Regulatory gene for reducing total protein of tobacco leaves and phenol content in smoke
A technique for regulating genes and total proteins, applied in the field of tobacco genetic engineering
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Embodiment 1
[0035] In this example, tobacco Ntε-LCY2 The process of gene cloning and silencing vector construction is briefly introduced as follows.
[0036] (1) Tobacco Ntε-LCY2 gene cloning
[0037] According to previous studies on the tobacco genome and related Ntε-LCY2 Gene research, select the specific coding sequence as the target fragment, and design the primer sequence for PCR amplification as follows:
[0038] Ntε-LCY2-F: 5′-TCTTAGGTGTGTGGAGGCAG-3′,
[0039] Ntε-LCY2-R: 5'-AGAATTTCCCTGAGGCAGCA-3'.
[0040] Using the cDNA of tobacco K326 leaves as a template, PCR amplification was carried out to obtain Ntε-LCY2 Gene;
[0041] The PCR amplification program was: pre-denaturation at 95°C for 3 min; denaturation at 95°C for 15 s, annealing at 55°C for 15 s, extension at 72°C for 30 s, and after 34 cycles, complete extension at 72°C for 5 min;
[0042] The PCR amplification products were detected by agarose gel electrophoresis, and the electrophoresis products were recovered for...
Embodiment 2
[0054] On the basis of Example 1, using the VIGS technology mediated by Agrobacterium, the inventors further transformed the constructed recombinant TRV2-Ntε-LCY2 vector into tobacco plants, and verified and analyzed the phenotypic changes of related plants. Specific experiments A brief introduction to the process is as follows.
[0055] (1) Transformation of Agrobacterium
[0056] It should be noted that, referring to the operation of Example 1 and the prior art, the inventor simultaneously prepared TRV2-GFP and TRV2-PDS recombinant vectors as positive and negative controls for transgenes. The specific transformation process is as follows:
[0057] The positive cloning plasmids of TRV2-GFP (vector control), TRV2-PDS (VIGS efficiency control) and TRV2-Ntε-LCY2 were transformed into Agrobacterium GV3101 competent cells by electric shock transformation respectively, using 50 mg / L Kan and The YEB plates with 50 mg / L Rif were cultured and screened, and after inverted culture at 2...
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