Method for synthesizing manganese dioxide nanowire by using filamentous phage template and application of manganese dioxide nanowire
A technology of manganese dioxide nanometer and filamentous bacteriophage, which is applied in the fields of catalysis, analytical chemistry and nanomaterials. It can solve the problems of mild preparation that have not been reported yet, and achieve good application prospects, uniform appearance and simple synthesis method.
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Embodiment 1
[0037] Preparation of M13 phage:
[0038] Take 1 μL of phagemid PC89 solution, transform it into Escherichia coli TG1 competent cells, inoculate a single colony in 2 mL of Amp-resistant SOC culture medium after plate culture, culture with shaking at 37 °C for 2 h, transfer to 400 mL of Amp In the resistant SOC culture solution, shake culture at 37 °C until the absorbance of the culture solution at 600 nm is about 0.4, add about 1×10 12 A helper phage M13KO7 was cultured with shaking for 1 h, then kanamycin with a final concentration of 25 µg / mL and isopropyl-β-d-thiogalactoside with a final concentration of 1 mM were added, and cultured with shaking at 37 °C overnight.
Embodiment 2
[0040] Purification of M13 phage:
[0041] Place the culture solution in a 70 °C water bath for 20 min, then divide into 50 mL centrifuge tubes, centrifuge for 15 min (rotating speed 5000rpm), collect the supernatant; add PEG8000 to 40 g / L, NaCl to 30 g / L, and store on ice For 1 h, centrifuge at 4°C for 5 min (12,000 rpm), discard the supernatant; dissolve the pellet with 5 mL of PBS, centrifuge at 4°C for 5 min (12,000 rpm), and discard the insoluble matter. Repeat the above method once, collect the supernatant, and store at 4°C. The concentration of M13 phage in the supernatant was determined by the common method of plate counting phage plaques.
Embodiment 3
[0043] Preparation of manganese dioxide nanowires based on filamentous bacteriophage M13 template:
[0044] (1) Mix the filamentous bacteriophage and the aqueous solution of manganese acetate evenly, and let it stand for 1 h;
[0045] (2) Add an aqueous solution of NaOH to the above-mentioned mixed solution and mix well, and generate a yellow-brown suspension after shaking for 24 h;
[0046] (3) Centrifuge the above reaction solution, remove the supernatant containing unreacted components, collect the precipitate, and store it at 4°C for future use; the purified manganese dioxide nanowires can also be collected by dialysis or filtration.
[0047] Another control experiment was done: manganese dioxide was synthesized in the absence of M13 phage, and other experimental conditions and steps were the same as the above experiment.
[0048] Such as figure 1 As shown, the mixed reaction solution of M13 bacteriophage and manganese acetate produced a large amount of precipitation aft...
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