Trichoderma harzianum strain and application in prevention and control of phytophthora capsici Leonian thereof
The technology of pepper blight and pepper blight is applied to Trichoderma harzianum strains and its application field in the prevention and control of pepper blight, and can solve the problems of fungicide resistance or even drug resistance, easy environmental pollution, and high cost of chemical control, Achieve the effect of increasing farmers' income, broad application prospects and enhancing economic added value
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Embodiment 1
[0054] Example 1. Obtainment and identification of Trichoderma harzianum HNA-12
[0055] 1. Obtaining strain HNA-12
[0056] 1. Sample collection
[0057] The samples were collected from the surface rhizosphere soil of pepper crops in Anyang, Henan.
[0058] Use soil borrowing equipment to remove 3-5cm of the topsoil in the field, dig out the soil together with the roots of the plants, pack them in polyethylene plastic bags, and bring them back to the laboratory for separation.
[0059] 2. Obtaining strain HNA-12
[0060] Air-dry the roots attached to the soil a little, tap the roots gently to make the attached soil fall off, dilute them gradually with sterile water, pipette 0.1 mL of the dilutions into the TSM medium plate, and use a sterile L-shaped coating The cloth rod is evenly coated and placed in a constant temperature incubator at 25-28°C for 3-4 days. Pick a single colony resembling Trichoderma and transfer it to a PDA plate for purification and culture. The mirror will initia...
Embodiment 2
[0067] Example 2. Inhibition of Trichoderma harzianum HNA-12 on pathogens
[0068] Experimental group: Inoculate Trichoderma harzianum HNA-12 and pathogenic bacteria cakes on the same PDA plate for confrontation culture (the vertical distance between the centers of the two bacterial cakes is 3 cm, and the diameter of the two bacterial cakes is 5 mm); The PDA plate of the pathogenic bacteria cake was used as the control group; after a certain period of dark culture at 25°C, the colony diameter of the pathogen (the average of the longest diameter and the shortest diameter) was measured and the inhibition rate was calculated. Inhibition rate = (colony diameter of pathogenic bacteria in the control group-colony diameter of pathogenic bacteria in the experimental group) / colony diameter of pathogenic bacteria in the control group * 100%. Three repeated treatments were set for each pathogenic bacteria, and three repeated treatments were set for the control, and the results were averag...
Embodiment 3
[0073] Example 3 Greenhouse biocontrol effect experiment of Trichoderma harzianum HNA-12
[0074] The pepper seeds are soaked in a warm soup at 55°C for 30 minutes, and then germinated. Select the same germinated seeds and sown in a culture bowl, 20 seeds per bowl; cultivate in a greenhouse (25-30°C) until the pepper plants grow 4 true leaves, grouping is as follows Operation (3 culture bowls per group):
[0075] Experimental group: each pepper plant was inoculated with 10 mL of Trichoderma harzianum HNA-12 spore suspension (the spore concentration was 5×10 6 Pieces / mL) and 10mL of Capsicum Phytophthora spore suspension (spore concentration is 5×10 6 Pcs / mL); The method of inoculation is to inject the spore suspension into the rhizosphere soil with a syringe;
[0076] Control group: Inoculate 10 mL of spore suspension of Phytophthora capsici per plant (spore concentration is 5×10 6 Pcs / mL); the method of inoculation is to inject the spore suspension into the rhizosphere soil with a s...
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