Tobacco leaf extract culture medium and application thereof
A technology of extraction liquid and medium, applied in the field of microorganisms, can solve the problems of high cost, complicated preparation, and expensive nicotine, and achieve the effects of low cost, convenient use, and simple preparation
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[0023] The present invention will be further described below in conjunction with the examples, but the protection scope of the present invention is not limited thereto.
[0024] The reagents described in the examples are all commercially available products, and the tobacco leaf fragments are purchased from Shandong Jinan General Group. The operation methods are general operation methods in the field unless otherwise specified.
Embodiment 1
[0026] Preparation of tobacco leaf extract:
[0027] Mix the tobacco leaf fragments and water according to the mass volume ratio (g / L) of 20:1 and 80:1, boil for 30 minutes, remove the precipitate by suction filtration, add water to make the volume to 1L, and prepare 2% tobacco leaf extract respectively and 8% tobacco leaf extract; after testing, 2% tobacco leaf extract contains nicotine 2.2g / L, and 8% tobacco leaf extract contains nicotine 9.5g / L.
[0028] (1) Preparation of tobacco leaf extract medium
[0029] ①The components of the strain activation medium (bacteria): 1L of 2% tobacco leaf extract, 3g of beef extract, 10g of peptone, 5g of NaCl, 20g of agar;
[0030] Components of the strain activation medium (fungus): 1 L of 2% tobacco leaf extract, 3 g of glucose, 5 g of peptone, 3 g of yeast powder, and 20 g of agar.
[0031] ② Components of the seed culture solution: 1 L of 2% tobacco leaf extract, 0.5 g of yeast powder.
[0032] ③ Components of the fermentation medi...
Embodiment 2
[0092] Cultivation of Aspergillus oryzae CGMCC NO.3687 with Nicotine Degradation Ability Using Tobacco Leaf Extract Medium
[0093] The preparation of the strain activation medium (fungus), seed culture solution and fermentation medium in this embodiment is the same as that in Example 1.
[0094](1) Select Aspergillus oryzae CGMCC NO.3687 and inoculate it into the strain activation medium (fungi) to activate for 40 hours. The culture temperature is 28° C. Then, take the activated Aspergillus oryzae CGMCC NO.3687 and inoculate it into the seed culture medium, and cultivate it for 30 hours. hour, the culture temperature is 28 DEG C to obtain the primary culture fluid; the primary culture fluid is transferred to the fermentation medium with an inoculum size of 5% (v / v) by volume, the culture temperature is 28 DEG C, and the shaking table speed is 150 rpm. After culturing for 40 hours, the mycelium was collected by suction filtration, the growth of the bacteria was measured, and ...
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