Culture medium and culture method for inducing callus differentiation through peony leaves

A technology of induction medium and differentiation medium, which is applied in the field of plant tissue culture, can solve problems such as failure to form root system, stem tip propagation without dedifferentiation process, vitrification, etc., and achieve the effect of saving manpower and reducing the risk of pollution

Inactive Publication Date: 2015-10-28
YANGZHOU UNIV
View PDF8 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Wang Jifeng et al. (Wang Jifeng, Li Qing, Meng Hui. Research on callus induction and differentiation of five peony varieties. Journal of Beijing Forestry University, 2011,32(3):213-216.) published a paper 'The callus of five peony varieties Callus was successfully induced and adventitious buds were differentiated in "Research on Induction and Differentiation of Wound Tissue", but the callus was severely browned, vitrified, and brittle, and the bud differentiation rate was low, only 7.95%.
CN1675992A discloses a method for asexual reproduction of shoot tips, but the shoot tips do not go through the dedifferentiation process and cannot form root systems, so they have no application value in production and scientific research

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
  • Culture medium and culture method for inducing callus differentiation through peony leaves
  • Culture medium and culture method for inducing callus differentiation through peony leaves
  • Culture medium and culture method for inducing callus differentiation through peony leaves

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0020] Example 1

[0021] This research was carried out with the peony tuogui type ‘Zifengyu’ planted in the peony germplasm resource nursery of the College of Horticulture and Plant Protection, Yangzhou University:

[0022] (1) Collection time: March 28, 2014;

[0023] (2) Material selection: select young leaves;

[0024] (3) Sterilization and inoculation of leaves:

[0025] After the tender leaves are collected, use a sterilization method combining alcohol and mercury. The specific steps are as follows:

[0026] ① Rinse the young leaves in running water for 10 minutes to remove the external soil, then wash them with detergent (Shanghai Hehuangbaicat Co., Ltd.), and rinse them with running water;

[0027] ②Place the young leaves on the ultra-clean workbench, put them in a beaker, disinfect with 75% alcohol for 30s, and rinse them with sterile water repeatedly for 5-6 times;

[0028] ③Use 0.1% mercury (Shanghai Sino-Western Chemical Plant) to disinfect for 3 minutes and rinse with sterile ...

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 a culture medium and culture method for inducing callus differentiation through peony leaves. The method comprises the following steps: in late March, selecting tender peony leaves; after sterilizing the leaves, inoculating the sterilized leaves to an induction medium, wherein the temperature is 25+/-2 DEG C; culturing in dark for 2 months; inducing to form callus; transferring the callus to a differential medium, wherein the temperature is 25+/-2 DEG C; the illumination time is 12 h.d<-1>; the illumination intensity is 1200+/-1001x; culturing for 2 months to obtain adventitious buds. According to the method, the callus initiation rate of peony leaves can reach up to 98.60%, the vitrification ratio is 0%, and the differentiation ratio of the adventitious buds can reach 58.99%; each callus block can form 4-10 adventitious buds, so that the technical problem that the ratios of adventitious bud differentiation is low when peony leaves are adopted as explants to induce callus is solved; the method provides technical support for carrying out peony gene engineering, and is wide in market prospect.

Description

technical field [0001] The invention belongs to the field of plant tissue culture, and in particular relates to a culture medium and a culture method for inducing callus differentiation through paeoniae officinalis leaves. Background technique [0002] Peony is a traditional famous flower in my country. Except for some areas in South China where the weather is hot and not suitable for growth, it is almost all over the gardens of the country, but most of them are conventional cultivated varieties, and there are few new varieties with novel characters. Therefore, Chinese peony growers And scientific research institutions are actively carrying out the work of peony variety improvement and new variety cultivation. The improvement of peony varieties and the cultivation of new varieties are mainly carried out through cross breeding. This traditional method has the disadvantages of long cycle, low efficiency, and inability to carry out directional improvement, which delays the pace ...

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
IPC IPC(8): A01H4/00
Inventor 赵大球陶俊王静史旻周春华
Owner YANGZHOU 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