Improved yield and stress tolerance in transgenic plants
A technology for transgenic plants and transgenic seeds, which is applied in the field of plant genomics and plant improvement, and can solve the problems of reduced yield variation of hybrid varieties, plant death, and increased yield of conventional varieties.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0228] It should be understood that the invention is not limited to the particular apparatus, machines, materials and methods described. While specific embodiments have been described, equivalents may be used in practicing the invention.
[0229] The foregoing general description of the invention will be more readily understood by reference to the following examples, which are included merely to illustrate certain aspects and embodiments of the invention and are not intended to be limiting of the invention. It will be appreciated by those skilled in the art that a polypeptide associated with a particular first trait may also be associated with at least one other, unrelated and inherent second trait that cannot be expressed through the first trait. predict.
Embodiment I
[0230] Example I. Item Types and Vector and Cloning Information
[0231] A number of constructs are used to modulate the activity of the sequences of the invention. A separate entry is defined as the analysis of a particular construct (for example, this may include the G1988 line constitutively overexpressing the sequences of the invention). In this study, the full-length wild-type gene was fused directly to a promoter driving its expression in transgenic plants. This promoter may be the native promoter of the gene or a constitutive promoter such as the cauliflower mosaic virus 35S promoter. Alternatively, promoters driving tissue-specific or conditional expression can be used in similar studies.
[0232] In this study, the expression of a given polynucleotide under a specific promoter was achieved by a direct promoter fusion construct in which the sequence was cloned directly behind the promoter of interest. An advantage of the direct fusion approach is that it allows simp...
Embodiment II
[0240] Example II. Transformation
[0241] Transformation of Arabidopsis was performed by an Agrobacterium-mediated protocol based on the method of Bechtold and Pelletier (1998). All experiments were performed using Columbia ecotypes unless otherwise indicated.
[0242] plant preparation . Arabidopsis seeds were sown in mesh covered pots. Thin out the seedlings 10 days after planting so that 6-10 evenly spaced plants remain per pot. The primary bolt was cut off one week before transformation to break the apical dominance and promote the formation of auxiliary shoots. Transformation typically takes place 4-5 weeks after sowing.
[0243] Bacterial Culture Preparation . Inoculated Agrobacterium stocks were either from single cloning plates or from glycerol stocks and grown to saturation with appropriate antibiotics. On the morning of transformation, the saturated culture was centrifuged and the bacterial pellet was resuspended in Infiltration Media (0.5X MS, 1X B5 vitam...
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