Pest control method
A technology for pests and Spodoptera litura, applied in the direction of botany equipment and methods, biochemical equipment and methods, insecticides, etc.
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no. 1 example
[0088] The first embodiment, the acquisition and synthesis of Vip3A gene
[0089] 1. Obtain the nucleotide sequence of Vip3A
[0090] Amino acid sequence (789 amino acids) of Vip3Aa-01 insecticidal protein, as shown in SEQ ID NO: 1 in the sequence listing; Vip3Aa-01 encoding the amino acid sequence (789 amino acids) corresponding to said Vip3Aa-01 insecticidal protein Nucleotide sequence (2370 nucleotides), as shown in SEQ ID NO:3 in the sequence listing. Amino acid sequence (789 amino acids) of the Vip3Aa-02 insecticidal protein, as shown in SEQ ID NO: 2 in the sequence listing; Vip3Aa-02 encoding the amino acid sequence (789 amino acids) corresponding to the Vip3Aa-02 insecticidal protein Nucleotide sequence (2370 nucleotides), as shown in SEQ ID NO:4 in the sequence listing.
[0091] 2. Obtain the nucleotide sequences of Cry1A and Cry1F
[0092] The Cry1Ab nucleotide sequence (2457 nucleotides) encoding the amino acid sequence (818 amino acids) of the Cry1Ab insecticidal...
no. 2 example
[0095] The second embodiment, construction of recombinant expression vector and transformation of recombinant expression vector into Agrobacterium
[0096] 1. Construction of a recombinant cloning vector containing the Vip3A gene
[0097] The synthetic Vip3Aa-01 nucleotide sequence was ligated into 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; Vip3Aa-01 is the promoter of Vip3Aa -01 nucleotide sequence (SEQ ID NO: 3); MCS is a multiple cloning site).
[0098] Then, the recombinant cloning vector DBN01-T was transformed i...
no. 3 example
[0113] The third embodiment, the acquisition and verification of corn plants transferred to Vip3A gene
[0114] 1. Obtaining corn plants transferred to the Vip3A gene
[0115] 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 DBN100066, DBN100003 and DBN100276 (including the promoter sequence of corn Ubiquitin gene, Vip3Aa-01 nucleotide sequence, Vip3Aa-02 nucleotide sequence, Cry1Ab nucleotide sequence, Cry1Fa nucleotide sequence , PMI gene and Nos terminator sequence) were transferred into the maize genome, and the maize plants transferred to the Vip3Aa-01 nucleotide sequence, the maize plants transferred to the Vip3Aa-01-Cry1Ab nucleotide sequence and the Vip3Aa -02-Cry1Fa nucleotide sequence of maize plants; meanwhile wild-type maize plants are used as con...
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