Optimized triterpenoid synthase coding gene and application thereof
A triterpene compound, coding technology, applied in application, genetic engineering, plant genetic improvement and other directions, can solve problems such as unsatisfactory expression and influence
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Embodiment 1
[0025] Example 1, the acquisition of the SnOsOSC7 gene after codon optimization
[0026] According to the existing sequence information of Os06g28820 / OsOSC7 in the NCBI database (GenBank Accession Number: KC416147, sequence 3 in the sequence table, which is the gene sequence of unoptimized codons), according to the codon preference information of Pichia pastoris, without changing Based on the precursor of the deduced protein sequence, an optimized new SnOsOSC7 gene was designed according to the high-frequency codons of yeast. Its nucleotide sequence is sequence 1 in the sequence table (gene sequence after codon optimization). The encoded protein is OsOSC7, and its amino acid sequence is sequence 2 in the sequence list.
[0027] Sequence 1 in the sequence listing was artificially synthesized, and the DNA molecule indicated by the sequence was cloned into the multiple cloning site of the cloning vector pGEM-T-EASY to obtain pGEM-SnOsOSC7.
[0028] Sequence 3 in the sequence lis...
Embodiment 2
[0029] Embodiment 2, the application of the SnOsOSC7 gene after codon optimization
[0030] 1. Acquisition of recombinant yeast containing SnOsOSC7
[0031] 1. Construction of yeast expression vector
[0032] 1) The pGEM-SnOsOSC7 and pPICZA vectors (Invitrogen, V19020) obtained in Example 1 were completely digested with restriction endonuclease Not I, respectively. The digestion system is: 5 μg plasmid, 2.5 μL 10× digestion buffer, 1 μL Not I, plus ddH 2 O Supplement the reaction system to 50 μL. The enzyme digestion reaction conditions are: enzyme digestion at 37°C for 1 hour.
[0033] 2) Separate the digested products by agarose electrophoresis, recover about 2.2kb fragments containing SnOsOSC7 and about 3kb pPICZA vector fragments, and dissolve them in 20μL ddH 2 in o.
[0034] 3) Perform ligation reaction on the two fragments obtained in step 2). The ligation reaction system is: 1 μL T 4 DNA ligase, 2 μL 10× ligase buffer, 3 μL recovered DNA fragment containing the ...
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