Bacillus amyloliquefacien and preparation method of polluted water reparation agent by using same
A technology for the preparation of amylolytic spores and strains, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, chemical instruments and methods, etc., and can solve problems such as complex production processes
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Embodiment 1
[0105] A method for preparing a polluted water restoration agent by using Bacillus amyloliquefaciens as a strain, the method comprising the following process steps:
[0106] A. Inoculate the activated Bacillus amyloliquefaciens CGMCCNo.3992 (Bacillus amyloliquefaciens) into a medium containing a carbon source after expanded culture, and add necessary nitrogen sources and nutrients;
[0107] B. Fermentation is carried out by the method of liquid deep aeration stirring fermentation + solid carrier adsorption;
[0108] C. Drying the fermented material after the fermentation is completed to prepare a polluted water restoration agent.
[0109] The activation process steps of the bacterial classification in the step A are as follows:
[0110] Inoculate Bacillus amyloliquefaciens CGMCC No.3992 (Bacillus amyloliquefaciens) on the slant of beef extract peptone medium test tube, culture at a temperature of 28°C-30°C for 48 hours, and transfer repeatedly 2-3 times to activate the strain...
Embodiment 2
[0123] Step A of the present embodiment is the same as step A of embodiment 1;
[0124] The medium in steps A and B is composed of 0.2% tryptone, 0.2% glucose, 0.2% yeast extract, 0.4% dipotassium hydrogen phosphate, 0.03% manganese sulfate and the rest of the water by mass percentage, and the conditions for fermentation and culture are the same as Example 1 is the same. After the fermentation is terminated, 1.0 times the volume of powdered zeolite and 1.0 times the volume of peat powder are added to the fermentation broth for adsorption, and air-dried at a temperature lower than 100°C until the water content of the material is below 12% by mass to obtain a polluted water restoration agent.
Embodiment 3
[0126] The strain activation step of step A is the same as that in Example 1. In the expanded culture, the expanded culture medium is composed of 0.3% tryptone, 0.3% glucose, 0.3% yeast extract, 0.4% dipotassium hydrogen phosphate, 0.03% manganese sulfate and excess Amount of water composed of natural pH. Dispense into Erlenmeyer flasks, and the sterilization condition of the expansion medium is 121°C autoclaving for 30 minutes, cooling to 25°C-35°C, inoculating Bacillus amyloliquefaciens strain CGMCCNo.3992 (Bacillus amyloliquefaciens), at 25°C- Shake flask culture at 30°C for 48 hours;
[0127] The solid fermentation medium in step B is respectively 10% crushed bran by mass percent, 88% powdery medical stone (0.1-2mm in particle diameter), 1.0% corn flour, 0.03% dipotassium hydrogen phosphate, 0.25 % ammonium sulfate, 1.0% humic acid and the balance of water. The sterilization condition of the solid fermentation medium is: autoclave at 121° C. for 60 minutes. After the ma...
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