Preparation and application of bacillus megatherium BM22 and spore powder thereof
A technology of Bacillus megaterium and BM22, applied in the field of microorganisms, can solve the problems of easily polluting the environment and destroying the ecology, and achieve the effects of good storage, low cost and good control effect
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Embodiment 1
[0028] Example 1 Isolation and Identification of Bacillus megaterium BM22
[0029] 1.1 Isolation, purification and preservation of endophytic bacteria
[0030] Healthy leaves of Eucommia ulmoides were collected from the black spot occurrence area of Eucommia ulmoides in Dayi, Sichuan. Rinse the collected samples with sterile water, weigh 1.0g of tissue, soak in 70% alcohol for 1-2min, then disinfect with 1-3% sodium hypochlorite solution for 3-5min, wash several times with sterile water, absorb Apply 100 μL of washing liquid for the last time to NA plate (3g beef extract, 10g peptone, 5g sodium chloride, 15-20g agar powder, 1000mL distilled water, pH 7.0, after mixing and dispensing, autoclave at 121°C for 30min), culture in the dark at 27°C 24h, used as a control for surface disinfection, to check whether the surface disinfection is thorough.
[0031] Cut the surface-sterilized bark tissue into pieces, put them into a sterile mortar, add sterilized quartz sand and 10mL of...
Embodiment 2
[0046] The preparation of embodiment 2 bacillus megaterium BM22 spore powder
[0047] The bacillus megaterium BM22 obtained according to embodiment 1 is made into spore powder preparation through seed culture and fermentation culture, specifically through the following methods:
[0048] The conventional method is to prepare beef extract peptone slant medium (beef extract 5g, peptone 10g, NaCl 3.5g, agar 18g, water 1000mL), inoculate Bacillus megaterium, and cultivate to make first-class seeds.
[0049] Nutritious succulent culture solution (beef extract 7g, peptone 10g, NaCl 5g, magnolia officinalis root bark soaking solution 1000mL) was autoclaved, and under oxygen control, bottled according to the proportion of 100mL liquid in a 300mL triangular flask, Inoculate Bacillus megaterium slant seeds in the state, inoculate 2 slant seeds per bottle, vibrate and cultivate, and make Bacillus megaterium liquid seeds. Wherein, 10 g of Photinia fragrans leaves are boiled in 1000 mL of ...
Embodiment 3
[0054] Example 3 Bacillus megaterium BM22 spore powder preparation spray method control test
[0055] According to the occurrence degree of erythema, it is divided into 4 occurrence areas (I: 5-10%; II: 11-30%; III: 31-60%; IV: >60%). In 4-5 months, the inoculum prepared in Example 2 adopts the concentration of spray method: 50 times of dilution, 100 times of dilution, 200 times of dilution, 400 times of dilution, 800 times of dilution, 1600 times of dilution, 2400 times of dilution to red leaves The leaves of Photinia were treated, sprayed evenly along the leaves, 100mL per plant, and sterile water was used as a control, repeated 3 times, and the incidence of Photinia fragrans was counted. 20 plants per treatment.
[0056] 15 days after treatment, conduct disease investigation and statistics according to the disease grading standards in Table 3, and calculate the control effect.
[0057] Table 3 Grading standard of Photinia erythema
[0058]
[0059] Incidence rate (%)=...
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