Soil paenibacillus and application thereof
A bacillus and soil technology, applied in the field of microorganisms, can solve the problems of limiting the amount of gellan gum used and its impact, and achieve the effects of unique properties, increased solution viscosity, and increased solution viscosity
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Embodiment 1
[0031] Isolation and identification of Paenibacillus edaphicus NUST16.
[0032] (1) Isolation of Paenibacillus edaphicus NUST16
[0033] The soil Paenibacillus edaphicus NUST16 of the present invention is isolated from coastal brown soil in Yancheng, Jiangsu. The method of separation is:
[0034] ① Screening of bacterial strains: Divide the soil samples into 10 groups, each group weighed 1g of soil samples and added them to the prepared liquid medium, put them in a constant temperature shaking incubator and culture them for 2 days at 200rpm and 30°C for enrichment. Then take 1mL bacterial liquid from each group of Erlenmeyer flasks and reintroduce it into a new liquid medium, culture for 2 days under the same conditions and enrich again. Then take 1 mL of the enriched bacterial solution from each group and add it to 9 mL of sterile water, mix well to make a bacterial suspension, and use 10-fold gradient dilution to take 10 -6 -10 -4 The diluted bacterial suspension was spr...
Embodiment 2
[0042] The cultivation of Paenibacillus edaphicus NUST16 and its application in the production of water-soluble exopolysaccharide.
[0043] Prepare medium, sucrose 5g, peptone 0.5g, NaH 2 PO 4 0.1g, CaCl 2 0.01g, MgCl 2 0.01g, KCl0.01g, FeCl 2 0.001g, CuSO 4 0.001g, MnSO 4 0.001g, ZnCl 2 0.001g, CoCl 2 0.001 g was dissolved in 1 L of deionized water, the pH was 6.0, 1% nutrient agar was added to sterilize at 121°C for 15 minutes, and then cooled to obtain a solid medium. After culturing the strain on agar solid medium at 30°C for 48 hours, colonies can be seen to grow. The colonies are round, translucent, shiny, sticky, and difficult to provoke. The strain secretes a large amount of exopolysaccharide. Scrape the colony on each 9cm plate and dissolve it with 30mL deionized water, then centrifuge at 5000×g for 20min, add 60mL ethanol-isopropanol mixture (volume ratio 1:1) to the supernatant to precipitate at room temperature, and collect the precipitate by filtra...
Embodiment 3
[0046] The cultivation of Paenibacillus edaphicus NUST16 and its application in the production of water-soluble exopolysaccharide.
[0047] Preparation medium, sucrose 50g, peptone 5g, NaH 2 PO 4 5g, CaCl 2 0.5g, MgCl 2 0.5g, KCl 0.5g, FeCl 2 0.05g, CuSO 4 0.05g, MnSO 4 0.05g, ZnCl 2 0.05g, CoCl 2 0.05 g was dissolved in 1L of deionized water, the pH was 7.0, sterilized at 121°C for 20 minutes, cooled for later use, added 1% nutrient agar, sterilized at 121°C for 15 minutes, cooled to obtain the corresponding solid medium. Pick a single colony of Paenibacillus soil NUST16 grown on the agar solid medium to the sterilized medium, culture it with shaking at 25°C for 24 hours to form a seed culture solution, and then add 7% of the seed culture solution to this spare medium Shake culture at 35°C for 48 hours to obtain fermentation broth. Add 3.5 times the volume of 95% ethanol-acetone mixture (volume ratio 1:1) to the fermentation broth, shake at room temperature, ...
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