A kind of production method of toxin tx4 (6-1) unlabeled recombinant protein
A technology of protein and recombinant bacteria, applied in the direction of microorganism-based methods, biochemical equipment and methods, recombinant DNA technology, etc., can solve the problems of low expression, the impact of biological safety analysis and research, and the impact of Tx4 insect resistance properties, etc. achieve high biological activity
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Embodiment 1
[0039] This embodiment provides an optimized artificially synthesized Tx4(6-1) gene, the specific sequence is shown in sequence 1 in the sequence listing, and the protein sequence corresponding to the gene is shown in sequence 2 in the sequence listing. The sequence before optimization in this example is based on the DNA sequence provided by the NCBI database, which is the natural DNA for the synthesis of Tx4(6-1) neurotoxin. According to the expression characteristics of Escherichia coli, the optimized DNA was optimized and synthesized. The NCBI database can only find the natural protein sequence (GenBank accession number 2108421A) of Tx4(6-1) without its corresponding nucleic acid sequence, so the optimized synthetic Tx4(6-1) Genes have no homologous DNA sequences.
[0040] Connect the genes before and after the above optimization to the pET series of E. coli expression vectors to obtain recombinant vectors. The above recombinant vectors verified by sequencing were transfor...
Embodiment 2
[0043] This embodiment provides a method for preparing protein, which specifically includes the following steps:
[0044] S1: Gene optimization, construction of prokaryotic expression vector and transformation: artificially synthesize the optimized mature scorpion insect neurotoxin Tx4(6-1) gene, and connect it to the expression vector pET32 to obtain the recombinant expression vector pET32 / Tx4(6-1) , the vector is constructed as figure 1 shown. The main vector construction steps are as follows:
[0045] (1) use B wxya I and H ind Ⅲ double enzyme cut recombinant vector Tx4(6-1) / pUC to obtain the target fragment PCP, the reaction system is as follows (endonucleases and buffers used were purchased from Dalian TAKARA Company):
[0046] carrier Tx4(6-1) / pUC 15 μL
[0047] 10×H buffer 5 μL
[0048] B wxya I 5U
[0049] h ind III 5U
[0050] Sterile water to 50μL
[0051] (2) with B wxya I and H ind Ⅲ Digest pET32 with double enzymes to obtain vector fragme...
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