Plant drought-induced artificial synthesis promoter SP2 and application thereof
A promoter, inducible technology, applied in the field of genetic engineering, can solve the problems of low expression activity and low specificity
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Embodiment 1
[0017] Example 1. Design of plant stress-inducible promoter SP2
[0018] By combining the soybean stress transcriptome sequencing data with the existing soybean stress expression profile data in Genbank, 63 target genes regulated by drought were screened out, and then they were listed for cluster module classification. After obtaining 4 clusters, the motif identification software was used to identify the motifs of each cluster, and finally 46 common expression elements of promoters related to stress regulation were obtained. Select G-box, ABRE, ABF, SORLIP1, CCA1, and E2F as the basic cis-elements, each element is repeated 4 times in series, and the two elements are separated by a random sequence of 7-9 bases. Synthetic Promoter 2, referred to as SP2, is constructed by connecting with 35S core promoter Core CaMV 35S, and its nucleotide sequence is SEQ ID No.1.
Embodiment 2
[0019] Example 2. Construction of promoter SP2 expression vector
[0020] The sequence of SP2 (SEQ ID No.1) was synthesized into the vector pUC57 by artificial synthesis method, and enzyme cutting sites were added at both ends of the sequence Bam H l and Hind III. The pUC57-SP2 vector and pBI121 plasmid were used respectively Bam H l and Hind III carried out double enzyme digestion, and after recovering the enzyme digestion products respectively, after connection, transformation and identification, the expression vector pBI121-SP2 (such as figure 1 ). The vector pBI121-SP2 was transformed into Agrobacterium EHA105 for infecting tobacco.
Embodiment 3
[0021] Example 3. Obtaining of Transgenic SP2 Tobacco
[0022] The leaf disc transformation method (Horsch et al. 1988) was followed. The Agrobacterium solution is diluted with sterilized water to 106-107 cells / mL (generally about 30 times diluted). Take sterile tobacco leaves, remove the main veins, cut the leaves into square shapes, then immerse them in the diluted bacterial solution, and infect for 8-10 minutes.
[0023] 1) Co-culture
[0024] After taking out the leaf explants, blot the bacteria solution on sterile filter paper, place the leaf surface down on the surface of the MS medium, and culture in the dark at 24°C-25°C for 2 days.
[0025] 2) Selective culture
[0026] Transfer the co-cultured leaves to the selective differentiation medium (containing 250 mg / L cephalosporin; 100 mg / L kanamycin), at 28°C, with 16 hours of light per day, and change the medium every 15-20 days.
[0027] 3) Rooting culture
[0028] When the differentiated resistant shoot grows to ab...
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