Trichoderma seed coating as well as preparation method and application thereof
A technology of Trichoderma and strains, applied in the prevention and treatment of root rot, sheath blight, preparation of biological control Trichoderma biological seed coating agent, field of corn stalk rot, can solve corn lodging, few studies , Restricting the promotion of corn mechanized production technology and other issues, to achieve the effects of promoting growth indicators, broad market prospects, and improving plant stress resistance
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Embodiment 1
[0031] 1. Plate strain activation: inoculate Trichoderma harzianum SH2303 on a PDA petri dish, and culture it upside down in a 28°C incubator for 4-5 days.
[0032] PDA medium: 200g potato boiled and filtered upper juice, 20g glucose, 20g agar powder, dilute purified water to 1L, fill each 250mL into 500mL Erlenmeyer flask, autoclave at 121℃ for 25min.
[0033] 2. Preparation of primary strains: 200g of potatoes, 20g of glucose, 1L of purified water, each 250mL was dispensed into a 500mL Erlenmeyer flask, and autoclaved at 121°C for 25min. The strains were inserted into the plate, placed in a shaker at 180 r / min, 28° C., and shaken for 5 days to obtain Trichoderma harzianum SH2303 liquid fermentation strains.
[0034] 3. Trichoderma liquid fermentation: corn flour 8kg, magnesium sulfate 80g, ferrous sulfate 1.2g, manganese sulfate 0.4g, zinc sulfate 0.32g, potassium dihydrogen sulfate 0.61kg, sodium nitrate 0.23kg, ammonium nitrate 176g, calcium chloride 160g, make up 200L wi...
Embodiment 2
[0042] 1. Plate strain activation: inoculate Trichoderma harzianum SH2303 on a PDA petri dish, and culture it upside down in a 28°C incubator for 4-5 days.
[0043] PDA medium: 200g potato boiled and filtered upper juice, 20g glucose, 20g agar powder, dilute purified water to 1L, fill each 250mL into 500mL Erlenmeyer flask, autoclave at 121℃ for 25min.
[0044] 2. Preparation of primary strains: 200g of potatoes, 20g of glucose, 1L of purified water, each 250mL was dispensed into a 500mL Erlenmeyer flask, and autoclaved at 121°C for 25min. The strains were inserted into the plate, placed in a shaking table at 180 r / min, 28° C., and shaken for 5 days to obtain Trichoderma liquid fermentation strains.
[0045] 3. Trichoderma liquid fermentation: corn flour 8kg, magnesium sulfate 80g, ferrous sulfate 1.2g, manganese sulfate 0.4g, zinc sulfate 0.32g, potassium dihydrogen sulfate 0.61kg, sodium nitrate 0.23kg, ammonium nitrate 176g, calcium chloride 160g, make up 200L with water, ...
Embodiment 3
[0056] 1. Plate strain activation: Inoculate Trichoderma viridans SH2303 on a PDA petri dish, and incubate it upside down in a 28°C incubator for 4-5 days.
[0057] PDA medium: 200g of potato boiled and filtered upper layer juice, 20g of glucose, 20g of agar powder, dilute to 1L with purified water, aliquot into 250mL Erlenmeyer flask, autoclave at 121°C for 25min.
[0058] 2. Preparation of primary strains: 200g of potatoes, 20g of glucose, 1L of purified water, aliquoted into 250mL Erlenmeyer flasks, and autoclaved at 121°C for 25min. Insert the strain on the plate, place it in a shaker at 180 r / min, 28° C., and shake the flask for 5 days to obtain the liquid fermentation strain of Trichoderma harzianum SH2303.
[0059] 3. Trichoderma liquid fermentation: corn flour 8kg, magnesium sulfate 80g, ferrous sulfate 1.2g, manganese sulfate 0.4g, zinc sulfate 0.32g, potassium dihydrogen sulfate 0.61kg, sodium nitrate 0.23kg, ammonium nitrate 176g, calcium chloride 160g, make up 200...
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