Trichoderma atroviride strain for producing myrosase and application thereof
A technology of Trichoderma dark green, Trichoderma dark green, applied in the application, fungicides, fungi and other directions, can solve the problems of low degradation, unstable fumigation effect, slow speed, etc., to achieve fast growth, strong soil and The effect of rhizosphere colonization ability and operability
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Embodiment 1
[0022]Jiangsu Academy of Agricultural Sciences screened a Trichoderma strain from the soil. The strain was preserved on December 23, 2011 in the General Microbiology Center of the China Committee for the Collection of Microbial Cultures. The address of the preservation unit is: 1 Beichen West Road, Chaoyang District, Beijing No. 3 Courtyard, Institute of Microbiology, Chinese Academy of Sciences, postal code 100101. The deposit number is CGMCC No.5609,
[0023] The characteristics of the strain are: cultured on a PDA plate at 30°C for 4 days to cover a plate with a diameter of 90 mm, the surface of the mycelium is loose and flat, and initially white; on the third day of cultivation, spores can be clearly seen, initially light green, Afterwards, it will gradually increase and become dark green. The spore-forming clusters are arranged in concentric ring patterns, and the back of the culture medium is brownish-yellow. It was identified as Trichederma atroviride by means of morph...
Embodiment 2
[0029] Preparation of culture medium
[0030] Preparation of test tube slant medium PDA: Weigh 200 grams of potatoes, peel them, cut into pieces and boil for half an hour, then filter with two layers of gauze, add 20 grams of glucose and 20 grams of agar, add water to 1000 milliliters after melting, pack The amount is 1 / 5-1 / 6 of the height of the test tube, plug the test tube mouth with a test tube stopper, autoclave at 121°C for 25 minutes, take it out while it is hot, and put it on a slope until it is cooled for later use. The height of the slope does not exceed 1 / 3 of the height of the test tube.
[0031] Preparation of liquid seed medium PDB: Weigh 200 grams of potatoes, peel them, cut into pieces and boil for half an hour, then filter with two layers of gauze, add 20 grams of glucose, make up water to 1000 milliliters, and then divide into liquid volumes It is an 80-100ml / 250ml triangular flask, plug the mouth of the bottle with a cotton plug, autoclave at 121°C for 25 mi...
Embodiment 3
[0034] The preparation of the dark green Trichoderma (Trichederma atroviride) solid microbial agent that produces myrosinase (the various culture medium that this embodiment relates to even embodiment 2 provides)
[0035] a) Activation of strains
[0036] The method for activating the bacterial strains preserved on the inclined plane of the test tube: the bacterial classification preserved on the inclined plane of the test tube is selected to inoculate a Trichoderma mycelium block of CGMCC No.5609 with a preservation number of about 5 mm in diameter and inoculated into the culture medium PDA on the inclined plane of the test tube for activation. Incubate in an environment of 28±2°C for 3-5 days before use.
[0037] The method of activating the strains preserved by freeze-drying in ampoule tubes: scrub the ampoule with 70% alcohol cotton ball in the ultra-clean workbench, then make a groove in the ampoule with a grinding wheel, wrap the ampoule with sterile gauze pad or sterile...
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