Bacillus amyloliquefaciens and application thereof in preventing and controlling peach bleeding disease
A technology for dissolving starch spores and peach liquid gum, applied in the application, bacteria, fungicides and other directions, can solve problems such as microorganisms or biological preparations that have not been reported, and achieve significant control effects, high inhibitory activity, and reduced incidence.
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Embodiment 1
[0024] Example 1 Isolation, screening and identification of Bacillus amyloliquefaciens H47CCTCCM2013283
[0025] 1.1 Isolation and screening of Bacillus amyloliquefaciens H47CCTCCM2013283
[0026] (1) Raw raw eucalyptus honey samples were collected from Fuxu County, Guangxi, China in March 2012;
[0027] (2) Dilute the above raw honey sample to 75% (w / w) with sterilized physiological saline, take 200 μL and spread it on LB agar medium, place it in an incubator at 30°C for 72 hours, and pick out a single colony that grows Streak on fresh LB plate medium for separation and purification, culture at 30°C for 48 hours, then pick a single colony to LB slant medium, and store at 4°C.
[0028] (3) Inoculate the pathogenic bacteria of peach gum disease, Botrytis aureus, on the PDA medium, and culture it at 25-30°C for 4-6 days; cut off the 5-10 mm bacterial cake from the edge of the colony of Botrytis aureus, and inoculate it on the newly prepared PDA plate for culture base center; ...
Embodiment 2
[0041] Example 2 Detection of the antagonistic effect of Bacillus amyloliquefaciens H47CCTCCM2013283 strain on Botrytis
[0042] Inoculate the Botrytis preserved on the slant on the PDA plate medium, and activate it under the light condition of 30°C for 7 days. After the Botrytis is overgrown on the plate, the culture is terminated, and the sterilized hole puncher with a diameter of 12.00mm is used for activation. Make a fungus cake at the edge of the pathogenic bacteria colony, put the fungus cake face up on one side of the confrontation culture plate, about 1cm close to the wall of the dish, pick a ring of Bacillus amyloliquefaciens H47CCTCCM2013283 activated on the LB slant medium for 24 hours with an inoculation needle , Draw a bacterial line parallel to the bacterial block in the confrontation plate, put the confrontation culture plate into a 30°C incubator for cultivation, and record the width of the inhibition zone after 5 days.
[0043] Test results: The width of the i...
Embodiment 3
[0044] Example 3 Preparation of Bacillus amyloliquefaciens H47CCTCCM2013283 Fermented Liquid and Anti-Gum Disease Biological Agent
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