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Preparation process of live bacillus mucilaginosus preparation

A technology for jelly-like spores and live bacteria preparations, which is applied to bacteria, microorganism-based methods, biochemical equipment and methods, etc. The effect of low air temperature and outlet air temperature, reducing the risk of fermentation contamination, and improving equipment utilization

Inactive Publication Date: 2015-02-11
HUBEI BIOPESTICIDE ENG RES CENT
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] 1. The filling coefficient of the fermentation tank is 60%-70%, and the utilization rate of the equipment is not high;
[0008] 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;
[0009] 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;
[0010] 4. The use of flocculation / plate-and-frame filtration or centrifugation technology will also cause the loss of active ingredients in the fermentation supernatant, resulting in a decline in the product effect;
[0011] 5. The inlet temperature of spray drying is generally set at 180°C to 200°C, and the outlet temperature is 80°C to 100°C. Under such a high working temperature, the number of bacteria in some varieties will decrease to a certain extent, which directly affects product quality
[0014] Fermentation and drying and granulation will produce a large amount of waste gas, which often contains volatile organic compounds (VOC), hydrogen sulfide, ammonia, mercaptans and other pollutants, accompanied by unpleasant stench. In the past, fermentation enterprises generally Discharge it directly or simply spray it with water, the two treatment methods will cause serious pollution to the environment

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Embodiment 1: (with 5m 3 Fermentation tank as an example)

[0038] 1) First-level seed culture: 2000ml of first-level seed culture medium is installed in a 5000ml triangular flask, sterilized by damp heat at 121°C for 15 minutes, and 10ml of live Bacillus jelly-like strains are inoculated in the first-level seed medium. Cultivate at 28°C for 16 hours; no bacterial contamination is found in the strain, and the shape of the bacteria is good, and then proceed to the next step. The raw materials and dosage of the medium used are: 0.5% starch, 0.5% beef extract, 3% peptone, and the pH of the medium is 7.5.

[0039] 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 16h; after inspection , if there is no contamination of the bacteria and the shape of the bacteria is good, proceed to the next step...

Embodiment 2

[0047] Embodiment 2, with embodiment 1, the difference is,

[0048] 1) The raw materials and dosage of the medium used for primary seed cultivation are: 0.5% starch, 3% beef extract, 0.5% peptone, and the pH of the medium is 6.5; sterilized by moist heat at 115°C for 30min, and cultured at 30°C for 12h after inoculation.

[0049] 2) The raw materials and dosage of the medium used for secondary seed cultivation are: 0.5% starch, 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 cultured at 30 ℃ for 12 hours after inoculation.

[0050] 3) The raw materials and consumption of the fermentation medium used are: molasses 1%, soybean meal 1.5%, corn steep liquor 1.5%, peptone 1.5%, dipotassium hydrogen phosphate 0.05%, magnesium sulfate 0.2%, manganese sulfate 0.002%, and the pH of the medium is 6.5; sterilize with damp heat at 115°C for 30 minut...

Embodiment 3

[0055] Embodiment 3, with embodiment 1, the difference is,

[0056] 1) The raw materials and dosage of the medium used for primary seed cultivation are: 2.5% starch, 1.5% beef extract, 2% peptone, the pH of the medium is 7.0; sterilized by moist heat at 115°C for 30min, and cultured at 30°C for 12h after inoculation.

[0057] 2) The raw materials and dosage of the medium used for secondary seed cultivation are: 2.5% starch, 1.5% yeast extract, 0.5% peptone, 0.05% dipotassium hydrogen phosphate, 0.1% magnesium sulfate, and the pH of the medium is adjusted to 7.0; 115 ℃ damp heat sterilization for 30 minutes, and cultured at 30 ℃ for 12 hours after inoculation.

[0058] 3) The raw materials and consumption of the fermentation medium used are: molasses 1.5%, soybean meal 1.2%, corn steep liquor 1.2%, peptone 2%, dipotassium hydrogen phosphate 0.05%, magnesium sulfate 0.2%, manganese sulfate 0.002%, and the medium pH is 7.0; sterilize with damp heat at 115°C for 30 minutes, and i...

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PUM

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Abstract

The invention relates to a preparation process of a live bacillus mucilaginosus preparation. The preparation process comprises the steps that bacillus mucilaginosus is inoculated into a fermentation medium to be cultured after being subjected to primary and secondary seed enlarged culture; the quantity and conversion rate of bacillus are increased through fed-batch of a carbon source in the fermentation process, thus obviously increasing the unit yield and reducing the unit cost; after fermentation is completed, the fermentation liquor is concentrated by using a vacuum film concentrator and the soluble synergistic substances, growth-stimulated substances and bacteriostatic active substances in the fermentation liquor can be effectively recovered; the concentrated fermentation liquor is dried and granulated by multistage low-temperature spray fluidized drying equipment, the granules are sorted and the fine powder is trapped by a cyclone separator and returns to be re-granulated, thus obtaining the bacillus mucilaginosus product, each gram of the powder of which has not less than 2.0*10<10> of CFU (colony-forming units); the tail gas is treated and is discharged up to the standard. The preparation process has the advantages that the active substances in the fermentation liquor can be furthest retained; the product quality and the equipment utilization rate are high; the biological activity is better maintained; the waste gas and the wastewater are discharged up to the standard; the preparation process can be used for large-scale industrial production.

Description

technical field [0001] The invention relates to a preparation process of a jelly-like bacillus living bacteria preparation. Background technique [0002] Bacillus mucilaginosus, commonly known as potassium bacteria, is a common soil bacterium in farmland. In the early 1950s, the Soviet scholar Aleksandrov first reported that this special bacterium was isolated from the soil, which not only has the ability to activate potassium in silicate minerals, but also can use phosphorus in apatite and fix atmospheric nitrogen. , so called silicate bacteria. The shape of the bacteria is thick and long rod, the end is round, the size is 1-1.2×4-7 microns, it does not move, the Gram staining is indeterminate, and there are often 1-2 large fat particles in the bacteria. In the nutrient-poor selective medium, the bacterium is covered with an oval hypertrophic capsule, the size of which is 5-7×7-10 microns, which is 10-20 times or even 50 times larger than the bacterium; There are even 2-...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/20C12R1/07
CPCC12N1/20
Inventor 刘芳饶犇廖先清周荣华陈伟刘晓艳张先进江爱兵杨自文
Owner HUBEI BIOPESTICIDE ENG RES CENT
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