Pyrimidine nucleoside phosphorylase gene and application thereof
A pyrimidine nucleoside phosphorylase gene and a pyrimidine nucleoside phosphorylase technology are applied to the pyrimidine nucleoside phosphorylase gene and its application fields, and can solve the problems of small amount of enzyme and the like
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Embodiment 1
[0033] The establishment of embodiment 1 genetically engineered bacteria
[0034]According to the Escherichia coli pyrimidine nucleoside phosphorylase gene (Genbank: NC_000913.3) announced by Genebank, the pyrimidine nucleoside phosphorylase gene fragment was artificially synthesized, and the gene fragment was used as a template to expand the fragment by PCR amplification (on both sides of the fragment) plus BamHI and EcoRI endonuclease fragments), its nucleotide sequence is shown in SEQ ID NO.3 (Genbank: NC_000913.3). And the gene was inserted into the pET-28a(+) plasmid by using the HindⅢ and BamHI endonuclease sites, and the ligated vector was transferred into Escherichia coli BL21(DE3) to establish the pyrimidine nucleoside phosphorylase genetically engineered bacteria. The primers for PCR amplification of the pyrimidine nucleoside phosphorylase gene are as follows: the upstream primer is 5'-GTCTGATGTTTTTCATCTCG-3' (SEQ ID NO.4), and the downstream primer is 5'-CCCGTTTTCCC...
Embodiment 3
[0044] The shaking flask culture of embodiment 3 recombinant escherichia coli
[0045] The recombinant Escherichia coli E.ColiBL21NP1506 obtained in Example 2 was inoculated into 50 mL of LB medium containing kanamycin (30 μg / mL) (peptone 10 g / L, yeast extract 5 g / L, NaCl 10 g / L, pH7. 0), cultured at 37°C for 6 hours in a shaker at 200 rpm. Transfer 3% bacterial cell culture solution to a 250 mL shake flask equipped with LB medium (containing 30 μg / mL kanamycin), and culture under the same conditions with shaking. When the OD600 value of the bacterial solution reaches about 0.6, add the inducer isopropyl βD-thiogalactopyranoside (IPTG) to a final concentration of 0.1mmol / L, and place the culture solution in a shaker at 28°C and 200rpm to induce Express for 6 hours. After expression, the cells were collected by centrifugation (8000rpm, 10min, 4°C), washed twice with phosphate buffer (pH7.5, 10mmol / L), dispersed in the same pre-cooled buffer, and ultrasonicated in an ice-water...
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