Tissue-culture fast propagation method of musella lasiocarpa plant

A technology for tissue culture, rapid propagation and ground gushing golden lotus, applied in the field of plant tissue culture, can solve the problems of limited number of sucking buds, difficult to clean and sterilize, difficult to obtain materials, etc., and achieve the effects of convenient disinfection and sterilization, and easy to obtain materials.

Inactive Publication Date: 2012-07-04
THE RES INST OF RESOURCES INSECTS RIRI OF THE CHINESE ACADEMY OF FORESTRY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The disadvantage of this method is: because the number of sucking buds on the T. chinensis plant is relatively limited, generally only 3 to 6 sucking buds will sprout from each T. chinensis plant, and the bases of the sucking buds are usually buried deep in the soil. Not only is it difficult to obtain materials, but it is often difficult to clean and sterilize because of carrying a large number of germs, and even impossible to perform tissue culture, so it is difficult to obtain sterile materials, which greatly affects the yield of T. The demand has hindered the promotion and application of this golden lotus with high ornamental value, great development potential and wide application.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] A, callus induction: take the inflorescences of Trollus chinensis that are about to open in the field, peel off the outer bracts, soak them in a sodium hypochlorite solution with a mass concentration of 2% on the ultra-clean workbench for 5 minutes, and rinse them with sterile water for 3 times , then soaked in mercuric chloride solution with a mass concentration of 0.1% for 20 minutes, rinsed with sterile water for 4 times, blotted the surface moisture with sterile filter paper, and then inserted into callus induction medium: modified MS, 1.0mg L -1 6-BA, 6.0mg·L -1 NAA, 20.0g·L -1 Sucrose, cultured in the dark at 25°C for 30 days, induced callus, and the callus induction rate was 64.0%;

[0036] B. Callus adventitious bud differentiation: inoculate the callus induced in step A in the callus adventitious bud differentiation medium: modified MS, 30.0g L -1 Sucrose, at a culture temperature of 25°C and a light time of 12h·d -1 , with an illumination intensity of 40 μm...

Embodiment 2

[0041] A, callus induction: get the nasturtium inflorescence that is just about to open in the field, peel off the outer bracts, soak it with 0.2% sodium hypochlorite solution for 15 minutes on the ultra-clean workbench, rinse it with sterile water for 5 times, and then use Soak in 1% mercuric chloride solution for 5 minutes, rinse with sterile water 8 times, blot the surface moisture with sterile filter paper, insert into callus induction medium: modified MS, 2.0mg L -1 6-B A, 3.0mg·L -1 NAA, 30.0g·L -1 Sucrose, cultivated in the dark at 20°C for 50 days, induced callus, and the callus induction was 76.0%;

[0042] B. Callus adventitious bud differentiation: inoculate the callus induced in step A in the callus adventitious bud differentiation medium: modified MS, 2.0mg L -1 6-BA, 0.02mg·L -1 NAA, 20.0g·L -1 Sucrose, at a culture temperature of 20°C and a light time of 8h·d -1 , with a light intensity of 30 μmol m -2 ·s -1 Under the condition of culturing for 40 days, t...

Embodiment 3

[0047] A, callus induction: take the nasturtium inflorescences that are just about to open in the field, peel off the outer bracts, soak them in 1% sodium hypochlorite solution for 10 minutes on the ultra-clean workbench, rinse them with sterile water 4 times, and then use Soak in 0.5% mercuric chloride solution for 15 minutes, rinse with sterile water 6 times, blot the surface moisture with sterile filter paper, insert into callus induction medium: modified MS, 6.0 mg L -1 6-BA, 1.0mg·L -1 NAA, 40.0g·L -1 Sucrose, cultured in the dark at 30°C for 40 days, induced callus, and the callus induction rate was 30.0%.

[0048] B. Callus Adventitious Bud Differentiation: Inoculate the above-mentioned induced callus in callus adventitious bud differentiation medium: modified MS, 3.0mg·L -1 6-BA, 0.04mg·L -1 NAA, 40.0g·L -1 Sucrose, at a culture temperature of 30°C and a light time of 10h·d -1 , with an illumination intensity of 50 μmol m -2 ·s -1 Under the condition of culturin...

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PUM

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Abstract

The invention provides a tissue-culture fast propagation method of a musella lasiocarpa plant, comprising the following steps of: inoculating inflorescences to be opened as explants into an induction medium to induce and culture calluses; then inoculating into an adventitious bud differential medium to be cultured and differentiated into buds; cutting the differentiated buds into single buds witha right amount of basal disc tissues, and inoculating into an enrichment medium to be cultured to obtain cluster buds; separately cutting the cluster buds into single plants, and inoculating into a rooting medium to be cultured into rooting seedlings; and acclimatizing the seedlings to obtain transplanting seedlings. The invention not only is easy and convenient for obtaining the materials, but also has large number of the explants because hundreds of the explants can be extracted from one inflorescence; the inflorescences tightly wrapped by bracts do not have germs because the germs are difficult to immerse into the inflorescences, therefore cleaning, disinfection and sterilization are very convenient; healthy transplanting seedlings are obtained through the sequential culture of the specifically-prepared induction medium, the adventitious bud differential medium, the enrichment medium and the rooting medium; and the survival rate reaches more than 90 percent after transplantation, therefore the demand quantity of the market on musella lasiocarpa can be completely satisfied.

Description

technical field [0001] The invention relates to a method for tissue culture and rapid propagation of plants, in particular to a method for tissue culture and rapid propagation of T. chinensis plants, and belongs to the technical field of plant tissue culture. Background technique [0002] Musella lasiocarpa, also known as Musella lasiocarpa, Musella lasiocarpa, is a large perennial herbaceous plant with rhizomes in the Musaceae genus Musella lasiocarpa. It is a unique single genus species in China, mainly distributed In the mountainous slopes of central and western Yunnan at an altitude of 1500-2500 meters, there are also a small amount of distribution in parts of Sichuan Province near Yunnan. Its flower shape is peculiar, the flower color is bright, and the ornamental period is as long as more than 200 days. It is a rare flower with great ornamental value and local characteristics. It also has various functions such as medicine, food, feed, textile, and water and soil conse...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A01H4/00
Inventor 刘秀贤李正红马宏万友名
Owner THE RES INST OF RESOURCES INSECTS RIRI OF THE CHINESE ACADEMY OF FORESTRY
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