Application of streptomyces lavendulae to preventing and treating dry rot of actinidia arguta
A technology of Streptomyces lavender and Actinidia jujube, which is applied in the field of agricultural biology, can solve the problems of fruit pesticide residues and environmental pollution, and achieve the effect of environmental friendliness and good control effect
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Embodiment 1
[0014] Example 1 Isolation and screening of antagonistic bacteria
[0015] 1. Separation and purification
[0016] From June 2013 to August 2015, 50 soil samples were collected from Fengcheng, Donggang, Kuandian and other places in Liaoning Province using the five-point sampling method. The collected soil samples were air-dried naturally. Take 10g of soil sample, place it in a conical flask filled with 90ml of sterile water, and shake it on a shaker for 20min. After standing for 30s, dilute 10 times successively to prepare 10 -4 Diluent. Micropipette pipette 10 -4 Put 0.1ml of the diluent on the solid plate of Gao's No. 1 medium, and spread it evenly with a sterile applicator. 25 ℃ constant temperature incubator upside down for 3-5 days. The strains with different colony forms on the plate were picked and transferred to Gao’s No. 1 medium to obtain pure culture, sealed in sterilized paraffin oil, and stored at 4°C for later use. Gaoshi No. 1 medium: 20.0g soluble starch...
Embodiment 2
[0020] Identification of embodiment 2 antagonistic strains
[0021] 1. Morphological identification and biochemical characteristics
[0022] Colony morphology: the aerial hyphae of strain DTJ-24 on Gao’s No. 1 medium are lilac-colored, and the hyphae in the base are colorless and have no soluble pigments; microscopic morphology: the hyphae in the base have no septum and no Fracture; the aerial hyphae are multi-branched, and the branches are relatively short, the spore filaments are long and spiral, and the spores are elliptical to cylindrical, with smooth surface.
[0023] Biochemical characteristics: Strain DTJ-24 can liquefy gelatin and hydrolyze starch weakly. Produces hydrogen sulfide, can decompose cellulose, peptonizes milk, and does not coagulate. Glucose and fructose can be used, but sucrose, inositol, mannitol, raffinose, and D-xylose are not used.
[0024] 2. 16SrDNA sequence analysis
[0025] The strain DTJ-24 was inoculated in Gaoshi No. 1 liquid medium, cultur...
Embodiment 3
[0027] Embodiment 3 Preparation of antagonistic bacteria aseptic fermentation filtrate
[0028] The strain DTJ-24 was inoculated in the liquid medium, the medium loading was 70%, the volume of the fermenter was 30L, the stirring speed was 150-200rpm / min, the ventilation rate was 15-20%, the temperature was 25-30℃, and the pH value was 6.5~ Under the condition of 7.5, constant temperature fermentation culture was carried out. After 5 days of fermentation, the fermentation liquid was centrifuged at 5000r / min to prepare a supernatant, which was filtered with a sterile filter membrane to prepare a sterile fermentation filtrate.
[0029] The formula of the liquid medium is as follows: yeast extract powder 4.0g / L, malt extract powder 10.0g / L, glucose 4.0g / L, water 1000ml, pH value 7.5.
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