Euonymus japonicus endophytic bacterium bacillus methylotrophicus and application thereof
A technology of boxwood and bacillus, applied in the application, bacteria, biocide and other directions, can solve the problems of pollution, bacteria resistance environment, etc.
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Embodiment 1
[0025] Example 1: Effect of HYEB5-6 on mycelial growth of Euonymus anthracnose
[0026] Inoculate the bacteria block of Euonymus anthracnose in the center of the PDA plate. At the same time, the purified HYEB5-6 was streaked at the left and right positions of the bacteria cake, and the control plate was only inoculated with the pathogenic fungus cake. The test was repeated 3 times. The inoculated plates were cultured in an incubator at 28°C for 3 days, and the antibacterial effect of HYEB5-6 on Euonymus anthracnose was determined. The result is as figure 2 , HYEB5-6 showed obvious inhibitory effect on the mycelial growth of Euonymus anthracnose.
Embodiment 2
[0027] Example 2: Inhibitory effect of HYEB5-6 on the mycelium growth of several plant pathogens
[0028] The pathogenic bacteria block was inoculated in the center of the PDA plate, and at the same time, the purified HYEB5-6 was spotted at the four corners 30 mm away from the bacterial cake. The control plate was only inoculated with the pathogenic fungal cake, and the test was repeated 3 times. Place the inoculated plates in an incubator at 28°C for 3-5 days, and measure the antibacterial effect of HYEB5-6 on the other seven pathogenic bacteria. The result is as image 3 , it can be seen from the figure that HYEB5-6 has obvious inhibitory effect on 7 kinds of pathogenic bacteria.
Embodiment 3
[0029] Example 3: Effects of metabolites of HYEB5-6 on the germination of conidia and the growth of germ tube mycelium of Euonymus anthracnose
[0030] A single colony of activated HYEB5-6 was inoculated into 100 mL of liquid NA medium, and cultured with shaking at 250 rpm at 28°C for 12 hours. The supernatant was collected after centrifugation, and the supernatant was filtered and sterilized through a 0.22 μm filter to obtain a sterile filtrate containing HYEB5-6 metabolites, which was diluted 5 times with sterile water for use. Inoculate Euonymus anthracnose bacteria HYCG2-3 on a fresh PDA plate, culture at 28°C for 5 days, cut off mycelium pieces with a diameter of 5mm from the edge of the colony and inoculate them into 100mL CMC liquid medium, culture with shaking at 28°C and 250rmp 3 days. Collect the conidia of Euonymus anthracnose and adjust the concentration to 10 6 individual / mL. Mix the above sterile filtrate with an equal volume to a concentration of 10 6After m...
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