Method for extracting selenocystine and selenomethionine from polyselenium plant Camelina officinalis
A technology of selenocystine and selenomethionine, which is applied in food science, metabolic diseases, drug combination and other directions, can solve problems such as waste of resources, and achieve the effects of high product extraction rate, wide application and simple technical process
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Embodiment 1
[0051] The present invention is a method for extracting selenocystine and selenomethionine from the broken rice chestnut of the selenium-accumulating plant. Water, ultrasonic for 60min, filtered, the filter residue was extracted twice with water, the residue was washed, the filtrate was combined, and the volume was adjusted to 200mL, and detected by HPLC-HG-AGS, the chromatographic conditions were: anion exchange column, A mobile phase 40mM, B mobile phase 60mM (Adjust pH value to 6.0 with formic acid), flow rate 1.0mL / min, adopt 0min~3min: 100%A; 3min~4min: 100%A→100%B; 4min~10min: 100%B; 10min~12.5min: Gradient elution of 100% A, selenocystine retention time is 2.42±0.25min, selenocystine content in the extract is 952.25mg / kg; use high-pressure preparation system to separate, the conditions are the same as the above chromatography, collect 2. For the solution between 10 and 2.70 minutes, put the eluate into a cellulose ester dialysis bag with a molecular weight cut-off of 10...
Embodiment 2
[0053] The present invention is a method for extracting selenocystine and selenomethionine from the selenium-accumulating plant Broken Camelina. The LHCl solution was shaken at 60°C for 90 minutes, the filter residue was extracted twice with water, the residue was washed, the filtrate was combined, the pH value was adjusted to 6-7 with NaOH solution, and the volume was adjusted to 200mL. The selenium in the extract was detected by HPLC-HG-AGS. The content of cysteine is 747.00mg / kg, and the content of selenomethionine is 216.34mg / kg. It is separated by a high-pressure preparation system, and the conditions are the same as the above chromatography. The selenocystine solution and 3. The selenomethionine solution between 10 and 3.70 minutes was weighed after dialysis and freeze-drying, respectively 5.35mg and 1.88mg, and the purity was 98.4% and 98.8%, respectively.
Embodiment 3
[0055] The present invention is a method for extracting selenocystine and selenomethionine from the selenium-accumulating plant cinnamon, the specific steps are as follows: Weigh 10 g of the selva sample with a selenium content of 2158.97 mg / kg, add 50mL1mol / L HCl, Ultrasonic extraction for 60 min, the filter residue was extracted twice again, the residue was washed, the filtrate was combined, the pH value was adjusted to 6-7 with NaOH solution, and the volume was adjusted to 200mL. The content of selenocystine in the extract was detected by HPLC-HG-AGS. 763.56mg / kg, the content of selenomethionine is 223.16mg / kg, separated by high-pressure preparation system, the conditions are the same as the above chromatographic conditions, selenocystine solution and selenomethionine solution are collected in sections, dialyzed, freeze-dried, weighed, They were 6.18mg and 1.95mg respectively, and the purity was 98.5% and 98.6%.
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