Tribonema and culture and application thereof
A technology of yellow silk algae and algae strains, applied in the fields of application, single-cell algae, animal feed, etc., can solve the problems of slow oil accumulation, unsuitable for production, and few research records, etc., and achieve the effect of fast oil accumulation
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Embodiment 1
[0034] Example 1 Screening and molecular identification of Xanthophyllum ENN172
[0035] 1. Screening of Xanthophylla ENN172 (Tribonema sp.)
[0036] In autumn, water samples were taken from lakes in northeastern Inner Mongolia. In the laboratory, BG11 medium diluted 1 / 10 was added to the water samples, enriched and cultured for 2-3 days under natural light and room temperature, and treated with sterile deionized water. The samples were diluted, and single algae filaments were taken for purification and culture in a 24-well plate. The medium was BG11 medium, the culture temperature was 25°C, and the light was natural light. The purified algae filaments in the orifice plate were transferred to the Erlenmeyer flask for expansion culture, and finally the pure algae strain of ENN172 was obtained.
[0037] Table 1BG11 medium composition
[0038] substance name
Amount per liter of deionized water
1.5g
K 2 HPO 4 ·3H 2 O...
Embodiment 2
[0062] The indoor cultivation of embodiment 2ENN172 algal strain
[0063] In a column reactor with an inner diameter of 5cm and a height of 60cm, cultured with sterile BG11 medium, the culture temperature was 25°C, the initial inoculation concentration was about 1g / L, and a mixture of filtered air and carbon dioxide was introduced. gas, wherein the content of carbon dioxide is 1-2% of the total mixed gas. The initial light intensity is 120umol / m 2 / s, in the later stage, according to the growth of biomass, the light intensity is increased to 200 umol / m 2 / s. Samples were taken every day for determination of biomass and fatty acid content in cells for a total of 4 days of culture.
[0064] Biomass determination method: Accurately measure 50 mL of algal liquid, filter it with a glass fiber membrane with a known initial weight after drying (pore size is 0.45um), rinse with 150 mL of deionized water for three times to remove ash, and then remove the attached algal cells. The g...
Embodiment 3
[0066] The oil production of embodiment 3ENN172 algal strain
[0067] The ENN172 algal species at the end of exponential growth was inserted into a column reactor with an inner diameter of 5 cm and a height of 60 cm. The initial inoculation amount of algal cells was about 1.5 g / L, and the medium used was BG11 medium deficient in nitrogen and phosphorus. The temperature is 25℃, and the initial light intensity is 150umol / m 2 / s, the subsequent light intensity is gradually increased to 200umol / m 2 / s, other parameters are the same as in Example 2. Samples were taken every day to measure the fatty acid content in the cells, and the biomass was measured every two days for a total of 4 days of culture. The measurement results are shown in 4.
[0068] Composition and content determination method of fatty acid: Weigh 25 mg of freeze-dried sample, add 2 mL of 2% H 2 SO 4 Anhydrous methanol-toluene solution. After filling with nitrogen, it was heated at 80°C for 2 hours. Then add ...
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