Embedded nano-iron/single microorganism compound bacterial agent and preparation method thereof
A composite bacterial agent and nano-iron technology, applied in microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of poor stability of nano-zero-valent iron, achieve low microbial toxicity, realize in-situ repair, use Simple and convenient effects
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Embodiment 1
[0034] (1) Preparation of triclosan-degrading bacterial liquid
[0035] Pick 2 rings of Pseudomonas stutzeri., transfer them to 30mL nutrient solution, culture the bacteria at 35°C for 2 days, and inoculate Pseudomonas stutzeri at a volume ratio of 10% Bacteria proliferation medium container, then cultivated at 35°C for 2 days, centrifuged at 5000rpm for 15min, and obtained the logarithmic growth phase cells of the above bacteria;
[0036] The logarithmic growth phase cells of the above-mentioned thalli are taken out, and with phosphate buffer (its main component sodium chloride 9.0g / L, potassium chloride 0.3g / L, dipotassium hydrogen phosphate 1.2g / L and potassium dihydrogen phosphate 0.3g / L, the rest is water) after washing twice, press and suspend in normal saline, refrigerate at 4°C for later use, and record it as cell A;
[0037] The nutrient solution for Pseudomonas stutzeri was beef extract 6.0g / L, NaCl 5.0g / L, peptone 10.0g / L, soybean powder 2.0g / L, pH 6.5, and the res...
Embodiment 2
[0054] (1) Preparation of triclosan-degrading bacterial liquid
[0055] Pick 2 rings of Pseudomonas stutzeri (Pseudomonas stutzeri.) (source is the same as in Example 1), which are transferred to 30mL nutrient solution respectively, and the bacteria are cultivated at 35°C for 2 days, with a volume ratio of 10%. Inoculate into the container of the proliferation medium of Pseudomonas stutzeri, then culture at 35°C for 2 days, centrifuge at a speed of 5000rpm for 15min, and obtain the logarithmic growth phase cells of the above bacteria;
[0056] The logarithmic growth phase cells of the above-mentioned thalli are taken out, and with phosphate buffer (its main component sodium chloride 9.0g / L, potassium chloride 0.3g / L, dipotassium hydrogen phosphate 1.2g / L and potassium dihydrogen phosphate 0.3g / L, the rest is water) after washing twice, press and suspend in normal saline, refrigerate at 4°C for later use, and record it as cell A;
[0057] The nutrient solution for Pseudomonas ...
Embodiment 3
[0073] (1) Preparation of triclosan-degrading bacterial liquid
[0074] Pick 2 rings of Pseudomonas stutzeri (Pseudomonas stutzeri.) (source is the same as in Example 1), which are transferred to 30mL nutrient solution respectively, and the bacteria are cultivated at 35°C for 2 days, with a volume ratio of 10%. Inoculate into a container of proliferation medium, then culture at 35°C for 2 days, centrifuge at a speed of 5000rpm for 15min, and obtain the logarithmic growth phase cells of the above bacteria;
[0075] The logarithmic growth phase cells of the above-mentioned thalli are taken out, and with phosphate buffer (its main component sodium chloride 9.0g / L, potassium chloride 0.3g / L, dipotassium hydrogen phosphate 1.2g / L and potassium dihydrogen phosphate 0.3g / L, the rest is water), washed twice, pressed and suspended in normal saline, and refrigerated at 4°C for later use. Denoted as cell A;
[0076] The nutrient solution for Pseudomonas stutzeri was beef extract 6.0g / L...
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