Process for preparing viable bacillus megaterium preparation

A technology of Bacillus megaterium and live bacteria preparations, which is applied in the field of preparation of live Bacillus megaterium preparations, can solve the problems of high processing cost, low equipment utilization rate, and product effect decline, and achieve low inlet air temperature and outlet air temperature , Reduce the risk of fermentation contamination and improve the utilization rate of equipment

Inactive Publication Date: 2014-12-24
HUBEI BIOPESTICIDE ENG RES CENT
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] 1. The filling coefficient of the fermentation tank is 60%-70%, and the utilization rate of the equipment is not high;
[0006] 2. Due to the batch fermentation used, the initial concentration of the fermentation medium is too high, the lag period after inoculation is longer, and more by-products are formed during the fermentation process, and the concentration of the fermentation product cannot increase, which eventually leads to higher fermentation costs;
[0007] 3. Flocculation/plate-and-frame filtration or centrifugation technology is generally used for the concentration of fermentation broth. These two technologies generally generate a large amount of wastewater, and the subsequent treatment costs are relatively high;
[0008] 4. The use of flocculation/plate-and-frame filtration or centrifugation technolog

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] Embodiment 1: (with 5m 3 Fermentation tank as an example)

[0037] 1) First-level seed culture: 2000ml of first-level seed medium is placed in a 5000ml Erlenmeyer flask, sterilized by moist heat at 121°C for 15 minutes, 10ml of Bacillus megaterium freeze-dried tube strains are inoculated into the first-level seed medium, and cultured at 28°C 12h; no contamination was found in the strain, and the shape of the bacteria was good, and then proceeded to the next step. The raw materials and dosage of the medium used are: 0.5% glucose, 0.5% beef extract, 3% peptone, and the pH of the medium is adjusted to 7.5.

[0038] 2) Secondary seed culture: 150L secondary seed medium is installed in a 400L fermenter, sterilized by moist heat at 121°C for 15 minutes, and 3000ml of primary seed is inoculated in the secondary seed medium; cultivated at 28°C for 12h; after inspection , if there is no contamination of the bacteria and the shape of the bacteria is good, proceed to the next st...

Embodiment 2

[0046] Embodiment 2, with embodiment 1, the difference is,

[0047] 1) The raw materials and dosage of the medium used for primary seed cultivation are: 0.5% glucose, 1% beef extract, 2.5% peptone, the pH of the medium is adjusted to 6.5; sterilized by moist heat at 115°C for 30min, and cultivated at 30°C for 10h after inoculation.

[0048] 2) The raw materials and dosage of the medium used for secondary seed cultivation are: 1% glucose, 1% yeast extract, 2.5% peptone, 0.05% dipotassium hydrogen phosphate, 0.1% magnesium sulfate, and the pH of the medium is adjusted to 6.5; 115 ℃ damp heat sterilization for 30 minutes, and inoculated at 30 ℃ for 10 hours.

[0049] 3) The raw materials and dosage of the fermentation medium used for fermentation are: glucose 1%, soybean meal 1%, corn steep liquor 2%, yeast powder 3%, dipotassium hydrogen phosphate 0.05%, magnesium sulfate 0.2%, manganese sulfate 0.002%, culture medium The pH is 6.5; sterilize with damp heat at 115°C for 30 minu...

Embodiment 3

[0054] Embodiment 3, with embodiment 1, the difference is,

[0055] 1) The raw materials and dosage of the medium used for primary seed cultivation are: 1% glucose, 2% beef extract, 2% peptone, the pH of the medium is adjusted to 7.0; sterilized by moist heat at 115°C for 30min, and cultured at 30°C for 10h after inoculation.

[0056] 2) The raw materials and dosage of the medium used for secondary seed cultivation are: glucose 1%, yeast extract 2%, peptone 2%, dipotassium hydrogen phosphate 0.03%, magnesium sulfate 0.08%, and the pH of the medium is adjusted to 7.0; 115 ℃ damp heat sterilization for 30 minutes, and inoculated at 30 ℃ for 10 hours.

[0057] 3) The raw materials and dosage of the fermentation medium used for fermentation are: glucose 1%, soybean meal 1.5%, corn steep liquor 1.5%, yeast powder 2%, dipotassium hydrogen phosphate 0.03%, magnesium sulfate 0.2%, manganese sulfate 0.002%, culture medium The pH is 7.0; sterilize with damp heat at 115°C for 30 minutes...

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Abstract

The invention relates to a process for preparing a viable bacillus megaterium preparation. According to the process, after bacillus megaterium undergoes first-stage germ amplification culture and second-stage germ amplification culture, the bacillus megaterium is inoculated to a fermentation culture medium for culture, and the number and conversion ratio of bacilli is increased through feeding a supplement carbon source during fermentation, so that the unit yield is increased remarkably, and the unit cost is reduced; at the end of fermentation, fermentation liquor is concentrated with a vacuum film concentrator, so that soluble synergistic substances, growth promoting substances and bacteriostatic active substances can be effectively recovered from the fermentation liquor; the concentrated fermentation liquor is subjected to drying and granulating by multi-level low-temperature spray-fluidized drying equipment, granules are subjected to sorting, fine powder gathered by a cyclone separator returns and is granulated again, and then, a bacillus megaterium product, of which the CFU of powder per gram is not less than 8.0*10<10>, is obtained; exhaust gas is treated and is discharged after reaching standard. The process has the advantages that effective substances in the fermentation liquor can be reserved to the maximum, the quality of the product is high, the equipment utilization ratio is high, the retention of biological activity is relatively good, waste gas and waste water are discharged after reaching standard, and large-scale industrial production can be achieved.

Description

technical field [0001] The invention relates to a preparation process of a live bacillus megaterium preparation. Background technique [0002] Bacillus megaterium, rod-shaped with rounded ends. singly or in short chains. 1.2~1.5×2.0~4.0 microns. able to exercise. Gram positive. Spores 1.0~1.2×1.5~2.0 microns, elliptic, mesogenic or subterminal. Slowly liquefies gelatin, peptonizes milk, hydrolyzes starch, and does not reduce nitric acid. Bacillus megaterium is a spore-forming bacillus, a gram-positive bacterium, an aerobic bacterium, and a common saprophytic bacterium in oil. [0003] Bacillus megaterium can be used to produce phosphorus-solving and potassium-fixing fertilizers. Bacillus megaterium has a good effect on degrading organic phosphorus in soil. It is a common strain for producing bio-organic fertilizers and a common strain for making water treatment agents. Apply it It has a unique effect on improving the fermentation and flavoring of tobacco leaves. Baci...

Claims

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Application Information

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IPC IPC(8): C12N1/20C12R1/11
Inventor 张光阳廖先清饶犇周荣华陈伟刘芳刘晓艳张先进杨自文
Owner HUBEI BIOPESTICIDE ENG RES CENT
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