Nannochloropsis oculata and application thereof
A kind of technology of pseudo-Ninochlorococcus and microbial strains, which is applied in the field of microorganisms
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Embodiment 1
[0052] Quizalofop-p-ethyl for Screening Nannochloropsis
[0053] 1. The growth inhibition of quizalofop-p-ethyl to Nannochloropsis
[0054] (1) Weigh 10 mg quizalofop-p-p-p-p powder and dissolve in 1 mL DMSO to obtain 26.8 μmol / mL inducer mother solution.
[0055] (2) Add the inducer mother solution to the MASM improved liquid medium, and prepare the liquid with the final concentration of quizalofop-p-ethyl at 0, 2.5mmol / L, 5mmol / L, 7.5mmol / L, 10mmol / L and 12.5mmol / L The culture media are respectively recorded as Q0, Q1, Q2, Q3, Q4, and Q5 groups in sequence, wherein, the culture medium Q0 without adding quizalofop-p-p is used as a control.
[0056] (3) According to the ratio of adding 2 mL of algae species to 100 mL of liquid culture medium, inoculate the algae liquid into the culture solution of the prepared 6 gradient concentrations of the Erlenmeyer flask, seal with a gas-permeable membrane, and record the shake flask as F 1 generation. Place the inoculated Erlenmeyer f...
Embodiment 2
[0068] Growth Performance Test
[0069] Prepare six 1000mL bottles of culture solution, sterilize at 121°C for 30 minutes, and cool it for later use; add each nutrient mother solution in the biological safety cabinet according to the above-mentioned MASM improved liquid medium formula to make a liquid medium; after the culture solution is prepared, press 5% of its volume (about 50mL) was respectively inserted into the algae fluids of groups Q0, Q1, Q2, Q3, Q4, and Q5, and each two were parallelized. 3000~6000lux, the mixed gas of air and 1%~2% carbon dioxide is introduced, and the culture bottle is marked as F 2 generation. Take aseptic samples regularly, measure the change in optical density, and draw the change graph of growth curve. After 14 days of cultivation, the culture bottle was taken out to collect the algae fluid, and the specific growth rate was measured. The algae liquid was collected by centrifugation, and the inorganic salts were washed with pure water for 3 ...
Embodiment 3
[0086] This example provides a method for preparing fatty acids. The algae strain Q5 in Example 2 is inoculated through a photocatalytic reactor for large-scale cultivation. The cultured product is extracted with chloroform / methanol and the corresponding ARA and EPA are separated by chromatography. The Nannochloropsis has high fatty acid content, stable genetic traits, and can efficiently and rapidly obtain a large amount of fatty acid products.
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