Method for accelerating rooting of masson pine tissue culture secondary sprout
A technology of subcultured buds and masson pine, applied in the field of promoting the rooting of masson pine tissue culture subcultured shoots, tissue culture seedlings, can solve the problem of low rooting rate of single buds, to improve the rooting situation of subcultured buds, good economic benefits and social benefits, the effect of promoting the rooting situation of subculture shoots
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Embodiment 1
[0025] 1. Experimental materials
[0026] The terminal buds of aseptic seedlings germinated from mature cone seeds of Pine masson in the same year were used as explants, and the cones were collected from Ningming, Guangxi Ningming, Tongmian provenance, which is a high-yielding and excellent Pine masson family line Ningming No.
[0027] 2. Experimental method
[0028] (1) Cluster bud induction
[0029] Inoculate the sterile explants into the modified MS+6-BA 3.0mg·L -1 +NAA 0.1mg·L -1 +Sucrose 30000mg·L -1 + Agar 3500mg·L -1 cultured on culture medium. After 26 days of culture, the average cluster bud induction rate reached 99.1%.
[0030] The basic composition of the improved MS medium is: KNO 3 1650mg·L -1 ; NH 4 NO 3 600mg·L -1 ;CaCl 2 2H 2 O260mg·L -1 ;MgSO 4 ·7H 2 O370mg·L -1 ; Ca(NO 3 ) 2 4H 2 O400mg·L -1 ;KH2 PO 4 170mg·L -1 ;MnSO 4 ·H 2 O22.3mg·L -1 ; ZnSO 4 ·7H 2 O8.6mg·L -1 ; CuSO 4 ·5H 2 O0.025mg·L -1 ;H 3 BO 3 6.2mg·L -1 Na 2 MoO ...
Embodiment 2
[0044] 1. Experimental materials
[0045] The terminal buds of aseptic seedlings germinated from mature cone seeds of Pine masson in the same year were used as explants, and the cones were collected from Ningming pine family Ningming No.
[0046] 2. Experimental method
[0047] (1) Cluster bud induction
[0048] Inoculate the sterile explants into the modified MS+6-BA 4.0mg·L -1 +NAA 0.1mg·L -1 +Sucrose 30000mg·L -1 + Agar 3500mg·L -1 cultured on culture medium. After 26 days of culture, the average cluster bud induction rate reached 98.4%.
[0049] The basic composition of the improved MS medium is the same as in Example 1.
[0050] (2) Cluster bud elongation
[0051] Transfer the induced clustered buds to the improved MS+NAA 0.3mg·L -1 +Sucrose 30000mg·L -1 + Agar 3500mg·L -1 on elongation medium to promote elongation of the culture. After 28 days of elongation culture, the cluster buds are 3-5cm high.
[0052] (3) Subculture bud culture
[0053] Cut out the si...
Embodiment 3
[0063] 1. Experimental materials
[0064] The top buds of aseptic seedlings germinated from the mature cone seeds of Pine masson in the same year were used as explants, and the cones were collected from Ningming 7, a high-yielding and excellent Pine masson family in the mother forest of Pine masson in Ningming, Guangxi.
[0065] 2. Experimental method
[0066] (1) Cluster bud induction
[0067] Inoculate the sterile explants into the modified MS+6-BA 4.0mg·L -1 +NAA 0.1mg·L -1 +Sucrose 30000mg·L -1 + Agar 3500mg·L -1 cultured on culture medium. After 26 days of culture, the average cluster bud induction rate reached 99.0%.
[0068] The basic composition of the improved MS medium is the same as in Example 1.
[0069] (2) Cluster bud elongation
[0070] Transfer the induced clustered buds to the improved MS+AC 4000mg·L -1 +Sucrose 30000mg·L -1 + Agar 3500mg·L -1 on elongation medium to promote elongation of the culture. After 28 days of elongation culture, the cluste...
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