Preparation method of high-purity stachyose
A stachyose and high-purity technology, applied in the field of high-purity stachyose preparation, can solve problems such as difficulty in finding and extracting high-purity stachyose, and achieve the effects of obvious competitive advantages, high purity and complete technology
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Embodiment 1
[0026] S1) After washing the fresh caddis worm, bake it at 70°C for 2 hours, then lower the temperature and keep it at 50°C for 24 hours to obtain the dried caddis worm;
[0027] S2) Add water three times the weight of the dried cadaveric product to the dried cadaveric product obtained in S1, extract at 80°C for 20 min, crush the caddis worm, continue leaching for 2 hours, and then filter to obtain the first Filtrate and first filter residue;
[0028] S3) in the first filtrate that S2 makes, add the yeast extract of first filtrate weight 0.2%, the casein of 0.2%, the K of 0.04% 2 HPO 4 and 0.03% calcium carbonate, and cooled to room temperature after high-temperature sterilization to obtain a culture solution;
[0029] S4) Add 1% Aspergillus suspension and 0.1% lactic acid bacteria to the culture solution prepared by S3, wherein the concentration of spores in the Aspergillus suspension is about 160 million / mL. After culturing for 40 hours, heat up to 80°C to inactivate the ...
Embodiment 2
[0037] S1) After washing the fresh caddis worm, bake it at 73°C for 2.5 hours, then lower the temperature and keep it at 53°C for 26 hours to obtain the dried caddis worm;
[0038] S2) Add water 4 times the weight of the dried caddis to the dried caddis produced in S1, extract at 90°C for 25 minutes, crush the caddis, continue to extract for 2.5 hours, and then filter to obtain the first a filtrate and a first filter residue;
[0039] S3) in the first filtrate that S2 makes, add the yeast extract of first filtrate weight 0.4%, the casein peptone of 0.3%, the K of 0.07% 2 HPO 4 and 0.09% calcium carbonate, and cooled to room temperature after high-temperature sterilization to obtain a culture solution;
[0040] S4) Add 2% Aspergillus suspension and 0.3% lactic acid bacteria to the culture solution prepared by S3, wherein the concentration of spores in the Aspergillus suspension is about 170 million / mL. After culturing for 45 hours, heat up to 90°C to inactivate the enzyme fo...
Embodiment 3
[0048] S1) After washing the fresh caddis worm, bake it at 75°C for 3 hours, then lower the temperature and keep it at 55°C for another 30 hours to obtain the dried caddis worm;
[0049] S2) Add water 5 times the weight of the dried cadaveric product to the dried cadaveric product obtained in S1, and extract at 100°C for 30 minutes, crush the cadaveric worm, continue leaching for 3 hours, and then filter to obtain the first Filtrate and first filter residue;
[0050] S3) in the first filtrate that S2 makes, add the yeast extract of first filtrate weight 0.6%, the casein peptone of 0.4%, the K of 0.1% 2 HPO 4 and 0.15% calcium carbonate, and cooled to room temperature after high-temperature sterilization to obtain a culture solution;
[0051] S4) Add 3% Aspergillus suspension and 0.4% lactic acid bacteria by weight to the culture solution prepared in S3, wherein the concentration of spores in the Aspergillus suspension is 180 million / mL, and stand at a constant temperature at...
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