Insecticidal protein, its coding gene and application
An insecticidal protein and insecticidal gene technology, applied in the field of insecticidal proteins, can solve the problems of environmental pollution, affecting the living conditions of the population, and the expression level and virulence of the PIC6 insecticidal protein have not been found.
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no. 1 example
[0078] The first embodiment, the acquisition and synthesis of PIC6-02 gene sequence
[0079] 1. Obtain the PIC6-02 gene sequence
[0080] The amino acid sequence (699 amino acids) of the PIC6-02 insecticidal protein is shown in SEQ ID NO: 2 in the sequence listing; the amino acid sequence (699 amino acids) encoding the insecticidal protein corresponding to the PIC6-02 is obtained according to the maize preference codon amino acids) nucleotide sequence (2100 nucleotides), as shown in SEQ ID NO:1 in the sequence listing. For maize codon usage bias, please refer to http: / / www.kazusa.or.jp / codon / cgi-bin / showcodon.cgi?species=381124.
[0081] 2. Synthesize the above-mentioned PIC6-02 nucleotide sequence
[0082] The PIC6-02 nucleotide sequence (shown as SEQ ID NO: 1 in the sequence listing) was synthesized by Nanjing GenScript Biotechnology Company; the synthesized PIC6-02 nucleotide sequence (SEQ ID NO: 1) The 5' end of the PIC6-02 nucleotide sequence (SEQ ID NO: 1) is also con...
no. 2 example
[0086] The second embodiment, construction of recombinant expression vector and transformation of recombinant expression vector into Agrobacterium
[0087] 1. Construction of recombinant cloning vector DBN01-T containing PIC6-02 nucleotide sequence
[0088] The synthesized PIC6-02 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; PIC6-02 It is the nucleotide sequence of PIC6-02 (SEQ ID NO: 1); MCS is the multiple cloning site).
[0089]Then, the recombinant cloning vector DBN01-T was tran...
no. 3 example
[0105] The third embodiment, the acquisition and verification of corn plants transferred to PIC6-02 nucleotide sequence
[0106] 1. Obtaining corn plants transferred to the PIC6-02 nucleotide sequence
[0107]According to the routinely used Agrobacterium infection method, the immature embryos of the aseptically cultivated corn variety Zong 31 (Z31) were co-cultured with the Agrobacterium described in 4 in the second example, so as to infect 2 and 3 in the second example. T-DNA (including the promoter sequence of corn Ubiquitin gene, PIC6-02 nucleotide sequence, PIC6-02 The substituted nucleotide sequence, PIC6-02 truncated nucleotide sequence, PIC6-02 added nucleotide sequence, natural sequence, PMI gene and Nos terminator sequence) were transferred into the maize genome, and the transferred PIC6- Corn plant with 02 nucleotide sequence, corn plant with PIC6-02 substituted nucleotide sequence, corn plant with PIC6-02 truncated nucleotide sequence, corn plant with PIC6-02 added...
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