Tea tree caffeine synthase gene promoter tcsp and its application
A technology of promoter and caffeine, applied in application, genetic engineering, enzyme and other directions, can solve the problems of insufficient expression of exogenous genes and inability to obtain transgenic plants ideally
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Embodiment 1
[0033] Cloning of caffeine synthase gene promoter TCSP in embodiment 1 tea tree
[0034] 1.1 Extraction of total genomic DNA (Biomiga kit)
[0035] (1) Weigh about 0.2g of the young leaves of Shucha tea tree into a pre-cooled mortar, add an appropriate amount of liquid nitrogen, and grind to powder.
[0036] (2) Transfer the powder to a 2ml centrifuge tube, immediately add 900μl Buffer P1 and 10μl β-mercaptoethanol, vortex briefly and place in a water bath at 65°C for 10 minutes, mixing by inversion 3-4 times. (Add 5 μl RNaseA before water bath)
[0037] (3) Add 140 μl Buffer P2, vortex and mix well. Centrifuge at 13000 rpm for 10 min.
[0038] (4) Carefully pipette the supernatant and transfer it to a new 2ml centrifuge tube to avoid suctioning up the precipitate. Add 0.5 times the volume of P3 and mix well, then add 0.5 times the volume of absolute ethanol to the mixture, and mix thoroughly by inversion.
[0039] (5) Insert a DNA adsorption column into a 2ml collection t...
Embodiment 2
[0105] Example 2 Construction of Tobacco Transgenic Plants and Verification of Promoter Activity
[0106]Use Gateway technology to introduce the promoter sequence into the plant expression vector (pKGWFS7), construct a recombinant plant expression vector, named pKGWFS7-TCSP, and use the Agrobacterium-mediated tobacco genetic transformation method to perform promoter activity by expressing the GUS gene functional verification.
[0107] 2.1 Vector construction and identification
[0108] (1) BP reaction
[0109]
[0110] The system was incubated overnight at 25°C. After the reaction, 2 μl of 2 μg / μl Proteinase K was added and treated at 37°C for 10 minutes, and then the BP reaction product (entry vector) was transferred into 50 μl of E. coli Trans1-T1. After screening on the LB plate, the plasmid was extracted after the positive single colony was detected and stored at -20°C.
[0111] (2) LR reaction
[0112]
[0113]
[0114] The system was incubated overnight at 2...
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