Bacillus atrophaeus and application of bacillus atrophaeus in prevention and control of Chinese wolfberry diseases
A technology of Bacillus rysophila and Bacillus, which is applied in the field of Bacillus fuencus and in the prevention and control of diseases of wolfberry, can solve the problems of severe drug resistance, achieve a wide antibacterial spectrum, do not pollute the environment, and are not easy to produce drug resistance Effect
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Embodiment 1
[0025] Acquisition and identification of Bacillus fuencus:
[0026] An isolated bacterium, isolated from the rhizosphere soil of Lycium barbarum, was identified as Bacillus atrophaeus ( figure 1 , Table 1), has been sent to the China Center for Type Culture Collection on October 18, 2021 for preservation, classification and name: Bacillus atrophaeus (Bacillus atrophaeus) GQ260; preservation number is CCTCC NO: M 20211286; place: China, Wuhan, Wuhan University.
[0027] In the present invention, Bacillus fumeus GQ260 may be referred to as GQ260 for short.
[0028] Morphological characteristics: the colony is round, milky white.
[0029] Physiological and biochemical characteristics of the strain:
[0030] Table 1 Physiological and biochemical characteristics of strain GQ260 – carbon source utilization
[0031]
[0032]
[0033]
[0034] +: Positive reaction; -: Negative reaction; W: Weak positive reaction
Embodiment 2
[0036] Fermentation of Bacillus Fuesus GQ260 (percentages in the following medium formula are mass fractions):
[0037] 1) First-level seed culture: 100ml of first-level seed medium is placed in a 500ml Erlenmeyer flask, sterilized by damp heat at 121°C for 20 minutes, and the strains from GQ260 freeze-dried tubes are inoculated into the first-level seed medium, and shaken at 35°C and 180rpm Shaking culture for 10 hours; the raw materials and dosage of the medium used for primary seed cultivation are: 1% glucose, 2% beef extract, 3% peptone, 0.5% sodium chloride, and the pH of the medium is 7;
[0038] 2) Secondary seed culture: 300L secondary seed medium is installed in a 500L fermenter, sterilized by moist heat at 121°C for 20 minutes, and 200ml of primary seed is inoculated into the secondary seed medium; cultured at 35°C for 10h; tank pressure is controlled 0.05Mpa, stirring speed 200rpm, aeration ratio 1:1, the raw materials and dosage of the medium used for secondary see...
Embodiment 3
[0042] Bacteriostatic activity of Bacillus fumarus GQ260 and its control effect on root rot and powdery mildew of Lycium barbarum
[0043] Fusarium solani, the pathogenic fungus of wolfberry root rot, was isolated from diseased wolfberry strains and stored on PDA slopes at 4°C, and other pathogenic fungi were stored on PDA slopes at 4°C. The slant strain was transferred to a PDA plate for activation, and cultured at 30°C for 6 days for later use. Place sterilized filter paper sheets at both ends of the PDA plate, and then drop 7 μL of GQ260 fermentation broth. After 24 hours, use a 4mm hole puncher to insert the above-mentioned pathogenic bacteria plate, and use sterile water as a blank control, and the distance between the pathogenic bacteria and the filter paper is 25mm. After the plate with the control was overgrown, the diameters of the colonies of each treatment and the control were counted, and the bacteriostatic rate was calculated.
[0044] Bacterial inhibition rate=...
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