Application of insecticidal protein
A protein and pest technology, applied in the field of insecticidal protein
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no. 1 example
[0090] The first embodiment, the acquisition and synthesis of genes
[0091] 1. Obtain Cry and Vip nucleotide sequences
[0092] The amino acid sequence (818 amino acids) of Cry1Ab-01 insecticidal protein, as shown in SEQ ID NO: 1 in the sequence listing; Cry1Ab-01 coding corresponding to the amino acid sequence (818 amino acids) of said Cry1Ab-01 insecticidal protein Nucleotide sequence (2457 nucleotides), as shown in SEQ ID NO:2 in the sequence listing. The amino acid sequence (615 amino acids) of Cry1Ab-02 insecticidal protein, as shown in SEQ ID NO:3 in the sequence listing; Cry1Ab-02 corresponding to the amino acid sequence (615 amino acids) of said Cry1Ab-02 insecticidal protein Nucleotide sequence (1848 nucleotides), as shown in SEQ ID NO:4 in the sequence listing.
[0093] The amino acid sequence (1156 amino acids) of the Cry1Ac-01 insecticidal protein, as shown in SEQ ID NO: 5 in the sequence listing; Cry1Ac-01 encoding the amino acid sequence (1156 amino acids) cor...
no. 2 example
[0099] The second embodiment, construction of recombinant expression vector and transformation of recombinant expression vector into Agrobacterium
[0100] 1. Construction of a recombinant cloning vector containing the Cry1A gene
[0101] 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 initiation 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: 2); MCS is the multiple cloning site).
[0102] Then, the recombinant cloning vector DBN01-T was transformed into Esche...
no. 3 example
[0120] The third embodiment, the acquisition of transgenic plants
[0121] 1. Obtaining transgenic corn plants
[0122] According to the commonly used Agrobacterium infection method, the immature embryos of the aseptically cultured corn variety Zong 31 (Z31) were co-cultured with the Agrobacterium described in 3 in the second embodiment, so that the T-DNA of recombinant expression vectors DBN100124, DBN100743, DBN100741, DBN100734, DBN100737 and DBN100736 (including the promoter sequence of corn Ubiquitin gene, Cry1Ab-01 nucleotide sequence, Cry1Ab-02 nucleotide sequence, Cry1Ac-01 nucleotide sequence sequence, Cry1Ac-02 nucleotide sequence, Cry1Ie nucleotide sequence, Cry1Ab / Ac nucleotide sequence, Cry1Ab+Vip3A nucleotide sequence, Hpt gene and Nos terminator sequence) into the maize genome, obtained Corn plants transferred to Cry1Ab-01 nucleotide sequence, corn plants transferred to Cry1Ab-02 nucleotide sequence, corn plants transferred to Cry1Ac-01 nucleotide sequence, tra...
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