Method for mixed fermentation of Schizochytrium sp.
A technology of Cryptodinium kouli and mixed fermentation, applied in the field of microbial fermentation, can solve the problems of reduced winterization efficiency, increased production cost, and reduced production efficiency, and achieve the effects of improving oil quality, increasing efficiency, and reducing energy consumption
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Embodiment 1
[0047] Production of docosahexaenoic acid by mixed culture of Schizochytrium sp.
[0048] 1. Preparation of seed solution
[0049] Each liter of seed medium contains raw materials of the following qualities:
[0050] Glucose 10g; Peptone 1g; Yeast extract 0.5g; Sodium glutamate 0.5g; Nacl 20g; MgSO 4 ·7H 2 O2g; Kcl 0.5g; (NH 4 ) 2 SO 4 0.1g; Cacl 2 2H 2 0 0.1g; KH 2 PO 4 0.1 g; pH=6.5.
[0051] Preparation of Seed Solution of Cryptidinium koulii
[0052] Under sterile conditions, according to the inoculation amount of 10% by volume, transfer the liquid-preserved strains into a cooled 250-ml Erlenmeyer flask containing 50 ml of sterile seed medium, and cultivate them at 20°C, 100rpm, and in the dark. Carry out the first activation until the cells enter the logarithmic growth phase; then transfer the culture solution into fresh sterile seed medium according to the inoculum volume of 10% by volume, and culture at 20°C, 100rpm, and dark conditions for the second Afte...
Embodiment 2
[0064]Production of docosahexaenoic acid by mixed culture of Schizochytrium sp.
[0065] 1. Preparation of seed solution
[0066] Each liter of seed medium includes the following quality raw materials: glucose 30g; yeast extract 3g; sodium glutamate 2g; peptone 1g; Nacl 15g; MgSO 4 ·7H 2 O 5g; Kcl 1g; (NH 4 ) 2 SO 4 0.2g; Cacl 2 2H 2 0 0.3g; KH 2 PO 4 0.3 g; pH=6.5.
[0067] Preparation of Seed Solution of Cryptidinium koulii
[0068] Under sterile conditions, according to the volume percentage of 20% inoculum, put the liquid preserved Cryptidium koelii into a 250 ml Erlenmeyer flask containing 50 ml of sterile seed medium, at 30°C, 200rpm, under dark conditions Cultivate until the cells enter the logarithmic growth phase to complete the first activation; then add the culture solution into fresh sterile seed medium according to the volume percentage of 20% inoculum, and cultivate at 30°C, 200rpm, and dark until the cells After entering the logarithmic growth phase ...
Embodiment 3
[0080] Production of docosahexaenoic acid by mixed culture of Schizochytrium sp.
[0081] 1. Preparation of seed solution
[0082] Each liter of seed medium contains raw materials of the following qualities:
[0083] Glucose 20g; Yeast extract 2g; Sodium glutamate 1g; Peptone 1g; Nacl 15g; MgSO 4 ·7H 2 O5g; Kcl1g; (NH 4 ) 2 SO 4 0.2g; Cacl 2 2H 2 0 0.3g; KH 2 PO 4 0.3 g; pH=6.5.
[0084] Preparation of Seed Solution of Cryptidinium koulii
[0085] Under sterile conditions, according to the volume percentage of 18% inoculum, the liquid preserved Cryptidium koelii was inserted into a 250-milliliter Erlenmeyer flask containing 50 milliliters of sterile seed medium, at 28°C, 180rpm, and dark conditions Cultivate until the cells enter the logarithmic growth phase to complete the first activation; then transfer the culture solution into fresh sterile seed medium according to the volume percentage of 18% inoculum, and cultivate at 28°C, 180rpm, and dark until the cells ...
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