Paenibacillus polymyxa fermentation product and its preparation method and application
A technology for polymyxa spore and fermented product, which is applied to the field of polymyxa spore fermented product and its preparation, can solve problems such as limited application, poor content penetration, etc., and achieves the promotion of plant growth, good control effect, increased Effects of Rice Yield
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Embodiment 1
[0047] Indoor bioassay of embodiment 1 Paenibacillus polymyxa
[0048] 1. Isolation of endophytes from rice
[0049] Pick healthy rice plants from the bad seedlings of rice and sheath blight diseased fields in Wenling and Jinhua, Zhejiang, take the leaves of the upper and lower middle parts of the plants, cut them into small pieces of 5 mm × 5 mm, disinfect them with 75% ethanol for about 1 min, and then Rinse 3 times with sterilized water to remove residual disinfectant, and finally put it on sterile absorbent paper to absorb excess water, then put it into a sterile mortar, add 6mL of BPS buffer to grind, take The supernatant was diluted 10, 50, and 100 times, and 200 μL of each dilution was applied to the LB plate. At the same time, verify that the last rinse water was applied to the LB plate to check whether the surface of the tissue was thoroughly disinfected. Incubate in the dark at 30°C for 1-2 days, and record Colony morphology, size and color.
[0050] The biological...
Embodiment 2
[0057] The fermentation process of embodiment 2 Paenibacillus polymyxa (ZJU-N)
[0058] See Table 1 for the medium used in the fermentation of this embodiment.
[0059] Table 1 The medium used for the fermentation of this embodiment is summarized
[0060]
[0061] Equipment: Paenibacillus polymyxa (ZJU-N) liquid complete fermentation equipment was purchased from Shanghai Chuyi Biotechnology Co., Ltd.
[0062] Fermentation process:
[0063] (1) Strain activation: pick a ring of Paenibacillus polymyxa ZJU-N and streak it on a solid plate for activation, and place the inoculated plate in a 30°C incubator for 72 hours;
[0064] (2) Seed culture: Pick an independent colony of Paenibacillus polymyxa activated in step (1) and inoculate it in a 250ml Erlenmeyer flask with 100ml seed culture solution, and cultivate it for 24h at a temperature of 30°C and a rotation speed of 160rpm ;
[0065] (3) Fermentation culture: insert the cultivated seed solution into a 15L fermenter conta...
Embodiment 3
[0067] The optimization of embodiment 3 fermentation process
[0068] The optimization of the fermentation medium in this embodiment: in the basal medium (tryptone: 5g / L; beef extract: 3g / L; yeast extract: 1g / L; NaCl: 3g / L; NaCl: 3g / L; 2 HPO 4 .12H 2 O: 1.5g; Ca(NO 3 ) 2 .4H 2 (2: 0.5g) on the basis of investigating several common carbon sources (the consumption of carbon source is the same as embodiment 2) on the influence of Paenibacillus polymyxa viable count, spore production amount and bacterial film secretion. See Table 2. All the other steps are identical to Example 2.
[0069] Table 2: Effects of different carbon sources on the number of viable bacteria, spore production and biofilm secretion of Paenibacillus polymyxa (ZJU-N)
[0070]
[0071] Note: The amount of biofilm secretion is more "+++", more "++", less "+", no secretion "-"
[0072] As can be seen from the above table 2, potato and sucrose are comparatively suitable carbon sources. Simultaneously,...
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