Method for synthesizing silver nanoparticles through pseudomonas poae acellular supernatant, product prepared by method and application of silver nanoparticles
A supernatant and cell-free technology, applied in the field of green biosynthetic nanomaterials, can solve problems such as ineffective effects, and achieve the effects of low price, small average particle size, and stable structure
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Embodiment 1
[0042] (1) Bacterial culture: Pick a single colony of Pseudomonas phlegm on the NA agar plate and put it in a 5ml test tube culture medium. After overnight shaking culture at 30°C and 200rpm, transfer it to NB liquid medium at a ratio of 1%. overnight culture at 30°C with a shaking rate of 200rpm;
[0043] (2) Collection of supernatant: centrifuge the bacterial suspension obtained in step (1) at 8000 rpm for 10 minutes and collect the supernatant to obtain cell-free supernatant (CFCS);
[0044] (3) Preparation of nano silver: get the bacterial supernatant obtained in step (2) and 1mM AgNO 3 The solution was fully mixed according to the ratio of 1:3, put into a 200rpm shaker and shaken in the dark for 48h, then the obtained reaction solution was passed through 8000rpm, centrifuged for 15min, washed 3 times with distilled water, and vacuum freeze-dried to obtain nano silver particles.
Embodiment 2
[0046](1) Bacterial culture: Pick a single colony of Pseudomonas phlegm on the NA agar plate and put it in a 5ml test tube culture medium. After overnight shaking culture at 30°C and 200rpm, transfer it to NB liquid medium at a ratio of 1%. overnight culture at 30°C with a shaking rate of 200rpm;
[0047] (2) centrifuge the bacterial suspension obtained in step (1) at 10000 rpm for 10 min and collect the supernatant to obtain a cell-free supernatant (CFCS);
[0048] (3) take the bacterial supernatant obtained in step (2) and 0.5mM AgNO 3 The solution was fully mixed according to the ratio of 1:5, and placed in a 200rpm shaker for 48h in the dark. Then the obtained reaction solution was subjected to 8000 rpm, centrifuged for 10 min, washed with distilled water for 3 times, and vacuum freeze-dried to obtain silver nanoparticles.
Embodiment 3
[0050] (1) Bacterial culture: Pick a single colony of Pseudomonas phlegm on the NA agar plate and put it in a 5ml test tube culture medium. After overnight shaking culture at 30°C and 200rpm, transfer it to NB liquid medium at a ratio of 1%. overnight culture at 30°C with a shaking rate of 200rpm;
[0051] (2) centrifuge the bacterial suspension obtained in step (1) at 9000 rpm for 15 minutes and collect the supernatant to obtain a cell-free supernatant (CFCS);
[0052] (3) get the bacterial supernatant that step (2) obtains and 1.5mM AgNO 3 The solution was fully mixed according to the ratio of 1:4, and placed in a 200rpm shaker for 48h in the dark. Then the obtained reaction solution was subjected to 10000 rpm, centrifuged for 15 min, washed with distilled water for 3 times, and vacuum freeze-dried to obtain silver nanoparticles.
[0053] The performance and bacteriostatic effect of the nano-silver particles obtained through the mediation of Pseudomonas phlegm in Example 1...
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