Diaminobutyrate-2-oxoglutarate transaminase and application thereof
A technology of ketoglutarate aminotransferase and diaminobutyric acid, which is applied in the field of genetic engineering and can solve problems such as high price
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Embodiment 1
[0037] Example 1: Extraction of PD-1 genomic DNA of Streptomyces albulus.
[0038] According to the instructions provided by the manufacturer, use Genomic DNA Purification Kit (Takara, Dalian) to extract the genomic DNA of Streptomyces albulus PD-1 (Streptomyces albulus PD-1, CCTCC NO: M2011043) in the logarithmic growth phase, and use 8g / L agarose gel electrophoresis to detect the bacterial genome.
Embodiment 2
[0039] Example 2, Cloning of the gene (dabat) of diaminobutyric acid-2-ketoglutarate aminotransferase and construction of recombinant bacteria.
[0040] 2.1 Dabat PCR amplification:
[0041] According to the genome sequence of Streptomyces coelicolor A3(2) published by GeneBank, the following pair of primers were designed:
[0042] Primer 1: 5’-CCG GAATTC ATGACCATCACCCAGCCCGA-3’
[0043] Primer 2: 5’-CCC AAGCTT TCAGGCGCAGTCGCGCACCG-3’
[0044] Introduce the EcoR I and Hind III restriction sites into the underlined part of the 5'end of the above primers, and use the total DNA of Streptomyces albulus PD-1 (Streptomyces albulus PD-1, CCTCC NO: M2011043) as a template for PCR amplification , PCR reaction composition is as follows (25μl system): 2.5μl 10×Ex Taq Buffer, 2μl dNTP, 2.5μl MgCl 2 , 2μl DMSO, 2μl template, 2μl each of primer 1 and primer 2, 0.5μl Ex Taq, 9.5μl ddH 2 O, the PCR reaction program is: denaturation at 95°C for 5 minutes, then 94°C for 30s, 58°C for 60s, 72°C for 90s,...
Embodiment 3
[0060] Example 3: Induced expression of diaminobutyric acid-2-ketoglutarate aminotransferase.
[0061] Recombinant E. coli BL21-pET-dabat was inoculated into 5 mL of LB liquid medium supplemented with 25 μg / mL kanamycin, cultured in a shaker at 37°C overnight; then transferred to 5% (v / v) inoculum In a 500mL shake flask containing 100mL LB medium (containing 25μg / mL kanamycin), culture in a shaker at 37°C until the OD600 is about 0.6, add IPTG for induction (IPTG final concentration 1mmol / L), and cool to 25~ After continuing to express for 12 hours at 30°C, the cells were collected by centrifugation.
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