Production method and application of high-yield gamma-aminobutyric acid
An aminobutyric acid, high-yield technology, applied in the fields of medical biology and food engineering, can solve the problems of chemical synthesis method with many by-products, unsuitable for industrial production, low GABA content, etc., and achieves improvement of brain function, good social and economic benefits, The effect of improving liver function
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Embodiment 1
[0045] Obtaining of Enterococcus raffinose strain M1 (CGMCC No.5584)
[0046] (1) Preliminary screening of the strains: from pickled cabbage soups naturally pickled in 12 regions in the three provinces of Northeast my country, using double-layer plate method, that is, containing 1% calcium carbonate and sodium glutamate, cultured at 30°C for 48 hours, and selected at high temperature. The colony with a transparent circle grown on a sodium glutamate plate with a high concentration was fermented statically. The fermentation temperature was 30°C and the fermentation time was 3 days. The content of GABA was detected by high-performance liquid chromatography, and a cotton seed with a yield of 16.95g / L was screened out. Enterococcus saccharomyces, numbered M3, was transferred on a slant and stored in a refrigerator at 4°C;
[0047] (2) Re-screening of strains: double-layer plate method is also used for re-screening, and M3 is picked from two rings from the slope to the seed medium, wh...
Embodiment 2
[0053] Production of GABA by Enterococcus raffinose strain M1 (CGMCC No.5584)
[0054] will activate the Entercoccus raffinosus CGMCC No.5584 strain was inoculated in the seed medium and the activation steps were as follows: pick two rings of M1 from the slope into the seed medium, wherein the seed medium (g / L): 10 sucrose, 10 peptone, yeast extract powder 5. Ammonium citrate 2, magnesium sulfate 0.58, manganese sulfate 0.25, sodium acetate 2, potassium dihydrogen phosphate 2;, culture at 30°C for 24 hours, and transfer to the fermentation medium when the amount of bacteria reaches the fermentation conditions.
[0055] Seed medium (g / L) and cultivation method: 10 sucrose, 10 peptone, 5 yeast extract powder, 2 ammonium citrate, 0.58 magnesium sulfate, 0.25 manganese sulfate, 2 sodium acetate, and 2 potassium dihydrogen phosphate. Seed culture conditions: 30 ° C incubator, static culture for 12 hours. According to the inoculation amount of 10-15%, it is inserted into a 10L fe...
Embodiment 3
[0058] Production of GABA by Enterococcus raffinose strain M1 (CGMCC No.5584)
[0059] will activate the Entercoccus raffinosus The CGMCC No.5584 strain was inoculated in the seed medium for cultivation, and was transferred to the fermentation medium when the bacterial mass reached the fermentation conditions.
[0060] Seed medium (g / L) and cultivation method: 10 sucrose, 10 peptone, 5 yeast extract powder, 2 ammonium citrate, 0.58 magnesium sulfate, 0.25 manganese sulfate, 2 sodium acetate, and 2 potassium dihydrogen phosphate. Seed culture conditions: 30 ° C incubator, static culture for 12 hours. According to the inoculation amount of 10-15%, it is inserted into a 10L fermenter.
[0061] Fermentation medium (g / L) and culture method: sucrose 20, yeast extract powder 15, sodium acetate 2, potassium phosphate 2, aluminum sulfate 0.3, magnesium sulfate 0.4, ammonium sulfate 0.2, Tween 80 0.2mL. The culture temperature of the fermenter was controlled at 30°C and the initial ...
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