A regulatory gene that reduces the total protein and phenol content of tobacco leaves
A technology for regulating gene and protein content, applied in the field of tobacco genetic engineering
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0035] Tobacco in this example Ntε-LCY2 The construction process of gene cloning and silencing vector 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 For gene research, select the specific coding sequence as the target fragment, and design the primer sequences 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 the template, PCR amplification was carried out to obtain Ntε-LCY2 Gene;
[0041] The PCR amplification program was as follows: pre-denaturation at 95°C for 3 min; denaturation at 95°C for 15s, annealing at 55°C for 15s, extension at 72°C for 30s, and after 34 cycles, complete extension at 72°C for 5min;
[0042] The PCR amplification products were detected by agarose gel electrophoresis, and the electrophoresis products were ...
Embodiment 2
[0054] On the basis of Example 1, using the VIGS technology mediated by Agrobacterium, the inventor further transformed the constructed recombinant TRV2-Ntε-LCY2 vector into tobacco plants, and made a verification analysis on the phenotypic changes of relevant plants. A brief introduction to the process is as follows.
[0055] (1) Transformation of Agrobacterium
[0056] It should be noted that, with reference to the operation of Example 1 and the prior art, the inventors simultaneously prepared TRV2-GFP and TRV2-PDS recombinant vectors as transgenic positive and negative controls, and the specific transformation process is as follows:
[0057] The positive cloned plasmids of TRV2-GFP (vector control), TRV2-PDS (VIGS efficiency control) and TRV2-Ntε-LCY2 were transformed into Agrobacterium GV3101 competent cells by electroporation, respectively. 50mg / L Rif YEB plate was cultured and screened. After 2d inversion culture at 28°C, colony PCR was used to screen Agrobacterium with...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com