Application of a compound for preventing and controlling cucumber fusarium wilt and tomato gray mold
A cucumber wilt and compound technology, applied in the field of microorganisms, can solve the problems of unsafe microbial source pesticide types and other problems
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Embodiment 1
[0020] Embodiment 1: (Isolation and Screening of Amylase Streptomyces Chromogenes D)
[0021] The present invention obtained the amylase chromogenic Streptomyces chromogen from the soil sample collected in Tianmu Mountain, Lin'an, Zhejiang Province in August 2006, through the steps of separation, cultivation, fermentation, activity determination and screening of effective strains for inhibiting plant fungal disease pathogens. diastatochromogenes) D, preservation.
[0022] Determination of antibacterial activity of amylase Streptomyces diastatochromogenes D: Take 1mL of its fermentation supernatant in a sterile petri dish, mix it with 9mL of PDA medium cooled to 50°C, and mix it evenly with 9mL of PDA medium cooled to 50°C. Place a 4mm-diameter cake of cucumber fusarium wilt or tomato gray mold on the base plane, connect the cake to the center of the petri dish (the diameter of the petri dish is 9cm), and place it in an incubator for 36 hours at 28°C. Sterile water treatment w...
Embodiment 2
[0025] Embodiment 2: (preparation method of amylase Streptomyces chromogenes D fermentation metabolite)
[0026] Follow these steps:
[0027] (1) Bacteria test tube slant activation culture: the slant medium is Gaoshi No. 1 medium, and its components and content are: K 2 HPO 4 0.5g, KNO 3 1g, MgSO 4 0.5g, 20g soluble starch, 0.5g NaCl, FeSO 4 0.01g, 20g of agar, add water to 1L after dissolving; pick a little amylase spores of Streptomyces chromogenicum D with an inoculation loop under aseptic conditions, and put them into the sterilized Gaoshi No. 1 medium test tube (15×150mm ), placed in an incubator at 28°C±1°C, activated for 96 hours, until the slant of the test tube is covered with spores;
[0028] (2) Fermentation culture: the fermentation medium contains 20g of soybean cake powder, 15g of corn flour, 10g of bran, and NH 4 NO 3 3g, (NH 4 ) 2 SO 4 5g, CaCO 3 5g, MgSO 4 1g, the balance is water; each 300mL triangular bottle is filled with 40mL fermentation brot...
Embodiment 3
[0031] Embodiment 3: (use amylase Streptomyces chromogenes D fermentation metabolite to prepare wettable powder)
[0032] in:
[0033] White carbon black: (produced by Shanghai Fuqi Chemical Co., Ltd.)
[0034] Nongdai 0203-B: (produced by Xingtai Lanxing Auxiliary Factory)
[0035] Sodium lignosulfonate: (produced by Shanghai Weicheng Chemical Co., Ltd.)
[0036] Light calcium carbonate: (produced by Shanghai Daewoo Biochemical Co., Ltd.)
[0037]The product contains 1.5% active compound [2,4-Dioxo-1-(3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-1,2,3,4-tetrahydro-pyrimidin-5 -yl]-methylamino-acetic acid, add 2% of white carbon black as an adsorbent, and add 1% of agricultural milk 0203-B and 3% of sodium lignosulfonate auxiliary materials, and finally make up to 100 with light calcium carbonate %, after mixing, the wettable powder (hereinafter referred to as "product A") was made by jet milling.
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