An antagonistic endophytic bacterium gh011 and its application
An endogenous bacteria and antagonism technology, applied in the field of microorganisms, can solve the problems of decreased control effect of chemical agents, endangering human and animal health, and pollution of agricultural products and the environment by chemical agents
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Embodiment 1
[0018] Potted tomato control using preparations to prevent tomato gray mold:
[0019] Step 1. Inoculate a single colony of GH011 strain in 200mL LB liquid medium, in a constant temperature shaking incubator at 28°C at 160 r min -1 After culturing for 24 h, the cultured bacterial solution was diluted to 4×10 8 cfu mL – 1 , preparing a preparation for preventing tomato gray mold;
[0020] Step 2: Take potted tomatoes that grow to 5-6 leaves and have the same growth, spray the front and back of the tomato leaves with the preparation for treating and preventing tomato gray mold, and use clean water as a control. After 24 hours, the spore suspension of tomato gray mold 1×10 7 spores / mL (Pour a little sterile water into the PDA plate covered with Botrytis cinerea, scrape off the spores on the surface of the agar, pour them into a sterile container, shake them fully, filter them with sterile gauze, and count them on the blood cell plate) spray inoculated on it. Tomato plants we...
Embodiment 2
[0026] Screening, isolation and purification of antagonistic endophytic bacteria GH011 strain:
[0027] Step 1, preparation of culture medium:
[0028] LB medium for bacterial plate culture (tryptone 10g / L; yeast extract 5g / L; sodium chloride 10g / L; agar powder 18g / L), LB liquid medium for liquid culture (without adding agar powder), fungi PDA medium (potato 200g / L; glucose 20g / L; agar powder 18g / L) was used for culture and plate confrontation test.
[0029] Step 2: Collect 3g leaves of healthy sweet-scented osmanthus plants, soak in 75% alcohol for 30s, then disinfect with 1% sodium hypochlorite for 3min, rinse with sterile distilled water for 5 times, take the last rinse solution 200μL, and spread on LB On the culture medium plate; the sterilized leaves were ground in a sterile mortar, mixed with 5ml of sterile distilled water, and 200 μL of the grinding liquid was taken and spread on the LB medium plate. Cultivate at 28°C and observe day by day. If there is no colony in t...
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