Endoplasmic reticulum-type ω-3 fatty acid desaturase gene and its application in Alpine mustard
A technology of alpine ionic mustard and desaturase, applied in the field of alpine ionic mustard endoplasmic reticulum type ω-3 fatty acid desaturase gene, to achieve high stress resistance, increase trienoic acid content, and strong response effect
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Embodiment 1
[0031] Example 1 Alpine mustard endoplasmic reticulum type ω-3 fatty acid desaturase gene, the amino acid sequence of the endoplasmic reticulum type ω-3 fatty acid desaturase encoded by the gene is as shown in the sequence table from the first position of SEQ ID NO.2 to Shown at position 386, its nucleotide sequence is shown at position 1 to 1161 of SEQ ID NO.1 in the sequence listing.
[0032] 1. Alpine ionic mustard CbFAD3 Gene cloning.
[0033] 1. Alpine ion mustard CbFAD3 Gene Conserved Sequence Amplification:
[0034] 1.1. Use Omega's Plant RNA Extraction Kit to extract total RNA from the callus of Japonica japonica.
[0035] 1.2. Use Takara's PrimeScript? 1st Strand cDNA synthesis kit for reverse transcription to obtain cDNA.
[0036] 1.3. The following degenerate primers were designed according to the gene sequence retrieved from the NCBI (National Center for Biotechnology Information) database:
[0037] Sense Primer: 5'-GGGCGGCKATTCCTAAGCAYT-3'(Degeneracy=4)
[0...
Embodiment 2
[0084] Example 2 Alpine mustard CbFAD3 Eukaryotic Expression of Genes in Saccharomyces cerevisiae INVScl
[0085] 1. Construction of eukaryotic expression vector pYES2- CbFAD3
[0086] 1.1. Design primers according to the sequence of the coding region as follows:
[0087] Z3-UP: 5'-GGATCCACCATGGTTGTTGCAATGGACCA-3'
[0088] Z3-DN: 5'-CGAGCTCTAATTGATTTTAGATTTGTCAG-3'
[0089] 1.2. Alpine mustard CbFAD3 Gene Amplification:
[0090] Reaction system (50 μl): cDNA 2.5 μl, TaKaRa LA Taq (5 U / μl) 0.5 μl, 10×LA Taq Buffer II (Mg2+ free) 5 μl, MgCl2 (25 mM) 5 μl, dNTP Mix (2.5 mM)8 μl, CbFAD3s (10μM) 1μl, CbFAD3a (10μM) 1μl, ddH 2 O 27 μl.
[0091] Reaction conditions: 94°C, 3min
[0092] (94°C, 1min; 56°C, 15s; 63°C, 15s; 72°C, 1min) 30 cycles
[0093] 72℃, 10min
[0094] 1.3. Alpine mustard CbFAD3 The gene recovery method is the same as 1.4.1 in Example 1.
[0095] 1.4. Enzyme digestion and ligation of CbFAD3 gene and expression vector pYES2 plasmid:
[0096] (1) The re...
Embodiment 3
[0115] Example 3 Transforming Alpine mustard CbFAD3 Acquisition of Genetic Tobacco
[0116] 1. Construction of eukaryotic expression vector pBI121- CbFAD3
[0117] 1.1. Design primers according to the sequence of the coding region as follows:
[0118] ZF3: 5'-GCTCTAGAATGGTTGTTGCAATGGACCA-3'
[0119] ZF3': 5'-CGAGCTCCTAATTGATTTTAGATTTGTCAG-3'
[0120] 1.2. Alpine mustard CbFAD3 Gene Amplification:
[0121] Reaction system is the same as 1.2 in embodiment 2
[0122] Reaction conditions: 94°C, 3min
[0123] (94°C, 1min; 60°C, 30s; 72°C, 1min) 30 cycles
[0124] 72℃, 10min
[0125] 1.3. Alpine mustard mustard CbFAD3 The gene recovery method is the same as 1.4.1 in Example 1.
[0126] 1.4. Enzyme digestion and ligation of CbFAD3 gene and expression vector pBI121 plasmid:
[0127] (1) The recovered product in 1.2 and the expression vector pBI121 plasmid (preserved in our laboratory) were double-digested with restriction endonucleases XbaI and SacI from Takara Company re...
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