Method for enhancing soil waterflooding effect to control pepper phytophthora blight
A technology for pepper blight and flooding, which is applied in the fields of botanical equipment and methods, chemicals for biological control, animal repellents, etc. The effect of low cost, simple operation and simple application process
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Embodiment 1
[0021] Preparation of Trichoderma Harzianum Culture Medium
[0022] The Trichoderma harzianum used in this example was screened by the Jiangsu Academy of Agricultural Sciences. The strain was preserved in the General Microbiology Center of the China Committee for the Collection of Microbial Cultures on May 24, 2013. The address of the preservation unit is: Beijing No. 3, No. 1, Beichen West Road, Chaoyang District, Institute of Microbiology, Chinese Academy of Sciences, Zip code 100101, and the preservation number is CGMCC No.7640.
[0023] Preparation of test tube slant medium: 100 grams of potatoes, 10 grams of glucose or sucrose, 10 grams of agar, 500 ml of water, and natural pH. Peel the potatoes, cut into pieces and boil for half an hour, then filter with 2 layers of gauze, add sugar and agar, heat and boil until the agar melts, make up the volume to 500ml, cool to about 60°C and divide into test tubes, the filling volume is 5 ml, plug the test tube mouth with a test tub...
Embodiment 2
[0027] Trichoderma harzianum ( Trichoderma harzianum ) Preparation of solid microbial agent (various media involved in this example are provided by Example 1)
[0028] A) Activation of strains
[0029] The method of activating the strains preserved on the slant of the test tube: Pick a piece of mycelium with a diameter of about 5mm from the strains preserved on the slant of the test tube and inoculate it into the PDA culture medium on the slant of the test tube for activation. After cultivating in an environment of 28±2°C for 3-5 days spare.
[0030] The method of activating the strains preserved by freeze-drying in ampoule tubes: scrub the ampoule with 70% alcohol cotton balls in an ultra-clean workbench, then make a groove in the ampoule with a grinding wheel, and use a sterile gauze pad or Wrap the ampoule with a sterile towel, then break the ampoule tube by hand and add 0.5-1.0ml of liquid medium PDB to it, slowly rotate the ampoule to rehydrate the freeze-dried bacteri...
Embodiment 3
[0037] Growth inhibition test of Trichoderma harzianum on Phytophthora capsici
[0038] Test method: Trichoderma harzianum and Phytophthora capsici were separately inoculated on PDA plates, and after 3 days of constant temperature cultivation at 30°C, fresh mycelium blocks (5 mm in diameter) were obtained from each strain, and Trichoderma harzianum and Phytophthora capsici were inoculated separately. The silk pieces were inoculated into the same PDA plate (each plate was inoculated with 1 Trichoderma harzianum mycelium piece and 1 Phytophthora capsici mycelium piece), and the distance between the two mycelium pieces was 5 cm, and they were cultured in a 30°C incubator observe.
[0039] See the test results figure 1 , as can be seen from the figure, the described Trichoderma harzianum has obvious growth inhibitory effect on Phytophthora capsici, and the described Trichoderma harzianum mainly inhibits or kills the pathogenic bacteria through hyperparasitism, that is, by secreti...
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