Mature chicken interferon-alpha gene capable of high-efficiency expression and preparation method of polypeptide thereof
A high-efficiency expression technology for alpha interferon, which is applied in the fields of botany equipment and methods, microorganism-based methods, biochemical equipment and methods, etc., can solve the problem of poor renaturation effect of recombinant chicken interferon alpha and recombinant chicken interferon alpha gene Low expression level and other problems, to achieve the effect of reducing production cost, good effect, improving efficiency and yield
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specific Embodiment approach 1
[0017] Specific embodiment one: the sequence of the mature chicken alpha interferon gene that can be highly expressed in this embodiment is:
[0018] ATGTGCAATC ATCTGCGTCC GCAAGATGCG ACCTTTAGCC ATGATAGCCT GCAGCTGCTG
[0019] CGCGATATGG CGCCGACCCT GCCGCAGCTG TGCCCGCAGC ATAACGCGAG CTGCAGCTTT
[0020] AACGATACCA TCCTGGATAC CAGCAACACC CGCCAGGCCG ATAAACCACCATGATATC
[0021] CTGCAGCATC TGTTTAAAAT CCTGAGCAGC CCGAGCACCC CGGCGCATTG GAACGATAGC
[0022] CAGCGCCAGA GCCTGCTGAA CCGCATTCAT CGCTATACCC AGCATCTGGA ACAGTGCCTG
[0023] GATAGCAGCG ATACCCGCAG CCGCACCCGC TGGCCGCGCA ACCTGCATCT GACCATTAAA
[0024] AAACATTTTA GCTGCCTGCA TACCTTTCTG CAGGATAACG ATTATAGCGC GTGCGCGTGG
[0025] GAACATGTGC GCCTGCAGGC GCGCGCGTGG TTTCTGCATA TTCATAACCT GACCGGCAAC
[0026] ACCCGCACCTAA.
specific Embodiment approach 2
[0027] Specific embodiment two: the method for preparing the mature chicken interferon alpha polypeptide that can be highly expressed in this embodiment is realized according to the following steps: 1. Apply the online software http: / / gcua.schoedl.de / to analyze the mature chicken interferon alpha gene The rare codons in the mature chicken α-interferon gene were synonymously replaced by the E. coli preferred codons through the E. coli preferred codon table, and the optimized chicken α-interferon gene was synthesized 2. Cloning the optimized chicken interferon alpha gene into the expression vector pWL, and then transforming it into Escherichia coli competent cell Top10, inducing expression after screening, obtaining wet bacteria after centrifugation, and then carrying out inclusion body detection of wet bacteria Extraction and dissolution; 3. The dissolved inclusion bodies are renatured and purified by Sephadex G50, and the protein is collected to complete the preparation of mat...
specific Embodiment approach 3
[0033] Specific embodiment 3: The difference between this embodiment and specific embodiment 2 is that in step 2, the induced expression after screening is the culture of screening positive clone strains, and then the culture is inoculated in the culture medium containing 50 μg / ml Amp at a volume ratio of 1:100. In LB liquid medium, culture at 30°C with shaking until OD 600 0.6 to 0.8, then placed in a constant temperature water bath at 42°C to induce expression by heat shock, then continued to induce culture at 42°C for 4 hours, and centrifuged to obtain wet bacteria. Other steps and parameters are the same as in the second embodiment.
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