Method for improving rice yield traits by using genetic transformation
A rice production technology, applied in the field of genetic engineering, to achieve the effect of increasing production, low cost and high benefit
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0031] Functional verification of embodiment 1lrk1 gene
[0032] 1) Construction of lrk1 gene expression vector
[0033] Using pCAMBIA1304 as the expression vector, the Dongxiang wild rice lrk1 gene was inserted into the downstream of the 35S constitutive promoter of the pCAMBIA1304 vector. The structure diagram of the expression vector containing the lrk1 gene is as follows:
[0034] 2) lrk1 gene transformation experiments and results
[0035] 9311, one of the main parents of domestic super hybrid rice, is used as the transgenic recipient. The mature seeds of 9311 were dehulled and sterilized and inoculated on dedifferentiated plant tissue culture medium to induce callus. After 2-3 weeks of callus induction, the purified pCAMBIA1304 plasmid DNA containing lrk1 gene was introduced into 9311 callus cells by particle gun bombardment. Resistant cell lines were selected by continuous culture for 3-4 weeks on MS medium supplemented with 30 ppm hygromycin, and then the selected ...
Embodiment 2
[0045] Example 2 Method for transforming rice lrk1 gene into indica rice 9311
[0046] 1) Select the full-length ORF segment of lrk1 (see the sequence list), amplify it from Dongxiang wild rice by PCR method, synthesize an insert linker and clone it into the plant expression vector pCAMBIA1304, and obtain the lrk1 expression vector pCAMBIA1304 / lrk1.
[0047] 2) Culture medium for inducing rice callus
[0048] 1. Induction and subculture medium: MS+2mg / L 2,4-D.
[0049] 2. Hyperosmotic medium: MS+2mg / L 2,4-D+46.67g / L sorbitol+46.67g / L mannitol.
[0050] 3. The first round of screening medium: MS+2mg / L 2,4-D+30mg / L hygromycin.
[0051] 4. The second round of screening medium: MS+2mg / L 2,4-D+50mg / L hygromycin.
[0052] 5. Differentiation medium: MS+3mg / L 6-BA+0.5mg / L NAA+50mg / L hygromycin.
[0053] 6. Rooting and strong seedling medium: 1 / 2MS+0.1mg / L NAA
[0054] Note: 1. The above media all contain 30g / L sucrose + 2.5g / L agar, pH 5.8
[0055] 2. The culture conditions for ...
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