Method for controlling injurious insect
A technology for pests, oriental armyworms, applied in the fields of botanical equipment and methods, biochemical equipment and methods, pesticides, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
no. 1 example
[0088] The first embodiment, the acquisition and synthesis of Cry1A gene
[0089] 1. Obtain the Cry1A nucleotide sequence
[0090] The amino acid sequence (818 amino acids) of the Cry1Ab-01 insecticidal protein, as shown in SEQ ID NO: 1 in the sequence listing; the Cry1Ab-01 core 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:4 in the sequence listing. 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:5 in the sequence listing.
[0091] The amino acid sequence (1177 amino acids) of the Cry1A.105 insecticidal protein, as shown in SEQ ID NO: 3 in the sequence listing; Cry1A.105 encoding the amino acid sequence...
no. 2 example
[0098] The second embodiment, construction of recombinant expression vector and transformation of recombinant expression vector into Agrobacterium
[0099] 1. Construction of a recombinant cloning vector containing the Cry1A gene
[0100] 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 promoter of SP6 RNA polymerase; T7 is the promoter of T7 RNA polymerase; Cry1Ab-01 is the promoter of Cry1Ab -01 nucleotide sequence (SEQ ID NO: 4); MCS is a multiple cloning site).
[0101] Then, the recombinant cloning vector DBN01-T was transformed...
no. 3 example
[0118] The third embodiment, the acquisition and verification of corn plants transferred to the Cry1A gene
[0119] 1. Obtaining corn plants transferred to the Cry1A gene
[0120] 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 T-DNA in recombinant expression vectors DBN100124, DBN100053, DBN100003, DBN100075, DBN100029 and DBN100076 (including the promoter sequence of corn Ubiquitin gene, Cry1Ab-01 nucleotide sequence, Cry1Ab-02 nucleotide sequence, Cry1A.105 nucleotide sequence Acid sequence, Vip3Aa nucleotide sequence, Cry1Fa nucleotide sequence, Cry2Ab nucleotide sequence, PMI gene and Nos terminator sequence) were transferred into the maize genome, and the maize with Cry1Ab-01 nucleotide sequence was obtained Plants, corn plants transferred to Cry1Ab-02 nucleotide sequence, corn plants transf...
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