Detection method for pathogenicity of maize bacterial wilt source fusarium in maize seedling stage
A detection method, Fusarium technology, applied in the field of detection, can solve the problems of complex detection, inaccurate measurement results, and inaccurate results of the Guo-Maier method, and achieve the effect of simple detection method, shortened time, and accurate results
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[0044] Step 1, preparation of water-agar mixed medium
[0045] 1) Add 17g of agar to 1000mL of water, heat to dissolve the agar, then add 1.5g of calcium nitrate, 1.5g of potassium nitrate, 1g of ammonium dihydrogen phosphate and 0.5g of magnesium sulfate, stir well to form a mixed solution, and pack In 300mL Erlenmeyer flasks, each bottle is 100mL, sealed with propylene film and left with a vent hole, and then each Erlenmeyer flask containing the mixed solution is sent into an autoclave, at a pressure of 0.14MPa and a temperature of 121°C, Sterilize for 30 minutes to prepare nutrient agar medium for subsequent use;
[0046] 2) Under sterile conditions, add 100mL of deionized water to each sterilized nutrient agar medium in step 1), and then crush the nutrient agar medium to particles with a particle size of 0.5--0.8cm Stop at the same time, mix evenly to form a water-agar mixed medium, and set aside;
[0047] Step two, corn seedling cultivation
[0048] Take 1 part of corn...
Embodiment 1
[0074] A method for detecting the pathogenicity of corn solanacear pathogen Fusarium to corn seedling stage, the detection method is:
[0075] Step 1, preparation of water-agar mixed medium
[0076] 1) Add 17g of agar to 1000mL of water, heat to dissolve the agar, then add 1.5g of calcium nitrate, 1.5g of potassium nitrate, 1g of ammonium dihydrogen phosphate and 0.5g of magnesium sulfate, stir well to form a mixed solution, and pack In 300mL Erlenmeyer flasks, each bottle is 100mL, sealed with propylene film and left with a vent hole, and then each Erlenmeyer flask containing the mixed solution is sent into an autoclave, at a pressure of 0.14MPa and a temperature of 121°C, Sterilize for 30 minutes to prepare nutrient agar medium for subsequent use;
[0077] 2) Under sterile conditions, add 100mL of deionized water to each sterilized nutrient agar medium in step 1), and then crush the nutrient agar medium until the particle size is 0.5cm. Mix evenly to form a water-agar mixe...
Embodiment 2
[0099] A method for detecting the pathogenicity of corn solanacear pathogen Fusarium to corn seedling stage, the detection method is:
[0100] Step 1, preparation of water-agar mixed medium
[0101]1) Add 17g of agar to 1000mL of water, heat to dissolve the agar, then add 1.5g of calcium nitrate, 1.5g of potassium nitrate, 1g of ammonium dihydrogen phosphate and 0.5g of magnesium sulfate, stir well to form a mixed solution, and pack In 300mL Erlenmeyer flasks, each bottle is 100mL, sealed with propylene film and left with a vent hole, and then each Erlenmeyer flask containing the mixed solution is sent into an autoclave, at a pressure of 0.14MPa and a temperature of 121°C, Sterilize for 30 minutes to prepare nutrient agar medium for subsequent use;
[0102] 2) Under sterile conditions, add 100mL of deionized water to each sterilized nutrient agar medium in step 1), and then crush the nutrient agar medium until the particle size is 0.7cm. Mix evenly to form a water-agar mixed...
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