Derris centralis extract bactericide as well as preparation method and application thereof
A technology of extracts and fungicides, which is applied in the field of degeria genus extracts and fungicides and its preparation, can solve problems such as the lack of systematic research on the prevention and treatment of plant pathogenic fungi, and achieve broad-spectrum antifungal activity, low residue, and low cost. Effect
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Embodiment 1
[0019] Embodiment 1-Preparation of Deerhide vine extract fungicide
[0020] Take fresh Deutschia zhongnan branches and leaves, cut them into 9cm branch and leaf sections, dry them in an oven at 45°C, and then pulverize them with a pulverizer to obtain the branches and leaves of Zhongnan vines; according to the dosage ratio of 1.5g:30mL, take Add 1.5kg of deer vine branches and leaves powder, add 30L of methanol solution with a mass concentration of 80%, stir, soak for 48 hours, filter, add again a methanol solution with a mass concentration of 80%, repeat soaking twice, filter, and combine the filtrates to obtain a soaking solution. Using a rotary evaporator to concentrate under vacuum at 45°C, the methanol extract 1 of the branches and leaves of Deerhinensis was obtained;
[0021] Take fresh Deutschia zhongnan branches and leaves, cut them into 10cm branch and leaf sections, dry them in an oven at 50°C, and then pulverize them with a pulverizer to obtain the branches and leav...
Embodiment 2
[0024] Example 2-in vitro antifungal activity test
[0025] The bactericidal activity of the fungicides extracted from Deerhide vines was detected by the method of mycelial growth rate. Take by weighing quantitative Deerhinen chinensis extract bactericide, after fully dissolving with DMF, be mixed with the test drug solution, the test drug solution and the potato dextrose agar medium (PDA medium) are mixed, and the concentration of the extract is made into 2.00mg·mL -1 The drug-carrying medium was used as a control with the PDA medium with the same content of DMF. The pathogenic fungi were made into fungus cakes with a puncher with a diameter of 0.5 cm, inserted into the middle of the medium with the medicine, and three replicates were set. The transferred pathogenic bacteria were cultured in a constant temperature incubator at 28°C. When the diameter of the colony in the control group reached 5.0 cm or more, the diameter of the colony was measured by the cross method. The ...
Embodiment 3
[0033] Example 3-Determination of inhibitory activity of conidia germination of banana anthracnose bacteria
[0034] Weigh the quantitative methanol extract 2, petroleum ether phase extract, ethyl acetate phase extract, n-butanol phase extract and aqueous phase extract of the branches and leaves of Deereus chinensis, dissolve them in DMF, and configure the test solution. Add to PDA medium and mix well to make 1.0mg·mL -1 drug-carrying medium. Draw 1.0 mL of the drug-containing medium and place it on a glass slide. After solidification, smear the banana anthracnose spore suspension (1×10 7 cfu mL -1 ), with sterile water containing the same proportion of DMF as a control, each treatment set 3 repetitions, and the experiment was repeated 3 times. The treated glass slides were cultured in a constant temperature incubator at 28°C. The spore germination rate of the control group exceeded 95.00%. After that, the spore germination of each treatment component was observed under a ...
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