A functional vegetable seedling-raising biological matrix containing Bacillus subtilis g10 and its preparation method
A Bacillus subtilis and seedling raising biological substrate technology, applied in the field of agricultural microorganisms, can solve the problems of insufficient systematic and in-depth research, no large-scale promotion products, etc., achieving good growth promotion effect, obvious technical and functional advantages, and efficient growth promotion. effect of ability
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Embodiment 1
[0034] Embodiment 1, isolation and identification of bacterial strain
[0035] Take the root of pepper, cut it into small pieces about 3cm long, take 10g of plant root in a triangular flask filled with 90ml of sterile water, shake it in a shaker at 30°C and 170r / min for 20min, and make a soil suspension, 80°C After 20 minutes in water bath, dilute to 10 -1 、10 -2 、10 -3 、10 -4 、10 -5After waiting for different gradient dilutions, smear the plate, culture in the dark for 1d to 2d in the incubator, and then pick a single colony, after plate purification, a total of 150 strains were selected, and the auxin indoleacetic acid (IAA) produced by each strain was determined respectively (method References: Glickmann E, Dessaux Y. A critical examination of the specificity of the salkowski reagent for indolic compounds produced by phytopathogenic bacteria. [J]. Applied and environmental microbiology, 1995, 612) and the ability to produce ACC deaminase (method reference: Glick BR. Mo...
Embodiment 2
[0038] The production of embodiment 2 functional bacterium bacterial liquid
[0039] Inoculate strain G10 (CGMCC NO.9921) into PDA culture medium for liquid fermentation production. The conditions for fermentation production are: pH 7.0, fermentation temperature 30°C, stirring speed 170rpm / min, spores are formed in the middle and late stages of fermentation, and the fermentation time is 48h, so that the amount of bacteria or spores in the fermentation broth is ≥1×10 10 a / ml;
[0040] The preparation method of the PDA medium used is as follows, taking the preparation of 1L medium as an example: 200g of potatoes are peeled, cut into small pieces, put into water and boiled, boiled for 30min and then filtered, add 20g of ordinary sucrose to the filtrate and make it to 1000ml , natural pH, sterilized at 121°C for 20min.
Embodiment 3
[0041] Example 3, research and development of functional biological matrix
[0042] 3.1 Effect of biological matrix seedling cultivation with strain G10 as functional bacteria
[0043] Research and development of the substrate: the strain G10 was connected to the common seedling cultivation substrate and mixed evenly. Selective medium for functional strain G10 in the matrix: 10.0g peptone, 5.0g yeast powder, 10.0g NaCl, 2.0% agar, 1000mL deionized water, pH 7.2‐7.4, autoclaved at 121°C for 20min; 1% polymyxa Cycloheximide 2mL, 1% cycloheximide 4mL (antibiotics are added after the medium is cooled before being poured). The number of colonies of functional bacteria G10 is calculated by dry weight per gram of substrate. After counting, the number of functional bacteria in the biological matrix is about 6.73×10 7 CFU / g.
[0044] The treatments for the seedling raising experiment were as follows: 1) Common seedling raising medium (CK2); 2) Seedling raising medium (CK1) added ...
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