Rapid culture method of chrysophyceae
A culture method and technology of golden algae, applied in the field of rapid cultivation of golden algae, can solve the problems of low culture density, slow growth rate of culture, difficulty in cultivating golden algae biomass to meet the requirements of industrial processing and application, and achieve energy saving, The effect of stable efficiency
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[0056] Example 1
[0057] Cultivation of golden algae in a 7.5 L, New Brunswick (NBS) BioFlo310 fermentor.
[0058] Using this invention method to cultivate in a 7.5L fermentor, the highest cell number can reach 2.88×10 8 Cell biomass can reach 56g / L per mL.
[0059] Step 1: Photoautotrophic pre-cultivation of seeds
[0060] (1) Prepare the seed culture medium according to Table 1, and dispense them into 1L Erlenmeyer flasks with a volume of 300mL and sterilize at 121°C for 30 min.
[0061] (2) Inoculation, algae species Poterioochromonas malhamensis CMBB-01 was provided by the Institute of Hydrology, Wuhan Chinese Academy of Sciences, with an inoculation volume of 10 mL.
[0062] (3) Cultivate for 7 days, culture temperature 25-28 ℃, light intensity 30-50 μmol photons m -2 s -1 . When the seed color changes from golden yellow to dark brown, the dry weight can reach 2-3g / L.
[0063] Step 2: Fermentation tank culture
[0064] (1) Prepare the fermentation tank culture medium according to ...
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[0078] Example 2
[0079] Cultivation of golden algae in 125 L, New Brunswick (NBS) BioFlo610 type fermentor.
[0080] Using the method of the invention to carry out amplifying culture on a 125L fermentor, the cell biomass of Chrysophyllum algae can reach 45 g / L after 96 hours of culture.
[0081] Step 1: Seed preparation
[0082] After culturing for 96h in Example 1, figure 1 It is known that it is in the logarithmic phase and is suitable for vaccination. The golden algae at this time was taken out and used as the algae seed of this example.
[0083] Step 2: Fermentation tank culture
[0084] (1) Prepare the fermentation tank culture medium according to Table 2 (except ammonium chloride), calibrate the pH electrode, prepare 32 L per tank, fill 28L, 121 ℃, and sterilize for 30 min. The mass ratio of carbon / nitrogen in the medium is 28:1.
[0085] (2) After sterilization, cool down, adjust the temperature to 28 ℃, rotate speed 50 rpm, and ventilate 4.0 L min -1 After that, calibrate the ...
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[0104] Example 3
[0105] According to the cultivation method of Example 1, cultured in a 7.5L fermenter, and set up the experimental group with vitamins (tank 1 and tank 3) and the control group (tank 2 and tank 4) without vitamins, as shown in the following table:
[0106]
[0107] The cultivation method, conditions and operation steps of this example are all carried out with reference to Example 1. The experimental results are shown in image 3 . by image 3 The statistical results show that:
[0108] ①By image 3 It can be seen that tank 1 and tank 3 add vitamin B in 44 h 1 :0.375 mg / L, B H :0.25mg / L, B 6 :0.125 mg / L and B 12 : 0.125 mg / L (the concentration of vitamins after adding the culture system), the growth rate began to be significantly faster than tank 2 and tank 4. The average rate of the fermentation tank of tank 1 is 32.22×10 in 48-120 h 5 (Each per mL / h), the average speed of tank 2 fermentor is 7.4×10 5 (A mL -1 h -1 ), tank 1 is 4.4 times the cell growth rate of t...
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