Method for extracting beta-farnesene from fermentation broth
A fermentation broth and farnesene technology, applied in the field of extracting β-farnesene, can solve the problems of unsuitability for industrial production, low yield, time-consuming, etc., achieve a breakthrough in the separation and purification technology bottleneck, high product yield, and reduce production cost effect
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Embodiment 1
[0025] The preparation of embodiment 1 culture medium
[0026] A seed medium was prepared, and the components of the seed medium were: 10 g / L tryptone, 5 g / L yeast extract and 10 g / L NaCl.
[0027] Prepare the fermentation medium, the components of the fermentation medium are: 2.3g / L citric acid, 0.3g / L ferric amine citrate, 5g / L yeast extract, 20g / L glycerol, 2g / L glucose, 3.07g / L L MgSO 4 .7H 2 O, 7.24g / L KH 2 PO 4 .
Embodiment 2
[0028] Example 2 A method for extracting β-farnesene from fermentation broth
[0029] A method for extracting β-farnesene from fermentation broth, comprising the steps of:
[0030] S1, two-phase extraction fermentation
[0031] (1) Cultivation of primary seed bacteria: add the seed culture medium prepared in Example 1 to the seed tank, insert Escherichia coli K-12MG1655 seed solution according to the inoculum amount of 1% after sterilization, and control the pH to 6.5, Rotate and shake for 12 hours, and transplant to the breeding tank when the biomass is 2-4%;
[0032] (2) Cultivation of secondary seed bacteria: add 30L of the seed medium prepared in Example 1 to the breeding tank, insert the primary seed liquid of E. coli according to the inoculation amount of 1% after sterilization, control the pH to 6.5, and rotate Shake culture for 18 hours, and transplant to the fermenter when the biomass reaches 5-8%;
[0033] (3) Cultivation of strains in the fermenter: add 100L of t...
Embodiment 3
[0041] Example 3 A method for extracting β-farnesene from fermentation broth
[0042] A method for extracting β-farnesene from fermentation broth, comprising the steps of:
[0043] S1, two-phase extraction fermentation
[0044] (1) Cultivation of primary seed bacteria: add the seed culture medium prepared in Example 1 to the seed tank, insert Escherichia coli K-12MG1655 seed solution according to the inoculum amount of 1% after sterilization, and control the pH to 6.5, Rotate and shake for 12 hours, and transplant to the breeding tank when the biomass is 2-4%;
[0045] (2) Cultivation of secondary seed bacteria: add 30L of the seed medium prepared in Example 1 to the breeding tank, insert the primary seed liquid of E. coli according to the inoculation amount of 1% after sterilization, control the pH to 6.5, and rotate Shake culture for 18 hours, and transplant to the fermenter when the biomass reaches 5-8%;
[0046] (3) Cultivation of strains in the fermenter: add 100L of t...
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