Pythium irregulare strain for producing eicosapentaenoic acid
A technology of eicosapentaenoic acid and Pythium, applied in the field of bioengineering, can solve the problems of unstable quantity and quality of polyunsaturated fatty acids, reduce consumer acceptance, etc., and achieve the effect of stable properties
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Embodiment 1
[0027] Analysis of Fatty Acid Composition of Pythium maloestrogens
[0028] Pythium malatus Python irregular JN168 adopts liquid fermentation and adopts standard PDA medium. The fermentation temperature was 25°C, and the fermentation ended after 4 days. The mycelium was collected by suction filtration, freeze-dried to constant weight, and the mycelium was ground with a mortar. Take about 0.1g of dried mycelium and add it to a test tube with a cover. Add 5 mL of 0.4 mol / L potassium hydroxide-methanol solution to it, keep it in a water bath at 50°C for 1 hour, then add 5 mL of 14% boron trifluoride-methanol solution, keep it in a water bath at 50°C for 1 hour, add 5 mL of n-hexane Extract with alkane, and finally add 2 mL of saturated sodium chloride solution to wash with water, pipette the upper layer solution and use GC-MS for detection.
[0029] Chromatographic conditions: Finnigan Trace MS (USA) gas chromatography-mass spectrometer. A DB-MAX capillary column (30m×0.25m...
Embodiment 2
[0034] Determination of the best carbon source
[0035] Pythium slant Python irregular The JN168 strain was inoculated on the plate, and then cultured in an incubator at 25°C. The plate medium composition is: glucose 20g / L, yeast powder 5g / L, agar 20%. After 3 days, scrape the mycelia on the plate into sterile water, shake and break the mycelium, and inoculate it into the seed medium with a 10% inoculum amount, cultivate it on a shaker at 25°C for 48 hours, and then inoculate it with a 10% inoculum amount. In the fermentation medium, culture on a shaker at 25°C for 96 hours. Using a single factor to investigate the best carbon source for accumulating eicosapentaenoic acid, using fructose, maltose, sucrose, lactose, D-galactose, glycerol, corn flour, or potato starch instead of glucose in the basic fermentation medium for liquid Fermentation, dry weight and eicosapentaenoic acid production were measured. Basic fermentation medium composition (w / v): glucose 60g / L, yeast pow...
Embodiment 3
[0039] Determination of the best nitrogen source
[0040] Pythium slant Python irregular The JN168 strain was inoculated on the plate, and then cultured in an incubator at 25°C. The plate medium composition is: glucose 20g / L, yeast powder 5g / L, agar 20%. After 3 days, scrape the mycelia on the plate into sterile water, shake and break the mycelium, and inoculate it into the seed medium with a 10% inoculum amount, cultivate it on a shaker at 25°C for 48 hours, and then inoculate it with a 10% inoculum amount. In the fermentation medium, culture on a shaker at 25°C for 96 hours. Using a single factor to investigate the best nitrogen source for the accumulation of eicosapentaenoic acid, use ammonium nitrate, ammonium sulfate, yeast extract, peptone, peanut cake powder or bean cake powder to replace the yeast powder in the basic fermentation medium for liquid fermentation, and measure Dry weight and eicosapentaenoic acid production. Basic fermentation medium composition (w / v)...
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