Trichoderma asperellum strain and application thereof
A technology of Trichoderma aculeatus and strains, applied in the fields of application, fungicides, fungi, etc., can solve the problems of unfavorable large-scale popularization and application, cumbersome preparation process, etc., achieve good biocontrol potential, prevent and control pepper blight, and strong parasitism Effect
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Embodiment 1
[0025] Isolation, purification, identification and preservation of the bacterial strain of embodiment 1
[0026] 1. Isolation and purification of Trichoderma
[0027] After fully mixing the soil collected from the capsicum rhizome soil of the disease, a small amount of soil particles were removed and placed on a PDA plate containing chloramphenicol, with 4 soil particles on each plate, and repeated three times. Incubate in the dark at 25°C. After Trichoderma spores, pick them out on a new PDA plate in time.
[0028] The strains for short-term storage are placed in PDA inclined test tubes and stored in a refrigerator at 4°C. Long-term storage of Trichoderma in a -20°C refrigerator (spores + 17% skimmed milk powder + silica gel particles).
[0029] 2. Identification of Trichoderma species
[0030] The biological characteristics of this strain are: the colony is cultured on PDA solid medium at 25°C, and it expands to 9cm in 3-4 days. The initial stage is white and sparse, and...
Embodiment 2
[0052] Embodiment 2 confrontation culture method
[0053] Trichoderma aculeatus Thz01 and Phytophthora capsici strains were transferred to PDA medium for activation. After Phytophthora capsici grew for 48 hours, a 0.5 cm diameter punch was used to cut the fungus cake at the edge of the colony, and the fungus cake was inoculated into the culture dish. At one end, after culturing at 25°C for 48 hours, inoculate the well-drilled Trichoderma strains to the other end of the petri dish, and treat each Trichoderma strain three times. At the same time, use only Phytophthora as a blank control, and observe whether there is an antagonistic effect after culturing for 7 days. And take pictures and record.
[0054] The results of confrontation culture experiment between Trichoderma aculeatus Thz01 strain and Phytophthora capsici strain are shown in figure 1 . No. 1 is the control, the plate on the left of plates 2, 3, and 4 is Phytophthora capsici, and the plate on the right is Trichoder...
Embodiment 3
[0055] Embodiment 3 prevents and treats capsicum blight
[0056] Preparation of biocontrol agent: Trichoderma aculeatus Thz01 was used to make biocontrol agent by using feed wheat grains as a substrate. The specific steps are:
[0057] (1) Strain activation: Trichoderma aculeatus Thz01 was inoculated into PDA medium and cultured at 25°C for 5 days;
[0058] (2) Preparation of seed liquid: after the activation of the bacterial strain, the spores were scraped off and scraped into sterilized water to prepare a live bacteria concentration of 10 7 The spore suspension of each / mL is the seed liquid;
[0059] (3) Inoculate the seed liquid into boiled and sterilized wheat grains, cultivate them for 15 days, and turn them in time during the culture period, so that the wheat grains can be fully grown with Trichoderma aculeatus Thz01 spores to prepare biocontrol agents; The dosage of seed solution is 3mL based on kilogram of wheat grains.
[0060] The prepared biocontrol preparation ...
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