Simple method for culturing haematococcus pluvialis to produce astaxanthin
A technology of Haematococcus pluvialis and astaxanthin, which is applied in the field of cultivating Haematococcus pluvialls to produce astaxanthin, which can solve the problem that the annual output is difficult to exceed 20 tons, the composition of the medium is complicated, the algal cell adhesion and shading, etc. problems, to achieve the effect of easy expansion of production capacity, low cost, and cheap procurement
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Embodiment 1
[0025]Culture solution preparation: select clean fresh water, filter, boil, then cool, add nitrogen and phosphorus-containing nutrient salts to prepare a culture solution with a nitrogen content of 6 mg / L and a phosphorus content of 0.2 mg / L for use. In the present embodiment, also can be in the culture fluid: the content of nitrogen is 2mg / L, and the content of phosphorus is 0.1mg / L; Or the content of nitrogen is 3mg / L, and the content of phosphorus is 0.1mg / L; Or the content of nitrogen is 4mg / L, the phosphorus content is 0.15mg / L; or the nitrogen content is 8mg / L, the phosphorus content is 0.3mg / L; the nitrogen content is 10mg / L, the phosphorus content is 0.4mg / L, etc.; but It is better to have a nitrogen-to-phosphorus weight ratio greater than 25.
Embodiment 2
[0027] The first step is cultivated: in the Erlenmeyer flask of 5000 milliliters, pack the nutrient solution of 3000 milliliters embodiment 1, in aseptic room inoculate Haematococcus pluvialls to the nutrient solution in the conical flask then, make every milliliter of nutrient solution Pluvialls The number of cells of Haematococcus is 1000-6000, and it is better to detect about 3000 / ml. Use soft light, control the light intensity on the surface of the Erlenmeyer flask in the range of 1500Lux-3000Lux, and control the culture temperature at 15°C-25°C. At this time, it is better to control the culture temperature at 16°C to 20°C, and the light hours are controlled at 10 hours to 18 hours for static cultivation. The light hours are preferably about 12 hours, and the cell density of the cultured Haematococcus pluvialis reaches 50,000 to 100,000 per milliliter to obtain primary vegetative growth. It is better to detect about 80,000 per milliliter in the primary vegetative growth, an...
Embodiment 3
[0031] It is basically the same as Example 2, except that in the second step of cultivation, nylon bags are used instead of plastic buckets, and in the third step of cultivation, halogen salts are used instead of mineral salts, and the concentration of halogen salts in the liquid in the pond is 0.3% to 0.5% by weight. %, H 2 o 2 The weight percent concentration is 0.002% to 0.005%, FeCl 2 The weight percent concentration of the nitrogen is 0.006% to 0.008%, and the weight ratio of nitrogen and phosphorus is about 0.1.
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