A kind of Paenibacillus qbjp-f4 and its application
A technology of QBJP-F4 and Paenibacillus, which is applied in the field of agricultural microorganisms, can solve the problems of insufficient systematic and in-depth research, and the lack of large-scale promotion of products, etc., to achieve good growth-promoting effects, survivability, and growth-promoting effects
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Embodiment 1
[0032] Embodiment 1, isolation and identification of bacterial strain
[0033] Take 5g of soil in a triangular flask filled with 45ml of sterile water, and shake it in a shaker at 30°C and 170r / min for 20min to make a soil suspension. After 20min in a water bath at 80°C, dilute to 10 -1 、10-2 、10 -3 、10 -4 、10 -5 After waiting for different gradient dilutions, smear the plate, incubate in the dark for 1d to 2d in the incubator, and then pick a single colony, after purification on the plate, select 12 strains in total, and measure the ability of each strain to produce the auxin indole acetic acid (IAA) (Method reference: Glickmann E, DessauxY. A critical examination of the specificity of the salkowski reagent forindolic compounds produced by phytopathogenic bacteria. [J]. Applied and environmental microbiology, 1995, 612). Using the same method, a strain QBJP-F4 with excellent growth-promoting ability was obtained as a result of primary screening and re-screening, which was ...
Embodiment 2
[0036] Embodiment 2, the production of functional bacteria fermented liquid
[0037] The strain QBJP-F4 (CGMCC NO.12887) was inoculated into PDA culture medium for liquid fermentation production. The conditions of fermentation production were: pH 7.0, fermentation temperature 30°C, stirring speed 170rpm / min, spores formed in the middle and late stages of fermentation, The fermentation time is 48 hours, so that the amount of bacteria or spores in the fermentation broth is ≥1×10 10 a / ml;
[0038] The preparation method of the PDA culture medium used is as follows, taking the preparation of 1L medium as an example: 200g potatoes are peeled, cut into small pieces, put them in water and boil them, boil them for 30min and then filter them, add 20g ordinary sucrose to the filtrate and make the volume to 1000ml , natural pH, sterilized at 121°C for 20min.
Embodiment 3
[0039] Example 3, research and development of functional biological matrix
[0040] The effect of biological matrix seedling cultivation with strain QBJP-F4 as functional bacteria
[0041] Research and development of the substrate: the fermentation broth of the bacterial strain QBJP-F4 prepared in Example 2 was inoculated (according to 5v / w% of the dry weight of the substrate, the same below) into the common seedling cultivation substrate, and mixed evenly. The functional strain QBJP-F4 in the matrix was counted by selective medium, and the formula of selective medium was: peptone 10.0g, yeast powder 5.0g, NaCl 10.0g, agar 2.0%, deionized water 1000mL, pH 7.2-7.4, 121 ℃ autoclave for 20min. 1% polymyxin 2mL, 1% cycloheximide 4mL (the antibiotics are added after the medium is cooled before being poured). The number of colonies of functional bacteria QBJP-F4 is calculated by dry weight per gram of substrate. After counting, the number of functional bacteria in the biological ...
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