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Dendrobium devonianum rapid propagation seedling survival culture medium series and tissue culture method

A technology of Dendrobium denticola and proliferation medium, which is applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of high cost, long period of test tube seedling formation, low germination rate and the like

Active Publication Date: 2015-09-23
临沧市云瑞堂生物科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Due to the lack of endosperm, the seeds need to symbiosis with fungi to germinate, and the germination rate is very low (less than 5%) under natural conditions
[0003] At present, there have been relevant reports on the tissue culture research of Dendrobium dendrobii, but the high cost of tissue culture and the long cycle of planting in test tubes are the bottlenecks restricting the industrialization of Dendrobium dendrobium production

Method used

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  • Dendrobium devonianum rapid propagation seedling survival culture medium series and tissue culture method
  • Dendrobium devonianum rapid propagation seedling survival culture medium series and tissue culture method
  • Dendrobium devonianum rapid propagation seedling survival culture medium series and tissue culture method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] Preparation of liquid A: Weigh 16.7g of ammonium nitrate, 19.2g of potassium nitrate, 3.7g of magnesium sulfate, and 1.7g of potassium dihydrogen phosphate, then add to 1L of water and mix to dissolve.

[0040] Preparation of liquid B: Weigh 4.4g of calcium chloride, then put it into 1L of water and mix to dissolve.

[0041] Prepare liquid C: weigh 0.4g of glycine, 0.4g of vitamin B1, 0.5g of niacin and 0.5g of pyridoxine hydrochloride VB6 into 800ml of water, mix and dissolve to obtain mixed solution I, then weigh 20g of inositol and mix with 200ml of water to dissolve To obtain the mixed solution II, just mix the mixed solution I and the mixed solution II.

[0042] Preparation of liquid D: Weigh 5.56g of ferrous sulfate and 7.46g of disodium ethylenediaminetetraacetate, dissolve them in water, and then mix them to prepare a 1L solution.

[0043] Prepare L liquid: Weigh 16.9g / L manganese sulfate, 8.6g / L zinc sulfate, 6.2g / L boric acid, 0.083g / L potassium iodide, 0.025...

Embodiment 2

[0064] The content and preparation method of liquid A, liquid B, liquid C, liquid D, liquid L, liquid M1 and liquid M2 are the same as in Example 1.

[0065] Preparation of seeding medium: Weigh 1000ml of A liquid, 1000ml of B liquid, 100ml of C liquid, 100ml of D liquid, 20ml of L liquid and 8ml of M1 liquid, then add 380g of sucrose, 74g of agar, 34g of carbon powder With 1900g crushed bananas, add 10 liters of water and heat at high temperature, then mix at 80°C, bottle, sterilize in an autoclave, and cool.

[0066] Preparation of proliferation medium: Weigh 1000ml of liquid A, 1000ml of liquid B, 100ml of liquid C, 100ml of liquid D, 20ml of liquid L, 8ml of liquid M1 and 5ml of liquid M2, then add 380g of sucrose, 74g Agar, 34g of carbon powder and 1900g of crushed bananas, plus 10 liters of water, heated at high temperature, then mixed at 80°C, bottled, sterilized in an autoclave, and cooled.

[0067] Preparation of strong seedling medium: Weigh 1000 ml of liquid A, 100...

Embodiment 3

[0083] The content and preparation method of liquid A, liquid B, liquid C, liquid D, liquid L, liquid M1 and liquid M2 are the same as in Example 1.

[0084] Preparation of seeding medium: Weigh 1000ml of A liquid, 1000ml of B liquid, 100ml of C liquid, 100ml of D liquid, 20ml of L liquid and 8ml of M1 liquid, then add 420g of sucrose, 78g of agar, 38g of carbon powder With 2100g of crushed apples, add 10 liters of water and heat at high temperature, then mix at 80°C, bottle, sterilize in an autoclave, and cool.

[0085] Preparation of proliferation medium: Weigh 1000ml of liquid A, 1000ml of liquid B, 100ml of liquid C, 100ml of liquid D, 20ml of liquid L, 8ml of liquid M1 and 5ml of liquid M2 and mix well, then add 420g of sucrose, 78g of Agar, 38g of carbon powder and 2100g of crushed apples, plus 10 liters of water, heated at high temperature, then mixed at 80°C, bottled, sterilized in an autoclave, and cooled.

[0086] Preparation of strong seedling medium: Weigh 1000 ml...

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Abstract

The invention provides dendrobium devonianum rapid propagation seedling survival culture medium series and a tissue culture method. The dendrobium devonianum rapid propagation seedling survival culture medium series comprise a sowing culture medium, a multiplying culture medium, a seedling strengthening culture medium, a differentiated seedling culture medium and a rooting culture medium. The tissue culture method comprises the steps that seeds are cultivated in a sprouting culture medium firstly, light treatment is directly conducted without darkness cultivation treatment, after the seeds spout and form protocorms, the protocorms are subjected to induction in a protocorms multiplying inducing culture medium to produce callus tissues, and the callus tissues further form protocorm-like bodies; the protocorm-like bodies are subjected to differentiation to form young seedlings; the young seedlings are transplanted into the seedling strengthening culture medium, after the young seedlings grow up to be big seedlings, the big seedlings are cultivated in the rooting culture medium to be dendrobium devonianum mature seedlings. By means of the dendrobium devonianum rapid propagation seedling survival culture medium series and the tissue culture method, the cultivating time of dendrobium devonianum can be shortened, not only is the operation simple, but also the method is not limited by the time and the place, and the continuous division growth of the protocorm-like bodies can guarantee anniversary production, and the large-scale industrial production and application are facilitated.

Description

technical field [0001] The invention relates to a breeding method of medicinal plant seedlings, in particular to a series of mediums for rapid propagation of dendrobium dendrobium and a tissue culture method. Background technique [0002] Dendrobium dendrobii is a perennial herb that likes shade and shade. It likes to grow in warm, humid, semi-shady and semi-sun environment with an annual rainfall of more than 1,000 mm and an average January temperature higher than 8°C. , the suitable growth temperature is 15 to 28 degrees, and the suitable growth air humidity is above 60%. The seeds of Dendrobium dendrobii are as fine as dust, and one capsule contains as many as 1 million seeds. Due to the lack of endosperm, the seeds need to symbiosis with fungi to germinate, and the germination rate is very low (less than 5%) under natural conditions. The natural reproductive capacity of Dendrobium candidum is extremely low, and conventional reproduction is difficult. Over the years, th...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A01H4/00
Inventor 陈茂云
Owner 临沧市云瑞堂生物科技有限公司
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