Preparation method of natural spice 2-phenethyl alcohol
A technology of natural fragrance and phenethyl alcohol, applied in microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problem that the product separation cannot be separated by an adsorption chromatography organic solvent extraction and separation method, destroy the aroma quality of 2-phenethyl alcohol, Difficulty in product separation process and other problems, to achieve the effect of overcoming poisoning and inhibition, reducing industrial operation procedures, and having broad application prospects
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Embodiment 1
[0030] The yeast in Example 1 of the present invention is Candida krusei (krusei Candida) preserved in the China Industrial Microorganism Culture Collection Management Center, with a preservation number of CICC 1674. The yeast culture temperature is 28-30°C, and it is a high-temperature aroma-producing yeast. .
[0031] Seed medium: glucose 15g / L, bean sprouts juice 4g / L, peptone 5g / L, yeast extract 3g / L, K 2 HPO 4 .3H 2 O 0.75g / L, the solvent is water, the pH is natural, and sterilized by high-pressure steam at 121°C for 20min. After the seed medium was cooled to 28°C, Candida krusei CICC 1674 was inoculated on the seed medium, cultured on a shaking table for 24 hours, the rotating speed of the shaking table was 150r / min, and the inoculation amount of the seed liquid inoculated to the fermentation medium was 5% by volume.
[0032] Fermentation shake flask medium: glucose 30g / L, peptone 5g / L, yeast extract 6g / L, K 2 HPO 4 .3H 2 O 0.75g / L, MgSO4.7H 2 O 0.5g / L, NH 4 Cl ...
Embodiment 2
[0037] The yeast in Example 2 of the present invention is Candida krusei (krusei Candida) preserved in the China Industrial Microorganism Culture Preservation Management Center with the preservation number CICC 1674. The yeast culture temperature is 28-30°C, and it is a high-temperature aroma-producing yeast. .
[0038] Seed medium: glucose 15g / L, wort juice 3g / L, peptone 5g / L, yeast extract 3g / L, K 2 HPO 4 .3H 2 O 0.75g / L, the solvent is water, the pH is natural, and sterilized by high-pressure steam at 121°C for 20min. After the seed medium was cooled to 28°C, Candida krusei CICC 1674 was inoculated on the seed medium, cultured on a shaking table for 24 hours, the rotating speed of the shaking table was 150r / min, and the inoculation amount of the seed liquid inoculated to the fermentation medium was 5% by volume.
[0039] Fermentation shake flask medium: glucose 30g / L, peptone 3g / L, yeast extract 8g / L, K 2 HPO 4 .3H 2 O 0.75g / L, MgSO4.7H 2 O 0.5g / L, NH 4 Cl 0.3g / L, ...
Embodiment 3
[0044] The saccharomyces selected in Example 3 of the present invention is Saccharomyces cerevisiae, which is preserved in China Industrial Microbiological Strain Preservation Management Center, with the preservation number CICC 1394. fragrant).
[0045] Seed medium: glucose 10g / L, bean sprout juice 5g / L, peptone 4g / L, yeast extract 3g / L, K 2 HPO 4 .3H 2 O 0.75g / L, the solvent is water, the pH is natural, and sterilized by high-pressure steam at 121°C for 20min. After the seed medium was cooled to 28°C, Saccharomyces cerevisiae CICC 1394 was inoculated on the seed medium, cultured on a shaking table for 24 hours, the rotating speed of the shaking table was 150r / min, and the inoculation amount of the seed liquid inoculated into the fermentation medium was calculated as 5%.
[0046] Fermentation shake flask medium: glucose 30g / L, peptone 3g / L, yeast extract 8g / L, K 2 HPO 4 .3H 2 O 0.75g / L, MgSO4.7H 2 O 0.5g / L, NH 4 Cl 0.3g / L, solvent is water, pH is natural, sterilized ...
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