Overcompensation cultural method improving content of proteins of heterotrophic microalgae
A technology of protein content and culture method, which is applied in the cultivation of chlorella and increases the protein production of chlorella, can solve the problem of low protein content of heterotrophic chlorella, and achieves favorable conditions for growth and protein accumulation and mild conditions , The effect of simple process
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Embodiment 1
[0039] the solid BG11 + Chlorella on plate medium was inoculated into sterilized BG11 + In the liquid culture medium, 25 ℃, 180rpm, culture 3 days, serve as primary seed liquid.
[0040] Inoculate the sterilized BG11 with a 10% (V / V) inoculum of the primary seed liquid + In liquid culture medium, cultured for 3 days, as the secondary seed solution. The culture conditions are the same as the seed solution.
[0041] The secondary seed solution was inoculated with 10% (V / V) inoculum in sterilized low nitrogen concentration of 3 mmol L -1 BG11 + medium. The culture conditions were as follows: temperature 25°C, shaker speed 180 rpm.
[0042] When Chlorella grows to the end of the exponential phase, that is, on the 3rd day of the culture process, the algae cells are collected by centrifugation at 4000rpm for 8 min under aseptic conditions.
[0043] Immediately resuspend the algal cells in an equal volume of fresh sterilized 18 mmol L -1 Continue culturing at 25°C in high nit...
Embodiment 2
[0047] the solid BG11 + Chlorella on plate medium was inoculated into sterilized BG11 + In the liquid culture medium, 25 ℃, 180rpm, culture 3 days, serve as primary seed liquid.
[0048] Inoculate the sterilized BG11 with a 10% (V / V) inoculum of the primary seed liquid + In liquid culture medium, cultured for 3 days, as the secondary seed solution. The culture conditions are the same as the seed solution.
[0049] The secondary seed solution was inoculated with 10% (V / V) inoculum in sterilized low nitrogen concentration of 3mmol L -1 BG11 + medium. The culture conditions were as follows: temperature 25°C, shaker speed 180 rpm.
[0050] When Chlorella grows to the end of the exponential phase, that is, on the 3rd day of the culture process, the algae cells are collected by centrifugation at 4500 rpm for 5 min under aseptic conditions.
[0051] Immediately resuspend the algal cells in an equal volume of fresh sterilized 15 mmol L -1 Continue culturing at 25°C in high nit...
Embodiment 3
[0055] The solid BG11 + Chlorella on plate medium was inoculated into sterilized BG11 + In the liquid culture medium, 25 ℃, 180rpm, culture 3 days, serve as primary seed liquid.
[0056] Inoculate the sterilized BG11 with a 10% (V / V) inoculum of the primary seed liquid + In liquid culture medium, cultured for 3 days, as the secondary seed solution. The culture conditions are the same as the seed solution.
[0057] The secondary seed solution was inoculated with 10% (V / V) inoculum in sterilized low nitrogen concentration of 3mmol L -1 BG11 + medium. The culture conditions were as follows: temperature 25°C, shaker speed 180 rpm.
[0058] When Chlorella grows to the end of the exponential phase, that is, on the 3rd day of the culture process, the algae cells are collected by centrifugation at 4500 rpm for 5 min under aseptic conditions.
[0059] Immediately resuspend the algal cells in an equal volume of fresh sterilized 12 mmol L -1 Continue culturing at 25°C in high nit...
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