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A kind of culture medium group and its application of the tissue culture rapid propagation of the plant

A technology of tissue culture rapid propagation and medium, applied in the application, plant regeneration, plant cells and other directions, can solve the problems of browning of tissue materials, high seed reproduction efficiency, difficult to collect, etc., to promote shoot rooting, efficient induction of healing. The effect of wounding tissue and efficiently inducing the formation and growth of buds

Active Publication Date: 2021-06-08
成都及禾生物科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0017] However, at present, when using the phytohormone ratio in the conventional plant tissue culture medium to breed the plants of the genus Cymbidium, the efficiency is very low, even not as high as the seed propagation efficiency
In addition, due to the small size of Maojiancao seeds, it is not easy to collect, and the seed germination rate is not high in the natural environment, which makes it difficult to reproduce the seeds; at the same time, because of its rich secondary metabolites, it contains a variety of enzymes and various small Molecular substances have seriously affected the effect of the phytohormone combination of conventional plant tissue culture, so that the conventional plant tissue culture method can not effectively achieve the efficiency of tissue culture for the breeding of Maojiancao
For example, the commonly used media for tobacco tissue culture cannot complete the regeneration of plants of the genus Pseudomonas genus, such as Maojiancao, Minshan Maojiancao, and Songye Qinglan. The induction medium cannot induce enough callus tissue. During the induction process, the tissue The browning of the material is also obvious

Method used

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  • A kind of culture medium group and its application of the tissue culture rapid propagation of the plant
  • A kind of culture medium group and its application of the tissue culture rapid propagation of the plant
  • A kind of culture medium group and its application of the tissue culture rapid propagation of the plant

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0041] 1. a culture medium group of the tissue culture rapid propagation of blue orchid plant, comprise induction medium, differentiation medium and rooting medium.

[0042] Among them, the induction medium includes 0.8MS medium, 6-BA 0.5mg / L, IAA 0.1mg / L, 2,4-D0.1mg / L, sucrose 30g / L, agar 5g / L, Vc 0.2mg / L , Sodium nitrosoferricyanide 2.0mg / L, pH=5.6;

[0043] Differentiation medium includes 1.5MS medium, 6-BA 0.8mg / L, NAA 0.1mg / L, IAA 0.1mg / L, sucrose 30g / L, agar 5g / L, pH=6.2;

[0044] Rooting medium includes 0.8MS medium, NAA 0.15mg / L, IBA 0.025mg / L, sucrose 20g / L, agar 5g / L, potato juice 2.0mL / L, activated carbon 1g / L, pH=5.8.

[0045] 2. The application method of the culture medium group of the tissue culture rapid propagation of a kind of blue orchid

[0046] Among them, the induction medium is used to induce culture of the explants of Maojiancao to obtain callus (the callus rate is 86.85%); the differentiation medium is used to differentiate and cultivate the callus to...

Embodiment 2

[0048] 1. a culture medium group of the tissue culture rapid propagation of blue orchid plant, comprise induction medium, differentiation medium and rooting medium.

[0049] Among them, the induction medium includes 1.5MS medium, 6-BA 1.0mg / L, IAA 0.3mg / L, 2,4-D 0.2mg / L, sucrose 30g / L, agar 5g / L, Vc 0.4mg / L , Sodium nitroferricyanide 6.0mg / L, pH=6.2;

[0050] Differentiation medium includes 0.8MS medium, 6-BA 0.5mg / L, NAA 0.05mg / L, IAA 0.05mg / L, sucrose 30g / L, agar 5g / L, pH=5.6;

[0051] Rooting medium includes 1.0MS medium, NAA 0.2mg / L, IBA 0.05mg / L, sucrose 25g / L, agar 5g / L, potato juice 3.0mL / L, activated carbon 1g / L, pH=6.2.

[0052] 2. The application method of the culture medium group of the tissue culture rapid propagation of a kind of blue orchid

[0053] Among them, the induction medium is used to induce the explants of Maojiancao to obtain callus (the callus rate is 94.48%); the differentiation medium is used to differentiate and cultivate the callus to obtain adve...

Embodiment 3

[0055] 1. a culture medium group of the tissue culture rapid propagation of blue orchid plant, comprise induction medium, differentiation medium and rooting medium.

[0056] Among them, the induction medium includes MS medium, 6-BA 0.8mg / L, IAA 0.2mg / L, 2,4-D 0.15mg / L, sucrose 30g / L, agar 5g / L, Vc 0.3mg / L, Sodium nitrosoferricyanide 4.0mg / L, pH=5.8;

[0057] Differentiation medium includes MS medium, 6-BA 0.7mg / L, NAA 0.08mg / L, IAA 0.08mg / L, sucrose 30g / L, agar 5g / L, pH=5.8;

[0058] Rooting medium includes 0.5MS medium, NAA 0.1mg / L, sucrose 15g / L, agar 5g / L, potato juice 1.0mL / L, activated carbon 1g / L, pH=5.6.

[0059] 2. The application method of the culture medium group of the tissue culture rapid propagation of a kind of blue orchid

[0060] Wherein, the induction medium is used for inducing culture to the explant of Mao Jiancao, to obtain callus (the callus rate is 88.15%); Differentiation medium is used for the differentiation culture of callus, to obtain adventitious ...

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Abstract

The invention relates to the technical field of plant cell induction and tissue culture, and discloses a culture medium group for tissue culture and rapid propagation of plants of the genus Cymbidium, including an induction medium, a differentiation medium and a rooting medium, and the induction medium includes 0.8 ~1.5MS medium, 6‑BA 0.5~1.0mg / L, IAA 0.1~0.3mg / L, 2,4‑D 0.1~0.2mg / L, Vc 0.2~0.4mg / L, nitrosoferricyanide Sodium 2.0~6.0mg / L, sucrose 25~30g / L and agar 5~7g / L, pH=5.6~6.2; the differentiation medium includes 0.8~1.5MS medium, 6-BA 0.5~1.0mg / L , NAA 0.05~0.1mg / L, IAA 0.05~0.1mg / L, sucrose 25~30g / L and agar 5~7g / L, pH=5.6~6.2; The rooting medium includes 0.5~1.0MS medium, NAA 0.1~0.2mg / L, IBA 0~0.05mg / L, sucrose 15~25g / L, agar 5~7g / L and potato juice 1.0~3.0mL / L; the invention also discloses the application of the medium group , the medium group achieves the effect of high-efficiency breeding of cultivated seedlings of the genus Cymbidium through the targeted limitation of the medium components and ratios of the multi-phytohormone combination.

Description

technical field [0001] The invention relates to the technical field of plant cell induction and tissue culture, in particular to a culture medium group for tissue culture and rapid propagation of plants of the genus Cymbidium and its application. Background technique [0002] Dracocephalum belongs to Labiatae, herbaceous, perennial, with woody rhizomes, and rarely annual. Stems often arise from rhizomes, erect, sparsely spread, often unbranched or with few branches, sparsely numerous branches, quadrangular. Leaves opposite, basal leaves with long stalks, cauline leaves with short stalks or sessiles, often heart-shaped ovate or oblong, or lanceolate, margins crenate or serrate, or entire, usually not Divided or pinnately nearly palmately parted. Verticels densely clustered into heads or spikes or sparsely arranged; flowers usually blue-purple, rarely white; bracts often obovate, often with sharp teeth or spines, rarely entire. The phytochemical composition of the genus Qin...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N5/04A01H4/00
CPCA01H4/001A01H4/008
Inventor 秦小波
Owner 成都及禾生物科技有限公司
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