Preparation method and use of agricultural bactericide containing parthenolide
A parthenolide, agricultural fungicide technology, applied in the directions of fungicides, botanical equipment and methods, biocides, etc., can solve the problem of less objects for activity research, achieve good inhibitory activity, low equipment requirements, and simple processing Effect
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Embodiment 1
[0020] 5kg of the whole herb of Pyrita chinensis was extracted three times with 75% ethanol at 60°C to obtain the total extract, which was adsorbed with A8 macroporous resin, eluted with water, 30%, 45%, 60%, and 90% ethanol respectively, and collected Macroporous resin 45%, 60% and 95% eluted parts, concentrated eluate to 1.5kg fluid extract, obtained extract containing parthenolide. The extract is separated and purified through silica gel column chromatography; gel column chromatography and recrystallization (ethyl acetate-methanol) to obtain parthenolide with a purity of more than 90%; 0.5kg surfactant (such as Polysorbate-80) and parthenolide are placed in a homogenizer, heated to 30°C, and 1kg of water is added into the homogenizer while stirring, stirred for 30 minutes, fully mixed, cooled to room temperature, and formed Emulsion in water to obtain parthenolide fungicide.
Embodiment 2
[0022] 10kg of the whole herb of Pyrita chinensis was extracted three times with 95% ethanol at 60°C to obtain the total extract, which was absorbed by D101 macroporous resin, eluted with water, 30%, 45%, and 85% ethanol respectively, and the macroporous resin was collected For 45% and 85% elution sites, concentrate the eluent to 3.0kg liquid extract, which is separated by silica gel column chromatography; gel column chromatography and recrystallization (ethyl acetate-methanol) and other means Purify and obtain parthenolide with a purity of more than 90%; put 0.5kg of surfactant (such as polyoxyethylene nonionic surfactant: OP-10) and parthenolide in a homogenizer and heat to 50°C, while stirring, add 1 kg of water into the homogenizer, stir for 30 minutes, mix well, cool to normal temperature, form water emulsion, and obtain parthenolide fungicide.
Embodiment 3
[0024] The parthenolide fungicide antimicrobial spectrum measurement prepared by embodiment 1:
[0025] The plant pathogenic bacteria tested included Sclerotinias clerotiorum, Fusarium graminearum, Botrytiscinerea, Colletotrichum gloeosporioides, Rhizoctonia solani, and Corn blight ( Helminthosporiummaydis), Botrytiscinerea, Fusariummoniliforme, Rhizoctoniacerealis, Alternariasolani, Verticilliumdahliae, Magnaportheoryzae , Phytophthora capsici, Phytophthorasojae, Xanthomonasoryzaepv.oryzae, Xanthomonasoryzaepv.oryzicola, Xanthomonascampetrispv.camestris, etc. 15 common plant pathogens. All the tested pathogenic bacteria were isolated strains collected in the field.
[0026] The virulence of 15 kinds of phytopathogenic bacteria was initially determined indoors by mycelium growth rate method (fungus, oomycete) or turbidity method (bacteria). Each strain was activated and cultured on PDA (fungus), V8 (oomycete) plate or NB (bacteria) culture medium. For fungi and oomycetes, u...
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