Study on Isolation, Effectiveness and Formulation of Native Trichoderma spp. from Jhum, Virgin and Cultivated Land of Nagaland

Chavan Digvijay Rajaram, S. Banik
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Abstract

Ten Trichoderma isolates named as Trichoderma isolate1 to Trichoderma isolate 10, were isolated from different soil samples collected from virgin, Jhum, cultivated, and fallow land of Medziphema block of Nagaland state by serial dilution agar plate method on Trichoderma selective medium (TSM). All the Trichoderma isolates were tested against Fusarium solani and Sclerotium rolfsii by dual culture method. All the isolates were highly effective against both the pathogens with 83-93 percent and 72-89 per cent growth inhibition of Fusarium solani and Sclerotium rolfsii, respectively. Among the tested Trichoderma isolates, Trichoderma isolate1 was observed most effective; therefore, it was mass multiplied in Potato Dextrose Broth and formulated in talc powder. The colony forming units were counted thrice to determine the number of viable conidia in product; the first counting was done on the same day of formulation, the second counting was done one month, and the last was done six months after formulation. It was observed that the colony forming units decreased from 13 × 106 c.f.u. to 5.66 × 106 c.f.u. after six months of storage from the initial formulation which indicates that even after six months of storage, the Trichoderma isolate 1 formulated by using talc powder still contained good number of viable conidia. Thus, from the overall results obtained from the present work, it can be concluded that Trichoderma spp. as a ubiquitous fungus and an effective biological control agent can be one of the paramount components of integrated disease management.
那加兰邦原生、原生和耕地木霉的分离、药效及配方研究
以木霉选择培养基(Trichoderma selective medium, TSM)为培养基,采用琼脂平板连续稀释法,从印度那加兰邦Medziphema区块的原始、Jhum、耕地和休耕地不同土壤样品中分离出10株木霉,分别命名为Trichoderma isolate1至Trichoderma isolate 10。采用双重培养法对分离的木霉进行了番茄枯萎菌和罗尔夫菌核菌的抑菌试验。所有分离菌株对茄枯菌和罗氏菌核菌的生长抑制率分别为83% ~ 93%和72% ~ 89%。实验分离的木霉菌株中,分离木霉1效果最好;因此,在马铃薯葡萄糖肉汤中大量繁殖,并在滑石粉中配制。对菌落形成单位进行三次计数,以确定产物中有活孢子的数量;第一次计数在配药当天进行,第二次计数在配药一个月后进行,最后一次计数在配药六个月后进行。结果表明,经过6个月的发酵,原配方的菌落形成单位由13 × 106 c.f.u.下降到5.66 × 106 c.f.u.,说明滑石粉配方的木霉分离物1在发酵6个月后仍含有大量的活孢子。因此,从本研究获得的总体结果可以得出结论,木霉作为一种普遍存在的真菌和有效的生物防治剂,可以成为综合疾病管理的重要组成部分之一。
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