Unlock instant, AI-driven research and patent intelligence for your innovation.

A kind of cultivation method of cassava axillary bud somatic cell embryo in vitro culture virus-free seedling

A technology of somatic cells and axillary buds, which is applied in the field of culture of cassava axillary bud somatic cell embryos in vitro cultured and detoxified seedlings, can solve the problems of peeling and transferring, which are easily broken and damaged, difficult to produce on a large scale, waste materials, and the like. The effect of chemical production, robust growth and fast peeling speed

Active Publication Date: 2021-03-23
TROPICAL CORP STRAIN RESOURCE INST CHINESE ACAD OF TROPICAL AGRI SCI
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, the growth point of the stem tip is not only small in length, but also very tender. During the peeling process, it is difficult to quickly find the exact location, and it is easily broken and damaged during the peeling and transfer process. The operation is very difficult, which not only wastes materials , and difficult to mass-produce

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of cultivation method of cassava axillary bud somatic cell embryo in vitro culture virus-free seedling
  • A kind of cultivation method of cassava axillary bud somatic cell embryo in vitro culture virus-free seedling
  • A kind of cultivation method of cassava axillary bud somatic cell embryo in vitro culture virus-free seedling

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0028] The present invention will be further understood by better understanding of the present invention with reference to the accompanying drawings.

[0029] First, the preparation of Acmv cassava patients

[0030] 1, material

[0031] African Cassavar Mosaic (ACMV) DNA-A, DNA-B Infective Cloning was preserved by the POAP Biotechnology Research Laboratory of Plant Physiological Ecology of Shanghai Life Academy of Life Sciences in the Chinese Academy of Sciences.

[0032] Agrobacterium Tumefaciens: lba4404

[0033] 2, injection method and grafting ACMV infected tapacow

[0034] Agrobacteria injection method: Cut the cassava group culture seedlings into the greenhouse, planted in the anti-insect net, the temperature is 25 ± 2 ° C, the relative humidity of 60%, 16H / 8H light / dark cycle. Agrobacteriobacillus LBA4404 containing Acmv-NOG DNA-A and DNA-B was overlined in Yeb solid medium (RIF 25 mg / L, STREP 100 mg / L, KaN 50 mg / L), and at 28 ° C for 48 hours. The bacteria of A a...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a culture method for cassava axillary bud somatic embryogenesis in-vitro culture of virus-free seedlings. The method comprises the following steps of performing pre-culturing, wherein cassava tender stems infected with ACMV are subjected to conventional surface disinfection, then, stems with auxiliary buds or incompletely-detoxified stems with auxiliary buds infected with virus test tube seedlings are cut and inoculated to an auxiliary bud expansion induction culture medium for performing dark culture for 3-7 d; performing somatic embryogenesis induction culture, whereinauxiliary buds expanded after culture are stripped and inoculated on a somatic embryogenesis induction culture medium for performing dark culture for 25-35 d; performing somatic embryogenesis matureculture, wherein somatic embryogenesis tissue blocks are inoculated to a somatic embryogenesis mature culture medium for performing illumination culture for 25-35 d; performing plant regeneration culture, wherein mature somatic embryogenesis tissue blocks are inoculated to a plant regeneration culture medium for performing illumination culture for 28-40 d. The virus-free efficiency and the breeding coefficient are high, explant materials are multiple, operation is easy, speed is high, the number of regeneration plants is large, the seedling rooting rate is high, and seedlings grow robustly.

Description

Technical field [0001] The present invention relates to the culture method of a cellular embryogenic cultured detoxification seedlings of cassava marsh bracket cells. Background technique [0002] MANIHOT ESCULENTA CRANTZ is Euphorbiae plant, the chromosome is 2N = 36, and the born shrub is 1-5m. Cassava is second only to rice, corn, and sorghum, the roots contain rich starch, which can be used as food, can also be used as industrial raw materials or feed. It is a main food source of 600 million people in the tropical area. Cassava originated in South America, in the 16th-18th century, in Africa, Asia and Oceania. Cassava is now widely distributed around the world's tropical and partial subtropical regions. Cow potatoes were introduced to my country 1820, and there were more than 180 years of cultivation history. At present, my country's cassava producing area includes Hainan, Guangdong, Guangxi, Fujian, Yunnan and other places in Sichuan, Guizhou, Hunan, Jiangxi, etc., existing ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): A01H4/00
CPCA01H4/001A01H4/005A01H4/008
Inventor 朱文丽陈松笔李开绵
Owner TROPICAL CORP STRAIN RESOURCE INST CHINESE ACAD OF TROPICAL AGRI SCI
Features
  • R&D
  • Intellectual Property
  • Life Sciences
  • Materials
  • Tech Scout
Why Patsnap Eureka
  • Unparalleled Data Quality
  • Higher Quality Content
  • 60% Fewer Hallucinations
Social media
Patsnap Eureka Blog
Learn More