A new gene of wheat grain lipoxygenase and its application
A technology of lipoxygenase and wheat grain, applied in the field of plant biology, can solve the problem of less research on wheat
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Embodiment 1
[0038] The screening of the specific primer pair of embodiment 1 wheat grain lipoxygenase new gene
[0039]Referring to the NCBI China Spring 3B chromosome sequence (HG670306.1), starting from the nucleotide sequence with the LH2 functional domain (Lipoxygenase homology 2 (beta barrel) domain) on the 3B chromosome, search for the closest start codon and A stop codon defines the open reading frame. Then the new lipoxygenase gene was divided into 6 sections, primers were designed and amplified by primer 3.0.
[0040] Experimental materials: Klein Proteo and Klein Chaja mature grains;
[0041] Primers: as shown in Table 1.
[0042] The specific method for extracting wheat Klein Proteo and Klein Chaja full-maturity grain genomic DNA is as follows:
[0043] (1) Smash it with a hammer and put it into a 1.5mL centrifuge tube, add 1mL sample extract, shake for 30 minutes, and make it fully mixed; the sample extract contains 288mM NaCl, 200mM Tris-HCl, 25mM EDTA, 0.5 % SDS.
[004...
Embodiment 2
[0054] Example 2 Using specific primer pairs (BJF, BJR) to detect lipoxygenase allelic types of wheat varieties / lines 11 wheat varieties / lines to be detected: Yumai 47 (Fengyou 3)a, Jinmai 54a, Jinmai Mai 50b, Yuanfeng 898b, Gaoyou 503 (Xiaoyan 503)a, 04zhong 70b, Ji 923235a, Neixiang 1822 (Yumai 17)b, Han 4589b, Xinmai 19b and Xinmai 9987b.
[0055] The grain genomic DNA of the above-mentioned 11 wheat varieties / lines was extracted by using the method for extracting genomic DNA from wheat matured grains in Example 1.
[0056] Using the genomic DNA of the grains of the above 11 wheat varieties / lines as templates, amplification was performed using specific primer pairs (BJF, BJR): the PCR reaction system contained 1 μL of genomic DNA (200 ng / μL), 0.4 μL of 10 mmol / L dNTP, 0.5 μL of 10 pmol upstream and downstream primers, 2 μL 10×Taq Buffer [200 mM Tris-HCl (pH 9.0), 200 mM KCl, 100 mM (NH 4 ) 2 SO 4 , 15mM MgCl 2 ], 0.4 μL of Taq DNA polymerase (2.5 U / μL), 0.6 μL of DMSO a...
Embodiment 3
[0060] Example 3 Detection of lipoxygenase alleles of 163 wheat varieties / lines
[0061] The grain genomic DNA of 163 wheat varieties / lines in Table 3 was extracted by using the extraction method of wheat full-maturity grain genomic DNA in Example 1.
[0062] The genomic DNA of the grains of 163 wheat varieties / lines in Table 3 was used as a template to amplify using specific primer pairs (BJF, BJR). The PCR reaction system and PCR reaction procedure were the same as in Example 2.
[0063] After PCR amplification, 5 μL of the above PCR amplification products were taken for 1% agarose gel electrophoresis (using 1×TAE buffer; ethidium bromide (EB) staining, 120V, 25min), after electrophoresis, gel electrophoresis The gel imaging system (MultiGeniusGel Documentation and Analysis System) scans the image and analyzes it with a computer. Then the amplified fragments were subjected to gel recovery monoclonal sequencing.
[0064] The lipoxygenase allelic types of the 163 wheat varie...
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