Agrobacterium-mediated method for culturing transgenic populus wutunensis plants
An Agrobacterium-mediated and transgenic technology, applied in the field of genetic engineering, can solve the problems such as the lack of Qingyang faction, and achieve the effect of convenient material acquisition.
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Embodiment 1
[0048] a. will cut 3 incisions along the vertical main veins of the leaves of the aseptic seedlings of Wutun Yang as transformed explants, the incisions are deep to the main veins, and the front is upwards, and put into the pre-cultivation medium, totally 50 blades, each Inoculate 9 to 11 leaves in the petri dish, inoculate 5 petri dishes in total, and culture in light for 2 days, the culture temperature is 26°C, the light intensity is 3400 Lux, and the light time is 16 hours / day;
[0049] The above pre-culture medium is: MS+6-BA 1.0mg / L+NAA 0.2mg / L+sucrose 30g / L+agar powder 8g / L;
[0050] b. Pick the colony of Agrobacterium AGLO with the bar gene and inoculate it into 10ml YEP liquid medium containing 50mg / L of kanamycin, culture at 26°C with shaking at 200rpm for 24 hours, and transfer 100μl of the bacterial solution to 30ml of YEP liquid medium was cultured with shaking at 200rpm, when the cells were 0D 600 When it reaches 0.8, collect the bacteria by centrifugation at 120...
Embodiment 2
[0078] The determination of embodiment 2 herbicide critical concentration
[0079] Since the Agrobacterium AGLO used for gene transformation has the bar gene, the positive plants transformed by Agrobacterium AGLO have resistance to herbicides, and herbicides are used as screening reagents to select transformed cells. For herbicide resistance, the critical concentration test of leaf resistance to herbicide was carried out, and the uniform leaves were placed on the medium containing 0.5, 1.0, 1.5, 2.0, 2.5mg / L PPT: MS+ 6-BA 1.0mg / L+NAA 0.2mg / L+sucrose 30g / L+agar powder 8g / L, the inoculation density was 5 leaves per petri dish, the selection culture temperature was 26°C, the light intensity was 3400Lux, and the light time was 16 hours / days. Observe the response of the leaves to a series of concentration gradient herbicides, and make statistics after culturing for 30 days to determine the critical concentration of the herbicides. The control medium is: MS medium supplemented wit...
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