A fungal agent prepared by using Trichoderma harzianum ta97 and its application in the prevention and treatment of cropping diseases
A technology of ta97 and inoculum, applied in the field of biological inoculants, can solve the problems of excessive soil pesticide residues, pollution of surrounding water resources, and incompatibility with green environmental protection, etc., and achieve the effect of prolonging the control effect time, improving performance and adhesion performance.
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Embodiment 1
[0031] Embodiment 1 African Trichoderma harzianum Ta97 measures the antagonism of four kinds of pathogenic bacteria
[0032] (1) Source of pathogenic bacteria
[0033] The pathogenic bacteria were collected from corn-wheat multi-cropping farmland in Jinan City, Shandong Province. According to morphological and molecular identification, Rhizoctonia solani is the pathogen of wheat and corn sheath blight, Alternaria sp. is the pathogen of wheat leaf blight and corn leaf blight, Fusarium oxysporum (Fusarium sp. oxysporum) and Fusarium moniliforme are root rot pathogens of wheat and corn.
[0034] (2) Standoff test
[0035]Introduce Trichoderma harzianum Ta97 and the above four pathogenic bacteria into PDA medium respectively, and activate twice at 25°C. After the second activation and growth for three days, punch the fungus cake from the edge of the colony with a 5mm hole punch; Put the mold Ta97 and Rhizoctonia solani on both ends of the center line of the same 9cm PDA plate, ...
Embodiment 2
[0037] Embodiment 2 Trichoderma harzianum Ta97 Trichoderma conidia powder preparation 1
[0038] The fermentation process of Trichoderma conidia powder is as follows:
[0039] (1) Obtaining the seed solution: Inoculate Trichoderma harzianum Ta97 preserved at -80°C on a PDA solid plate, activate it at 25°C for 3 days, take mycelium from the edge of the colony and inoculate it on the PDA plate again, and cultivate it at 25°C for 3 days. day, take the mycelium at the edge of the colony and culture it at 25°C for 3 days, which is the activated strain; put the activated strain on a PDA plate, and culture it alternately for 10 days at 25°C, 12 hours of light and 12 hours of semi-darkness, and take the spores , to prepare 10 7 conidia suspension per mL, inoculate the conidia suspension in the PDB culture medium, the volume ratio of the conidia suspension to the PDB culture medium is 1:100, and then at 25°C, 180rpm Under shaking culture for 4 days, it is the seed liquid, and the num...
Embodiment 3
[0043] Embodiment 3 Trichoderma harzianum Ta97 Trichoderma conidia powder preparation 2
[0044] (1) Obtaining the seed solution: Inoculate Trichoderma harzianum Ta97 preserved at -80°C on a PDA solid plate, activate it at 25°C for 3 days, take mycelium from the edge of the colony and inoculate it on the PDA plate again, and cultivate it at 25°C for 3 days. day, take the mycelium at the edge of the colony and culture it at 25°C for 3 days, which is the activated strain; put the activated strain on the PDA plate, and culture it alternately for 10 days at 25°C, 12 hours of light and 12 hours of darkness, and take the spores. Prepare 10 7 conidia suspension per mL, inoculate the conidia suspension in the PDB culture medium, the volume ratio of the conidia suspension to the PDB culture medium is 1:100, and then at 25°C, 180rpm Under shaking culture for 5 days, it is the seed liquid, and the number of viable bacteria in the seed liquid is 1×10 8 cfu / mL;
[0045] (2) Obtaining co...
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