Lysine bacillus for preventing and controlling kiwi berry canker and application thereof
A technology of Bacillus lysinus and kiwifruit canker, which is applied in the field of microbiology, can solve the problems affecting the field control effect of canker and the drug resistance of canker bacteria, and achieve the effects of stable properties, strong inhibitory effect, and simple separation and screening methods
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Embodiment 1
[0026] Example 1 Isolation and screening of Bacillus lysinica CCTCC M2016557
[0027] The bacterial source of Bacillus lysinus CCTCC M2016557 of the present invention comes from Hongbai Town, Shifang City, Sichuan Province (31.36° north latitude, 104.03° west longitude, 861 meters above sea level), and the sampling time was May 2015.
[0028] The separation method is: 1. Rinse the collected kiwi branches with clear water, disinfect the surface with 75% alcohol, air-dry at room temperature, cut an appropriate amount of sample with a sterilized blade, put it into a grinding bag, add an appropriate amount of normal saline, grind, After soaking for 3 minutes, take 100 μL of the supernatant of the plant grinding liquid and add it to the newly prepared KB medium, and use an inoculation loop to coat and streak.
[0029] The purification method is as follows: After cultivating the sample petri dish at room temperature for a certain period of time, wait for the colonies to grow in the ...
Embodiment 2
[0030] The identification of embodiment 2 lysinibacillus CCTCC M2016557
[0031] 1. Observation of culture status
[0032] Activate the preserved bacteria on KB solid medium, culture at room temperature, observe the growth of the colony, and record the characteristics of the colony, including color, growth speed, shape, texture, etc.;
[0033] It is finally found that: the Bacillus lysinus CCTCC M2016557 bacterial strain of the present invention is milky white, colloidal, with a smooth and moist surface, raised center, neat edges, and normal viscosity; its bacterial species morphology is shown in figure 1 shown; its scanning electron microscope picture is shown in the sequence table.
[0034] 2. Molecular biological identification
[0035] DNA extraction: use bacterial PCR universal primer 27F (primer sequence is:
[0036] Eubac27F[106]5'-AGAGTTTGATCMTGGCTCAG-3') and 1492R (primer sequences are:
[0037] Eubac1492R[106]5'-TACGGYTACCTTGTTACGACT-3') amplified the 16S rDNA of...
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