Method for increasing yield of haematococcaceae astaxanthin with saccharose as carbon source through co-culture
A technology of Haematococcus astaxanthin and astaxanthin, which is applied in the field of Haematococcus astaxanthin yield, can solve problems such as poor utilization of sucrose by Haematococcus, and achieves reduction of culture cost, improvement of utilization rate, and improvement of The effect of yield
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Embodiment 1
[0022] (1) Add 0.5g / L sucrose to BG11 medium, and sterilize;
[0023] (2) After the Haematococcus in the logarithmic growth phase was collected, it was added to the culture medium at a ratio of 5:1 and an initial biomass of 0.2g / L with Phaffia rhodozyme. Cultured for 4 days under the ventilation of 5vvm;
[0024] (3) At the later stage of cultivation, after 1 day of induction with ultraviolet light, the mixture of algae and bacteria was collected for the extraction of astaxanthin.
[0025] Processing effect test:
[0026] During the culture process, the yield of astaxanthin reaches 120mg / L / day, which is 30% higher than that under the pure culture of Haematococcus simplex using glucose as the carbon source.
Embodiment 2
[0028] (1) add waste molasses of 25g / L sucrose equivalent in SE medium, sterilize;
[0029] (2) After collecting Haematococcus pluvialis in the logarithmic growth phase, add Phaffia rhodozyme to the medium at a ratio of 20:1 and an initial biomass of 0.4g / L, at 15°C, pH8. Cultivate for 5 days under the ventilation of 0 and 1vvm;
[0030] (3) At the later stage of cultivation, after 2 days of high temperature induction, the mixture of algae and bacteria is collected for the extraction of astaxanthin.
[0031] Processing effect test:
[0032] During the culture process, the yield of astaxanthin reaches 80mg / L / day, which is 20% higher than that under the pure culture of Haematococcus simplex using glucose as the carbon source.
Embodiment 3
[0034] (1) add bagasse equivalent to 15g / L sucrose in Chu13 medium, and sterilize;
[0035] (2) After the Haematococcus in the logarithmic growth phase was collected, it was added to the culture medium with the ratio of 10:1 and the initial biomass of 0.1g / L to Phaffia rhodozyme. Cultured for 6 days under the ventilation of 20vvm;
[0036] (3) At the later stage of cultivation, after 3 days of induction with high light intensity, the mixture of algae and bacteria was collected for the extraction of astaxanthin.
[0037] Processing effect test:
[0038] During the culture process, the yield of astaxanthin reaches 100 mg / L / day, which is 25% higher than the pure culture of Haematococcus simplex with glucose as the carbon source.
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