A method for microalgae to start compensatory growth at ice temperature
A technology for compensating growth and microalgae, applied in the direction of microorganism-based methods, methods using microorganisms, biochemical equipment and methods, etc., can solve the problems of high production costs, low breeding efficiency, short breeding period, etc., and achieve industrial production. The effect of low efficiency and low processing cost
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Embodiment 1
[0057] This embodiment is a method of spiral algae ice temperature activation compensation growth, including the following steps:
[0058] 1) Incorporate the jacchite inoculated into a fresh Zhi culture medium at a cultivation concentration of 10 ml / L, cultured for 2 days at 32 ° C, 6000lux, pH = 9, which adapted to a new growth environment. For several days;
[0059] 2) Under Dark Condition, the culture temperature of the spiral algae in which the long-term long-term spiral algae is reduced at a rate of 1 ° C to -5 ° C at a rate of 1 ° C per 36 minutes; and the culture temperature is maintained for 12 h.
[0060] The spirulina cultured in the above step continued to cultivate 4 days at 32 ° C, 6000 lux. The day relative growth rate is detected, and the relative growth rate (OD) 0.210 is measured.
Embodiment 2
[0062] This embodiment is a method of laminating a saline algae ice temperature, including the following steps:
[0063] 1) Incorporate saline alga in a fresh DM medium in a fresh DM medium in a fresh DM medium, cultured under 32 ° C, 6000lux, pH = 7.5, which adapted to a new growth environment and enters logarithm growth. period.
[0064] 2) Under Dark Condition, the culture temperature in which a long period of saline alga in which a long period of life is lowered at a rate of 1 ° C per 36 minutes, and the culture temperature is maintained at a rate of 9 h.
[0065] The saline alga cultured in the above steps was continued for 4 days at 32 ° C, 6000 lux. It is detected that the day relative growth rate is detected, and the day relative growth rate (OD) 0.168 is measured.
Embodiment 3
[0067] This embodiment is a method of taking a chromophoreglutaneous ice temperature activation compensation growth, including the following steps:
[0068] 1) Inoculated into fresh BG-11 medium in a fresh BG-11 medium in a fresh BG-11 medium in the concentration of 10 ml / L, it was cultured under the culture conditions of 32 ° C, 6000 lux, pH = 7.1, so that it adapted to a new growth environment. For a long time.
[0069] 2) Under Dark Condition, the culture temperature of the chlorinated algae in which the long-term long-term chlorinated algae is reduced at a rate of 1 ° C to -5 ° C at a rate of 1 ° C per 36 minutes; the culture temperature is maintained.
[0070] The collaborate cultured in the above steps was continued for 4 days at 32 ° C, 6000 lux. It is detected that the day relative growth rate is detected, and the day relative growth rate (OD) 0.089 is measured.
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