Pseudo-ginseng seedling root biological coating agent, and preparation method and applications thereof
A coating agent and root growth technology, applied in botany equipment and methods, seed coating/seed dressing, chemicals for biological control, etc., can solve the biological coating of roots of Panax notoginseng species In order to achieve the effects of preventing diseases such as blight and root rot, avoiding skin damage, and reducing diseases such as blight and root rot
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Embodiment 1
[0024] Accurately weigh 90g of polyvinylpyrrolidone (PVP), heat 1000mL of water, and stir to make it fully dissolved; Subculture 2-3 times under the condition of 25~28℃ to obtain well-growing colonies) of Chaetomium globosa (C.globosum) and Chaetomium chaeteum (C.cupreum) by conventional solid culture method In PDA medium (200g potatoes peeled, cut into 1cm 3 Small pieces, boiled for 20-30min, filtered, added 10g of glucose and 20g of agar to the filtrate, made the volume to 1L with pure water, and cultivated for 18 days, until the upper part of the petri dish was covered with spores, took out with a crystallization knife, and separated the two The fungi were formulated to a concentration of 2.0х10 5 500 mL of spore suspension per spore / mL; accurately weigh 300 mg of indole acetic acid IAA, a root growth promoter of Panax notoginseng, dissolve it with a small amount of ethanol, add water to make the volume to 200 mL, and prepare a mother liquor of IAA with a concentration of ...
Embodiment 2
[0031] Accurately weigh 70g of hydroxypropyl methylcellulose (HPMC), heat 1000mL of water, and stir to make it fully dissolved; Subculture 2-3 times under the conditions of 25~28℃ to obtain well-growing colonies) Streptomyces misionensis (S.misionensis) and A.vancoresmycina (A.vancoresmycina) were cultured on conventional solid Methods respectively in trehalose‐proline (S 2 ) solid medium (trehalose 5g, proline 1g, (NH4) 2 SO 4 1g, NaCl 1g, CaCl 2 2g,K 2 HPO 4 1g, MgSO 4 .7H 2 O 1g, multivitamins: riboflavin 1mg, niacin 1mg, calcium pantothenate 1mg, inositol 1mg, biotin 1mg, P‐aminobenzoic acid 1mg, VB 1 1mg, VB 6 1mg, 20g agar, water up to 1000mL, pH 7.2) and LB solid medium (yeast powder 5g, tryptone 8g, NaCl4g, agar 15g, pH 6.8) for 48h, until the colonies covered the entire culture dish, with a crystallization knife Take it out, prepare the concentration of Streptomyces rice repair (S.misionensis) and pseudomycobacterium (A.vancoresmycina) respectively to be ...
Embodiment 3
[0038] Precisely weigh 80g of sodium alginate, heat 1000mL of water, and stir to dissolve it fully; Carry out subculturing 2-3 times under the condition of ℃, obtain well-growth bacterium colony) chaetomium globus (C.globosum), horn chaetomium (C.cupreum) respectively in PDA medium (potato 200g peeled, cut into 1cm 3 Small pieces, boiled for 20‐30min, filtered, added 10g of glucose and 20g of agar to the filtrate, adjusted to 1L with purified water, and the pH was natural) and proliferated for 18 days until the upper part of the petri dish was covered with spores. The fungi were formulated to a concentration of 2.0х10 5 Each 500 mL of spore suspension per spore / mL; A. vancoresmycina (A. vancoresmycina) was propagated and cultivated in LB solid medium (5 g of yeast powder, 8 g of tryptone, 4 g of NaCl, 15 g of agar, pH 6.8) for 48 h. Colonies covered the entire Petri dish, and were taken out with a crystallization knife, and A.vancoresmycina was formulated to a concentration ...
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