Fungicide composition and application thereof
A composition and aqueous solution technology, applied in the direction of application, bactericide, biocide, etc., can solve the problems of increased drug resistance of pathogenic bacteria, impact on food safety, environmental pollution, etc.
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Embodiment 1
[0021] Example 1 Determination of the antibacterial activity of 2-phenylethanol to mango leaf spot
[0022] Cultivate the mango stalk rot pathogen Botryosphaeria dothidea YB11-2 (Botryosphaeria dothidea) on a PDA plate, and after 3 days at room temperature, use a sterilized 5mm puncher to punch out the bacteria cake at the edge of the plate colony. Measure 20ml of melted PDA medium with a sterilized graduated cylinder, add 1ul, 10ul, 100ul, 1000ul of 2-phenylethanol respectively, mix evenly and pour it into a plate with a diameter of 9cm, and make 2-phenylethanol concentrations of 1ul / 20ml, 10ul / 20ml, 100ul / 20ml, 1000ul / 20ml PDA plate. The pathogenic bacteria cake with a diameter of 5 mm is transferred to the center of the plate with a sterilized toothpick, and cultivated in a 25 degree Celsius incubator. The pathogenic bacteria cultured without adding 2-phenylethanol was used as the control, and each treatment was repeated three times. When the petri dish was covered with ...
Embodiment 2
[0025] Example 2 The bacteriostatic activity assay of 2-phenylethanol to 11 kinds of pathogenic fungi
[0026] Select 11 kinds of pathogenic bacteria isolated from mango leaf spot (Table 1) and culture them on PDA plates. After culturing at room temperature for 3 days, use a sterilized 5mm puncher to punch bacteria cakes from the edge of the plate colonies. Measure 20ml of melted PDA medium with a sterilized graduated cylinder, add 1ul, 10ul, 100ul, 1000ul 2-phenylethanol respectively, mix well and pour into a plate with a diameter of 9cm to make 2-phenylethanol concentrations of 1ul / 20ml, 10ul / 20ml, 100ul / 20ml, 1000ul / 20ml plates. Transfer the pathogenic bacteria cake to the center of the plate with a sterilized toothpick, and cultivate it in an incubator at 25 degrees Celsius. Take the pathogenic bacteria cultivated without adding 2-phenylethanol as the control, and when the control group is full of petri dishes, use the cross method to measure the pathogenic bacteria colo...
Embodiment 3
[0032] Example 3 Control experiment of 2-phenylethanol mixed with prochloraz manganese salt on mango leaf spot
[0033] Prepare 5ml / l 2-phenylethanol respectively, two kinds of medicinal liquids of 1g / L prochloraz manganese salt are used as mother liquor, and mix in different ratios (9:1, 8:2, 7:3, 6:4, 5: 5, 4:6, 3:7, 2:8, 1:9) Select healthy mango leaves without obvious diseases and soak them in two kinds of mother solutions and mixed medicinal solutions in different proportions for 5 minutes. Use a sterilized 5mm hole puncher to punch out the bacteria cake on the edge of the YB11-2 plate colony. Use a sterilized toothpick to puncture mango leaves six times, and the wound is roughly circular. Use a sterilized toothpick to inoculate the bacteria cake into the puncture site, and the control group is inoculated with a blank agar block. The inoculated mango leaves were placed in plastic boxes with covers soaked with sterile water, and 6 mango leaves were placed in each plastic ...
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