High-yield cultivation method of botryococcus
A kind of botrytis culture, botrytis technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, single-cell algae, etc., can solve the problem of low cell growth rate and yield, reduce the number of devices and equipment, and reduce area production The effect of high efficiency and small footprint
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Embodiment 1
[0091] Example 1: Research on algae cell growth during heterotrophic, polytrophic and photoautotrophic culture of Botryococcus braunii cells
[0092] The botrytis of this example was cultured in heterotrophic, polytrophic and photoautotrophic cultures respectively in 500 ml shake flasks. The inoculation density of botrytis heterotrophic culture is 0.05g / l, the temperature is 25°C, and the rotational speed is 150rmp. The conditions of botrytis polyculture culture are the same as those of heterotrophic culture, except that there is light outside, and the light intensity is 80 μmolm -2 the s -1 . After 12 days of heterotrophic and mixed cultivation of grape algae, the glucose in the culture medium is exhausted, and the algae cell density is 0.70g / l and 0.78g / L, which can be used for the seeds of the next step of photoautotrophic cultivation; the seeds of grape algae are photoautotrophic The inoculation density during cultivation is 0.05g / l, the temperature is 25°C, and the lig...
Embodiment 2
[0093] Example 2: Comparison of Heterotrophic and Polycultured Culture Processes of Brown Botrytis (Botryococcus braunii) in a 5L Bioreactor under Different Culture Process Conditions
[0094] Add the heterotrophic or mixed culture medium and water to 2.5L in a 5L bioreactor and steam sterilize it, and then insert the botrytis when the temperature drops to 25° C., and start the heterotrophic or mixed culture. During mixed culture, the external light is 700 μmolm -2 the s -1 . In the case of heterotrophic or mixed culture, feed feeding is started, and the pH is kept constant at 8.0±0.3 by controlling the continuous flow of feed medium. The feed medium consisted of an organic carbon source (glucose), a nitrogen source (KNO 3 ), plant growth hormones, and inorganic salts and other nutrient salts. The added nutrient salts are the above-mentioned corresponding medium after concentration to promote the continued growth of microalgae. At the same time, timely monitor the content o...
Embodiment 3
[0096] Embodiment 3: Research on the photoautotrophic cultivation of botrytis heterotrophic seeds, polytrophic seeds and photoautotrophic seeds in indoor 2L photobioreactor
[0097] In the present embodiment, in the indoor 2L cylindrical air-lift photobioreactor, photoautotrophic cultivation of heterotrophic, polytrophic and photoautotrophic Botrytis seeds was carried out, and the conditions of heterotrophic, polytrophic and photoautotrophic seeds were measured respectively. Algae cell density, final oil and total hydrocarbon content and yield during culture. The inoculation density of heterotrophic, polytrophic and photoautotrophic seeds is 0.3g / l, the temperature of photoautotrophic culture is 25℃, and 2% CO 2 , The ventilation volume is 0.25vvm. In polyculture and photoautotrophic culture, the light intensity is 111 μmolm -2 the s -1 , continuous light. After 12 days of photoautotrophic culture, the algal cell density of heterotrophic seeds was 1.98g / l, the total hydroc...
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