Plant water treatment method of municipal wastewater at high altitude
A technology of urban domestic sewage and treatment method, applied in the field of water treatment of domestic sewage, can solve the problems of low oxygen content, freezing to death, difficult to repair, etc., and achieve the effect of enhancing oxygen binding capacity, improving cold resistance, and improving water treatment effect.
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specific Embodiment approach 1
[0013] Specific implementation mode 1: The plant water treatment method of high-latitude urban domestic sewage in this implementation mode is carried out according to the following steps:
[0014] 1. Construction of plant expression vectors;
[0015] 2. Constructing transgenic plants of A. japonicus;
[0016] 3. Cultivate and propagate transgenic plants of A. japonicus, and then transplant the transgenic plants of A. japonicus to high-latitude polluted water bodies for sewage treatment and restoration;
[0017] Wherein, in the first step, the plant expression vector contains a promoter superpromoter and a hyaline hemoglobin gene.
[0018] In this embodiment, the promoter superpromoter whose nucleotide sequence is shown in SEQ ID NO: 1 is first introduced into the vector p3300-Tnos, and then the synthetic hemoglobin gene (shown in SEQ ID NO: 2) and the promoter superpromoter are introduced into the vector The superpromoter vector p3300-Tnos was double digested with XbaI and S...
specific Embodiment approach 2
[0021] Specific embodiment two: the difference between this embodiment and specific embodiment one is: after the transgenic plants of A. sinensis in step three take root, the seedlings grow to a height of 3 cm for transplantation. Other steps and parameters are the same as those in Embodiment 1.
specific Embodiment approach 3
[0022] Embodiment 3: The difference between this embodiment and Embodiment 1 is that in Step 1, the promoter superpromoter is introduced into the vector p3300-Tnos to obtain the plasmid p3300-superpromoter-Tnos, and then the p3300-superpromoter-Tnos is extracted by alkaline lysis Plasmid, then use XbaI and SacI to carry out double enzyme digestion, the XbaI and SacI double enzyme digestion reaction system is 50 μL, consisting of 20 μL plasmid, 0.5 μL restriction endonuclease XbaI, 0.5 μL restriction endonuclease SacI, 5 μL 10× common enzyme digestion buffer and the balance of ddH 2 O composition; double enzyme digestion reaction: place in a water bath at 30°C for 2 hours. Other steps and parameters are the same as those in Embodiment 1.
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