Application of apple residue and apple leaf extract to prevention and control of phytopathogen
A technology of plant pathogenic bacteria and apple pomace, applied in the fields of application, plant growth regulator, botanical equipment and methods, etc., can solve the problems of resource loss, low probability of effective use, and odor, and achieve significant antibacterial activity and good control effect of effect
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Embodiment 1
[0008] Embodiment 1: Apple pomace ethanol extract prevents and treats tomato gray mold and canker
[0009] Taking tomato Botrytis cinerea and canker as objects, the control effect of apple pomace ethanol extract on the two diseases was evaluated by artificial inoculation technique in potted plants. Test crops: tomato. Pathogens tested: tomato gray mold (Botrytis cinerea), tomato canker (Clavibacter michiganensis subsp. Michiganensis).
[0010] Experimental design: the concentration of ethanol extract of apple pomace was diluted 200 times, the control agent for tomato gray mold was 50% procymidone wettable powder, and the control agent for canker was 500 million spores / g Pseudomonas fluorescens wettable powder , 1 water control (only inoculated with bacteria), 1 blank control. Each treatment was replicated 4 times, and each replicated 10 seedlings.
[0011] Test method: Spraying is used to apply pesticides, and after spraying treatment, pathogenic bacteria are artificially i...
Embodiment 2
[0016] Embodiment 2: The in vitro activity of apple pomace ethanol extract to different pathogenic bacteria
[0017] Using the method of measuring the inhibition zone of the drug-containing PDA medium (25°C, dark culture conditions), the six plant pathogenic fungi Fusarium graminearum, Rhizoctonia solani, Magnaporthe oryzae, Glososporum anthracnose, and Botrytis cinerea and tomato early blight inhibition test. The test results are as follows.
[0018]
Embodiment 3
[0019] Embodiment 3: the indoor inhibitory action of monomer compound of the present invention to Botrytis cinerea
[0020] Tested species: Botrytis cinerea
[0021] Experimental method: the test bacteria were activated on PDA (potato dextrose agar medium) for 72 hours. The polyphenol compound obtained by separation and extraction was prepared into a dilution solution with a concentration of 62.5 µg / ml to 2000 µg / ml by 2-fold concentration dilution method, and then mixed evenly (v / v) with the drug solution and PDA medium at a ratio of 1:9 to obtain a concentration of 6.25 µg / ml~200µg / ml drug-containing medium, each treatment was poured into 4 flat plates (diameter 9cm), after cooling, 6mm bacteria cake was placed in the center of the plate, cultured at 25±1°C, and the blank control bacteria When the cake grew to the edge of the plate, the diameter of the colony of each treatment was measured by the cross method of vernier calipers, and the bacteriostatic rate of each treatmen...
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