Docosahexaenoic acid-producing strain and mutation and screening method and application thereof
A docosahexaenoic acid and production strain technology, which is applied in the biological field, can solve problems such as difficulty in resisting competitive pressure, and achieve the effects of saving screening costs, clear purpose, and improving work efficiency
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Embodiment 1
[0048] Embodiment 1: The cultivation of seed.
[0049] Inoculate Cryptidinium dinoflagellate (ATCC 30772) with docosahexaenoic acid production ability into the seed medium at an inoculation amount of 1% (v / v), and cultivate it for three generations at 25°C, and take the third generation after culturing for 40 hours. Substitute liquid.
Embodiment 2
[0050] Embodiment 2: the pretreatment of seed solution.
[0051] Dilute 1 mL of the bacterial solution obtained in Example 1 with 9 mL of sterile artificial seawater with a concentration of 30 g / L, place it in a sterilized Erlenmeyer flask covered with glass beads, shake it at room temperature for 5 min, and make the algae Somatic cells were dispersed, filtered through sterilized 6-layer gauze, serially diluted, and counted until the cell concentration was 1.5×10 4 individual / mL.
Embodiment 3
[0052] Embodiment 3: UV mutagenesis
[0053] Spread the bacterial solution obtained in Example 2 on a sterile plate to ensure that the thickness of the bacterial solution is about 2 to 3 mm, and carry out mutagenesis at a distance of 30 cm from a 30W ultraviolet lamp for 1, 3, 5, 9, and 15 minutes, and obtain 5 strains to be screened strain.
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