Use of trichothecenes in resisting tobacco pathogenic fungi
A technology of tobacco pathogenic fungi and trichothecenes, which is applied in the fields of application, fungicides, and chemicals for biological control, etc., can solve problems such as singleness, decline in resistance of tobacco varieties, and aggravation of tobacco hazards, so as to improve the quality of tobacco yield effect
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Embodiment 1
[0026] This example is used to illustrate the effect of using trichothecenes to inhibit the growth of tobacco pathogenic fungi.
[0027] The spores of Alternaria alternata and Alternaria alternata were prepared to form a spore suspension of appropriate concentration (under a 10×10 low power microscope, 30-40 spores per field of view). Trichothecene was prepared into a certain concentration of acetone aqueous solution, then mixed with the spore suspension in equal volume, and one drop was added dropwise on the concave glass slide. Each treatment was repeated 3 times. After moisturizing culture at 28°C for 18 hours, check the control spores Germination situation. When the germination rate of the control spore reaches 85%, check the spore germination rate of all treatments. The spore germ tube length is greater than half of the spore length as germination, and the trichothecene concentration when the spore germination inhibition rate is 100% is found. That is the minimum inhibitory...
Embodiment 2
[0029] This example is used to illustrate the effect of using trichothecenes to inhibit the growth of tobacco pathogenic fungi hyphae.
[0030] The plate growth rate method was used to determine the inhibitory effect of trichothecenes on the growth of the hyphae of Alternaria alternata and Alternaria alternata. The steps are as follows:
[0031] Prepare trichothecenes with sterile water at concentrations of 500μg / ml, 250μg / ml, 125μg / ml, 62.5μg / ml, 31.25μg / ml, 15.625μg / ml, 7.8125μg / ml, 3.90625μg / ml Solution, use sterile water as control (CK).
[0032] Pour 10 mL of each diluted solution into 8 bottles of sterilized culture medium (each bottle contains 90 mL of culture medium, and the drug solution is diluted 10 times). After mixing, pour the culture medium into a petri dish with a diameter of 9 cm. A series of concentration gradient drug-containing culture plates, 5 replicates for each concentration, and stand by after condensation. Use a sterile stainless steel puncher with a diame...
Embodiment 3
[0042] This example is used to illustrate the determination of the effect of trichothecenes on the prevention and control of tobacco pathogenic fungi infection in greenhouse pots.
[0043] Select healthy tobacco plants with the same growth at the 8-9 leaf stage to determine the protective and therapeutic effects.
[0044] Protective effect: spray trichothecene (sprayed at a concentration of 200μg / mL), 24 hours later, the spray method inoculation concentration is 3×10 5 A / mL spore suspension of tobacco pathogenic fungi (Alternaria alternata or Alternaria alternata), a 1% glucose solution was set as a blank control, and the spraying rates of the three were all 50 mL / plant. After inoculation, they were placed in a 28°C incubator and kept for 6 days.
[0045] Therapeutic effect: inoculation concentration of spray method is 3×10 5 A / mL spore suspension of tobacco pathogenic fungi (Alternaria alternata or Alternaria alternata), set a 1% glucose solution as a blank control, and then placed ...
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