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A Bacillus coagulans strain and a liquid fermentation enzyme production method thereof

A technology for Bacillus coagulans and fermentation culture, which is applied in the field of Bacillus coagulans with high production of β-galactosidase and its liquid fermentation, can solve the problems of low activity and lack of β-galactosidase, and achieves easy and convenient process operation. , the effect of reducing production costs and high industrial value

Active Publication Date: 2019-01-15
SHANDONG LONGKETE ENZYME PREPARATION
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, the enzyme activity of β-galactosidase produced by natural enzyme-producing strains is generally low, and the resources of excellent natural strains are scarce. Therefore, it is of great significance to breed new excellent strains with high enzyme production.

Method used

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  • A Bacillus coagulans strain and a liquid fermentation enzyme production method thereof
  • A Bacillus coagulans strain and a liquid fermentation enzyme production method thereof
  • A Bacillus coagulans strain and a liquid fermentation enzyme production method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0055] Example 1 Screening of the starting strain

[0056] (1) Take 2g of soil sample from the breeding base of the dairy farm, add it to a small triangular flask containing 50mL of cooled sterile water, shake it at 200r / min for 20min, then put it in a water bath at 80°C for 10min, and shake it constantly Mix the soil samples in the triangular flask, let it stand for 5 minutes, absorb 100 μL of the supernatant, and gradually dilute to 10 -1 ~10 -9 Concentration, select 10 -3 , 10 -4 , 10 -5 , 10 -6 Concentration coated beef extract peptone plate, cultivated at 37°C for 24h, and continued to cultivate at 30°C for 24h.

[0057] (2) According to the characteristics of the shape, size, surface structure, edge structure, texture, gloss, transparency, color and soluble pigment of the microbial colony, use the inoculation loop to pick out the isolated single colony and move it to the screening culture Base plate, and numbered, 34 ℃ for 48h.

[0058] The screening medium consis...

Embodiment 2

[0064] Mutation breeding of embodiment 2 bacterial strains

[0065] (1) After absorbing and activating the starting strain, collect the bacteria by centrifugation, resuspend the bacteria with 5% glycerol, count with a hemocytometer until the bacterial concentration is 10 7 -10 8 cells / mL, as the starting bacterial suspension.

[0066] (2) Turn on the normal temperature and pressure plasma system, wipe the inside and outside of the operating room with alcohol cotton, and turn on the ultraviolet light for 30 minutes to sterilize. After the sterilization, take 10 μL of the bacterial suspension and spot it on the rough surface of the slide, and transfer the slide to the operating room table with tweezers under sterile conditions. Open the helium gas valve, set the gas flow and mutagenesis time for mutagenesis. The mutagenesis time was set as 90s, 120s, 150s, 180s, 210s respectively. After each mutagenesis, the slides were placed in an EP tube containing 990 μL sterile saline, ...

Embodiment 3

[0078] Example 3 Production of endo-β-galactosidase by liquid fermentation and its extraction and purification

[0079] (1) First-level seed cultivation: put the Bacillus coagulans mutant strain BR-171 into a 500-ml shake flask, with a medium capacity of 100 ml, a rotary shaker at 180 rpm, and a culture temperature of 34-35°C , culture time 11h;

[0080] (2) secondary seed cultivation: the primary seed is inserted into a 500 milliliter secondary seed shake flask according to the inoculum size of 10%, and the cultivation condition is the same as that of the primary seed;

[0081] (3) Tertiary seed cultivation: insert the secondary seeds into a 3000 ml third-stage seed shake flask with 10% inoculum size, 800 ml of culture medium, 100 rpm on a rotary shaker, and a culture temperature of 34-35°C , culture time 11h;

[0082] (4) One-level seed tank cultivation: the three-level seeds are inserted into the first-level seed tank with a total volume of 50L with 3.5% inoculum size, th...

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Abstract

The invention belongs to the technical field of fermentation engineering, in particular to a Bacillus coagulans strain having a high beta-galactosidase yield and a liquid fermentation technique thereof. The strain is a Bacillus coagulans mutant strain BR-171 with an accession number of CGMCC No.14413. The strain can produce the beta-galactosidase stably in a high efficiency. Through deep fermentation in a fermentation tank having a volume of 50 L, and fermentation culture with material supplement for 84 h, the enzyme yield can be 4000 u / ml or above. The optimum pH of the beta-galactosidase produced by the strain is 5.0, and activity can still be 80% or more in a pH range of 2.5-8.5. The pH tolerance of the beta-galactosidase is suitable for most dairy products. The optimum temperature of the beta-galactosidase is 60 DEG C, and the residual activity of the beta-galactosidase can be 88.4 after incubation at 65 DEG C for 2 h, which indicates that the beta-galactosidase has significant heat resistance. The beta-galactosidase has high industrial value in dairy industry.

Description

Technical field: [0001] The invention belongs to the technical field of fermentation engineering, and in particular relates to a bacillus coagulans with high β-galactosidase production and liquid fermentation technology thereof. Background technique: [0002] Bacillus coagulans, a Gram-positive bacterium, belongs to the phylum Firmicutes (or Firmicutes). Bacillus coagulans belongs to the genus Bacillus in taxonomy, the cells are rod-shaped, terminal spores, without flagella, decompose sugars to generate L-lactic acid, and are homolactic acid fermenters. The optimum growth temperature is 45-50°C, and the optimum pH is 6.6-7.0. Bacillus coagulans is a facultative anaerobic bacterium that can grow in both aerobic and anaerobic environments, can adapt to a low-oxygen intestinal environment, has a high tolerance to acid and bile, can carry out lactic acid fermentation, and produces The L-lactic acid can lower the pH value of the intestinal tract, inhibit harmful bacteria, and p...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/20C12N9/38C12R1/07
CPCC12N9/2471C12Y302/01023
Inventor 王兴吉郭庆文王克芬张杰钱娟娟郭庆亮
Owner SHANDONG LONGKETE ENZYME PREPARATION
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