Noni sphingomonas xenophaga preserving culture medium and preparation method thereof
The technology of sphingomonas and noni sphingosine is applied in the field of preservation medium of noni sphingomonas and its preparation, and can solve the problem that sphingomonas is late and research stays in the primary stage , ecological value and economic value are rarely paid attention to
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Embodiment 1
[0011] The formula of the culture medium is: 0.8% dry powder of nutrient broth, dilute to 1000ml with 1% noni dried fruit aqueous solution, and adjust the pH to 4.0-6.0.
[0012] Take 10.0g noni dried fruit, add 1000ml water to boil for 10min, add water to 1000ml, add 8.0g nutrient broth dry powder, boil to dissolve, adjust pH to 4.0-6.0, then subpackage and sterilize at 121°C for 20min.
[0013] Use an inoculation loop to pick a loop from the seed slant to inoculate, and store it in a 4°C refrigerator after culturing for 2 days. Take it out after storage for 70 days, the culture medium is brown-black, and a large amount of off-white bacteria is deposited on the bottom of the test tube. After shaking well, dip an inoculation loop bacteria solution and streak it onto a fresh solid medium. After 2 days of cultivation, off-white colonies grow on the streaked place It shows that the Sphingomonas noni preserved in this medium still has activity.
Embodiment 2
[0015] The formula of the culture medium is: dry powder of nutrient broth, 0.8% agar, 0.5%, dilute to 1000ml with 5% noni dried fruit aqueous solution, and adjust the pH to 4.0-6.0.
[0016] Take 50.0g of noni dried fruit, add 1000ml of water and boil for 10min, add water to 1000ml, add 8.0g of nutrient broth dry powder and 5.0g of agar, boil and dissolve, adjust the pH to 4.0-6.0, then subpackage and sterilize at 121°C for 20min.
[0017] Use an inoculation needle to pick the bacteria from the seed slope for puncture inoculation. After 2 days of cultivation, the bacteria can be seen growing along the puncture line, and then stored in a refrigerator at 4°C. After 70 days of storage, take it out, use an inoculation loop to take the thallus on the puncture line and streak it onto a fresh solid medium, and grow gray-white colonies after 2 days of cultivation, indicating that the thallus is still active.
[0018] The preservation culture medium prepared by the method of Embodiment...
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