Candida tropicalis and application thereof, and production method for long chain diprotic acid
A Candida, long-chain dibasic acid technology, applied in the field of fermentation, can solve problems such as affecting the development of the biological method long-chain dibasic acid industry, slow metabolism of strains, and inability to carry out fermentation, and achieves obvious industrialized value advantages and simplification. Extraction process, the effect of reducing pressure on resources and the environment
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[0068] A fifth aspect of the present invention provides a method for preparing a long-chain dibasic acid, comprising the following steps:
[0069] S1: fermentation to prepare long-chain dibasic acid fermentation broth; and
[0070] S2: extracting and purifying the obtained long-chain dibasic acid fermentation broth to obtain the long-chain dibasic acid;
[0071] Wherein, step S1 adopts the method for producing long-chain dibasic acid by fermentation according to the fourth aspect of the present invention to prepare the long-chain dibasic acid fermentation broth.
[0072] In the preparation method of the long-chain dibasic acid of the present invention, the obtained long-chain dibasic acid fermentation broth can be obtained by using the existing extraction and purification process to obtain the final long-chain dibasic acid product.
[0073] In one embodiment of the method for preparing long-chain dibasic acids according to the present invention, the extraction and purificatio...
Embodiment 1
[0088] Example 1 The acquisition of Candida tropicalis CAT H1614 strain
[0089] Connect the starting strain CCTCC NO:M 203052 glycerol tube into the shake flask filled with YPD culture solution, add 0.01% 5-fluorouracil, and culture at 30°C and 200rpm for 16-24h with shaking. Take the well-grown culture medium to collect the bacteria by centrifugation and wash with saline several times, and finally suspend the cells with an equal amount of LiCl aqueous solution. Take an appropriate amount of cell suspension and place it in a sterile plate to irradiate mutagenesis with ultraviolet light, the power of the ultraviolet lamp is 15W, the irradiation distance is 20cm, and the irradiation time is 90s. The mutated strains were cultured on a plate containing YPD medium at a culture temperature of 29° C. for a culture time of 50 h, and picked well-grown single clones to a culture medium containing a primary screening medium (substrate long-chain alkanes were included in the culture medi...
Embodiment 2~7
[0090] Examples 2-7 Fermentation of Candida tropicalis CAT H1614 in a 10L fermenter to produce different dibasic acids
[0091] Get the glycerol tube bacterial classification of Candida tropicalis CAT H1614 and inoculate in the seed bottle that 30ml YPD liquid culture medium (glucose 2%, yeast extract 1%, peptone 2%) is housed, pH is natural, under 29 ℃, 220rpm shaker Cultured for 1 day. Get shake flask seed access and be equipped with 5L seed culture medium (sucrose 2%, corn steep liquor 0.3%, yeast extract 0.5%, KH 2 PO 4 0.8%, urea 0.3%) in the seed tank, the inoculation amount is 10%, the initial pH value of the system after inoculation is 6.0, at 29°C, the ventilation rate is 0.4vvm, the tank pressure is 0.08MPa, and the culture is 18h. natural drop to 3, OD 620 When growing to 0.7, inoculate into 6L fermentation medium 1 (4% of glucose, 0.5% of corn steep liquor, 0.4% of yeast extract, 1% of potassium nitrate, 0.1% of potassium dihydrogen phosphate, 0.12% of urea, 0....
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