Root induction method in kiwi fruit tissue culture
A tissue culture and kiwifruit technology is applied in the field of plant tissue culture to achieve the effects of high light utilization rate, developed root system and high survival rate
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Embodiment 1
[0018] The method of the present invention is used to carry out tissue culture with Actinidia xuxiang leaves as tissue culture material.
[0019] 1. Select the emerald green, thick leaves on the strong kiwifruit plant, which are relatively close to the stem tip, as the explant material, and wash them with clean water;
[0020] Sterilize with 0.1% mercuric chloride solution for 10 minutes, then sterilize with 75% alcohol for 5 minutes, and wash with sterile water for 3-5 times;
[0021] Cut the treated leaves into squares with a side length of 1.5 cm, put them on the induction medium,
[0022] Light 800LX, 10h per day, temperature 25±2°C, humidity 70%, culture for about 50 days to form kiwifruit callus.
[0023] The induction medium is: MS medium + sucrose 20g / L + agar 6g / L + 6-BA0.8mg / L + NAA (naphthalene acetic acid) 0.2mg / L + 2,4-D (2,4-dichlorophenoxy Acetic acid) 0.5mg / L culture medium;
[0024] 2. Inducing Cluster Buds
[0025] Divide the callus into small pieces with...
Embodiment 2
[0030] The leaves of Actinidia kiwifruit were used as tissue culture materials, and different methods were used for tissue culture.
[0031] Experimental group: use the method for inducing rooting in Step 4 of Example 1 of the present invention;
[0032] Control group 1: the medium used in the step of inducing rooting is: 0.7mg L -1 IBA, 30mg·L -1 Sucrose, 7mg·L -1 1 / 2 MS medium of agar, the others are the same as the experimental group.
[0033] Control group 2: the medium used in the step of inducing rooting is: in 1 / 2MS+NAA0.2mg L -1 , and the others are the same as the experimental group.
[0034] Control group 3: the light time used in the rooting induction step is 10h, the temperature is 25±2°C, the humidity is 85%, and the others are the same as the experimental group.
[0035] Control group 4: the carbon dioxide concentration used in the rooting induction step is 1200ppm, and the others are the same as the experimental group.
[0036]
Embodiment 3
[0038] A special rooting device for tissue culture, such as Figure 3 to Figure 5 As shown, it includes: a box body 1, a box cover 2 and a root bed 3, the box cover 2 is connected with the box body 1 through a hinge 26, and can be turned over relative to the box body 1; Composed of partitions, the root bed 3 has several mutually independent well-shaped root bed areas 30 for accommodating medium, the bottom surface of the box cover 2 is provided with LED lights 20, the box body 1 A number of ventilation holes 10 are opened on the side wall, and the location of the ventilation holes 10 is higher than the top surface of the root bed 3 . The roots grown by the kiwifruit seedlings can be separated by the root bed 3, which avoids the entanglement of their root systems after the cultivation of the seedlings is completed, and it takes time and effort to separate them and easily damages the root system.
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