Anti-Verticillium dahliat protein from Sea Island cotton and its coding gene and application
A verticillium wilt and coding technology, applied in the field of genetic engineering, can solve the problems of susceptibility or disease resistance, poor disease resistance of verticillium wilt, and achieve the effect of improving disease resistance and high application value
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Embodiment 1
[0071] Embodiment 1, the acquisition of GbAt11 gene
[0072] 1. Verticillium dahliae V 991 Induced Sea Island Cotton Leaves
[0073] Verticillium dahliae V 991 Cultivate in Cha's medium for 15 days, filter with gauze, count the filtrate with a counting plate under a microscope, and then adjust the spore concentration to 1×10 6 / mL. Take the young leaves of sea island cotton 7124 and soak them in 1×10 6 / mLV991 spore suspension, record the time when the leaves start to soak, and take out the leaves at 0h, 3h, 6h, 12h and 24h after soaking, wrap them in tin foil, freeze them with liquid nitrogen, and store them in a -80°C refrigerator stand-by.
[0074] 2. Extraction of sea island cotton RNA
[0075] Use the EASYspin Plant RNA Rapid Extraction Kit to extract sea island cotton RNA:
[0076] (1) Mix 500 μl lysate RLT (beta-mercaptoethanol has been added) and 50 μl PLANTaid in a 1.5ml centrifuge tube.
[0077] (2) Grind the sample in liquid nitrogen, transfer about 50 mg of...
Embodiment 2
[0099] Example 2, the acquisition and functional analysis of GbAt11 transgenic cotton
[0100] 1. The acquisition and identification of GbAt11 transgenic cotton
[0101] 1. Acquisition of recombinant expression vector pSPT-02-GbAt11
[0102] Design primers At11-Sal1 and At11-KpnI according to the GbAt11cDNA sequence (sequence 2), the sequences are as follows:
[0103] At11-Sal1: 5'-CG GTC GAC ATGTCGATCGCGTTGGAACG-3' (underlined is the SalI enzyme recognition site, and the subsequent sequence is the 1st to 20th position of sequence 2);
[0104] At11-KpnI:5'-CG GGTACC GTTATATTCACGTACATCAGCC-3' (the underlined mark is the KpnI enzyme recognition site, and the subsequent sequence is the reverse complementary sequence from the 744th to the 765th position of Sequence 2).
[0105] Using the recombinant plasmid pMD18-GbAt11 obtained in Example 1 as a template, PCR amplification was performed with primers At11-Sal1 and At11-KpnI.
[0106] After the reaction, the obtained PCR pro...
Embodiment 3
[0191] Example 3, Obtaining and Functional Analysis of GbAt11 Transgenic Arabidopsis
[0192] 1. Acquisition and identification of GbAt11 transgenic Arabidopsis
[0193] 1. Acquisition of recombinant expression vector super1300-MYC-GbAt11
[0194] Design primers At11-Sal1 and At11-KpnI according to the GbAt11cDNA sequence (sequence 2), the sequences are as follows:
[0195] At11-Sal1: 5'-CG GTC GAC ATGTCGATCGCGTTGGAACG-3' (underlined is the SalI enzyme recognition site, and the subsequent sequence is the 1st to 20th position of sequence 2);
[0196] At11-KpnI:5'-CG GGTACC GTTATATTCACGTACATCAGCC-3' (the underlined mark is the KpnI enzyme recognition site, and the subsequent sequence is the reverse complementary sequence from the 744th to the 765th position of Sequence 2).
[0197] Using the recombinant plasmid pMD18-GbAt11 obtained in Example 1 as a template, PCR amplification was performed with primers At11-Sal1 and At11-KpnI.
[0198] After the reaction, the obtained P...
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