Reducing enzyme of nitryl, phenylnitryl, encoding gene and application
A technology of nitrobenzene nitrate and coding gene, applied in the directions of oxidoreductase, application, genetic engineering, etc., can solve the problems of environmental pollution and high cost
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Embodiment 1
[0021] Embodiment 1, the acquisition of the nitrophenyl nitroreductase gene of the present invention
[0022] Pick the single colony of Comamonas testosteroni CNB1 CGMCC No.1028 strain on the LB plate into the LB culture medium, shake culture at 30°C, collect the bacteria, extract the genomic DNA, and partially digest it with MboI Fragments around 30kb. SuperCos 1 was used as a vector (purchased from Stratagene Company, USA). The vector was digested with XbaI, dephosphorylated, and then cut into two fragments of 6.8 kb and 1.1 kb with BamHI enzyme. Partially digested genome fragments and processed vectors were incubated at 16°C with T 4 DNA ligase ligation. The ligated fragments were packaged with Gigapack III XL packaging protein (purchased from Stratagene Company, USA). Transfected into Escherichia coli XL 1-blue MR (purchased from Stratagene Company, USA) to establish a Cosmid gene library. Use 2-aminophenol as a substrate to screen the library, culture in 2-aminopheno...
Embodiment 2
[0023] Embodiment 2, expression and functional identification of nitrophenyl nitroreductase of the present invention
[0024] 1, the expression of nitrophenyl nitroreductase of the present invention
[0025] Genomic DNA of Comamonas testosteroni (Comamonas testosteroni) CNB1 CGMCC No.1028 strain was extracted and used as a template in primer 1: 5'-GACGTTT CATATG CCGACCAGCCCGTTC-3' (underlined bases are NdeI recognition sites, bold start codons) and primer 2: 5'-TG GGATCC Under the guidance of TAATTCGTGGACGAAGGTGG-3' (the underlined base is the BamHI recognition point, and the bold is the stop codon), PCR amplifies the nitrophenyl nitroreductase gene of the present invention. Among them, the 50μl PCR reaction system is: template (60ng / μl) 0.5μl; dNTP (each 10mM) 1μl; primer (each 25μM) 1μl; 10× buffer 5μl; ddH 2 O 42.1 μl; Taq (5U / μl) 0.4 μl. Wherein, the 10× buffer comes from TaKaRa Taq kit (TaKaRa Company, Code No.: DR100A). The PCR temperature conditions were first 94°C...
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