Method for mutagenizing micro algae to generate docosahexaenoic acid by use of ion beam bioengineering
A technology for the yield of docosahexaenoic acid and docosahexaenoic acid, which is applied in the field of bioengineering, can solve the problems of unfavorable downstream separation and purification, complicated autotrophic culture equipment, and low concentration of active ingredients, and achieves Good economic and social benefits, wide application range, cheap fermentation raw materials
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Embodiment 1
[0011] A method for producing docosahexaenoic acid by using ion beam bioengineering to induce microalgae to produce docosahexaenoic acid, comprising the steps of:
[0012] 1) Chemical mutagenesis: choose Cryptidinosa as the starting algae species, cultivate it on a slope according to the conventional method, cultivate the inoculum bottle in a culture room at 25°C, and dilute the microalgae in the seed solution cultivated for about three days with artificial seawater solution, The dilution is controlled within 100 times. Then the diluted microalgae suspension obtained is mixed with the chemical mutagen solution nitrosoguanidine solution in a specific ratio. Below 25°C, treat for 20 minutes; then centrifuge in a centrifuge for 5 minutes, discard the supernatant, and then add artificial seawater.
[0013] Wherein, the concentration of the nitrosoguanidine solution used in the present invention is 0.1 g / L, and the volume ratio of the chemical mutagen to the microalgae suspension ...
Embodiment 2
[0017] A method for producing docosahexaenoic acid by using ion beam bioengineering to induce microalgae to produce docosahexaenoic acid, comprising the steps of:
[0018] 1) Chemical mutagenesis: choose Cryptidinosa as the starting algae species, cultivate it on a slope according to the conventional method, cultivate the inoculum bottle in a culture room at 25°C, and dilute the microalgae in the seed solution cultivated for about three days with artificial seawater solution, The dilution is controlled within 100 times. Then the diluted microalgae suspension obtained is mixed with the chemical mutagen solution nitrosoguanidine solution in a specific ratio. Below 27°C, treat for 25 minutes; then centrifuge in a centrifuge for 5 minutes, discard the supernatant, and then add artificial seawater.
[0019] Wherein, the concentration of the nitrosoguanidine solution used in the present invention is 0.2 g / L, and the volume ratio of the chemical mutagen to the microalgae suspension ...
Embodiment 3
[0023] A method for producing docosahexaenoic acid by using ion beam bioengineering to induce microalgae to produce docosahexaenoic acid, comprising the steps of:
[0024] 1) Chemical mutagenesis: choose Cryptidinosa as the starting algae species, cultivate it on a slope according to the conventional method, cultivate the inoculum bottle in a culture room at 25°C, and dilute the microalgae in the seed solution cultivated for about three days with artificial seawater solution, The dilution is controlled within 100 times. Then the diluted microalgae suspension obtained is mixed with the chemical mutagen solution nitrosoguanidine solution in a specific ratio. Below 30°C, treat for 30 minutes; then centrifuge in a centrifuge for 5 minutes, discard the supernatant, and then add artificial seawater.
[0025] Wherein, the concentration of the nitrosoguanidine solution used in the present invention is 0.3 g / L, and the volume ratio of the chemical mutagen to the microalgae suspension ...
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