Clonal tissue culture breeding method of Liquidambar formosana hance
A clonal and tissue culture technology, applied in the field of tree tissue culture and tissue culture breeding, can solve the problems of large forest differentiation, easy aging of ear picking mother plants, long seedling cultivation period, etc., and achieve good ecological and social benefits. , the effect of good promotion and application prospects and short seedling cultivation cycle
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Embodiment 1
[0043] Liquidambar clonal tissue culture breeding method is characterized in that: comprises the steps:
[0044](1) Disinfection of explant materials: Take the young shoots of the year, remove the leaves, cut into sections, so that each section is a stem section with 1-2 axillary buds, and the stem sections are first sterilized with 0.2% and cleaned in an ultrasonic cleaner Treat for 20 minutes, wash 6 times with sterile water, then use 0.1% mercury liter, 2-5 drops of Tween 80, treat for 3 minutes, wash 6 times with sterile water, and then set aside;
[0045] (2) Bud induction: inoculate the sterilized stem section in step (1) on the bud induction medium, and after 6 days of cultivation, the axillary buds will start to germinate and new shoots will grow. The induction medium is DCR 改 +6-BA 0.5mg+NAA 0.05mg;
[0046] (3) Proliferation of buds: After culturing the new shoots grown in step (2) for 30 days, they were cut off, cultured on the subculture medium, and cultured on t...
Embodiment 2
[0051] Liquidambar clonal tissue culture breeding method is characterized in that: comprises the steps:
[0052] (1) Disinfection of explant materials: Take the young shoots of the year, remove the leaves, cut into sections, so that each section is a stem section with 1-2 axillary buds, and the stem sections are first sterilized with 0.2% and cleaned in an ultrasonic cleaner Treat for 30 minutes, wash 6 times with sterile water, then use 0.1% mercury liter, 2-5 drops of Tween 80, treat for 5 minutes, wash 6 times with sterile water, and set aside;
[0053] (2) Bud induction: inoculate the sterilized stem section in step (1) on the bud induction medium, and after 15 days of cultivation, the axillary buds will start to germinate and new shoots will grow. The induction medium is DCR 改 +6-BA 0.5mg+NAA 0.5mg;
[0054] (3) Proliferation of buds: After culturing the new shoots grown in step (2) for 30 days, they were cut off, cultured on the subculture medium, and cultured on the p...
Embodiment 3
[0059] Liquidambar clonal tissue culture breeding method is characterized in that: comprises the steps:
[0060] (1) Preparation of explant materials: take the young shoots of the year, remove the leaves, cut into sections, so that each section is a stem section with 1~2 axillary buds, and the stem sections are first sterilized with 0.2% and cleaned in an ultrasonic cleaner Treat for 25 minutes, wash with sterile water 6 times, then use 0.1% mercuric chloride, 2-5 drops of Tween 80, treat for 4 minutes, wash with sterile water for 6 times and set aside;
[0061] (2) Induction of buds: inoculate the sterilized stem segments in step (1) on the bud induction medium, and after 10 days of cultivation, germination begins at the axillary buds and new shoots grow. The induction medium is DCR 改 +6-BA 0.5mg+NAA 0.25mg;
[0062] (3) Proliferation of buds: after culturing the new shoots grown in step (2) for 30 days, cut them off, then culture them on the subculture proliferation medium...
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