Biocontrol fungus for preventing and controlling plant mycosis and its preparation process
A phytopathogenic and fungal technology, applied in botany equipment and methods, plant growth regulators, chemicals for biological control, etc., can solve the problem of high development costs of new varieties of fungicides, toxicity of wild and non-target organisms, New varieties of fungicides are expensive, etc., to achieve the effect of no poisonous harm to humans and animals, no phytotoxicity to crops, and stable product quality
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Embodiment 1
[0017] Example 1: Isolation and identification of LCH0606 strain
[0018] Fresh camphor tree stems are collected from Zijin Mountain in Nanjing, Jiangsu Province, washed with tap water, dried and cut into small pieces of about 1cm. Sequentially immerse in 75% ethanol and 40% formaldehyde solution to disinfect the surface for 3 minutes each, then wash 3 times with sterile water to remove surface contamination bacteria, then cut the stem longitudinally with sterile scissors, put the cut side down on the potato sucrose On the agar plate, 5 stem segments per plate, 5 plates in total. Cultivate at 30°C, observe the appearance of new colonies every day for a total of 7 days, pick a single colony, and purify by streaking. In addition, put 2 to 3 uncut stems or leaves in the same potato sucrose medium plate as a control to test whether the surface sterilization is thorough. The obtained strains were preserved in a -80°C refrigerator by glycerin preservation method for future use.
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Embodiment 2
[0021] Embodiment two: the preparation method of Bowman's bacteria liquid
[0022] The seed medium was potato sucrose medium, and a single colony of activated LCH0606 was picked and inoculated into 4 mL potato sucrose medium (15 mL test tube) for culture, and cultured on a shaker at 37° C. and 100 rpm for 12 hours. Inoculate 1% seed solution in 400mL potato sucrose medium shake flask (1L), culture on a shaker at 37°C and 100rpm for 48-60h, and the obtained bacterial solution is centrifuged at 5000-6000rpm to remove bacteria, and then it becomes Baumann's bacterial solution.
Embodiment 3
[0023] Embodiment three: the preparation method of baumannycin
[0024] The Bowmansin solution described in Example 2 was adsorbed by macroporous resin X-5, eluted with 80% ethanol, and dried by rotary evaporation under reduced pressure to obtain baumannin. The amount of macroporous resin used was 1% of the Baumannii solution, and the flow rate of sample loading and elution was 4 mL / min. The yield of baowmanicin was 568mg / L.
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