CgWRKY57 gene of cymbidium goeringii, and application of gene
A gene and amino acid technology, applied in Chunlan CgWRKY57 gene and its application field, achieves the effect of wide application prospect
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Embodiment 1
[0020] The material used in this example is the leaves of Chunlan 'Songmei', which are quickly frozen in liquid nitrogen after harvest and stored in an ultra-low temperature refrigerator (-80°C).
[0021] 1) Extraction of total RNA from Chunlan leaves
[0022] According to the instructions of the TaKaRa plant total RNA extraction kit, the specific operation is as follows:
[0023] The ultra-low temperature frozen leaves of Chunlan were quickly transferred to a mortar pre-cooled with liquid nitrogen, and the tissue was ground with a pestle, during which liquid nitrogen was continuously added until it was ground into powder; the powdered sample was added to a 450 μl In a 1.5 mL sterilized tube of Buffer PE, pipette repeatedly until there is no obvious precipitation in the lysate; centrifuge the lysate at 12,000 rpm at 4°C for 5 minutes; pipette the supernatant carefully into a new 1.5 mL sterilized tube middle. Add 1 / 10 volume of Buffer NB to the supernatant, shake and mix wit...
Embodiment 2
[0045] Research indicates WRKY57 The gene was expressed in every tissue and organ of Chunlan ( figure 2 a), but the expression level of the gene is the highest in Chunlan root, indicating that the gene is functionally active in the root. Through the expression analysis of the leaves of Chunlan low temperature stress treatment ( figure 2 b), to prove CgWRKY57 Genes in Chunlan leaves can respond to low temperature stress, and play an important regulatory role in this process.
[0046] The plant material used in this embodiment is Arabidopsis ( Arabidopsis thaliana ) Col (Columbia) wild-type seeds.
[0047] The Escherichia coli strain used in this example was Trans5α; the Agrobacterium strain was GV3101, which were used to transform Arabidopsis thaliana; the plant expression vector used in the experiment was pBI121. The strains used were purchased from Quanshijin Biotechnology Company and Price Biotechnology Company.
[0048] 1) CgWRKY57 Construction of gene overexpres...
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