Preparation method of antialcoholism product
A product and inoculum technology, applied in microorganism-based methods, biochemical equipment and methods, functions of food ingredients, etc., can solve problems such as high cost and reduce cost, achieve less retention, improve metabolism, and sweetness. Moderate effect
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Embodiment 1
[0037] 1) Strain cultivation: Inoculate Saccharomyces cerevisiae strains into a fermenter with strain medium, the liquid volume is 10%, the inoculum volume is 7%, the air volume is 1:0.6, pH 7, and the rotation speed is 200 rpm / min. The culture temperature was 28 ℃, cultured for 16 h, and the strain culture solution was obtained;
[0038] 2) Centrifuge the strain culture solution prepared in step 1), discard the supernatant to obtain a precipitate, wash twice with 0.066 mol / L disodium hydrogen phosphate buffer, keep the bacterial cells, add 5% 50 mM Tris -Cl (pH 8.0), 0.2 % 1 mM EDTA, 2 % 100 mM NaCl buffer solution, use Constant high-pressure cell disruptor to disrupt cells to obtain a solution containing alcohol dehydrogenase and acetaldehyde dehydrogenase;
[0039] 3) Preparation of corn husk enzymatic hydrolysis solution: After crushing corn husks, pass through a 60-mesh sieve, add purified water at a weight ratio of 1:8, adjust the pH value to 6.0, and stir at 120 rpm / min...
Embodiment 2
[0051] 1) Strain cultivation: Inoculate Saccharomyces cerevisiae strains into a fermenter with strain medium, the liquid volume is 10%, the inoculum volume is 7%, the air volume is 1:0.6, pH 7, and the rotation speed is 200 rpm / min. The culture temperature was 30 ℃, cultured for 16 h, and the strain culture solution was obtained;
[0052] 2) Centrifuge the strain culture solution prepared in step 1), discard the supernatant to obtain a precipitate, wash with 0.066 mol / L disodium hydrogen phosphate buffer 3 times, keep the bacterial cells, add 5% 50 mM Tris -Cl (pH 8.0), 0.2 % 1 mM EDTA, 2 % 100 mM NaCl buffer solution, use Constant high-pressure cell disruptor to disrupt cells to obtain a solution containing alcohol dehydrogenase and acetaldehyde dehydrogenase;
[0053] 3) Preparation of corn husk enzymatic hydrolysis solution: After crushing corn husks, pass through a 60-mesh sieve, add purified water at a weight ratio of 1:3, adjust the pH value to 5.0, and stir at 50 rpm / mi...
Embodiment 3
[0065] 1) Strain cultivation: Inoculate Saccharomyces cerevisiae strains into a fermenter with strain medium, the liquid volume is 10%, the inoculum volume is 7%, the air volume is 1:0.6, pH 7, and the rotation speed is 200 rpm / min. The culture temperature was 29 ℃, cultured for 16 h, and the strain culture solution was obtained;
[0066] 2) Centrifuge the strain culture solution prepared in step 1), discard the supernatant to obtain a precipitate, wash twice with 0.066 mol / L disodium hydrogen phosphate buffer, keep the bacterial cells, add 5% 50 mM Tris -Cl (pH 8.0), 0.2 % 1 mM EDTA, 2 % 100 mM NaCl buffer solution, use a constant high-pressure cell disruptor to disrupt cells to obtain a solution containing alcohol dehydrogenase and acetaldehyde dehydrogenase;
[0067] 3) Preparation of corn husk enzymatic hydrolysis solution: After crushing corn husks, pass through a 60-mesh sieve, add purified water at a weight ratio of 1:12, adjust the pH value to 5.5, stir at 80 rpm / min, ...
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