Herbicide resistance protein, its encoding gene and use
A herbicide and protein technology, applied in genetic engineering, plant gene improvement, application, etc., can solve the problem of undiscovered 24DT11 herbicide resistance protein expression level, herbicide tolerance report, etc., to achieve increased flexibility and high flexibility sexual effect
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no. 1 example 、24D
[0097] The first embodiment, the acquisition and synthesis of 24DT11 gene sequence
[0098] 1. Obtain the 24DT11 gene sequence
[0099] The amino acid sequence (292 amino acids) of the 24DT11 herbicide resistance protein is shown in SEQ ID NO: 2 in the sequence listing; the amino acid sequence (292 amino acids) corresponding to the 24DT11 herbicide resistance protein encoding is obtained according to the plant preference codon amino acids) nucleotide sequence (879 nucleotides), as shown in SEQ ID NO:1 in the sequence listing.
[0100] 2. Synthesize the above-mentioned 24DT11 nucleotide sequence
[0101] The 24DT11 nucleotide sequence (shown as SEQ ID NO: 1 in the sequence listing) was synthesized by Nanjing KingScript Biotechnology Co., Ltd.; the 5' of the synthesized 24DT11 nucleotide sequence (SEQ ID NO: 1) The end is also connected with a SpeI restriction site, and the 3' end of the 24DT11 nucleotide sequence (SEQ ID NO: 1) is also connected with a KasI restriction site. ...
no. 2 example
[0102] The second embodiment, construction of Arabidopsis thaliana and soybean recombinant expression vector
[0103] 1. Construction of recombinant cloning vector DBN01-T containing 24DT11 nucleotide sequence
[0104] The synthetic 24DT11 nucleotide sequence was connected 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 of the product of Promega Company to obtain the recombinant cloning vector DBN01-T, which Build process such as 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; 24DT11 is the 24DT11 nucleoside acid sequence (SEQ ID NO: 1); MCS is the multiple cloning site).
[0105]Then, the recombinant cloning vector DBN01-T was transformed into Escherichia coli T1 competent cells (...
no. 3 example
[0113] The third embodiment, the acquisition of Arabidopsis plants transferred to 24DT11 nucleotide sequence
[0114] 1. Transformation of recombinant expression vector into Agrobacterium
[0115] The constructed recombinant expression vectors DBN100411 and DBN100411N (control sequence) were transformed into Agrobacterium GV3101 by liquid nitrogen method, and the transformation conditions were: 100 μL Agrobacterium GV3101, 3 μL plasmid DNA (recombinant expression vector); placed in liquid nitrogen 10 minutes at 37°C in a warm water bath for 10 minutes; Inoculate the transformed Agrobacterium GV3101 in LB test tubes and culture at 28°C and 200rpm for 2 hours, and apply Rifampicin containing 50mg / L and 50 mg / L of kanamycin on the LB plate until a positive single clone grows, pick a single clone and culture it and extract its plasmid, digest DBN100411 with restriction endonuclease SmaI and EcoRV, and carry out enzyme digestion verification. DBN100411N (control sequence) was dige...
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