Method for extracting plukenetia volubilis seed protein
A technology of star oil vine and protein, which is applied in the field of protein extraction from star oil vine seeds, and can solve the problems of little research on protein
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Embodiment 1
[0011] Crush the star oil vine cake, pass through a 100-mesh sieve, degrease with n-hexane for 4 h, and place it in a fume hood for 12 h, and evaporate the solvent to obtain a degreasing powder.
[0012] Weigh 5 g of defatted powder, add 150 ml of sodium hydroxide solution (pH 12), stir magnetically at 50 °C for 120 min, then centrifuge at 4000 r / min for 20 min, repeat the extraction once for the precipitate, and combine the two extractions supernatant. The pH of the above supernatant was adjusted to 3.5 with dilute acid, settled at 4 °C for 10 h, the separated precipitate was filtered and washed three times with distilled water, and finally dried in a freeze dryer to obtain 2.478 g of protein, with an extraction rate of 76.47%.
Embodiment 2
[0014] Crush the star oil vine cake, pass through a 80-mesh sieve, degrease with n-hexane in a fat extractor for 4 hours, and then place it in a fume hood for 12 hours, and evaporate the solvent to obtain a degreased powder.
[0015] Weigh 5 g of defatted powder, add 150 ml of sodium hydroxide solution (pH 9), stir magnetically at 50 °C for 120 min, then centrifuge at 4000 r / min for 20 min, repeat the extraction once for the precipitate, and combine the two extractions supernatant. The pH of the above supernatant was adjusted to 5 with dilute hydrochloric acid, settled at 4 °C for 10 h, the precipitate separated by filtration was washed with distilled water three times, and finally dried in a freeze dryer to obtain 1.812 g of protein, with an extraction rate of 55.92%.
Embodiment 3
[0017] Crush the star oil vine cake, pass through a 60-mesh sieve, degrease with n-hexane in a fat extractor for 4 hours, then place it in a fume hood for 12 hours, and evaporate the solvent to obtain a degreased powder.
[0018] Weigh 5 g of defatted powder, add 150 ml of sodium hydroxide solution (pH 12), stir magnetically at 60 °C for 120 min, then centrifuge at 4000 r / min for 20 min, repeat the extraction once for the precipitate, and combine the two extractions supernatant. The pH of the above supernatant was adjusted to 4 with dilute hydrochloric acid, settled at 4 °C for 10 h, the separated precipitate was filtered and washed with distilled water three times, and finally dried in a freeze dryer to obtain 2.201 g of protein, with an extraction rate of 67.92%.
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