Cultivating method of disease-resistant TaM2K transgenic wheat, and related biological materials of cultivating method
A technology of transgenic plants and disease resistance, applied in genetic engineering, plant genetic improvement, botany equipment and methods, etc., can solve problems such as lack and slow progress
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[0073] The preparation method of bacterial wheat kernels: soak the wheat kernels for 5-6 hours, boil them for 20 minutes, fill up the triangular flask, inoculate the mycelia block of the pathogenic bacteria of wheat sheath blight into the triangular flask after sterilization, and cultivate at a constant temperature of 25°C until The mycelia are densely covered with grains.
[0074] The preparation method of bacterial toothpick: put the toothpick segment upright and fill it with a small beaker, pour liquid MS medium into it, inoculate the mycelia block of wheat sheath blight pathogenic bacteria into the small beaker after sterilization, and cultivate it at a constant temperature of 25°C until the mycelia Densely strewn with toothpicks.
Embodiment 1
[0075] Embodiment 1, sheath blight resistant wheat kinase TaM2K and cloning of its coding gene
[0076] 1. Cloning of TaM2K gene
[0077] The inventors of the present invention isolated and cloned a wheat disease resistance-related protein from sheath blight resistant wheat CI12633, as shown in sequence 1 of the sequence listing, and named it TaM2K protein, which belongs to wheat kinase. The gene encoding TaMK protein is named TaM2K gene, and its cDNA is shown in sequence 2 of the sequence listing. In sequence 2 of the sequence listing, nucleotides 39-1145 are open reading frames.
[0078] Specific cloning steps: extract the total RNA from the stem of wheat CI12633 inoculated with the pathogenic bacteria of wheat sheath blight, and reverse-transcribe the RNA to synthesize the first-strand cDNA according to the procedure of the first-strand cDNA synthesis kit of Tiangen Biochemical Company, as The template for gene cloning was amplified with primers TaM2K-OF: 5'-GGAGCCAGCCTCG...
Embodiment 2
[0093] Embodiment 2, acquisition and disease resistance identification of transgenic TaM2K wheat resistant to sheath blight
[0094] 1. Construction of recombinant expression vector
[0095] 1. Extract the total RNA from the stem of wheat CI 12633 and reverse transcribe to obtain cDNA.
[0096] 2. Using the cDNA obtained in step 1 as a template, using a primer pair composed of TaM2K-O-F1 and TaM2K-O-R1, carry out PCR amplification under the action of the high-fidelity amplification enzyme PrimeSTAR, and recover the PCR amplification product.
[0097] TaM2K-O-F1: 5'-cG GGATCC ATGCGTCCGGGCGGGCCG-3';
[0098] TaM2K-O-R1: 5'-c GAGCTC gtggtggtggtggtggtgGCACGGCGGGGCGGCGAGGG-3'.
[0099] PCR reaction program: 94°C pre-denaturation for 5 minutes; 35 cycles of 98°C for 10s, 60.8°C for 30s, 68°C for 1.5min; 68°C for 10min.
[0100] 3. Take the PCR amplification product obtained in step 2, perform double digestion with restriction endonucleases BamHI and SacI, and recover the dige...
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