Culture method for improving embryonic birth rate of cabbage stalk
A technology for cabbage and cultivation methods, applied in horticultural methods, botanical equipment and methods, plant regeneration and other directions, can solve problems such as affecting the rate of embryo production, unsatisfactory cultivation effect, affecting the quality of embryos, etc., so as to improve the utilization efficiency. Effect
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Embodiment 1
[0024] (1) In this example, the head cabbage and rape inflorescences were picked from the experimental field of Zhenjiang Institute of Agricultural Sciences, and the varieties are not limited.
[0025] (2) Culture medium preparation: culture medium including different stages of microspore culture, its components and the weight of each component contained in each liter of medium are:
[0026] B5 washing medium: B5 liquid medium 1L + sucrose 30 g / L, pH 6.0, high temperature and high pressure sterilization; wherein, B5 liquid medium, in 1L, consists of: NaH 2 PO 4 2H 2 O 169.5mg, KNO 3 2500mg, (NH 4 ) 2 SO 4 134mg, MgSO 4 ·7H 2 O 500mg, MnSO 4 4H 2 O 10mg, H 3 BO 3 3mg, ZnSO 4 ·7H 2 O 2mg, KI 0.75mg, Na 2 MoO 4 2H 2 O 0.25mg, CuSO 4 ·5H 2 O 0.025mg, CoCl 2 ·6H 2 O 0.025mg, Na 2 -EDTA 37.3mg, FeSO 4 ·7H 2 O 27.8mg, CaCl 2 .2H 2 O 150mg, VB 1 10mg, VB 6 1mg, VPP 1mg, inositol 100mg and the rest in distilled water.
[0027] NLN-13 induction medium: N...
Embodiment 2
[0046] The difference between the medium in this example and the medium in Example 1 is as follows, B5 liquid medium 1L + sucrose 30g / L, pH 6.0, high temperature and high pressure sterilization; NLN-13 induction medium: NLN-13 liquid medium 1L + sucrose 130g / L, pH 6.1, filter sterilized; embryoid solid differentiation medium: B5 medium + sucrose 20g / L, agar 11 g / L, pH 6.0, high temperature and high pressure sterilization; rooting medium: MS medium + White sugar 20g / L, agar 7g / L, pH 5.9, high temperature and high pressure sterilization;
[0047] The present embodiment cultivates head cabbage as follows:
[0048] Step 1, picking healthy, no pests and diseases, flower buds from late mononucleate to early binucleate on the inflorescence of cabbage and rape inflorescence as donor plants for microspore culture, the petal and anther length ratio of cabbage inflorescence is 1.2, rapeseed The petal and anther length ratio of the inflorescence is 0.75, the two kinds of flower buds are ...
Embodiment 3
[0060] The difference between the medium in this example and the medium in Example 1 is as follows: B5 liquid medium 1L + sucrose 30g / L, pH6.0, high temperature and high pressure sterilization; NLN-13 medium: NLN-13 liquid medium 1L + sucrose 130g / L, pH 6.1, filter sterilized; embryoid body solid differentiation medium: B5 medium + sucrose 20g / L, agar 12 g / L, pH 6.0, high temperature and high pressure sterilization; rooting medium: MS medium + white sugar 20g / L, agar 7g / L, pH 5.9, high temperature and high pressure sterilization;
[0061] The present embodiment cultivates head cabbage as follows:
[0062] Step 1, pick the flower buds that grow healthy on the head cabbage inflorescence and rapeseed, no damage by diseases and insect pests, late mononucleate to early binucleate as the donor plant for microspore culture, the petal and anther length ratio of the head cabbage inflorescence is 1.1, rapeseed The petal and anther length ratio of the inflorescence is 0.75. The two kin...
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