karnataka), India
2 Department of Biotechnology, College of Agriculture, University of Agricultural Sciences, Dharwad (Karnataka), India
     

   Subscribe/Renew Journal


Thirty three isolates of Trichoderma belonging to different species which were previously screened against Sclerotium rolfsii, Fusarium oxysporum and Rhizactonia solani were used for checking chitinolytic activity using agarose plate containing glycol chitin. Differences were observed among species and isolates of the same species with respect to chitinase production after induction with colloidal chitin and chitin degradation. Among all the isolates, T. virens IABT 1010, T. koningii IABT1016, T. polysporum IABT1018 were found to be more efficient chitinase producers. In all the isolates, chitinase production started within 24 hours of induction, but maximum production reached in 48 hours. Therefore, culture filtrates taken after 48 hours of induction can be used for routine screening of the Trichoderma isolates.

Keywords

Trichoderma, Chitinolytic Activity, Glycol Chitin, Colloidal Chitin.
Subscription Login to verify subscription
User
Notifications
Font Size


Abstract Views: 205

PDF Views: 0




  • Screening of Trichoderma Isolates for Chitinolytic Activity Using Glycol Chitin Plate Assay

Abstract Views: 205  |  PDF Views: 0

Authors

Ganapathi Bhat
Central Food Technological Institute, Mysore (Karnataka), India
Sumangala Bhat
Department of Biotechnology, College of Agriculture, University of Agricultural Sciences, Dharwad (Karnataka), India
M. S. Kuruvinashetti
Department of Biotechnology, College of Agriculture, University of Agricultural Sciences, Dharwad (Karnataka), India

Abstract


Thirty three isolates of Trichoderma belonging to different species which were previously screened against Sclerotium rolfsii, Fusarium oxysporum and Rhizactonia solani were used for checking chitinolytic activity using agarose plate containing glycol chitin. Differences were observed among species and isolates of the same species with respect to chitinase production after induction with colloidal chitin and chitin degradation. Among all the isolates, T. virens IABT 1010, T. koningii IABT1016, T. polysporum IABT1018 were found to be more efficient chitinase producers. In all the isolates, chitinase production started within 24 hours of induction, but maximum production reached in 48 hours. Therefore, culture filtrates taken after 48 hours of induction can be used for routine screening of the Trichoderma isolates.

Keywords


Trichoderma, Chitinolytic Activity, Glycol Chitin, Colloidal Chitin.