Method for enhancing content of tanshinone in salvia miltiorrhiza hairy root by double-key enzyme genetic transformation
A technology for tanshinone content and hairy roots, applied in biochemical equipment and methods, genetic engineering, plant genetic improvement, etc., can solve the problems of low accumulation of active ingredients, high cost, poor stability, etc., and achieve the goal of increasing the total tanshinone content, Alleviate the shortage of drug sources and have reliable effects
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Embodiment 1
[0073] (1) Extraction of total RNA from Salvia miltiorrhiza and synthesis of the first strand of cDNA:
[0074] The RNApreppureplantkit provided by TIANGEN was used to extract total RNA from the transgenic hairy roots of Salvia miltiorrhiza, and the extraction steps followed the instructions in the kit. The fresh weight of Salvia miltiorrhiza transgenic hairy roots used to extract total RNA is about 0.1 g, and the DNA in the sample has been removed with DNase working solution during the extraction process. Measure the relative absorbance value of the extracted RNA on a spectrophotometer, and calculate the purity and concentration of the extracted RNA. After calculation based on the concentration of different RNA samples, the first-strand cDNA was synthesized with reverse transcriptase XL (AMV) using 0.5 μg RNA as the initial amount, and the operation steps were in accordance with the instructions provided by Promega.
[0075] (2) wxya with SmGGPPS Design of coding sequenc...
Embodiment 2
[0078] Contains Danshen wxya and SmGGPPS Construction of plant expression vectors for genes.
[0079] (1) Intermediate vector pCAMBIA1304 + The build:
[0080] Using pBI121 and pCAMBIA1304 as materials, construct the plant expression vector pCAMBIA1304 + . Specifically, pBI121 and pCAMBIA1304 were digested with HindIII / EcoRI; the pBI121-GUS expression cassette and the large fragment of pCAMBIA1304 were recovered; ligation transformation was carried out, and single-clonal colonies were picked to extract plasmids for digestion and verification. The results showed that the plant expression vector pCAMBIA1304 + The build was successful.
[0081] (2) Plant expression vector pCAMBIA1304 + - SmGGPPS The build:
[0082] The successful pCAMBIA1304 constructed above + Based on the cloned from Salvia miltiorrhiza SmGGPPS gene replacement GUS Gene. Specifically, BamHI / SacI double enzyme cut pMD18T- SmGGPPS and pCAMBIA1304 + ;Recycle SmGGPPS gene an...
Embodiment 3
[0087] Agrobacterium rhizogenes mediated wxya with SmGGPPS Genetic transformation of Salvia miltiorrhiza to obtain transgenic hairy roots.
[0088] (1) Containing plant expression vector pCAMBIA1304 + - wxya - SmGGPPS Obtaining Agrobacterium rhizogenes engineering bacteria;
[0089] The plant bivalent expression carrier pCAMBIA1304 that contains SmHMGR and SmGGPPS gene in embodiment 2 + - wxya - SmGGPPS Transformed into Agrobacterium rhizogenes C58C1, picked a single clone colony for PCR verification. The results showed that containing wxya with SmGGPPS The plant expression vector of the gene has been successfully constructed in Agrobacterium rhizogenes strain C58C1.
[0090] (2) Mediated by Agrobacterium rhizogenes wxya , SmGGPPS Genetic transformation of salvia miltiorrhiza:
[0091] ① Pre-cultivation of explants: cut leaves of healthy and sterile seedlings of Salvia miltiorrhiza (0.5 cm 2 ), inoculated onto the pre-culture medium (MS), and c...
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