Instant yolk oligopeptide-phosphatide type DHA double-effect dietary supplement and preparation method thereof
A technology of dietary supplement and phospholipid type, which is applied in the field of instant type egg yolk oligopeptide-phospholipid type DHA double-effect dietary supplement and its preparation field, can solve the problem of the preparation of egg yolk oligopeptide-phospholipid type DHA double-effect dietary supplement which has not yet been seen methods, etc., to achieve the effects of high biological activity and intestinal absorption and utilization rate, high product yield, good water solubility and solubility stability
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Embodiment 1
[0042] 1) Insert the strain of Schizochytrium SD006 (the strain is described in the patent document No. 201410203041.0) stored in the glycerol tube into a 500mL shake flask equipped with 100mL seed medium (see Table 1), at 30 Cultivate on a shaker at ℃ for 24 hours to obtain first-grade seeds; put the first-grade seeds into a 5L fermenter equipped with 1L of seed medium (see Table 1), and culture on a shaker at 30°C for 24 hours to obtain second-grade seeds; ferment to 50L Add 20L of fermentation medium (see Table 2) into the tank, and insert activated secondary seed liquid. During the fermentation process, the temperature was controlled at 28° C., and the fermentation was carried out for 60 hours. During the fermentation process, 50% (w / v) corn steep liquor solution was fed, and the pH value of the system was maintained at 6.5 by feeding 2M NaOH or 14% citric acid solution.
[0043] Table 1 Schizochytrium produces the seed medium formula of DHA
[0044]
[0045] The ferm...
Embodiment 2
[0066] 1) The Schizochytrium SD006 (201410203041.0) strain stored in a glycerol tube was inserted into a 500mL shake flask containing 100mL seed medium (see Table 1), and cultured on a shaker at 30°C for 24h to obtain first-grade seeds; The primary seeds were placed in a 5L fermenter with 1L of seed medium (see Table 1), and cultured on a shaker at 30°C for 24 hours to obtain secondary seeds; 20L of fermentation medium was added to the 50L fermenter (see Table 3) , into the activated secondary seed solution. During the fermentation process, the temperature was controlled at 35° C., and the fermentation was carried out for 80 hours. During the fermentation process, 50% (w / v) corn steep liquor solution was fed, and the pH value of the system was maintained at 6.5 by feeding 2M NaOH or 14% citric acid solution.
[0067] Table 3 The fermentation medium formula of Schizochytrium producing DHA
[0068]
[0069]
[0070] 2) After the fermentation is finished, the Schizochytrium...
Embodiment 3
[0079] 1) Insert the Schizochytrium SD006 (201410203041.0) strain stored in a glycerol tube into a 500mL shake flask containing 100mL seed medium (see Table 1), and culture it on a shaker at 30°C for 24h to obtain first-grade seeds; Put the primary seeds into a 5L fermenter with 1L of seed medium (see Table 1), and culture them on a shaker at 30°C for 24 hours to obtain secondary seeds; add 20L of fermentation medium to the 50L fermenter (see Table 4) , into the activated secondary seed solution. During the fermentation process, the temperature was controlled at 30° C., and the fermentation was carried out for 80 hours. During the fermentation process, 50% (w / v) corn steep liquor solution was fed, and the pH value of the system was maintained at 6.5 by feeding 2M NaOH or 14% citric acid solution.
[0080] The fermentation medium formula of table 4 Schizochytrium producing DHA
[0081]
[0082] 2) After the fermentation is finished, the Schizochytrium fermented liquid in t...
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