Medium for prolonging life of fruit flies and preparation and use methods thereof
A culture medium, Drosophila technology, applied in the application, resistance to vector-borne diseases, animal feed, etc., can solve the problems of large amount of addition, difficult separation and purification, limited application prospects, etc., to achieve the effect of prolonging lifespan
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Embodiment 1
[0035] see figure 1 , a preparation method of a medium for prolonging the lifespan of fruit flies, comprising the steps of:
[0036] (1) Obtaining the fruiting bodies of Phellinus sanghuang: The fruiting bodies of Phellinus sangellia were collected from Jilin, and were identified as Phellinus sphaerifolia by experts in the classification of edible fungi.
[0037] (2) Preparation of Phellinus Phellinus water body fluid: boil the dried Phellinus Phellinus fruiting body small particles and water in a ratio of 1:10 in boiling water at 100°C for 2 hours, centrifuge at room temperature for 30 minutes at 12,000 rpm, and filter the residue for secondary extraction , combined and collected the supernatant into a 50mL sterilized tube;
[0038] (3) Place the centrifuge tube containing the supernatant in a freeze dryer to freeze-dry it into a dry powder for later use; the freezing temperature of the freeze dryer is -55°C, and the drying time is 15 days;
[0039] (4) First configure the ...
Embodiment 2
[0051] Adopt the method for embodiment 1, the application in Drosophila melanogaster cultivation, specifically as follows:
[0052] (1) Drosophila: Drosophila melanogaster;
[0053] (2) Treatment method: starve the fruit flies for 2-4 hours first, anesthetize the newly eclovened fruit flies with carbon dioxide, pick out 10 male and female fruit flies, and place the bottle on its side to prevent the fruit flies from sticking to the bottle. On the culture medium, after the fruit flies wake up, the culture bottle can be placed in a constant temperature incubator for cultivation, and each treatment is repeated 3 times:
[0054] (3) Culture method: Put the control group and the Phellinus japonica water extract group into the same culture, set the temperature at 25±1°C, and the relative humidity is about 60%, light:dark=12h:12h; add Phellinus japonica water The concentration used in the extract group was 1 μg / ml.
[0055] (4) Observing the control group and the treatment group: ob...
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