Salicornia europaea SeVHA-A protein and encoding gene and application thereof
A technology that encodes genes and proteins, applied in applications, genetic engineering, plant genetic improvement, etc., can solve problems such as soil salinization exacerbated by cultivation measures
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Embodiment 1
[0053] Embodiment 1, the preparation of gene and protein
[0054] 1. Gene preparation
[0055] 1. Cloning of Salicornia seVHA-A gene
[0056] (1) Acquisition of 3'RACE gene fragment
[0057] The total RNA of Salicornia salicornia leaves was extracted by Trizol mini-extraction method, and the first-strand cDNA was synthesized by a reverse transcription kit (Quanshi Jinbio). SeV-1F / 3'oligdT was amplified by PCR with primers to obtain the 3' terminal fragment of cDNA. The specific PCR reaction conditions are as follows: 94°C 5min; 2 cycles: 94°C 30sec, 68°C 30sec, 72°C 1min; 2 cycles: 94°C 30sec, 66°C 30sec dT=-2°C, 72°C 1min; 25 cycles: 94°C 30sec, 54°C 30sec, 72°C 1min; 72°C 10min.
[0058] Upstream degenerate primer SeV-1F: 5'-CCTCTA(A / T / G)CTC(G / C / T)ACTGGACAGCG-3'. The downstream primer is 3'oligdT.
[0059] The obtained PCR products were subjected to agarose gel electrophoresis, and DNA fragments with similar sizes to the expected bands were recovered and sequenced afte...
Embodiment 2
[0088] Embodiment 2, the application of gene
[0089] 1. Overexpression—transformation of wild-type Arabidopsis
[0090] 1. Recombinant expression vector
[0091] The plant expression vector pBI121 was disclosed in the document "Overexpression of Organellar and Cytosolic AtHSP90 in Arabidopsis thaliana Impairs Plant Tolerance to Oxidative Stress. Hongmiao Song, Pengxiang Fan, Yinxin Li. Plant Mol Biol Rep (2009) 27: 342-349." Publicly available from Institute of Botany, Chinese Academy of Sciences. The plant expression vector pBI121 used contained a Kana (kanamycin) selection marker, and SeVHA-A and AtVHA-A genes were respectively inserted for gene function verification in Arabidopsis thaliana.
[0092]The SeVHA-A gene obtained in Example 1 was inserted between the Xba I and Sma I restriction sites of the plant expression vector pBI121, and the resulting recombinant expression vector was denoted as pBI121-SeVHA-A; sequencing verification, the results were in pBI121-SeVHA- T...
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