Method for separating and extracting D-lactic acid from D-sodium lactate fermentation broth
A fermented liquid and sodium lactate technology, which is applied in the direction of microorganism-based methods, separation/purification of carboxylic acid compounds, fermentation, etc., can solve the problems of many unit operations, long process routes, and low product quality, and achieve low operating energy consumption, No waste liquid pollution, high product quality effect
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Embodiment 1
[0038] The preparation method of D-sodium lactate fermented liquid comprises the following steps that are connected in sequence:
[0039] (1) Plate culture: Inoculate Bacillus BS1-5 into plate medium for anaerobic culture, culture temperature 30°C, culture time 48h;
[0040] (2) Seed cultivation: inoculate the bacillus grown on the plate in step (1) into the seed medium for anaerobic cultivation, the cultivation temperature is 30°C, and the cultivation time is 24h;
[0041] (3) fermentation acid production: the seed culture liquid obtained in step (2) is inoculated into the fermentation medium for fermentation acid production, the inoculum size is 15%, the fermentation temperature is 30 ° C, and nitrogen is introduced to maintain its anaerobic environment, using The neutralizer controls the pH of the fermentation system at 6.0.
[0042] The components of the plate medium are (g / L): glucose 10, yeast extract 1, anhydrous sodium acetate 1, anhydrous magnesium sulfate 0.1, potas...
Embodiment 2
[0047] (1) Plate culture: Inoculate Bacillus BS1-5 into plate medium for anaerobic culture, culture temperature 45℃, culture time 20h;
[0048] (2) Seed cultivation: inoculate the bacillus grown on the plate in step (1) into the seed medium for anaerobic cultivation, the cultivation temperature is 45°C, and the cultivation time is 12h;
[0049] (3) fermentation acid production: the seed culture liquid obtained in step (2) is inoculated into the fermentation medium for fermentation acid production, the inoculum size is 3%, the fermentation temperature is 45 ° C, and nitrogen is introduced to maintain its anaerobic environment, using The neutralizer controls the pH of the fermentation system at 7.0.
[0050] The components of the plate medium are (g / L): glucose 30, yeast extract 3, anhydrous sodium acetate 4, anhydrous magnesium sulfate 0.4, potassium dihydrogen phosphate 3, agar 25.
[0051] The components of the seed medium are (g / L): glucose 40, yeast extract 3, peptone 3, a...
Embodiment 3
[0055] (1) Plate culture: Inoculate Bacillus BS1-5 into plate medium for anaerobic culture, culture temperature 37°C, culture time 24h;
[0056] (2) Seed cultivation: inoculate the bacillus grown on the plate in step (1) into the seed medium for anaerobic cultivation, the cultivation temperature is 37°C, and the cultivation time is 20h;
[0057] (3) fermentation acid production: the seed culture liquid obtained in step (2) is inoculated into the fermentation medium for fermentation acid production, the inoculum size is 10%, the fermentation temperature is 37 ° C, and nitrogen is introduced to maintain its anaerobic environment, using The neutralizer controls the pH of the fermentation system at 6.5.
[0058] The components of the plate medium are (g / L): glucose 20, yeast extract 2, anhydrous sodium acetate 2, anhydrous magnesium sulfate 0.3, potassium dihydrogen phosphate 2, agar 20.
[0059] The components of the seed medium are (g / L): glucose 20, yeast extract 2, peptone 2,...
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