Trichoderma fungus with nematicide activity as well as preparation method and application thereof
A Trichoderma, nematicide technology, applied in the direction of nematicides, botany equipment and methods, microbe-based methods, etc., can solve limited problems and achieve good effect of nematicidal activity
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Embodiment 1
[0032] The isolation and identification of embodiment 1 Trichoderma viridans (H.virens H22)
[0033] The medium formula is CMA medium: 20g corn flour, 15g agar powder, 1000ml water.
[0034] Sprinkle 1.0g soil sample (taken from the mangrove rhizosphere in Shenzhen Bay, Guangdong Province) on the culture medium, insert about 1000 second-instar larvae (J2) of Meloidogyne incognita, culture them at 25°C for 3 days, examine them under the microscope and pick them up with a needle Single fungal conidia on and around the dead insect body were placed on a CMA plate containing 50 ppm of streptomycin sulfate, and the fungus was purified.
[0035] The bacterial strain morphological characteristic of described Trichoderma viridans (Hypocrea virens H22) is: initial stage is white on PDA, and mid-term color becomes light green gradually, has well-developed aerial hyphae, and later stage produces a large amount of fractional sporophytes and conidia , conidiophores are opposite or alternat...
Embodiment 2
[0058] The solid culture of embodiment 2 Trichoderma viridans (H.virens H22)
[0059] The medium formula is potato agar medium (PDA medium): 200g potato, 20g glucose, 20g agar powder, 1000mL water;
[0060] In each 90mm petri dish, pour about the thick PDA medium that accounts for the height of 1 / 3 of the petri dish, Trichoderma viridans (H.virens H22) mycelium is inoculated on the PDA medium, after sealing with parafilm Cultivate at 25-28°C for 2-3 days. Store the strains in a refrigerator at 4°C until use, or use them directly with spore culture solution.
Embodiment 3
[0061] The liquid culture of embodiment 3 Trichoderma viridans (H.virens H22)
[0062] The medium formula is CMA culture medium: corn flour 20g, distilled water 1000mL.
[0063] Each 500mL triangular flask was filled with 200mL of CMA culture solution, sterilized by damp heat at 121°C for 20min, and after cooling, 5 pieces of activated Trichoderma viridans discs were inserted into each bottle, and cultured in the dark at 180rmp 27°C for 8 days. Centrifuge at 12000rmp for 10min to obtain a supernatant, which is stored in a refrigerator at 4°C until use.
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