SCREENING OF ENDOPHYTIC FUNGI FOR THEIR ABILITY TO PRODUCE EXTRACELLULARCELLULASES Original Article
Dakshayani Siddalinga Devaru Seethikal, Ramasandra Govind Sharathchandra, Sudisha
Abstract
Dakshayani Siddalinga Devaru Seethikal, Ramasandra Govind Sharathchandra, Sudisha
Abstract
Objective: Screening endophytic isolates from woody perennial medicinal plants of Western Ghats for production of extracellular cellulases Methods: Endophytes were isolated using normal microbiological methods and their colonization frequency and dominance were calculated using statistical methods. Efficiency of growth on complex cellulosic substrates was evaluated on media supplemented with specific substrates. Enzyme assays with identified endophytic fungi were carried from their secretome. Results: Forty endophytic fungal isolates were obtained using standard isolation methods from different medicinal plants from a biodiversity hotspot in the Western Ghats region of Karnataka, India. The isolated endophytic fungi were then identified based on their morphological characters. The percentage of dominant endophytes (���� ) was calculated based on the colonization frequency. Among the isolated fungi, colonization frequency of F. solani and Talaromycessp. was found to be highest, at5.5 and 5.6 respectively. Each of the identified fungi was grown on (Carboxyl Methyl Cellulase) CMC and seven among the 40 isolates were found to grow luxuriantly as measured by radial growth. The identities of these fungi were morphologically re-confirmed and were completely carbon drained by growing them on a low nutrient medium. These fungi were later evaluated for their growth on avicel and microcrystalline cellulose. Fusariumsolani and Talaromycessp. were significantly better in their growth when compared to other endophytes tested. Further, the cellulosome complex of enzymes was analysed in the secretome of Fusariumsolani and Talaromycessp. Total filter paper activity of Fusariumsolani was found to be FPU/ml, 76 FPU/ml and 70 FPU/ml at 24, 48 and 72 h respectively. Similarly, Filter paper activity of Talaromycessp. was found to be 89, 86 and 78 FPU/ml at 24h, 48h and 72h respectively. Endogluconase activity of Fusariumsolani was found to be 63CMCase, 60and 61CMCase at 24, 48 and 72hours of incubation respectively, which was greater than Talaromycessp. Similarly, Exogluconase and Beta-glucosidase activities were also found to be high in Talaromycessp. when compared to Fusariumsolani at all the time intervals tested. Conclusion: The results from the present study reveals that Fusariumsolani and Talaromycessp. are extremely potent producers of cellulases and can thus be used for eco-friendly and economic hydrolysis of biomass for biofuel purposes.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective: Screening endophytic isolates from woody perennial medicinal plants of Western Ghats for production of extracellular cellulases Methods: Endophytes were isolated using normal microbiological methods and their colonization frequency and dominance were calculated using statistical methods. Efficiency of growth on complex cellulosic substrates was evaluated on media supplemented with specific substrates. Enzyme assays with identified endophytic fungi were carried from their secretome. Results: Forty endophytic fungal isolates were obtained using standard isolation methods from different medicinal plants from a biodiversity hotspot in the Western Ghats region of Karnataka, India. The isolated endophytic fungi were then identified based on their morphological characters. The percentage of dominant endophytes (���� ) was calculated based on the colonization frequency. Among the isolated fungi, colonization frequency of F. solani and Talaromycessp. was found to be highest, at5.5 and 5.6 respectively. Each of the identified fungi was grown on (Carboxyl Methyl Cellulase) CMC and seven among the 40 isolates were found to grow luxuriantly as measured by radial growth. The identities of these fungi were morphologically re-confirmed and were completely carbon drained by growing them on a low nutrient medium. These fungi were later evaluated for their growth on avicel and microcrystalline cellulose. Fusariumsolani and Talaromycessp. were significantly better in their growth when compared to other endophytes tested. Further, the cellulosome complex of enzymes was analysed in the secretome of Fusariumsolani and Talaromycessp. Total filter paper activity of Fusariumsolani was found to be FPU/ml, 76 FPU/ml and 70 FPU/ml at 24, 48 and 72 h respectively. Similarly, Filter paper activity of Talaromycessp. was found to be 89, 86 and 78 FPU/ml at 24h, 48h and 72h respectively. Endogluconase activity of Fusariumsolani was found to be 63CMCase, 60and 61CMCase at 24, 48 and 72hours of incubation respectively, which was greater than Talaromycessp. Similarly, Exogluconase and Beta-glucosidase activities were also found to be high in Talaromycessp. when compared to Fusariumsolani at all the time intervals tested. Conclusion: The results from the present study reveals that Fusariumsolani and Talaromycessp. are extremely potent producers of cellulases and can thus be used for eco-friendly and economic hydrolysis of biomass for biofuel purposes.
Key concepts: Plant use of endophytic fungi in defense, Cellulase, Biology, Colonization, Botany, Dominance (genetics), Cellulose, Microbiology