Bacillus for preventing wheat diseases, as well as preparation and use thereof
A technology for bacillus and wheat take-all disease, applied in botany equipment and methods, microbe-based methods, biochemical equipment and methods, etc., can solve the problem of little research on bacillus, and achieve strong inhibition of the main pathogenic fungi of wheat Active, non-toxic and side effects, easy to operate
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Embodiment 1
[0035] Embodiment 1: Isolation and identification of E1R-j bacterial strain
[0036]Rinse the naturally growing wheat root system collected from Changwu County, Shaanxi Province with tap water and spread it out to dry. Take 1 / 4 of the root system from each plant and cut it into pieces. Mix the root samples of all plants and weigh 1g for surface disinfection (70% alcohol for 60s→ 3. Treat in 125% NaClO for 6min → 70% alcohol for 30s → rinse with sterile water 3-5 times). Take 200 μL of the sterile water rinsed for the last time and spread it on the PDA plate to test whether the surface disinfection is thorough. Grind the surface-sterilized sample material with 9 mL of sterile water in a sterilized mortar until it becomes a paste, take the original solution, diluted 100-fold solution and 1000-fold solution, shake well, and apply 200 μL on the mixture with carbendazim (50 μg / mL, 25% wettable powder, produced by Zhejiang Yifan Agrochemical Factory) on the PDA plate, each treatme...
Embodiment 2
[0039] Embodiment 2: the preparation method of E1R-j bacterial strain thalline
[0040] Inoculate the E1R-j strain stored at -80°C on NA medium, culture it at 25-28°C for 2 days, inoculate its single colony into 100mL LB (Luria-Bertani: 10g peptone; 10g yeast powder; 5g NaCl; 1000mL distilled water , adjust pH=7.2) in the culture solution, shake and cultivate in the dark at 37°C and 150rpm for 18-24h, then inoculate 1% seed solution into 100mL of LB culture solution, and cultivate in the dark at 28°C and 150rpm for 48h, the obtained bacteria After the solution was centrifuged at 8000rpm for 20min, the precipitate obtained was the bacterial cell of the E1R-j strain.
Embodiment 3
[0041] Embodiment 3: the preparation method of the antibacterial active substance of E1R-j bacterial strain
[0042] Inoculate the E1R-j strain stored at -80°C on NA medium, and after culturing at 25-28°C for 2 days, inoculate its single colony into 100mL LB culture medium, culture at 37°C and 150rpm in the dark for 18-24h, then Inoculate 1% of the seed liquid into 100mL of LB culture liquid, culture at 28°C and 150rpm in the dark for 40-48h with shaking, and centrifuge the obtained bacterial liquid at 8000rpm for 20min. Salt out, overnight at 4°C, centrifuge at 12000rpm for 30min to dialyze and concentrate the precipitate.
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