Tissue Culture and Rapid Propagation Method of Orchid chinensis
A technique for straight-lipped orchid and tissue culture, which is applied in the field of tissue culture and plant reproduction to achieve the effects of ensuring the multiplication coefficient and seedling quality, improving the seedling rate, and cooperating closely.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2017-12-19
- Estimated Expiration
- Not applicable · inactive patent
Abstract
Description
Technical field
[0001] The invention belongs to the field of tissue culture and plant propagation, and in particular relates to a method for tissue culture and rapid propagation of C. vulgaris. Background technique
[0002] Bulbophyllum delitescens Hance (Bulbophyllum delitescens Hance) is a plant of the Orchidaceae Glycine max, with thick rhizomes, creeping roots, internodes covered by membranous sheaths or fibers remaining after the sheath rots, one at every 3-11cm interval Fake bulb. Scape originates from rhizome nodes with pseudobulbs, umbels with 2-4 flower petals sickle-lanceolate, apex is truncated and concave notch with 1 short awn in the center, with 3 veins , The whole edge. The lips are fleshy, tongue-like, and curved outwards. The flowers are unique and have a long flowering period, which is of great ornamental value. Seed reproduction is difficult to germinate due to incomplete embryo development. Coupled with the pressure of artificial excavation, the deteriora...
Examples
example 1
[0030] A method of tissue culture and rapid propagation of straight lip curly orchids includes the following steps:
[0031] Step 1. Take the newly germinated buds of C. serrata as explants and place them in the first culture medium to obtain sterile test tube plantlets; wherein, the first culture medium includes: Huabao No. 1 medium , 0.3mg / L methionazine, 1.5mg / L naphthaleneacetic acid, 1.5mg / L polyvinylpyrrolidone, 25g / L sucrose and 4.5g / L agar;
[0032] Step 2. Place the sterile test-tube plantlet obtained in step 1 in a second medium for culturing to obtain a clumping bud of the test-tube plantlet; wherein, the second medium includes: Huabao No. 1 medium, 0.5 mg / L A Thiadazine, 1.0mg / L naphthaleneacetic acid, 0.2mg / L kinetin, 1.5mg / L polyvinylpyrrolidone, 25g / L sucrose and 4.5g / L agar;
[0033] Step 3. Place the test-tube clumping buds obtained in step 2 in the third medium to obtain robust seedlings; wherein, the third medium includes: MS, 0.1 mg / L naphthalene acetic acid, 1.2...
example 2
[0047] A method of tissue culture and rapid propagation of straight lip curly orchids includes the following steps:
[0048] Step 1. Take the newly germinated buds of C. serrata as explants and place them in the first culture medium to obtain sterile test tube plantlets; wherein, the first culture medium includes: Huabao No. 1 medium , 0.7mg / L methionazine, 2.5mg / L naphthaleneacetic acid, 2.5mg / L polyvinylpyrrolidone, 35g / L sucrose and 5.5g / L agar;
[0049] Step 2. Place the sterile test-tube plantlet obtained in step 1 in a second medium for cultivation, to obtain a clumping bud of the test-tube plantlet; wherein, the second medium includes: Huabao No. 1 medium, 1.5 mg / L A Thiadazine, 2.5mg / L naphthaleneacetic acid, 0.5mg / L kinetin, 2.5mg / L polyvinylpyrrolidone, 35g / L sucrose and 5.5g / L agar;
[0050] Step 3. Place the test-tube clumping buds obtained in step 2 into the third medium to obtain robust seedlings; wherein, the third medium includes: MS, 0.3 mg / L naphthalene acetic acid...
example 3
[0064] A method of tissue culture and rapid propagation of straight lip curly orchids includes the following steps:
[0065] Step 1. Take the newly germinated buds of C. serrata as explants and place them in the first culture medium to obtain sterile test tube plantlets; wherein, the first culture medium includes: Huabao No. 1 medium , 0.5mg / L methionazine, 2mg / L naphthaleneacetic acid, 2mg / L polyvinylpyrrolidone, 30g / L sucrose and 5g / L agar;
[0066] Step 2. Place the sterile test tube plantlet obtained in step 1 in a second medium for cultivation to obtain a cluster of test tube plantlets; wherein the second medium includes: Huabao No. 1 medium, 0.5-1.5 mg / L Thioridazine, 1.0-2.5mg / L naphthaleneacetic acid, 0.2-0.5mg / L kinetin, 1.5-2.5mg / L polyvinylpyrrolidone, 25-35g / L sucrose and 4.5-5.5g / L Agar
[0067] Step 3. Place the test-tube clumping buds obtained in step 2 in the third medium to obtain robust seedlings; wherein, the third medium includes: MS, 0.2 mg / L naphthalene acetic...