Method for preparing gamma-linolenic acid-rich grease through sea squirt-associated Penicillium citrinum Asc2-4 fermentation
A technology of Penicillium citrinum and linolenic acid is applied in the field of preparing oil rich in γ-linolenic acid, can solve the problems of high cost, poor stability, complicated production process and the like, and achieves the effects of tenacious vitality, low cost and simple process
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Embodiment 1
[0059] Example 1 Isolation and identification of ascidian symbiotic fungus Penicillium citrinum Asc2-4
[0060] 1. Strain isolation
[0061] (1) Sample: sea squirt, collected from quicksand shrimp pond in Leizhou City, Guangdong Province.
[0062] Take 10 g of sea squirt viscera, homogenize it with a homogenizer, put it into 90 mL of sterile sea water, shake and mix well. Then use sterile seawater to press 10 -2 ~10 -6 Dilute and spread on solid medium, culture at 28°C for 24-72 hours, and isolate single colonies.
[0063] The above-mentioned single colony was further inoculated into a liquid seed medium, cultured on a shaker at 28°C for 72 hours, and the fat particles in the mycelia were observed under a microscope. Suction filter and dry the fermented mycelium, extract the oil in the mycelium by acid-heat method, measure the content of gamma-linolenic acid in the oil with a gas chromatograph, and select the strain with the highest gamma-linolenic acid content as the bact...
Embodiment 2
[0074] Example 2 Preparation of gamma-linolenic acid oil by fermentation of ascidian symbiotic fungus Penicillium citrinum Asc2-4
[0075] 1. A method for preparing gamma-linolenic acid oil by fermenting the ascidian symbiotic fungus Penicillium citrinum Asc2-4, comprising the following steps:
[0076] (1) Strain activation (solid strain culture):
[0077] Transfer the strains preserved in freeze-dried tubes or sand tubes to potato dextrose agar slant medium, and culture them at 25°C for 5 days to activate the strains;
[0078] (2) Seed liquid preparation (liquid strain culture):
[0079] The slant strains were made into spore suspension and inoculated in the seed medium for cultivation. The seed medium was potato dextrose medium, the inoculation amount was 3%, the pH was 5.5-6.5, the cultivation temperature was 28°C, and the cultivation time was 2 days ;
[0080] (3) Fermentation culture
[0081] 1) Fermentation medium preparation: Accurately weigh potatoes according to t...
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