Hair weeds bacterial culture and culturing product
A cell culture and cell technology, applied in the direction of plant cells, fermentation, unknown raw materials, etc., can solve the problems of ecological environment deterioration, difficult development, vegetation destruction, etc., and achieve the effect of protecting the ecological environment and saving natural resources
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Embodiment 1
[0016] (1) Separation of the Nostocella cells:
[0017] Weigh 1g of Nostocella in a triangular flask, sterilize the surface, and rinse with sterile water. Add filter-sterilized isolated enzyme solution 30mL under sterile conditions, the enzyme solution contains 0.5% pectinase, 0.8% mannitol, and 1% dextran sulfate potassium. The Erlenmeyer flask was placed on a shaker with a rotation speed of 120r / min, a stroke of 4-5cm, a temperature of 25°C, and a time of 2 hours, during which the enzyme solution was replaced every 30 minutes. After the third enzyme solution was replaced, glass beads with a diameter of 2mm were added to the Erlenmeyer flask. Two hours later, the enzymolysis solution was filtered with 800-mesh metal mesh, and the filtrate was centrifuged at 3000r / min for 15 minutes to collect the cells of Nostocchia.
[0018] (2) Cultivate the Nostocella cell species:
[0019] After washing with medium for 3 times, the Nostocella cells were inserted into the medium, the med...
Embodiment 2
[0023] Weigh 1g of Nostocchi, put it in a mortar after surface sterilization, add about 30mL of sterile saline or culture medium, grind it fully under sterile conditions, filter with 800-mesh metal mesh, centrifuge the filtrate, collect Nostoc cells, and culture Fat vegetables cell species. The cell species were preserved at 10°C, or inserted into the culture medium after expansion, the inoculum size was 20%, the pH was 9, the culture temperature was 30°C, and the light was cultivated for 15 days, and the rest were the same as in Example 1.
Embodiment 3
[0025] Lettuce cells were stored at 12°C. After the expansion of the cell species, insert it into the reactor with a 15% inoculum. The composition of the medium: 1.6% sodium bicarbonate, 0.12% sodium nitrate, 0.03% ammonium nitrate, add dipotassium hydrogen phosphate, calcium chloride, magnesium sulfate, pH8 .75, 32°C, 4500lux light intensity, light-to-dark ratio 16:8, light culture for 12 days. All the other are with embodiment 1 or embodiment 2.
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