Application of Pestalotiopsis guepinii Stey. toxin in herbicide
A technology of Polychaeta pseudodiscoides and herbicides, applied in the direction of herbicides and algicides, applications, biocides, etc., can solve problems such as unseen
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Embodiment 1
[0022] Inoculate the Polychaeta pseudodiscoides bacterial strain preserved by the inventor on a PDA plate, cultivate it under dark conditions at 25-30°C, and when the colony is about ф80mm, use a sterile puncher (ф5mm) to cut out the outer edge hyphae of the colony to prepare Mushroom cake. Put the PD medium in a 250mL Erlenmeyer flask, 150mL per bottle, quantitatively inoculate 3 pieces of bacteria cake, and culture at 150r / min at 25°C in the dark for 15 days. The mycelium is filtered out by double-layer absorbent cotton gauze from the culture solution of Trichosporum pseudodiscoides, and the crude toxin culture filtrate is obtained. Take 3000mL of the crude toxin culture filtrate, extract with 1500mL, 1000mL, and 500mL of ethyl acetate respectively, combine the extracted ethyl acetate, concentrate and dry it, and then dilute to 600mL with methanol to obtain the crude toxin. Add 100g of 1601 to 200mL of crude toxin, then add 700mL of water, and stir well to obtain 1000mL of ...
Embodiment 2
[0024] Inoculate the Polychaeta pseudodiscoides bacterial strain preserved by the inventor on a PDA plate, cultivate it under dark conditions at 25-30°C, and when the colony is about ф80mm, use a sterile puncher (ф5mm) to cut out the outer edge hyphae of the colony to prepare Mushroom cake. Put the corn flour culture medium in a 250mL Erlenmeyer flask, 150mL per bottle, quantitatively inoculate 3 pieces of bacteria cake, and culture at 150r / min at 25°C for 15 days in the dark. The mycelium is filtered out by double-layer absorbent cotton gauze from the culture solution of Trichosporum pseudodiscoides, and the crude toxin culture filtrate is obtained. Take 5000mL of the crude toxin culture filtrate, extract with 2500mL, 1500mL, and 1000mL of ethyl acetate respectively, combine the extracted ethyl acetate and concentrate it to near-dryness, then dilute to 1000mL with methanol to obtain the crude toxin. Add 120g of 1601 to 350mL of crude toxin, then add 530mL of water, and stir ...
Embodiment 3
[0029]Inoculate the Polychaeta pseudodiscoides bacterial strain preserved by the inventor on a PDA plate, cultivate it under dark conditions at 25-30°C, and when the colony is about ф80mm, use a sterile puncher (ф5mm) to cut out the outer edge hyphae of the colony to prepare Mushroom cake. Put the corn-soybean flour medium in 250mL Erlenmeyer flasks, 150mL per bottle, quantitatively inoculate 3 pieces of bacteria cakes, and culture them at 150r / min at 25°C in the dark for 15 days. The mycelium is filtered out by double-layer absorbent cotton gauze from the culture solution of Trichosporum pseudodiscoides, and the crude toxin culture filtrate is obtained. Take 4000mL of the crude toxin culture filtrate, extract with 2000mL, 1000mL, and 1000mL of ethyl acetate respectively, combine the extracted ethyl acetate and concentrate to dryness, then dilute to 800mL with methanol to obtain the crude toxin. Add 150g of 1601 to 500mL of crude toxin, then add 350mL of water, and stir well ...
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