Cytochrome P450 gene participated in anabolism of tanshinone compound as well as coding product and application thereof
A technology of biosynthesis and tanshinone, applied in the direction of plant gene improvement, application, plant products, etc.
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Embodiment 1
[0016] Example 1: Cloning of Cytochrome P450 Genes in Salvia Miltiorrhiza
[0017] 1. The root of Salvia miltiorrhiza in full flowering stage was taken, the total RNA of Salvia miltiorrhiza was extracted by Trizol method, and the 5' and 3' end sequences of CYP76AH3 gene were obtained by using the 5' and 3' RACE kits of invitrogen to amplify respectively.
[0018] 2. Cloning and sequencing of full-length cDNA
[0019] The 5' and 3' RACE results were spliced, the ORF region was searched, full-length gene primers were designed, and cDNA was used as a template for amplification. Agarose gel electrophoresis showed that a specific fragment appeared at about 1500bp, the target fragment was recovered by the agarose gel recovery kit (Takara), cloned into the pGEM-T easy vector (Promega), positive clones were identified and verified by sequencing) (Beijing Huada Gene) for the construction of expression vectors.
Embodiment 2
[0020] Example 2, Bioinformatics of CYP76AH3 Gene Sequence
[0021] The length of the full-length open reading frame (ORF) of the cytochrome P450 gene CYP76AH3 gene of the Danshen diterpene synthetic metabolic pathway involved in the present invention is 1485bp, encoding 494 amino acids, and the detailed sequence is shown in SEQ ID No.1 and SEQ ID in the sequence listing No.2. The full-length open reading frame of CYP76AH3 was searched for homology in the NCBI database by BLAST program. The comparison analysis of the gene at the amino acid level showed that the amino acid sequence of the protein encoded by the Danshen CYP76AH3 gene had low homology with other species.
Embodiment 4
[0022] Example 4, Eukaryotic expression and functional analysis of CYP76AH3 gene
[0023] 1. Construction of yeast expression vector
[0024] By designing primers with EcoR I and Spe I restriction sites, the open reading frame of the cloned Danshen cytochrome P450 gene was inserted into the EcoR I and Spe I of the yeast expression vector pESC-His by using PCR method Between the restriction sites, the recombinant plasmid pESC-CYP76AH3 was obtained, which was verified by sequencing at Beijing Huada Gene Company.
[0025] 2. Induced expression
[0026] The constructed pESC-CYP76AH3 plasmid was transformed into YJ35, an engineered strain of the ferruginous yeast, and the expression was induced by galactose.
[0027] 3. Activity analysis of CYP76AH3 in Danshen
[0028] Introduce the CYP76AH3 gene expression vector into the Saccharomyces cerevisiae engineering strain producing ferruginol, pick 3 single clones and inoculate them in 5ml SD liquid medium, 30°C, 200rmin -1 Cultivate f...
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