Bacillus velezensis ZF2 and application thereof to control of plant diseases
A technology of ZF2 and Bacillus, applied in the fields of application, plant growth regulator, and microbial-based methods, can solve the problems of high dependence on chemical control, lack of disease-resistant varieties, and reduced sensitivity
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Embodiment 1
[0064] Embodiment 1, the separation, purification and identification of biocontrol bacillus ZF2
[0065] 1. Isolation of biocontrol bacillus
[0066] Rinse the cucumber plants with water, disinfect the surface with 1% sodium hypochlorite aqueous solution for 1 min, and then rinse the cucumber plants with sterile water for 3 times. Put about 2g of the surface-sterilized cucumber plant into a sterilized mortar, add a small amount of sterilized quartz sand and 10ml of sterile water for full grinding, take 1ml of the grinding juice, add it to a test tube containing 9ml of sterile water, and mix After homogeneity, serially dilute to 10 -6 concentration, will be 10 -4 、10 -5 、10 -6 The concentration of bacterial solution was maintained in a water bath at 80°C for 30 minutes to kill most of the non-bacillus bacteria. Take 100 μl of LB solid plates, apply 3 plates for each concentration, and incubate at 28°C. After culturing for 1 day, different single colonies were picked and st...
Embodiment 2
[0089] Embodiment 2, the functional research of bacterial strain ZF2
[0090] 1. Application of strain ZF2 in antibacterial
[0091] 1) Determination of fungal inhibition spectrum
[0092] The method refers to the screening of antagonistic bacteria in Example 1.
[0093] 2) Determination of bacterial inhibition spectrum
[0094] The antibacterial spectrum test of pathogenic bacteria adopts the method of double-layer culture. The strain ZF2 was inoculated in liquid LB medium, and cultured with shaking at 28°C for 16 hours to obtain a ZF2 bacterial suspension. In the center of a 90 mm glass PDA plate, a hole was punched with a 10 μl pipette tip, and 5 μl of ZF2 bacterial suspension was placed in it, and incubated at 28° C. for 24 hours. Invert the Petri dishes, add 3ml of chloroform to each Petri dish in a fume hood, and ventilate for 12h. The pathogenic bacteria were shaken and cultured in NB medium at 28°C for 48 hours, 100 μl of bacterial suspension was added to 5 ml of ...
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