Method for promoting single-needle algae accumulated grease by nitrogen deficiency combined with strigolactones
A technology of strigolactone and monospermia, which is applied in the field of biodiesel, can solve the problems of long growth cycle of microalgae algae cells, influence on growth and oil accumulation, and cannot be applied on a large scale, and is beneficial to the growth of microalgae. and the accumulation of oil and fat content, the effect of promoting the accumulation of oil and fat, and the effect of promoting the accumulation of oil and fat content
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Embodiment 1
[0025] Prepare a nitrogen-deficient autotrophic BG-11 medium as the basic medium for oleaginous microalgae, adjust the pH value to 6.8-7.0; sterilize under high pressure and high temperature for 20 minutes, insert Monospiritoleum oleaginum, and control the algae cell concentration at 0.7 g / L, without adding SLs, the light culture temperature is 25°C, the light intensity is 3500 lux, the shaker speed is 150r / min, and light shake flask culture is carried out. The maximum oil content of the monospora oleaginous cultured in this example reached 46.18%; the maximum biomass reached 0.86g / L.
Embodiment 2
[0027] Prepare the self-supporting BG-11 basic medium as the basic medium for oleaginous microalgae, adjust the pH value to 6.8-7.0; sterilize at high pressure and high temperature for 20 minutes, insert the oleaginous monospora, and control the algae cell concentration at 0.7g / L, SLs were added to the culture medium so that the final SLs concentration was 1 μM, the light culture temperature was 25° C., the light intensity was 3500 lux, and the shaker speed was 150 r / min, and light shake flask culture was carried out. The maximum oil content of Monopodella oleaginum cultivated in this control example reached 48.76%; the maximum biomass reached 0.91g / L.
Embodiment 3
[0029] Prepare a nitrogen-deficient autotrophic BG-11 medium as the basic medium for oleaginous microalgae, adjust the pH value to 6.8-7.0; sterilize under high pressure and high temperature for 20 minutes, insert Monospiritoleum oleaginum, and control the algae cell concentration at 0.7 g / L, SLs were added to the medium so that the final SLs concentration was 1 μM, the light culture temperature was 25°C, the light intensity was 3500 lux, and the shaker speed was 150 r / min, and light shake flask culture was carried out. The maximum oil content of the monospora oleaginous cultured in this example reached 53.71%; the maximum biomass reached 0.90 g / L.
[0030] The culture solution obtained in Comparative Example 1 and Examples 1 to 3 was enriched by centrifugation (3500r / min, 10min), washed repeatedly with distilled water twice, then freeze-dried and weighed; add freeze-dried algae powder with 2 times the mass of quartz sand and grind for 20min Afterwards, the oil was extracted w...
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