Biological preparation method of all-trans free astaxanthin
A technology for biological preparation and astaxanthin, applied in organic chemical methods, animal feed, animal feed, etc., can solve problems such as being unsuitable for human consumption, and achieve the effects of enhancing bioavailability, improving safety, and increasing application.
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Embodiment 1
[0027] (1) Preparation of astaxanthin nutritious biological raw material: Mix Haematococcus pluvialis algae powder and basal feed evenly in a blender at a mixing ratio of 10:90. After feeding layer hens for 15 days, collect eggs every day.
[0028] (2) Collect poultry eggs and separate egg yolks Pretreatment: Deshell the poultry eggs, separate egg whites and egg yolks with an egg separator, collect egg yolks, take about 30 g of egg yolks and stir evenly for 3 minutes.
[0029] (3) The supernatant liquid was collected for the first protein precipitation: add 150ml of absolute ethanol, and stir and extract for 1 hour. After stirring and extracting, place in a warm water bath at 40° C. for 1 hour, centrifuge in a centrifuge cup at a speed of 3000 rpm for 3 minutes, and collect the supernatant.
[0030] (5) The astaxanthin extract was concentrated under reduced pressure at a vacuum degree of -0.1Mpa, and the solvent was removed. Obtain astaxanthin protein complex extract, such as...
Embodiment 2
[0032] (1) Obtaining astaxanthin poultry eggs: Mix Haematococcus pluvialis non-broken wall algae powder and laying hen basal feed evenly in a blender at a ratio of 10:90, and feed sea laying hens for 20 days, daily Collect eggs.
[0033] (2) Egg yolk collection and pretreatment: shelling the astaxanthin poultry eggs, separating egg whites and egg yolks with an egg separator, collecting egg yolks, putting the egg yolks into a mixing tank for fully stirring.
[0034] (3) Primary protein precipitation: After stirring evenly, add absolute ethanol, stir and extract for 1 hour. After stirring and extracting, extract in a warm water bath at 37°C for 1 hour. After extraction, centrifugation was carried out at a rotational speed of 2000 rpm for 5 minutes, and the supernatant was collected.
[0035] (4) The supernatant obtained in step 3) is subjected to secondary protein precipitation to collect the supernatant: adding hydrochloric acid to the supernatant obtained in step (3) to adju...
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