Simple high-efficiency haematococcus pluvialis nutritive cell culturing and harvesting method
A technology for culturing Haematococcus pluvialis and cells, applied in the field of Haematococcus pluvialis vegetative cell culture and harvesting, can solve the problems of difficult collection, low solubility, poor applicability, etc., and achieve improved induction efficiency and efficient harvesting , the effect of easy operation
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Embodiment 1
[0021] (1) Add 30mM bicarbonate and 5mM carbonate to BG-11 complete nutrient medium to obtain nutrient medium.
[0022] (2) Inoculate Haematococcus pluvialis into the nutrient medium of step (1), and then pass a mixed gas of carbon dioxide and filtered air into the algae liquid. The carbon dioxide content in the mixed gas is 0.5~5%, to maintain the algae liquid The pH value is 7.0~8.0; the culture temperature of vegetative culture is 20~25℃, and the light intensity is 50~80μmol / m 2 / s.
[0023] (3) After 10 days of vegetative culture, before the end of vegetative culture, stop feeding carbon dioxide, and only feed filtered air, and continue suspension culture for 12 hours.
[0024] (4) When the pH value of the algae solution rises to 11, stop feeding the filtered air, settle naturally for 1 hour, remove the clarified medium in the upper layer, collect the vegetative cells in the lower layer, and obtain concentrated algae cells.
[0025] (5) Inoculate the concentrated algal c...
Embodiment 2
[0030] (1) Add 10 mM bicarbonate and 1 mM carbonate to BG-11 complete nutrient medium to obtain a nutrient medium.
[0031] (2) Inoculate Haematococcus pluvialis into the nutrient medium of step (1) to obtain the inoculated algae liquid, and pass a mixed gas of carbon dioxide and filtered air into the algal liquid, and the carbon dioxide content in the mixed gas is 0.5~ 5%, maintain the pH value of algae liquid at 7.0~8.0; the culture temperature of vegetative culture is 20~25℃, and the light intensity is 50~80μmol / m 2 / s.
[0032] (3) After 10 days of vegetative culture, before the end of vegetative culture, stop feeding carbon dioxide, and only pass through filtered air, and continue suspension culture for 6 hours.
[0033] (4) When the pH value of the algae liquid rises to 10, stop passing through the filtered air, let it settle naturally for 1.5 hours, remove the clarified medium in the upper layer, collect the vegetative cells in the lower layer, and obtain concentrated ...
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