A trichoderma ta-9 strain and its application in rice disease control
A technology for trichoderma dark green and rice disease, applied in the field of microorganisms, can solve the problems affecting food safety, decline, and the control effect of rice sheath blight resistance, and achieves high content, simple and easy fermentation process, and is beneficial to long-term The effect of time storage
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Embodiment 1
[0026] Example 1: A method for isolating and obtaining Trichoderma atroviride TA-9 strain.
[0027] The formula of PDA medium is: potato 200g / L, glucose 20g / L, water 1L, agar 20g / L (solid medium). Peel the potatoes and cut them into small pieces, add 1L of water and boil for 30 minutes, filter with 2 layers of gauze, add glucose to the filtrate, add water to make up to 1L, add agar to make a solid medium and boil, divide and heat at 121°C Sterilize.
[0028] Include the following steps:
[0029] (1) Strain isolation, purification and preservation. A total of 200 rice balls were collected in many rice fields in Nanjing City 7-10 days after harvesting and scattered in the field. After drying in the shade, they were half-buried in moist sterilized quartz sand and cultured at 28°C for 15-20 days. The parasitic fungi grow on the surface of the rice ball. Carefully pick the parasitic fungi on the surface of the rice ball and place them on a PDA plate containing 50 μg / mL chloramph...
Embodiment 2
[0034] Example 2: Preparation of chlamydospore and conidia fermented product of Trichoderma dark green TA-9 strain.
[0035] Move Trichoderma TA-9 into the PDA slant medium and culture it at 28-30°C for 7 days; wash the conidia on the PDA slant medium with sterile water, and adjust the concentration of the spore liquid after counting with a hemocytometer to 1.0×10 6 pcs / mL; Prepare liquid fermentation medium, its components are: 15g corn flour, 20g oat flour, adjust pH to 5.0, dilute to 1L with water, put each 200mL into 1L Erlenmeyer flask, sterilize with moist heat at 121℃ for 30min . Add 2mL of the above-mentioned conidia spore liquid to every 200mL of liquid fermentation medium, shake culture at 30°C and 160r / min for 7-9d under dark conditions, and break up the fermentation culture to obtain 5.4×10 7 Chlamydospores / mL and 1.6×10 8 The fermentation broth of conidia per mL can be diluted and added with surfactant for spray application.
Embodiment 3
[0036] Example 3: Control effect of Trichoderma dark green TA-9 fermentation product on rice sheath blight.
[0037] This experiment was carried out on potted rice. Transplant the seedlings of the well-raised rice variety King Kong 30 into pots (30 cm in diameter and 40 cm in height), plant 3 holes in each pot, and 5 seedlings in each hole. The fertilizer and water are managed according to the routine, and the fertilizer and water conditions of each pot are guaranteed to be consistent.
[0038] Inoculate the dish of Rhizoctonia solani wild-type strain RH-2 with a diameter of 5mm on a PDA plate, culture at 28°C for 3-4 days, cut up the medium and inoculate it into a Erlenmeyer flask equipped with sterilized matchsticks. Continue culturing at 28°C for 3-4 days, and shake and mix once a day during this period, so that the hyphae of Rhizoctonia solani can be attached to loose matchsticks.
[0039] The matchstick with Rhizoctonia solani was inserted into the leaf sheath of the pen...
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