A strain of Trichoderma guizhou and its application
A technology of Trichoderma and mycelium, applied in fungi, fungicides, chemicals for biological control, etc., can solve problems such as excessive heavy metals, destruction of ecological balance, and decline in soil fertility
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Embodiment 1
[0043] Embodiment 1, the isolation, purification and identification of Trichoderma strain
[0044] 1. Isolation and Purification of Trichoderma
[0045] Take soil samples from the forest area of Milin County, Nyingchi Prefecture, Tibet, weigh 1g of soil samples, and dilute to 10 with sterile water -1 、10 -2 and 10 -3 Three concentration gradients, each concentration gradient takes 200 μl and spreads on PDA medium (potato 200g, glucose 20g, agar 20g, distilled water to 1000ml, sterilized at 121 ℃ and added to the medium at a final concentration of 300mg / l chloramphenicol) on the surface of a 9cm diameter petri dish. After inverting the plate and incubating at 25°C for 1–3 days, pick a single colony and transfer it to PDA slant medium.
[0046] 2. Species identification of Trichoderma strains
[0047] Biological features: see figure 1 , on CMD medium, after 3 days of culture at 25 ° C, the colony radius is 70–73 mm, and the plate is full in 3 days. The colonies are gr...
Embodiment 2
[0066] Embodiment 2, the application of Trichoderma
[0067] 1. Confrontation with plant pathogenic bacteria
[0068] Guizhou Trichoderma TC952 and Botrytis cinerea (Zhao Juan, Liu Ting, Liu Weicheng, et al. were selected from the preserved slant medium respectively. Screening and identification of Streptomyces against Botrytis cinerea [J]. Microbiology Bulletin, 2019,46 (10): 2548-2558), Fusarium graminearum (the fungus is stored in the China Agricultural Microorganism Culture Collection Center, the preservation number is: ACCC 31053) and Rhizoctonia solani (Rhizoctonia solani ACCC 36124) 3 plant pathogenic bacteria in Activate on the PDA medium, then use a 5mm diameter puncher to cut the bacterial block at the edge of the activated colony as the inoculum, and inoculate it on a 9cm petri dish containing PDA. The inoculum of TC952 and plant pathogenic bacteria are separated on the PDA plate 5 cm, and a plate inoculated with only plant pathogenic bacteria at one end was used a...
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