Proliferation culture medium for Jinbian cymbidium faberi

A technology for multiplying culture medium and culture medium, applied in horticulture, botanical equipment and methods, gardening tools/equipment, etc., can solve the problems of low number of induced buds and value-added coefficient, slow reproduction speed, no more than 5%, etc. To achieve the effect of promoting cell division and expansion, promoting cell division, and enhancing plasticity

Inactive Publication Date: 2020-07-03
安徽智野生物科技发展有限公司
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] Orchid, a traditional famous flower in China, is rich in germplasm resources, widely distributed, and has high ornamental value. Its propagation method is generally branch propagation, which can only be carried out once every 3-4 years. The propagation speed is slow and it is difficult to meet the market demand. , although the orchid seeds are small, the number is amazing. There are millions of seeds in a capsule. The number of orchid seeds is very large, but because the orchid seeds are very small and powdery, their structure can only be seen clearly under a microscope. There is no endosperm, only a simple embryo, which is surrounded by a loose, transparent, impermeable seed coat. The embryo contains very little nutrients, most of which are lipid substances. The orchid seeds that exist under natural conditions can only be suitable for The fungal infection can successfully germinate, and the germination rate is very low, generally not more than 5%.
[0003] Cymbidium, also known as Jiuzilan, Jiujielan, and Xialan, is a large species of orchids in China. It is one of the oldest and most popular orchids. Because of its elegant plant type, strong fragrance, and beautiful flower shape, it is popular in Southeast Asia. Regarded as a high-end potted flower, Cymbidium grows naturally in hillside forests. Most of the cultivated varieties are domesticated from wild species or selected from natural variation. Among them, Cymbidium in Phnom Penh is rarer and has great ornamental value, so Phnom Penh The artificial proliferation of Cymbidium has gradually come into people's sight. In the process of proliferation and cultivation of Phnom Penh Cymbidium, plant proliferation medium is needed. The traditional plant proliferation medium needs to add a lot of trace elements and auxin in the preparation process. To ensure the normal proliferation of plants, the use of a large amount of trace elements and auxins increases the cost of medium preparation, and the traditional plant proliferation medium is not effective for plant proliferation. The number of induced buds and The value-added coefficients are all very low, which makes it difficult to increase the proliferation and cultivation of Phnom Penh Cymbidium, and the plant multiplication efficiency is low, and the quality of Phnom Penh Cymbidium cultivated is low

Method used

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  • Proliferation culture medium for Jinbian cymbidium faberi
  • Proliferation culture medium for Jinbian cymbidium faberi
  • Proliferation culture medium for Jinbian cymbidium faberi

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] A kind of Phnom Penh Cymbidium proliferation medium, the formula composition is as follows: 1 / 2MS medium, sugar 20g / L, coconut milk 100mL / L, NAA 5mg / L, 6-BA 15mg / L, agar 5g / L, nutrition 10mL / L;

[0036] The preparation steps of the proliferation medium are as follows:

[0037] Step S1: Weigh the corresponding components according to the above formula;

[0038] Step S2: Stir and heat the MS medium and agar until the MS medium and agar are completely melted to obtain a molten liquid. Add sugar, coconut juice, NAA, 6-BA, and nutrient solution to the molten liquid, and stir until the sugar and coconut Mix the juice, NAA, 6-BA, and nutrient solution evenly to obtain a mixed solution;

[0039] Step S3: adding sodium hydroxide solution to the mixed solution prepared in step S2 until the pH value of the mixed solution reaches 5.5 to prepare a culture solution;

[0040] Step S4: Put the culture solution prepared in step S3 into an Erlenmeyer flask and put it in a sterilization pot, ster...

Embodiment 2

[0047] A medium for the growth of Cymbidium euphorbiae, the formula composition is as follows: 1 / 2MS medium, sugar 30g / L, coconut milk 110mL / L, NAA 8mg / L, 6-BA 18mg / L, agar 8g / L, nutrition 15mL / L;

[0048] The preparation steps of the proliferation medium are as follows:

[0049] Step S1: Weigh the corresponding components according to the above formula;

[0050] Step S2: Stir and heat the MS medium and agar until the MS medium and agar are completely melted to obtain a molten liquid. Add sugar, coconut juice, NAA, 6-BA, and nutrient solution to the molten liquid, and stir until the sugar and coconut Mix the juice, NAA, 6-BA, and nutrient solution evenly to obtain a mixed solution;

[0051] Step S3: adding sodium hydroxide solution to the mixed solution prepared in step S2 until the pH value of the mixed solution reaches 5.5 to prepare a culture solution;

[0052] Step S4: Put the culture solution prepared in step S3 into an Erlenmeyer flask and put it into a sterilization pot. After ...

Embodiment 3

[0054] A growth medium for Cymbidium euphorbiae, the formula composition is as follows: 1 / 2MS medium, sugar 40g / L, coconut milk 120mL / L, NAA 12mg / L, 6-BA 20mg / L, agar 10g / L, nutrition 20mL / L;

[0055] The preparation steps of the proliferation medium are as follows:

[0056] Step S1: Weigh the corresponding components according to the above formula;

[0057] Step S2: Stir and heat the MS medium and agar until the MS medium and agar are completely melted to obtain a molten liquid. Add sugar, coconut juice, NAA, 6-BA, and nutrient solution to the molten liquid, and stir until the sugar and coconut Mix the juice, NAA, 6-BA, and nutrient solution evenly to obtain a mixed solution;

[0058] Step S3: adding sodium hydroxide solution to the mixed solution prepared in step S2 until the pH value of the mixed solution reaches 5.5 to prepare a culture solution;

[0059] Step S4: Put the culture solution prepared in step S3 into an Erlenmeyer flask and put it into a sterilization pot. After steri...

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Abstract

The invention discloses a proliferation culture medium for Jinbian cymbidium faberi. The formula of the proliferation culture medium comprises the following composition components of a 1 / 2 MS culturemedium, sugar of 20-40g / L, coconut juice of 100-120mL / L, NAA of 5-12mg / L, 6-BA of 15-20mg / L, agar of 5-10g / L and a nutrient solution of 10-20mL / L. In the process of preparing the proliferation culturemedium, the nutrient solution is prepared. The nutrient solution can open a DNA-histone compound body in plant cells or open a DNA double helix structure, DNA and RNA polymerase can be combined, transcription is performed, further a new protein can be synthesized through translation, and growth of plant cells is promoted. The nutrient solution is used, so that the proliferation efficiency of theJinbian cymbidium faberi is high. Compared with a conventional heteroauxing culture medium, for the prepared culture medium disclosed by the invention, the number of induced buds of the Jinbian cymbidium faberi can be increased, the number of plants cultured within the same culturing time is larger, and growth time required by the Jinbian cymbidium faberi is shorter. The quality of the Jinbian cymbidium faberi after being subjected to proliferation can be high.

Description

Technical field [0001] The invention belongs to the technical field of orchid culture, and specifically relates to a propagation medium for Cymbidium euphorbiae. Background technique [0002] Orchid, a traditional Chinese flower, has rich germplasm resources, is widely distributed, and has high ornamental value. Its propagation method is generally ramification propagation, which can only be carried out once 3-4 years, and the propagation speed is slow, which is difficult to meet market needs Although the orchid seeds are very small, the number is amazing. There are millions of seeds in a capsule. The number of orchid seeds is very large. However, because the orchid seeds are very small and powdery, their structure can only be seen under a microscope. There is no endosperm, only a simple embryo, with a loose, transparent, and impermeable seed coat on the outside. The embryo contains few nutrients, most of which are lipids. The orchid seeds that exist under natural conditions are o...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A01H4/00
CPCA01H4/001
Inventor 闻智磊
Owner 安徽智野生物科技发展有限公司
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