Application of purple acid phosphatase gene GmPAP35 of soybean
A technology of acid phosphatase and soybean, which is applied in the field of genetic engineering to achieve the effect of improving soybean phosphorus efficiency, promoting carbon metabolism ability, and improving plant phosphorus efficiency
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Embodiment 1
[0024] Embodiment 1 GmPAP35 gene expression pattern analysis
[0025] By quantitative PCR technology, it was confirmed that GmPAP35 gene was strongly expressed by low phosphorus. The length of the open reading frame of the GmPAP35 gene is 1989bp, encoding a protein of 662 amino acids.
[0026] The plant materials are planted in greenhouse nutrient solution hydroponic cultivation. First, seeds with full grains and complete seed coats are selected, and after the seeds are sterilized by chlorine gas fumigation (100mL sodium hypochlorite + 4mL concentrated HCl) for 13.5hrs, the seeds are germinated by the rolling paper tube method. After the cotyledons are fully unfolded, the healthy and consistent seedlings are moved to the soybean nutrient solution with a pH of about 5.8. Two weeks later, when the seedlings grow the first complete three compound leaves, the phosphorus level treatment is carried out. Phosphorus treatments included low phosphorus (5 μM) (LP) and high phosphorus (...
Embodiment 2
[0036] Cloning of embodiment 2GmPAP35 gene
[0037] Using the soybean leaf cDNA as a template, the upstream specific primer 5′- CTCGAG ATGATTCCCGATCTACCCCTC-3'(SEQ ID NO:5) and downstream specific primer 5'- ACTAGT TCAAGTTTCCTCAGTCTTCAC-3' (SEQ ID NO: 6) amplified the full-length ORF sequence of 1989bp of the GmPAP35 gene, and sequenced and compared the obtained GmPAP35 coding sequence, see Glyma20g03260.1, and the corresponding protein sequence, see Glyma20g03260.1.
Embodiment 3
[0038] Example 3 Overexpression GmPAP35 vector construction
[0039] Construction of overexpression vector: using soybean leaf cDNA as template, using upstream specific primer 5'- CTCGAG ATGATTCCCGATCTACCCCTC-3'(SEQ ID NO:5) and downstream specific primer 5'- ACTAGT TCAAGTTTCCTCAGTCTTCAC-3′(SEQ ID NO:6) amplifies the full-length ORF sequence of GmPAP35 gene 1989bp, after the PCR fragment is recovered and sequenced correctly, the fragment and the target vector are digested with Xho I and Spe I, and the GmPAP35 gene is connected to the destination vector pTF101.1.
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