Aspirin-containing banana rooting-promoting culture medium

一种阿司匹林、培养基的技术,应用在香蕉组织培养领域,能够解决培出根率低等问题

Inactive Publication Date: 2017-06-30
黄庆辉
View PDF0 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, banana is a kind of popular fruit, and it is also the main food in some areas. It has a huge market demand. It is necessary to carry out research on the rapid propagation of bananas. It can not only solve the huge market demand, but also be able to To a certain extent, good banana varieties are preserved. Tissue culture is one of the methods for rapid propagation of bananas. However, the rooting rate of existing banana tissue culture is too low to meet the current growth rate of demand.

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

[0020] Prepare the 1 / 2MS medium of the experimental group according to the following steps:

[0021] Step S10, using an electronic scale to prepare a 1000-fold 1 / 2MS medium stock solution according to the 1 / 2MS medium standard formula;

[0022] Step S20, take 1 / 2MS medium mother liquor to prepare 1 / 2MS medium, and add PP according to the formula 333 (Paclobutrazol), lanthanum nitrate, aspirin solution, NAA (naphthalene acetic acid), agar powder and white sugar, use hydrochloric acid or sodium hydroxide to adjust the pH of the medium;

[0023] Step S30, sterilize the culture medium at 121°C for 20 minutes in a high-temperature and high-pressure steam sterilizer, take out the culture medium and leave it to cool in the ultra-clean workbench;

[0024] Step S40, prepare a vitamin solution according to the formula, and filter and sterilize it;

[0025] In step S50, when the medium is cooled to 60°C, the reagent prepared in step S40 is added to the medium, shake evenly, stand still, and cool a...

Embodiment 2

[0029] The difference between the second embodiment and the first embodiment is that the concentration of the medium formula is adjusted.

[0030] Prepare the 1 / 2MS medium of the experimental group according to the following steps:

[0031] Step S10, using an electronic scale to prepare a 1000-fold 1 / 2MS medium stock solution according to the 1 / 2MS medium standard formula;

[0032] Step S20, take 1 / 2MS medium mother liquor to prepare 1 / 2MS medium, and add PP according to the formula 333 (Paclobutrazol), lanthanum nitrate, aspirin solution, NAA (naphthalene acetic acid), agar powder and white sugar, use hydrochloric acid or sodium hydroxide to adjust the pH of the medium;

[0033] Step S30, sterilize the culture medium at 121°C for 20 minutes in a high-temperature and high-pressure steam sterilizer, take out the culture medium and leave it to cool in an ultra-clean workbench;

[0034] Step S40, prepare a vitamin solution according to the formula, and filter and sterilize it;

[0035] In s...

Embodiment 3

[0039] Prepare the 1 / 2MS medium of the experimental group according to the following steps:

[0040] Step S10, using an electronic scale to prepare a 1000-fold 1 / 2MS medium stock solution according to the 1 / 2MS medium standard formula;

[0041] Step S20, take 1 / 2MS medium mother liquor to prepare 1 / 2MS medium, and add PP according to the formula 333 (Paclobutrazol), lanthanum nitrate, aspirin solution, NAA (naphthalene acetic acid), agar powder and white sugar, use hydrochloric acid or sodium hydroxide to adjust the pH of the medium;

[0042] Step S30, sterilize the culture medium at 121°C for 20 minutes in a high-temperature and high-pressure steam sterilizer, take out the culture medium and leave it to cool in the ultra-clean workbench;

[0043] Step S40, prepare a vitamin solution according to the formula, and filter and sterilize it;

[0044] In step S50, when the medium is cooled to 60°C, the reagent prepared in step S40 is added to the medium, shake evenly, stand still, and cool 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 an aspirin-containing banana rooting-promoting culture medium, with a 1 / 2MS culture medium as a basic culture medium, an aspirin solution, NAA (naphthylacetic acid), PP333 (paclobutrazol), lanthanum nitrate, vitamin, an agar powder and white granulated sugar are added; the aspirin solution is added in the culture medium, the composition components and proportion of the hormones are adjusted and rare earth elements are added, so the banana rooting rate and the rooting quality are improved; the culture medium has the advantages of high rooting rate and good root growth quality.

Description

Technical field [0001] The invention belongs to the technical field of banana tissue culture, and particularly relates to a banana-containing aspirin-containing medium for promoting root emergence. Background technique [0002] Banana (scientific name: Musa nana Lour.) Musa, Musa, also refers to its fruit. It is widely cultivated and eaten in tropical regions. Bananas are fragrant and nutritious, and can be harvested all year round. They are also highly valued in temperate regions. The plant is a large herb, emanating from the rhizome, forming a false stem with a height of 3-6 meters (10-20 feet) from the lower part of the leaf sheath; the leaves are oblong to elliptical, and some are as long as 3 to 3.5 meters (10 ~11.5 feet), 65 cm (26 inches) wide, with 10 to 20 clusters of stem tops. Drooping spikes [1] , Extracted from the top of the fake stem, with many flowers, light yellow; infructescence is bent down, the result is 10-20 bunches, about 50-150. The plants wither afte...

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 Applications(China)
IPC IPC(8): A01H4/00
CPCA01H4/001A01H4/008
Inventor 不公告发明人
Owner 黄庆辉
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