A strain containing Bacillus dead valley and its prepared functional vegetable seedling biological matrix
A technology of Bacillus dead valley and biological substrate for seedling cultivation, which is applied in the field of agricultural microorganisms, can solve the problems of slow development of biological substrate for seedling cultivation, and achieve the effects of good growth promotion effect, obvious functional advantages, and obvious technical advantages
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Embodiment 1
[0035] Isolation and identification of embodiment 1 bacterial strain
[0036] Take the root of watermelon, cut it into small pieces about 3cm in length, take 10g of the plant root, put it 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 LB plate, culture in the dark for 1 to 2 days in the incubator, and then pick a single colony, after plate purification, a total of 126 pure bacteria were selected, and the auxin indole acetic acid produced by each strain was determined respectively. IAA) (method reference: 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 (meth...
Embodiment 2
[0039] The production of embodiment 2, N23 fermented liquid
[0040] Inoculate strain N23 (CGMCC NO.9920) into PDA culture medium for liquid fermentation production. The conditions for fermentation production are: pH 6.5, fermentation temperature range 30°C, stirring speed 170 rpm, spores are formed in the middle and late stages of fermentation, and fermentation The time is 48 hours, so that the amount of bacteria or spores in the fermentation broth is ≥1×10 10 a / ml;
[0041] 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
[0042] Example 3, research and development of functional biological matrix
[0043] 3.1 The effect of biological matrix seedlings with strain N23 as functional bacteria
[0044] Research and development of the substrate: the strain N23 was inoculated (according to 5% of the dry weight of the substrate, the same below) into the common seedling cultivation substrate, and mixed evenly. The count of functional strain N23 in the matrix adopts selective medium: 10.0g peptone, 5.0g yeast powder, 10.0g NaCl, 2.0% agar, 1000mL deionized water, pH 7.2-7.4, autoclaved at 121℃ for 20min; more than 1% Colistin 2mL, 1% cycloheximide 4mL (antibiotics are added after the medium is cooled before being poured): the number of colonies of functional bacteria N23 is calculated by dry weight per gram of substrate. After counting, the number of functional bacteria in the biological matrix is about 3.35×10 7 CFU / g.
[0045] The seedling raising test is processed as follows: 1) common seedling ra...
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