A method for establishing a lily embryogenic callus regeneration system with pedicels as explants

An embryogenic callus and explant technology, applied in the directions of plant regeneration, botanical equipment and methods, horticultural methods, etc., can solve problems affecting lily genetic engineering improvement, strict requirements for tissue culture and disinfection, destruction of rare and endangered species, etc. To achieve the effect of good callus embryos, high embryogenicity and tender explants

Inactive Publication Date: 2016-03-30
ZHEJIANG UNIV
View PDF4 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, the embryogenic callus regeneration system of lily is also the decisive basis of the genetic transformation system of lily, which in turn affects the genetic engineering improvement of lily.
[0003] At present, the establishment of lily callus regeneration system mostly uses the scales of field bulbs as explants. The disadvantage is that the bulbs have been in the soil environment for a long time and carry many germs, which makes the tissue culture disinfection strict and the pollution rate is high.
In addition, when it is necessary to establish a laboratory in vitro system of wild lily germplasm, bulbs are used as explants, and bulbs can only be dug after flowering. There are two outstanding shortcomings: first, the determination of the location and species of wild lily. The identification largely depends on the eye-catching floral organs and their characteristics. After the flowering period, all or part of the aboveground parts of wild lilies have withered. Confusion; secondly, digging bulbs is equivalent to the complete collection of wild resources, and it is even more difficult to restore damage to rare and endangered species

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] Example 1 Establishment of lily embryogenic callus regeneration system with oriental lily 'Sorbonne' pedicels as explants

[0049] (1) At the flower bud stage, take 1.5cm-long young lily flower buds with 1cm-long pedicel, refrigerate them in a sealed bag at 4 degrees Celsius, and take them out for processing after refrigerating for a week.

[0050] (2) Soak the flower buds in tap water with detergent for 5 minutes, rinse them under running water for 75 minutes, clean them, and use 1% w / v sodium hypochlorite solution with 0.1% v / v Tween on the ultra-clean workbench , disinfect the surface for 8 minutes, and then rinse with sterile water 3 times. Cut off the 1 cm long pedicel, cut off the browned part of its end to produce a fresh incision, scratch the surface with a scalpel, inoculate after incision or trauma, and make the wound surface contact the surface of the callus induction medium as much as possible. The callus induction medium inoculated with explants was cultur...

Embodiment 2

[0056] Example 2 Establishing Lilium Embryogenic Callus Regeneration System Using Oriental Lily 'Sorbonne' Pedicels as Explants

[0057] (1) At the flower bud stage, take 0.5cm-long young lily flower buds with 1.2cm-long pedicels, seal them in a bag and refrigerate them in a refrigerator at 4 degrees Celsius for a week before proceeding to follow-up operations.

[0058] (2) Soak the flower buds in tap water added with detergent for 18 minutes, rinse them under running water for 30 minutes, and wash them with 1% (w / v) Disinfect the surface with sodium hypochlorite solution for 12 minutes, and then rinse with sterile water for 3 times. Separate the flower buds with tweezers and a scalpel, cut the 1cm long pedicel, cut off the browned part of its end to produce a fresh incision, inoculate it on the callus induction medium after scratching, incision or trauma on its surface with the scalpel, and make The wound surface should be in contact with the surface of the culture medium a...

Embodiment 3

[0064] Example 3 Establishment of lily embryogenic callus regeneration system with oriental lily 'Sorbonne' pedicels as explants

[0065] (1) At the flower bud stage, young lily flower buds with a length of 2 cm and a pedicel with a length of 1.5 cm were taken, sealed in a bag and refrigerated at 4 degrees Celsius. After a week of refrigeration, the explants were taken out for processing.

[0066](2) Soak the flower buds in tap water added with detergent for 30 minutes, rinse them under running water for 120 minutes, and wash them with 1% (w / v) Tween added with 0.1% (v / v) v) Disinfect the surface with sodium hypochlorite solution for 15 minutes, and then rinse it with sterile water for 3 times. Separate the flower buds with tweezers and a scalpel, cut the 1cm long pedicel, cut off the browned part of its end to produce a fresh incision, inoculate it on the callus induction medium after scratching, incision or trauma on its surface with the scalpel, and make The wound surface ...

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 relates to the technical field of quick reproduction of plants, and aims to provide a method for establishing a lily embryogenic callus regeneration system by using pedicles as explants. The method comprises the following steps: material acquisition, callus-induced culture medium preparation, explant inoculation and callus induction, small plant regeneration, successive transfer culture of small plants, and transplanting of small plants. The method has the characteristics of low pollution rate, high callus inductivity, large callus conglomeration, favorable callus embryogenic property, high regeneration capacity and high reproducibility; especially, as the pedicles are used as the explants, the pollution rate can be lowered to 0, the callus inductivity of up to 100% can be obtained, the callus conglomeration reproducibility is up to 100%, the embryogenic property is high, and every 1cm of pedicle explant can obtain 60-80 small plants.

Description

technical field [0001] The invention relates to the technical field of rapid plant propagation, in particular to a method for establishing a lily embryogenic callus regeneration system with pedicels as explants. Background technique [0002] Lilium embryogenic callus regeneration system has the highest proliferation rate and multiplication rate compared with other regeneration systems such as bud regeneration system, which is of great significance for the preservation of excellent germplasm. In addition, the embryogenic callus regeneration system of lily is also the decisive basis of the genetic transformation system of lily, which in turn affects the genetic engineering improvement of lily. [0003] At present, most of the lily callus regeneration systems are established with the scales of field bulbs as explants. The disadvantage is that the bulbs have been in the soil environment for a long time and carry many germs, so the requirements for tissue culture disinfection are...

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
Inventor 张琳夏宜平
Owner ZHEJIANG UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products