Streptomycete S1-5 and uses thereof
A technology of streptomyces and plant pathogenic fungi, applied in the direction of application, bacteria, biocides, etc., can solve the problems of no streptomyces and achieve the effects of less resistance to drugs, lower agricultural costs, and high killing activity
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Embodiment 1
[0026] Example 1: Obtaining fermentation broth
[0027] (1) Slope culture: Use PDA medium, coat the slant with Streptomyces S1-5 strain, and cultivate for 2 to 3 days at 30°C to obtain the slant strain;
[0028] (2) Seed culture: inoculate the slant strains to Gao's No. 1 medium and cultivate for 2 to 3 days at 30°C to obtain Streptomyces S1-5 colonies;
[0029] (3) Fermentation culture: Preparation of original fermentation medium: 20 mL of 1% soybean meal powder infusion, 20 g glucose, 3.0 g peptone, 2.0 g calcium carbonate, 2.5 g sodium chloride, and 1000 ml distilled water. Scrape the spores from the colony of Streptomyces S1-5 cultured on Gao's medium No. 1 and place them in sterile water, shake for 10 minutes, and make a concentration of 1×10 8 The spore suspension per ml was inserted into the fermentation medium at a 10% (V / V) inoculum amount, and a 250 ml Erlenmeyer flask was placed on a shaker and cultured on a constant temperature shaker for 5 days to obtain a fermentatio...
Embodiment 2
[0030] Example 2: Obtainment and determination of fermentation broth extract
[0031] Take 50ml of the fermentation broth, centrifuge at 5000r / min for 10min, and add an equal volume of absolute ethanol to the supernatant to form the crude extract of the biologically active substance supernatant. The filter cake was washed twice with distilled water and centrifuged, the supernatant was discarded, the filter cake was reduced to the volume of the fermentation broth by adding absolute ethanol, after soaking for 1 hour, centrifuged at 5000r / min for 10 minutes, and the supernatant was taken as the crude mycelium of the biologically active substance. Extract. The two crude extracts and the supernatant after centrifugation of the fermentation broth were tested for bacteriostasis and acaricidal tests, and the same ethanol aqueous solution was used as a control.
[0032] Antibacterial effect determination method: (Four kinds of plant pathogenic fungi are gifted by the Department of Plant Pr...
Embodiment 3
[0041] Example 3: Obtainment and determination of biologically active substances
[0042] After the fermentation broth of Streptomyces S1-5 is centrifuged, the supernatant is taken, and an equal volume of ethyl acetate is added for extraction, and the upper layer is concentrated under reduced pressure and collected. Collect the lower layer for bacteriostasis determination, use ethyl acetate as the eluent to run the column, the eluent is petroleum ether / ethyl acetate, column chromatography silica gel (200-300 mesh) as the stationary phase, use the dry method to pack the column, Collect the eluent at the lower end of the test tube, 10 mL per tube, 10 tubes in total. Biological activity tracking: the collected 10 tubes of eluate and the extracted lower layer solution were used filter paper method to determine their bacteriostasis against the test bacteria (Alternaria longifolia and Rhizoctonia solani, courtesy of the Department of Plant Protection, Zhejiang University) Effect (result...
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