Application of glycosyltransferase gene UGT85A5 of Arabidopsis thaliana to improvement of salt tolerance of plants
A technology of glycosyltransferase and Arabidopsis sugar, which is applied to the application of the Arabidopsis glycosyltransferase gene UGT85A5 in improving the salt tolerance of plants, the glycosyltransferase gene and its application field, which can solve the problem of Arabidopsis thaliana. Glycosyltransferase gene has not been reported and other problems, to achieve the effect of improving salt tolerance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0016] Example 1 Arabidopsis glycosyltransferase gene UGT85A5 molecular cloning
[0017] 1. Arabidopsis glycosyltransferase gene UGT85A5 clone
[0018] Obtained through the public website http: / / www.cazy.org UGT85A5 cDNA sequence of the gene. Primers were designed according to the cDNA sequence, wherein the forward primer was 85A5-F: 5'-GCGTCTAGAATGGCGTCTCATGCTGTTAC-3'; the reverse primer was 85A5-R: 5'-GCGGAGCTCCTACTCCCCCTAAAAGAACCT-3'. Arabidopsis RNA was extracted using TRIzol kit and amplified by RT-PCR UGT85A5 The full-length cDNA sequence of the gene. The RT-PCR amplification program was as follows: 94°C for 2 min; 94°C for 40 s, 55°C for 40 s, 72°C for 1 min, a total of 36 cycles; finally, 72°C for 7 min. will get UGT85A5 The gene cDNA was cloned into the pBluescript II SK(+) vector (a universal vector) after enzyme digestion and ligation, which is called pK85A5 intermediate vector, and then the full-length PCR verification and double enzyme digestion verificatio...
Embodiment 2
[0024] Example 2 Arabidopsis glycosyltransferase gene UGT85A5 transgenic application
[0025] 1. contains UGT85A5 Construction of cDNA expression vector for coding region
[0026] use Xba I and Sac Ⅰ Obtained by double digestion of pK85A5 intermediate vector UGT85A5 full-length sequence, and then with the Xba I and Sac ⅠThe part of pBI121 vector digested with double restriction enzymes was connected to get the glycosyltransferase gene driven by CaMV 35S promoter UGT85A 5 plant overexpression vector, this vector is named pB85A5. Finally, through gene PCR verification and double enzyme digestion verification, it was identified that the construction of the plant expression vector was correct.
[0027] 2. Agrobacterium-mediated Plant Genetic Transformation
[0028] Firstly, the plant expression vector pB85A5 was transformed into Agrobacterium LBA4404, and it was verified by PCR and double enzyme digestion that the vector had been transformed into Agrobacterium.
[...
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