Scopoloa acutangula 1,4-tetramethylenediamine-nitrogen-methyltransferase 1 and its coding protein and application
A technology of methyltransferase and butanediamine, applied in 1 field, can solve problems such as unseparated clones
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Embodiment 1
[0040] Example 1 (cloning of three points three tor 1,4-butanediamine-nitrogen-methyltransferase gene 1)
[0041] 1. Tissue separation (isolation)
[0042] Three-thirds of the plants come from Lijiang, Yunnan, and the young roots are immediately frozen in liquid nitrogen for preservation.
[0043] 2. RNA isolation (RNA isolation)
[0044] Take part of the tissue and grind it with a mortar, add it to a 1.5mL EP tube filled with lysate, shake it fully, and then transfer it into a glass homogenizer. After homogenization, transfer to 1.5mL EP tube, and extract total RNA (Trizol Reagents, GIBCO BRL, USA). The quality of total RNA was identified by formaldehyde denaturing gel electrophoresis, and then the RNA content was determined on a spectrophotometer.
[0045] 3. Cloning of Full-length cDNA
[0046] According to the PMT amino acid conserved sequence of Scopolamine and other Solanaceae plants, degenerate primers were designed, and using the principle of homologous gene clonin...
Embodiment 2
[0054] Example 2 (Sequence information and homology analysis of three-point three 1,4-butanediamine-nitrogen-methyltransferase gene 1)
[0055] The length of the full-length cDNA of the new three-thirds 1,4-butanediamine-nitrogen-methyltransferase gene 1 of the present invention is 1353bp, and the detailed sequence is shown in SEQ ID NO.1, wherein the open reading frame is located at the core of position 117-1133 glycosides. According to the full-length cDNA, the amino acid sequence of three-point 1,4-butanediamine-nitrogen-methyltransferase is deduced, with a total of 338 amino acid residues, a molecular weight of 37.223KD, and a pI of 5.50. For the detailed sequence, see SEQ ID NO.2 .
[0056] The full-length cDNA sequence of three-thirds 1,4-butanediamine-nitrogen-methyltransferase gene 1 and its encoded protein were published in Non-redundant GenBank+EMBL+DDBJ+PDB and Non-redundant GenBank CDS translations using BLAST program Nucleotide and protein homology search in +PD...
Embodiment 3
[0069] Example 3 (Prokaryotic expression and purification of three-thirds 1,4-butanediamine-nitrogen-methyltransferase 1 or polypeptide in Escherichia coli)
[0070] In this example, the full-length three-thirds AaPMT1 coding sequence or fragment was constructed into a commercially available protein fusion expression vector to express and purify the recombinant protein.
[0071] 1. Construction of prokaryotic expression vector and transformation of Escherichia coli
[0072] According to the nucleotide sequence of three-thirds of AaPMT1, design primers to amplify the protein coding region, and introduce restriction enzyme sites on the forward and reverse primers respectively (this depends on the selected pET32a(+) vector), In order to construct the expression vector. Using the amplified product obtained in Example 1 as a template, after PCR amplification, the AaPMT1 gene was cloned into the pET32a(+) vector (Novagen) under the premise of ensuring the correct reading frame. Th...
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