High-density euglena culture method
A technology for high-density culture and euglena, which is applied in the field of euglena preparation, can solve the problems of slow growth of euglena, inability to become a dominant species, unfavorable scale production, etc. The effect of the production cycle
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Embodiment 1
[0025] The high-density cultivation method of euglena of the present invention comprises the following steps:
[0026] The first step is to expand the algae species. Prepare the euglena concomitant culture medium in a 5.0L Erlenmeyer flask, and sterilize it in an autoclave at 121°C for 20 minutes. Then inoculate the algal species in the seed bottle into the above-mentioned sterilized and cooled medium, and the inoculation amount of the euglena algae species expansion is 10%. Shake the flask every 4 hours for the expansion of algae, and irradiate with an artificial LED light source at a light intensity of 2500 lx, and cultivate for 3 days. The formula of euglena adjunct culture medium contains: 1.0g of peptone, 0.9g of yeast powder, 0.05g of potassium dihydrogen phosphate, 0.1g of magnesium sulfate, 0.06g of calcium chloride, 1mL of Fe-EDTA mother solution, and trace amount in each liter of medium. Element mother solution 1mL and vitamin mother solution 1mL, control pH to 6; ...
Embodiment 2
[0031] The difference from Example 1 is that in the second step, an artificial LED light source is used to irradiate with a light intensity of 3000lx; the aeration ratio is 1:1v / vm, the carbon dioxide content accounts for 1%, and the culture is cultivated for 3 days.
[0032] According to biochemical testing, the concentration of euglena cells prepared in this example is 2.4 million / mL.
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