Sorghum drought response gene SbJAZ1 and recombinant vector and expression method thereof
A recombinant vector and gene technology, which can be used in chemical instruments and methods, botanical equipment and methods, biochemical equipment and methods, etc., and can solve the problems that have not yet been reported on JAZ protein research.
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Embodiment 1
[0032] Example 1: Acquisition and Analysis of Sorghum Drought Response Gene SbJAZ1
[0033] According to the reported protein sequence of the rice JAZ1 gene, blastP searched the sorghum genome database (https: / / phytozome) to find the sorghum homologous gene SbJAZ1 (gene number is Sb08g005080, and its nucleotide sequence is shown in SEQ ID NO.1). Search the NCBI database with the SbJAZ1 protein (its amino acid sequence is shown in SEQ ID NO.2), download the JAZ1 gene in other species, and use MEGA 7.0 software to construct a no root phylogenetic tree, by figure 1 It can be seen that SbJAZ1 and maize JAZ1 are clustered together and have the closest relationship. It can be seen that the SbJAZ1 gene is a drought-responsive gene in sorghum.
Embodiment 2
[0034] Example 2: Construction and Identification of Sorghum Drought Response Gene SbJAZ1 Recombinant Vector
[0035] 1. Extract sorghum RNA and reverse transcribe cDNA
[0036] The sorghum BTx623 material was taken, the total RNA at the seedling stage was extracted with an RNA extraction kit (Tiangen Biochemical Technology (Beijing) Co., Ltd.), and cDNA was obtained by reverse transcription with a reverse transcription kit (Promega).
[0037] 2. Using cDNA as a template to amplify the SbJAZ1 gene;
[0038] Primers were designed to amplify the SbJAZ1 gene using cDNA as a template.
[0039] Primers are as follows:
[0040] Upstream primer: SbJAZ1-F: GC GAATTC ATGGCCGCCGAGCAG underlined is the EcoRI restriction site;
[0041] Downstream primer: SbJAZ1-R:CG AAGCTT The underline of TCAGCTGAGGCTGAGCGC is the HindIII restriction site;
[0042] The upstream and downstream primers are shown in SEQ ID NO.3 and 4 respectively.
[0043]The PCR amplification system used for gene a...
Embodiment 3
[0048] Example 3: Induced expression of SbJAZ1 protein
[0049] 1. Obtain the recombinant prokaryotic expression strain of SbJAZ1
[0050] The single clone successfully sequenced in Example 2 was selected and inoculated into 50ug / mL kanamycin liquid medium, cultured overnight at 37°C and 200rpm, and the pET-28a - The SbJAZ1 recombinant expression vector was extracted, and the recombinant expression vector plasmid was transformed into Escherichia coli expression strains BL21(DE3), JM109(DE3), BL21(DE3)pLysS, Tuner(DE3), Rosetta(DE3), and the expression of SbJAZ1 protein was detected.
[0051] 2. Cultivate the activated strain overnight
[0052] The above-mentioned recombinant prokaryotic expression strains were activated by culturing overnight. For example, transfer BL21(DE3), JM109(DE3), Tuner(DE3) strains to 50ug / mL kanamycin liquid medium, transfer Rosetta(DE3), BL21(DE3)pLysS strains to 50ug / mL In mL kanamycin+50ug / mL chloramphenicol liquid medium, cultivate the activate...
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