A kind of rapid propagation method of rabbit ear orchid leaf tissue culture
A technology of tissue culture and rabbit ear orchid, applied in the field of plant propagation, can solve the problems of internal and external pollution, germination and simultaneous rooting, low reproduction coefficient, etc., to achieve large-scale production, ensure the quality of seedlings, and ensure the multiplication coefficient Effect
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2017-03-29
Abstract
Description
technical field
[0001] The invention relates to a plant propagation method, in particular to a rapid propagation method of rabbit ear orchid leaf tissue culture. Background technique
[0002] Cymbidium lancifolium (Cymbidium lancifolium), also known as broad-leaved orchid, is a semi-epipphytic plant of the orchid family first published in "Exotic Flora" by British scholar Hooke in 1823. It is distributed in Guangdong, Guangxi, Sichuan, and Yunnan. , Guizhou, China Taiwan and Tibet and other provinces, Japan, Vietnam, Nepal, India and Malaysia are also distributed.
[0003] Rabbit ear orchid is a national first-level key protected wild plant. It is one of the Chinese orchids with great ornamental value, with peculiar leaf shape, elegant flowers, quiet fragrance and green and white flower color. In addition, the whole herb can also be used as medicine. It can be harvested throughout the year, washed, cut into sections and used fresh or dried. Carbuncles, sores, furuncles, r...
Examples
Embodiment 1
[0020] An example of the tissue culture rapid propagation method of rabbit ear blue of the present invention, comprises the following steps:
[0021] (1) Selection and disinfection of explants: take the explants of tender leaves of Rabbit ear orchids, remove the leaves, soak in 2% aqueous solution of detergent for 5 minutes, rinse with linear tap water for 15-30 minutes, add 2- 3 drops of Tween-20 in 100mL of 0.1% mercuric chloride for 8-10 minutes, rinsed with sterile water for 3-5 times, and finally, removed surface moisture with sterile filter paper to obtain explants, wherein sterile water was treated with high temperature and high pressure Sterilized distilled water;
[0022] (2) The first generation of explants was induced to obtain sterile test-tube plantlets: the explants obtained in step (1) were placed in the ultra-clean workbench, and the surface of the leaves was scratched with a scalpel and inoculated into the MS induction medium, and the culture temperature was ...
Embodiment 2
[0028] An example of the tissue culture rapid propagation method of rabbit ear blue of the present invention, comprises the following steps:
[0029] (1) Selection and disinfection of explants: take the explants of tender leaves of Rabbit ear orchids, remove the leaves, soak in 2% aqueous solution of detergent for 5 minutes, rinse with linear tap water for 15-30 minutes, add 2- 3 drops of Tween-20 in 100 mL of 0.1% mercuric chloride were sterilized for 8-10 minutes, rinsed with sterile water for 3-5 times, and finally the surface moisture was removed with sterilized filter paper to obtain explants. Wherein, sterile water is distilled water sterilized by high temperature and high pressure.
[0030] (2) The first generation of explants was induced to obtain sterile test-tube plantlets: the explants obtained in step (1) were placed in the ultra-clean workbench, and the surface of the leaves was scratched with a scalpel and inoculated into the MS induction medium, and the culture ...
Embodiment 3
[0036] An example of the tissue culture rapid propagation method of rabbit ear blue of the present invention, comprises the following steps:
[0037] (1) Selection and disinfection of explants: take the explants of tender leaves of Rabbit ear orchids, remove the leaves, soak in 2% aqueous solution of detergent for 5 minutes, rinse with linear tap water for 15-30 minutes, add 2- 3 drops of Tween-20 in 100 mL of 0.1% mercuric chloride were sterilized for 8-10 minutes, rinsed with sterile water for 3-5 times, and finally, surface moisture was removed with sterile filter paper to obtain explants. Wherein, sterile water is distilled water sterilized by high temperature and high pressure.
[0038] (2) The first generation of explants was induced to obtain sterile test-tube plantlets: the explants obtained in step (1) were placed in the ultra-clean workbench, and the surface of the leaves was scratched with a scalpel and inoculated into the MS induction medium, and the culture temper...