Glyphosate-resistant gene, special expression vector and its application in obtaining glyphosate-resistant transgenic wheat
A technology of transgenic plants and transgenic cell lines, which is applied in the field of obtaining glyphosate-resistant transgenic wheat, can solve the problems of limiting the scope of use and use time
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Embodiment 1
[0037] Embodiment 1, optimization of GR79 gene and synthetic fusion gene wCTP:GR79m
[0038] The GR79 gene was isolated from a glyphosate-resistant strain in an extremely polluted environment, provided by the Institute of Biotechnology, Chinese Academy of Agricultural Sciences. The following aspects are mainly considered during optimization: wheat codon bias, GC content, and guide peptide. The guide peptide of the present invention is the chloroplast guide peptide (wCTP) from wheat RubisCO small subunit. See the gene sequence and GC content characteristics before and after optimization. The homology between the sequence optimized according to wheat codon bias and the original nucleotide sequence is 73.62%, and the codon usage before and after optimization is as follows: Figure 7 .
[0039] The fusion gene of the optimized GR79m gene and the gene combination of chloroplast guide peptide (wCTP) is named wCTP:GR79m, and its nucleotide sequence is the 2192-3675th nucleotide fr...
Embodiment 2
[0042] Embodiment 2, the application of wCTP:GR79m gene in anti-glyphosate
[0043] 1. Construction of pCS167-wCTP:GR79m overexpression vector
[0044] The specific construction method of pCG185-UMN vector is as follows: amplify about 2500bp Ubi:MCS:Nos fragment from pAHC-PSK, add PacI sites at both ends of the primers, insert the PacI sites in pCG185T-DNA after digestion with PacI , to obtain the intermediate vector pCG185-UMN.
[0045] The optimized gene was synthesized by Shanghai Sangon and cloned into the pUC57 vector to obtain the vector plasmid pUC57-wCTP:GR79. Digest pUC57-wCTP:GR79 with SpeI to recover a 1503bpwCTP:GR79m fragment, and connect the recovered fragment to the pCG185-UMN vector with SpeI digestion to remove P, to obtain an expression vector driven by the Ubiqutin promoter, named pCG185-wCTP:GR79m, the construction process Such as figure 1 a.
[0046] The recombinant plasmid pCG185-wCTP:GR79m was identified by digestion with SpeI, and the results were a...
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