Method for separation and purification of D-lactic acid from D-ammonium lactate fermentation broth
A technology for separation, purification and fermentation liquid, applied in the field of biological engineering, can solve the problems of low product quality, long process route, many unit operations, etc., and achieve the effects of high product quality, low operating energy consumption, and no waste liquid pollution.
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Embodiment 1
[0039] The preparation of D-ammonium lactate fermented liquid is as follows:
[0040] (1) Plate culture: Bacillus BS1-5 was inoculated into the plate medium for anaerobic culture, the culture temperature was 30°C, and the culture time was 48 hours;
[0041] (2) Seed culture: Inoculate the bacillus cultured on the plate in step (1) into the seed medium for anaerobic culture, the culture temperature is 30° C., and the culture time is 24 hours;
[0042] (3) Fermentation acid production: inoculate the seed culture solution obtained in step (2) into the fermentation medium to carry out fermentation acid production, the inoculum size is 15%, the fermentation temperature is 30 ° C, and nitrogen is fed to maintain its anaerobic environment. The neutralizer controls the pH of the fermentation system at 6.0.
[0043] The composition of the above-mentioned plate medium is (g / L): 10 glucose, 1 yeast extract, 1 anhydrous sodium acetate, 0.1 anhydrous magnesium sulfate, 1 potassium dihydro...
Embodiment 2
[0048] (1) Plate culture: Inoculate Bacillus BS1-5 into plate medium for anaerobic culture, culture temperature is 45°C, culture time is 20h;
[0049] (2) Seed culture: Inoculate the bacillus cultured on the plate in step (1) into the seed medium for anaerobic culture, the culture temperature is 45° C., and the culture time is 12 hours;
[0050] (3) Fermentation acid production: inoculate the seed culture liquid obtained in step (2) into the fermentation medium to carry out fermentation acid production, the inoculum size is 3%, the fermentation temperature is 45°C, feed nitrogen to maintain its anaerobic environment, adopt The neutralizer controls the pH of the fermentation system at 7.0.
[0051] The composition of the above-mentioned plate medium is (g / L): 30 glucose, 3 yeast extract, 4 anhydrous sodium acetate, 0.4 anhydrous magnesium sulfate, 3 potassium dihydrogen phosphate, and 25 agar.
[0052] The above-mentioned seed medium composition is (g / L): glucose 40, yeast ext...
Embodiment 3
[0056] (1) Plate culture: inoculate Bacillus BS1-5 into plate medium for anaerobic culture, culture temperature is 37°C, culture time is 24h;
[0057] (2) Seed culture: Inoculate the bacillus cultured on the plate in step (1) into the seed medium for anaerobic culture, the culture temperature is 37°C, and the culture time is 20h;
[0058] (3) Acid production by fermentation: Inoculate the seed culture solution obtained in step (2) into the fermentation medium to produce acid by fermentation, the inoculum size is 10%, the fermentation temperature is 37° C., and nitrogen is fed to maintain its anaerobic environment. The neutralizer controls the pH of the fermentation system at 6.5.
[0059] The composition of the above-mentioned plate medium is (g / L): 20 glucose, 2 yeast extract, 2 anhydrous sodium acetate, 0.3 anhydrous magnesium sulfate, 2 potassium dihydrogen phosphate, and 20 agar.
[0060] The composition of the above seed medium is (g / L): 20 glucose, 2 yeast extract, 2 pe...
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