Agrobacterium tumefaciens-mediated sesame cotyledon transgenic method
An Agrobacterium-mediated, transgenic technology, applied in the field of genetic engineering operations, can solve the problems of low genetic transformation efficiency of sesame, low survival rate of transgenic regenerated plants, etc., achieve good application and promotion value, improve transgenic efficiency, and shorten the transformation cycle.
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Embodiment 1
[0050] In this example, the pBI121 empty expression vector (the vector itself contains kanamycin resistance and the selection marker GUS reporter gene, that is, in the genetic transformation, the GUS gene is equivalent to the target gene) as an example, takes the main sesame variety Yuzhi 11 in my country as an example. As the transgenic raw material, the construction method of Agrobacterium-mediated sesame cotyledon transgenic genetic transformation system is introduced as follows.
[0051] (1) Obtaining explants
[0052] Select plump and clean Yuzhi No. 11 mature grains, and rinse them twice with sterile water after sterilizing with 75% ethanol for 90 s on a sterile operating table; then, after sterilizing with 3% sodium hypochlorite for 15 minutes, wash with sterile water for 5 minutes. Second-rate;
[0053] Put the sterile seeds in sterile water, under the conditions of room temperature (about 25 ℃) and dark conditions, shake and cultivate at 100 r / min for 12 hours to ensu...
Embodiment 2
[0120] In order to illustrate the versatility of the genetic transformation system provided in this application, the inventors further take the pFGC5941 expression vector (containing the glufosinate-ammonium resistance gene Bar) as an example, and briefly introduce the construction process and experimental results of the related genetic transformation system as follows.
[0121] The relevant experimental operations refer to Example 1, and only some of the different operations are briefly described as follows.
[0122] In step (3), since the pFGC5941 expression vector carries the glufosinate-ammonium resistance gene, the formula of the resistance screening medium M3 is adjusted as follows:
[0123] MS + 6-BA 2.5mg / L + IAA 1.0 mg / L + ABA 1.0 mg / L + AgNO 3 5.0 mg / L + cephalexin 300 mg / L + resistance screening substance glufosinate ammonium 1 mg / L + plant supplement 5.0 g / L + agar powder 7.5 g / L, pH=5.8.
[0124] When further PCR detection and judgment are performed on transgeni...
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