Variability in Production of Extracellular Hydrolytic Enzymes by Trichoderma spp. and Induction of Resistance in Gram (cicer arietinum)
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DOI:
https://doi.org/10.18311/jbc/2008/3798Keywords:
β, -1, 3 Glucanase, Cellulase, Chi Tinase, Induced ResistanceTrichodermaspp.Abstract
Ten isolates of Trichoderma spp. isolated from rhizosphere region Of different crops were evaluated for their ability to produce extracellular hydrolytic enzymes, viz., β-1, 3 glucanase, chitinase and cellulase enzymes with different concentrations ef carbon sources, pM, and temperature levels and the induction of systemic resistance in gram seedlings. Highest chitinase and β-1, 3 glucanase activity were observed in TR2 isolate whereas TH2 isolate exhibited highest activity of cellulase. TH1 and TH5 were the next best isolates in their chtinase enzyme activity. Similarly, TR1 and TH1 isolates followed the TR2 for β-1, 3-glucanase activity. The activity of cellulase was highest in TH2 isolate followed by TH5 and TR2, which were statistically significant. The enzyme β-1,3 glucanase was produce in media with pH 4.0 to 8.0 with an optimum pH5.5. The optimum pH for chitinase and cellulase enzyme activity was recorded at 5.0. With the variable temperatures, i.e., 20, 25, 30, 35 and 40°C, the enzyme activities of all three enzymes showed highest at 30°C. The activities of enzymes β-1,3 glucanase and chitinase was recorded highest at 3.0 and 4.0% concentrations of glucan and chitin, respectively whereat 0.75% concentration of cellulose showed highest cellulase activity. The highest induced resistance by Trichoderma isolates in gram seedlings, was recorded by TR1, through the increase activity of PAL and β-1,3 glucanase and TH1 by enhance activity of peroxidase enzyme.Downloads
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Published
2008-06-14
How to Cite
Bhagat, S., & Pan, S. (2008). Variability in Production of Extracellular Hydrolytic Enzymes by <I>Trichoderma</I> spp. and Induction of Resistance in Gram (<I>cicer arietinum</I>). Journal of Biological Control, 22(1), 57–66. https://doi.org/10.18311/jbc/2008/3798
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