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Process for preparing viable bacillus firmus preparation

A technology of Bacillus firmus and live bacteria preparations, which is applied in the field of preparation of live Bacillus firmus 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

[0004] 1. The filling coefficient of the fermentation tank is 60%-70%, and the utilization rate of the equipment is not high;
[0005] 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;
[0006] 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;
[0007] 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;
[0008] 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
[0011] 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

[0034] Embodiment 1: (with 5m 3 Fermentation tank as an example)

[0035] 1) Primary seed culture: 2000ml of primary seed medium is placed in a 5000ml Erlenmeyer flask, sterilized by moist heat at 121°C for 15 minutes, and 10ml of Bacillus firmus freeze-dried tube strains are inoculated into the primary seed medium, and cultured at 35°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 for primary seed cultivation are: 0.5% glucose, 0.5% beef extract, 3% peptone, 0.5% sodium chloride, and the pH of the medium is adjusted to 7.5.

[0036] 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 35°C for 12h; after inspection , if there is no contamination of the bacteria and the shape of the b...

Embodiment 2

[0044] Embodiment 2, with embodiment 1, the difference is,

[0045] 1) The raw materials and dosage of the medium used for primary seed cultivation are: 1% glucose, 1% beef extract, 2.5% peptone, 1% sodium chloride, and the pH of the medium is adjusted to 6.5; Incubate at 28°C for 16h.

[0046] 2) The raw materials and dosage of the medium used for secondary seed cultivation are: glucose 1%, yeast extract 1%, peptone 2.5%, dipotassium hydrogen phosphate 0.05%, sodium chloride 1%, magnesium sulfate 0.1%, medium Adjust the pH to 6.5; sterilize with damp heat at 115°C for 30 minutes, and incubate at 28°C for 16 hours after inoculation.

[0047] 3) The raw materials and dosage of the fermentation medium used are: glucose 1%, soybean meal 1%, corn steep liquor 1%, yeast powder 3%, peptone 3%, dipotassium hydrogen phosphate 0.05%, magnesium sulfate 0.2%, manganese sulfate 0.002% , calcium carbonate 0.5%, medium pH 6.5; 115 ℃ damp heat sterilization for 30 minutes, 28 ℃ culture 46h...

Embodiment 3

[0052] Embodiment 3, with embodiment 1, the difference is,

[0053] 1) The raw materials and dosage of the medium used for primary seed cultivation are: 1.5% glucose, 2% beef extract, 2% peptone, 0.8% sodium chloride, and the pH of the medium is adjusted to 7.0; Incubate at 30°C for 14h.

[0054] 2) The raw materials and dosage of the medium used for secondary seed cultivation are: glucose 1.5%, yeast extract 2%, peptone 2%, dipotassium hydrogen phosphate 0.04%, sodium chloride 0.8%, magnesium sulfate 0.08%, medium Adjust the pH to 7.0, sterilize with damp heat at 115°C for 30 minutes, and incubate at 30°C for 14 hours after inoculation.

[0055] 3) The raw materials and dosage of the fermentation medium used are: glucose 1.5%, soybean meal 1.5%, corn steep liquor 2%, yeast powder 2%, peptone 3%, dipotassium hydrogen phosphate 0.03%, magnesium sulfate 0.2%, manganese sulfate 0.002% , calcium carbonate 0.3%, medium pH 7.0; 115 ℃ damp heat sterilization for 30 minutes, 32 ℃ cu...

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PUM

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Abstract

The invention relates to a process for preparing a viable bacillus firmus preparation. According to the process, after bacillus firmus undergoes first-stage germ amplification culture and second-stage germ amplification culture, the bacillus firmus 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 firmus product, of which the CFU of powder per gram is not less than 1.0*10<11>, 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 firmus preparation. Background technique [0002] Bacillus firmus (Bacillus firmus) is a saprophytic gram-positive bacterium that exists widely in soil, water, plant surfaces and other natural environments, is easy to obtain, has endogenous spores, strong resistance to stress, and rapid reproduction , Simple nutritional requirements, safe for crops and the environment, can produce a variety of antibacterial substances, and have strong inhibitory effects on many fungi and nematodes. [0003] At present, domestic manufacturers have produced Bacillus firmus products, but the quality of related products is generally not high. At present, the common production method of Bacillus firmus preparations is to use related Bacillus firmus production strains, ferment and cultivate them in batches, and when most or all of them form spores, concentrate them by plate-and-frame filtration or centrifugat...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/20C12R1/07
Inventor 廖先清饶犇周荣华陈伟刘芳张先进江爱兵张光阳杨自文
Owner HUBEI BIOPESTICIDE ENG RES CENT
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