Pest control method
A technology for pests and Spodoptera frugiperda, applied in the field of pest control
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
no. 1 example
[0078] The first embodiment, the acquisition and synthesis of Cry1Ab gene
[0079] 1. Obtain the Cry1Ab nucleotide sequence
[0080] The amino acid sequence (818 amino acids) of the Cry1Ab-01 insecticidal protein, as shown in SEQ ID NO: 1 in the sequence listing; Cry1Ab-01 encoding the amino acid sequence (818 amino acids) corresponding to the Cry1Ab-01 insecticidal protein Nucleotide sequence (2457 nucleotides), as shown in SEQ ID NO:3 in the sequence listing.
[0081] The amino acid sequence (615 amino acids) of the Cry1Ab-02 insecticidal protein, as shown in SEQ ID NO: 2 in the sequence listing; Cry1Ab-02 encoding the amino acid sequence (615 amino acids) corresponding to the Cry1Ab-02 insecticidal protein Nucleotide sequence (1848 nucleotides), as shown in SEQ ID NO:4 in the sequence listing.
[0082] 2. Synthesis of the above Cry1Ab nucleotide sequence
[0083] The Cry1Ab-01 nucleotide sequence (as shown in SEQ ID NO: 3 in the sequence listing) and the Cry1Ab-02 nucleo...
no. 2 example
[0084] The second embodiment, construction of recombinant expression vector and transformation of recombinant expression vector into Agrobacterium
[0085] 1. Construction of a recombinant cloning vector containing the Cry1Ab gene
[0086] The synthesized Cry1Ab-01 nucleotide sequence was connected to the cloning vector pGEM-T (Promega, Madison, USA, CAT: A3600), and the operation steps were carried out according to the instructions of the pGEM-T vector produced by Promega Company to obtain the recombinant cloning vector DBN01-T , its construction process is as follows figure 1 Shown (wherein, Amp represents the ampicillin resistance gene; f1 represents the replication origin of phage f1; LacZ is the LacZ start codon; SP6 is the SP6 RNA polymerase promoter; T7 is the T7 RNA polymerase promoter; Cry1Ab-01 is the Cry1Ab-01 nucleotide sequence (SEQ ID NO: 3); MCS is the multiple cloning site).
[0087] Then, the recombinant cloning vector DBN01-T was transformed into Escherichi...
no. 3 example
[0096] The third embodiment, the acquisition and verification of corn plants transferred to Cry1Ab gene
[0097] 1. Obtaining corn plants transferred to the Cry1Ab gene
[0098] According to the commonly used Agrobacterium infection method, the immature embryos of the aseptically cultured maize variety Zong 31 (Z31) were co-cultured with the Agrobacterium described in 3 in the second example, so that the The T-DNA in recombinant expression vectors DBN100124 and DBN100106 (including the promoter sequence of maize Ubiquitin gene, Cry1Ab-01 nucleotide sequence, Cry1Ab-02 nucleotide sequence, PMI gene and Nos terminator sequence) were transferred to maize chromosome In the group, corn plants transformed with the Cry1Ab-01 nucleotide sequence and corn plants transformed with the Cry1Ab-02 nucleotide sequence were obtained; meanwhile, wild-type corn plants were used as controls.
[0099] For Agrobacterium-mediated transformation of maize, briefly, immature immature embryos are isol...
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