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A kind of aseptic seeding and tissue culture method of micro-spotted primula moss

A technology of primrose and aseptic sowing, applied in the field of bioengineering, can solve problems such as lack of artificial breeding technology, and achieve the effects of high seed germination rate, fast seedling formation and good seedling quality

Active Publication Date: 2019-01-08
GUANGXI ZHUANG AUTONOMOUS REGION ACAD OF AGRI SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Aiming at the lack and insufficiency of the existing micro-spotted primula artificial breeding technology, the present invention provides a method for aseptic sowing and tissue culture of micro-spotted primula. The method has the advantages of high seed germination rate, fast seedling growth, The quality of seedlings is good, and a large number of tissue culture seedlings can be obtained in a short period of time. It is an effective way for the production of seedlings of Primula microspot and the protection of resources.

Method used

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  • A kind of aseptic seeding and tissue culture method of micro-spotted primula moss

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Embodiment 1

[0027] A kind of aseptic seeding and tissue culture method of micro-spotted primula moss, comprising the steps:

[0028] (1) Aseptic germination of seeds: take the fruit pods of the mature and uncracked Primula spp., rinse them under running water for 10 minutes with detergent, and use 75% alcohol on the ultra-clean workbench. Soak the fruit pods in medium for 30 seconds, rinse them with sterile water for 3 times, then soak the fruit pods with 0.1% mercuric chloride solution for 12 minutes, rinse them with sterile water for 3 times, cut the fruit pods on the inoculation tray, and gently clean them with a sterilized spoon. The seeds are put into the seed germination medium, and the sown seeds are cultivated in the dark in the light incubator until the seeds germinate, and then transferred to the light culture in the culture room; the temperature of the dark culture is 17°C; The light culture temperature is 23°C, and the light is 1000lx; the germination medium is MS+GA 3 1.0mg...

Embodiment 2

[0035] A kind of aseptic seeding and tissue culture method of micro-spotted primula moss, comprising the steps:

[0036](1) Aseptic germination of seeds: take the fruit pods of the mature and uncracked Primula spp., rinse them under running water for 15 minutes after soaking them with detergent, and use 75% alcohol on the ultra-clean workbench. Soak the fruit pods in medium for 40 seconds, rinse them with sterile water for 5 times, then soak the fruit pods with 0.1% mercuric solution for 15 minutes, rinse them with sterile water for 5 times, cut the fruit pods on the inoculation tray, and gently clean them with a sterilized spoon. Dial the seeds into the seed germination medium, and cultivate the sown seeds darkly in the light incubator until the seeds germinate, and then transfer them to the light culture in the culture room; the temperature of the dark culture is 20°C; The light culture temperature is 25°C, and the light is 1400lx; the germination medium is MS+GA 3 2.0mg / L...

Embodiment 3

[0043] A kind of aseptic seeding and tissue culture method of micro-spotted primula moss, comprising the steps:

[0044] (1) Aseptic germination of seeds: take the fruit pods of the mature and uncracked Primula spp., rinse them under running water for 13 minutes after soaking them with detergent, and use 75% alcohol on the ultra-clean workbench. Soak the fruit pods in medium for 35 seconds, rinse them with sterile water for 3-5 times, then soak the fruit pods with 0.1% mercury liter solution for 14 minutes, rinse them with sterile water for 4 times, cut the fruit pods on the inoculation tray, and use a sterilized spoon Gently dial the seeds into the seed germination medium, and cultivate the sown seeds darkly in the light incubator until the seeds germinate, and then transfer them to the light culture in the culture room; the temperature of the dark culture is 18°C; The above light culture temperature is 24°C, and the light is 1200lx; the germination medium is MS+GA 3 1.5mg / ...

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Abstract

The invention belongs to the field of bioengineering technology and specifically relates to a tissue culture method of Primulina minutimaculata. The aseptic germination and tissue culture method of Primulina minutimaculata comprises the following steps: aseptic germination, initial culture, adventitious buds proliferation culture, callus differentiation, rooting culture, and acclimatization and transplanting. The tissue culture method of Primulina minutimaculata has characteristics of high seed germination rate, fast seedling formation, good seedling quality and the like, can be adopted to obtain lots of tissue culture seedlings within a short period of time, and is an effective approach to seedling production and resource protection of Primulina minutimaculata.

Description

technical field [0001] The invention belongs to the technical field of bioengineering, and in particular relates to a method for aseptic sowing and tissue culture of micro-spotted primula lettuce. Background technique [0002] Primulina minutimaculata is a perennial herbaceous plant of the genus Primulina in the family Gesneriaceae. Distributed in Longzhou, Tian, ​​etc., Guangxi, born on rocks under forests in rocky mountains, at an altitude of 200-450m, flowering period is April-May. Although the distribution range of Primula microspot in Longzhou and Tiandeng is relatively wide, the distribution is sporadic, and the population is small, the number of individual plants is small, and self-renewal is difficult. In addition, due to the serious damage to the habitat due to the construction of mountains and roads, the population has rapidly retreated, and it is currently in an endangered state, and the IUCN classification is critically endangered. [0003] Primula microspot ha...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A01H4/00
CPCA01H4/008
Inventor 闫海霞邓杰玲卜朝阳黄昌艳何荆洲关世凯陶大燕
Owner GUANGXI ZHUANG AUTONOMOUS REGION ACAD OF AGRI SCI