Method for producing lipid through mixed culture of microalgae
A mixed culture and microalgae technology, which is applied in the field of biotechnology and bioenergy, can solve the problems of low efficiency, achieve high carbon sequestration efficiency, alleviate the greenhouse effect and exhaust pollution problems, and achieve the effects of high biomass and oil content
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Embodiment 1
[0017] The preparation of embodiment 1 microalgae seed liquid
[0018] BG11 medium was used for microalgae culture, and the formulation of the medium was shown in Table 1 and Table 2.
[0019] Table 1BG11 medium
[0020]
[0021] * Composition of A5+Cosolution in Table 2 and Table 1
[0022]
[0023] First prepare the BG11 liquid medium according to Table 1 and Table 2, adjust the pH of the medium for cultivating Scenedesmus obliquus FSH-Y2 to 10, adjust the pH of the medium for cultivating Monostipella SS-B1 to 7.5, and then Scenedesmus obliquus FSH-Y2 and Single needle sp. SS-B1 were inoculated in the above medium respectively. Cultivate in a constant temperature light shaker, the culture temperature is 25°C, the light cycle is 24h, the light-dark time ratio is 14:10, the light intensity is 5000Lux, 120rpm shaking culture to the logarithmic growth phase, and Scenedesmus obliquus FSH-Y2 is obtained Seed solution and Monostipella SS-B1 seed solution, the above seed so...
Embodiment 2
[0024] The preparation of embodiment 2 microalgae oil
[0025] (1) In the photobioreactor, add the FSH-Y2 seed solution prepared in Example 1 and the microalgae medium, the volume ratio of the FSH-Y2 seed solution to the medium is 1:10, and the medium is BG11 medium, The pH value of the culture medium was controlled at 10, the light intensity of the culture was 5000Lux, the light cycle was 24h, the light-dark time ratio was 14:10, and a mixed gas of nitrogen and carbon dioxide was introduced, and the carbon dioxide content was 5v%.
[0026](2) After culturing for 2 days, insert the seed solution of Monospina SS-B1 prepared in Example 1, the volume ratio of the seed solution to the medium is 1:10, the pH of the medium is controlled at 8, and nitrogen and carbon dioxide are introduced into the solution. Mixed gas, where CO 2 The content is 30v%.
[0027] (3) After cultivating for 7 days, enter the stable period, end the culturing, harvest the microalgae cells by centrifugation...
Embodiment 3
[0028] The preparation of embodiment 3 microalgae oil
[0029] (1) In the photobioreactor, add the FSH-Y2 seed solution prepared in Example 1 and the microalgae medium, the volume ratio of the FSH-Y2 seed solution to the medium is 1:5, and the medium is BG11 medium, The pH value of the culture medium was controlled at 12, the light intensity of the culture was 5000Lux, the light cycle was 24h, the light-dark time ratio was 14:10, and a mixed gas of nitrogen and carbon dioxide was introduced, and the carbon dioxide content was 5v%.
[0030] (2) After culturing for 3 days, insert the seed solution of Monospina SS-B1 prepared in Example 1, the volume ratio of the seed solution to the medium is 1:10, the pH of the medium is controlled at 10, and nitrogen and carbon dioxide are introduced into the solution. Mixed gas, where CO 2 The content is 25v%.
[0031] (3) After cultivating for 7 days, enter the stable period, end the culturing, harvest the microalgae cells by centrifugatio...
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