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 problems such as high cost and environmental pollution
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Embodiment 1
[0021] Embodiment 1, the acquisition of the nitrophenyl nitroreductase gene of the present invention
[0022] Pick a single colony of Comamonas testosteroni CNB1 CGMCC No.1028 strain on LB plate into LB culture medium, shake culture at 30°C, collect the bacteria, extract genomic DNA, and partially digest with Mbo I Fragments up to about 30kb. SuperCos 1 was used as a vector (purchased from Stratagene Company, USA). The vector was first digested with Xba I, dephosphorylated, and then cut into two fragments of 6.8 kb and 1.1 kb with BamH I enzyme. The partially digested genome fragment and the treated vector were ligated with T4 DNA ligase at 16°C. 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-aminophenol aqueous sol...
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 BamH I recognition point, and the bold is the stop codon), the nitrophenyl nitroreductase gene of the present invention is amplified by PCR. 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 (5 U / μl) 0.4 μl. Wherein, the 10× buffer comes from TaKaRa Taq kit (TaKaRa Company, Code No.: DR100A). The PCR temperature conditions were fi...
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