Preparation method of Gamma-aminobutyric acid
A technology of aminobutyric acid and seeds, applied in the field of preparation of γ-aminobutyric acid, can solve the problems of severe reaction conditions, potential safety hazards, difficult application, etc., so as to reduce environmental pollution, protect the environment, and avoid the use of corrosive solvents Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0043] The preparation process of the corn cob hydrolyzate adopted in the present embodiment is:
[0044] 1) Acid hydrolysis of corncobs: hydrolyzing corncobs in a sulfuric acid solution with a concentration of 5% by volume to obtain an acidolysis solution, the hydrolysis temperature is 200°C, and the hydrolysis time is 300 minutes;
[0045] 2) Solid-liquid separation: solid-liquid separation of the acid hydrolysis solution to obtain the first sugar solution rich in xylose and corn cob acid hydrolysis slag;
[0046] 3) Enzymatic hydrolysis of acid hydrolysis residue: use one or more of cellulase, xylanase or cellobiase to enzymatically hydrolyze the acid hydrolysis residue of corncobs to obtain an enzymatic hydrolysis solution; the enzyme dosage is: Gram acid hydrolysis residue 50PFIU cellulase, 30IU cellobiase, 200PFIU xylanase; during the enzymolysis process, the pH is controlled at 7.0, the temperature is 60°C, and the enzymolysis time is 240 hours;
[0047] 4) Solid-liqui...
Embodiment 2
[0055] The γ-aminobutyric acid preparation process of the present embodiment is as follows:
[0056] First, the γ-aminobutyric acid production strain Lactobacillus brevis CGMCC NO.1306 (Lactobacillus brevis CGMCC NO.1306) was connected to the hydrolyzate containing 20% of corncob, 0.4% of yeast extract, 0.8% of peptone, 0.3% of corn steep liquor, and 2% of agar cultured at 30°C for 26 hours.
[0057] Then adopt plate cultured gamma-aminobutyric acid to inoculate one loop into the liquid seed medium containing 25% of corncob hydrolyzate, 0.4% of yeast extract, 0.8% of peptone, and 0.2% of corn steep liquor for cultivation, pH is controlled at 5.2, shaker Cultivate for 20 hours, the rotation speed of the shaker is 220 rpm, and the culture temperature is 33°C.
[0058] After the shake flask seeds are cultivated, inoculate them into the liquid seed medium of the seed tank containing 30% corn cob hydrolyzate, 0.3% yeast extract, 0.5% peptone, and 0.2% corn steep liquor for venti...
Embodiment 3
[0062] The γ-aminobutyric acid preparation process of the present embodiment is as follows:
[0063] First, the γ-aminobutyric acid production strain Lactobacillus brevis CGMCC NO.1306 (Lactobacillus brevis CGMCC NO.1306) was connected to the corncob hydrolyzate containing 25%, yeast extract 0.3%, peptone 0.8%, corn steep liquor 0.3%, agar 2% cultured at 30°C for 18 hours.
[0064] Then adopt plate cultured gamma-aminobutyric acid to inoculate one loop into the liquid seed medium containing 20% of corn cob hydrolyzate, 0.3% of yeast extract, 0.7% of peptone, and 0.4% of corn steep liquor for cultivation, pH is controlled at 5.5, shaker Cultivate for 24 hours, the rotation speed of the shaker is 180 rpm, and the culture temperature is 30°C.
[0065] After the shake flask seeds have been cultivated, inoculate them into the liquid seed medium of the seed tank containing 25% corncob hydrolyzate, 0.2% yeast extract, 0.5% peptone, and 0.2% corn steep liquor for ventilated culture...
PUM
Property | Measurement | Unit |
---|---|---|
recovery rate | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information

- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com