Improved polyoxin fermentation culture medium and fermentation process
A fermentation medium, polyoxin technology, applied in the direction of fermentation, microorganism-based methods, biochemical equipment and methods, etc., can solve the problem that the viscosity and the elimination of foam during sterilization cannot be scientifically controlled, and there is no special research Over-fermentation medium quality stability, medium quality instability and other issues, to achieve the effect of shortening the fermentation cycle, reducing air demand, and reducing ventilation
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[0031] Example 1
[0032] The fermentation medium of the present invention: weigh 1.5% corn flour, 2.0% soybean meal powder, 2.0% caramel, and KH according to the formula 2 PO 4 0.1%, NaCl 0.1%, CaCO 3 0.3%, (NH 4 ) 2 SO 4 0.5%, antifoaming agent 0.035%, pH was adjusted to 6.5 before adding anticannoning agent, and sterilized at 121°C for 30 minutes to obtain the fermentation medium of the present invention.
Example Embodiment
[0033] Example 2
[0034] The fermentation medium of Example 1 adopts the fermentation process of the present invention as follows: Inoculate the slant spores of Streptomyces aureus with the model number 4896 into a seed shake flask at 28° C. and 220 rpm for 30 hours, and then bottle it into shake flask seeds. The shake flask seeds were inoculated into the first-level seed tank at 28°C for 24h, and then transplanted into the sterilized fermentation medium prepared in Example 1. At 28°C, 110rpm, tank pressure 0.05MPa, and ventilation volume 0.5-1.0L / Min continues to ferment. Feeding (NH 4 ) 2 SO 4 And ammonia water, add nitrogen source while adjusting the pH to maintain at 6.3-6.5, and put it in the tank when the culture is 113h.
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[0035] Example 3
[0036] The experimental results of Comparative Examples 1 and 2 and Examples 1 and 2 are compared as follows:
[0037] figure 1 In order to use the original fermentation process of the original fermentation medium, that is, Comparative Example 2, the diagram of the hypha at 30 hours shows that it forms a small net, and the hypha is long and less. figure 2 In order to use the fermentation process of the fermentation medium of the present invention, that is, the diagram of the hyphae at 30h, it can be seen that the hyphae form medium to large meshes, with long hyphae and complex cross-linking, less hyphae, and deep staining. .
[0038] image 3 In order to use the original fermentation process of the original fermentation medium, that is, Comparative Example 2, the diagram of the hypha at 68 hours shows that it forms a large network with long hyphae and complex cross-links. Figure 4 In order to use the fermentation process of the fermentation medium of the present ...
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