Method for synthesizing natamycin through solid-state fermentation of industrial and agricultural byproducts
A technology of natamycin and solid-state fermentation, which is applied in the field of industrial biology, can solve the problems that the inherent defects of liquid submerged fermentation cannot be effectively solved, the concentration of natamycin products is low, and the pressure on environmental protection of enterprises is increased, and energy consumption can be achieved. Reduced power consumption, low power consumption, and no pollution
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Embodiment 1
[0051] A 250mL triangular flask was used as a fermentation vessel, 10g of bran, rice bran, bagasse or wheat straw was used as a carbon source, 5g of rapeseed cake was used as a nitrogen source, 0.45g of rice husk was used as a fluffy carrier, and 0.45g of industrial glycerin was used as an auxiliary carbon source. Configure 16g of dry weight solid-state fermentation medium. Add 70% (v / w, g / L, where w is the total mass of carbon source, nitrogen source, auxiliary carbon source and fluffy carrier, the same below) water to the solid-state fermentation medium, and autoclave at 126°C Sterilize in the pot for 30min. Inoculate the 42-52h seed culture solution of Streptomyces luteus Z28 with an inoculum amount of 15% (v / w) in the above medium, and place it in a constant temperature incubator at 28°C for fermentation and cultivation for 7 days. Turn over twice to ensure oxygen supply, and the final natamycin production concentration reaches 9.53, 3.04, 6.10, 2.06 mg·g -1 Dry weight (...
Embodiment 2
[0053] Use a 250mL triangular flask as a fermentation vessel, 10g of bran as a carbon source, 5g of rapeseed cake, soybean cake, rice distiller's grains or oyster mushroom residue as a nitrogen source, 0.45g of rice husk as a fluffy carrier, and 0.45g of industrial glycerin as an auxiliary Carbon source, configure 16g dry weight solid fermentation medium. Add 70% (v / w) water to the solid-state fermentation medium, and sterilize in an autoclave at 126° C. for 30 minutes. Inoculate the 42-52h seed culture solution of Streptomyces luteus Z28 with an inoculum amount of 15% (v / w) in the above medium, and place it in a constant temperature incubator at 28°C for fermentation and cultivation for 7 days. Turn over twice to ensure oxygen supply, and the final natamycin production concentration reaches 9.53, 6.96, 1.56, 3.34 mg·g -1 dry weight.
Embodiment 3
[0055] Use a 250mL triangular flask as the fermentation container, the mass ratio of carbon source and nitrogen source is 3:1, 2:1, 1:1, 1:2, 1:3, and the total mass of carbon source and nitrogen source is 15g, 0.45g rice husk It is a fluffy carrier, 0.45g of industrial glycerin is used as an auxiliary carbon source, and 16g of dry weight solid fermentation medium is configured. Add 70% (v / w) water to the solid-state fermentation medium, and sterilize in an autoclave at 126° C. for 30 minutes. Inoculate the 42-52h seed culture solution of Streptomyces luteus Z28 with an inoculum amount of 15% (v / w) in the above medium, and place it in a constant temperature incubator at 28°C for fermentation and cultivation for 7 days. Turn over twice to ensure oxygen supply, and the final natamycin production concentration reaches 2.32, 9.53, 4.51, 1.80, 1.13 mg·g -1 dry weight.
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