Thlaspiarvense L. fatty acid elongase and coding gene thereof
A technology of fatty acid elongation enzyme and coding gene, which is applied in the fields of molecular biology and genetic engineering, and can solve problems such as the complex content of erucic acid
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Embodiment 1
[0016] Embodiment 1, the cloning of gene TaFAE1
[0017] To clone TaFAE1, the specific steps are as follows:
[0018] 1. Acquisition of TaFAE1 gene
[0019] Cultivated under normal conditions, after the true leaves grow, the leaves are collected, DNA is extracted from the leaves, polymerase chain reaction is carried out, and the TaFAE1 gene is finally obtained.
[0020] 1. Extraction of Genome DNA
[0021] Take about 0.2g of fresh young living plant leaves, fully grind them under liquid nitrogen freezing conditions, transfer them to a 1.5mL centrifuge tube, add 500μL CTAB extract, and bathe in water at 65°C for 45min, during which time they are inverted and mixed 3 times; add 500μL volume Chloroform-isoamyl alcohol with a ratio of 24:1, mixed evenly, 12000r·min -1 Centrifuge for 15 min; take the supernatant, add 2 times the volume of absolute ethanol, and put it in the refrigerator at -20°C overnight; 4000r min -1 Centrifuge for 15min to precipitate DNA; wash twice with 70...
Embodiment 2
[0031] Example 2, Functional Verification of TaFAE1 Gene
[0032] 1. High expression of TaFAE1 gene in yeast
[0033] In order to demonstrate the coding function of the TaFAE1 gene, the present invention clones the TaFAE1 gene between the BamHI and KpnI sites of pYES2 / NT C from Invitrogen, and transforms the yeast strain InvSc1 to obtain high-level expression.
[0034] The present invention utilizes the multiple cloning sites of the pYES2 / NT C high-efficiency expression vector of Invitrogen Company to realize the high-efficiency expression of TaFAE1. The enzyme cleavage site used in this experiment makes the 5' end of the product expressed by the pYES2 / NT C expression vector add 6 consecutive His fusion proteins, and these 6 consecutive His constitute the specific binding site of i-NTA gel. Therefore, the expression product can be purified by affinity chromatography.
[0035] The pMD-TaFAE1 recombinant vector carrying the TaFAE1 gene and the pYES2 / NT C expression vector were...
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