Solid medium for producing plasmin by using cordyceps sobolifera and plasmin production method using same
A technology of solid medium and plasmin, which is applied in the field of microorganisms, can solve the problems that Paecilomyces cicadae has not been reported, and achieve the effect of easy preparation and simple formula
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Embodiment 1
[0032] A culturing method (screening method) of a solid medium for producing plasmin by utilizing cicada flowers:
[0033] 1 Medium used
[0034] (1) Basic medium: 30 g of glucose, 1 g of potassium dihydrogen phosphate, 3 g of yeast extract, 0.2 g of magnesium sulfate 7hydrate, and 1000 g of water. 1000 g of water is equivalent to 1000 mL of water.
[0035] (2) Plasmin solid induction medium: Add 10g of the following different induction components to the basic medium: peptone, acid hydrolyzed casein, tryptone, starch, casein, Malt extract (malt extract), milk powder, soy peptone (Soytone), prepared into different components of plasmin induction medium. Finally, 1.5% agar was added to the above various media. Conventional high temperature sterilization (1.1 atmosphere pressure, sterilization at 121 ℃ for 20 minutes).
[0036] (3) Potato dextrose agar (PDA): Cut 200 g of potatoes into small pieces, add water to boil for 15 minutes, then filter with 2 layers of gauze, discard...
Embodiment 2
[0060] Example 2: qianrongm plasmin activity (U / mL)
[0061] Optimization of the induction components of solid medium for plasmin production by Cicada flower:
[0062] 1 Medium used
[0063] (4) Basic medium: 30 g of glucose, 1 g of potassium dihydrogen phosphate, 3 g of yeast extract, 0.2 g of magnesium sulfate 7-hydrate, and 1000 g of water. 1000 g of water is equivalent to 1000 mL of water.
[0064] (5) Plasmin solid induction medium: add peptone and tryptone to the basic medium, respectively. The test content gradient of peptone is 7, which are 5g, 7.5g, 10g, 12.5g, 15g, 17.5g, 20g; the test content gradient of tryptone is 7, which are 5g and 7.5g respectively. , 10g, 12.5g, 15g, 17.5g, 20g. The plasmin-inducing medium with different components was prepared according to the above components. Finally, 1.5% agar was added to the above various media. Conventional high temperature sterilization (1.1 atmosphere pressure, sterilization at 121 ℃ for 20 minutes).
[0065] (...
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