A racetrack-type bioreactor suitable for sunshine industrialization
A bioreactor, racetrack-style technology, applied in specific-purpose bioreactor/fermenter, combination of bioreactor/fermenter, microorganism-based methods, etc., can solve the problem of large cement pool area and poor light utilization sufficient, high cost of breeding, etc., to avoid pollution, improve light utilization, and increase the effect of cultivating density
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Embodiment 1
[0028] Embodiment 1: Haematococcus pluvialis (Haematococcus pluvialis) cultivation
[0029] (1) experimental device is prepared: two lengths are 5m, and the width is 1m oval runway pond, and experimental group is device of the present invention, and matched group is cement open runway pond;
[0030] (2) Inoculation: On the first day, the Haematococcus pluvialis liquid was inoculated in the experimental group and the control group, so that the cell inoculation density was 2.5×10 4 cells / ml; and MCM culture solution is added to the pool, the height of the culture solution is 0.15m (liquid volume 750L); the average temperature and light intensity during the culture period: 13°C at 8:00, 130μmol / m 2 / s, 25°C at 13:00, 380μmol / m 2 / s, 13°C at 17:00, 150μmol / m 2 / s;
[0031] (3) Control management: the control group uses impeller stirring to make the culture solution mix and circulate in the pool, and the rotation speed in the whole culture cycle is 30r / min, without carbon dioxid...
Embodiment 2
[0033] Embodiment 2: Isochrysis galbana (Isochrysis galbana) culture
[0034] The method is the same as in Example 1, except that in step 2, the cell seeding density is 2×10 4 cells / ml; after 10 days of culture, the cell density of Isochrysis globosa in the experimental group reached 1.9×10 5 cells / ml, the cell density of Isochrysis globosa in the control group reached 1.1×10 5 cells / ml. Compared with the control group, the concentration of cell culture in the experimental group increased by 72.7%.
Embodiment 3
[0035] Embodiment 3: Phaeodactylum tricornutum Bohlin (Phaeodactylum tricornutum Bohlin) cultivation
[0036] The method is the same as in Example 1, except that in step 2, the cell seeding density is 1.5×10 4 cells / ml; after 10 days of culture, the cell density of Phaeodactylum tricornutum in the experimental group reached 1.7×10 5 cells / ml, the cell density of Phaeodactylum tricornutum in the control group reached 1.1×10 5 cells / ml. Compared with the control group, the concentration of cell culture in the experimental group increased by 54.5%.
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