CN103641543A - Culture medium for prevention of astragalus mongolicus test-tube sprout etiolation - Google Patents
Culture medium for prevention of astragalus mongolicus test-tube sprout etiolation Download PDFInfo
- Publication number
- CN103641543A CN103641543A CN201310593212.0A CN201310593212A CN103641543A CN 103641543 A CN103641543 A CN 103641543A CN 201310593212 A CN201310593212 A CN 201310593212A CN 103641543 A CN103641543 A CN 103641543A
- Authority
- CN
- China
- Prior art keywords
- culture medium
- test
- corresponding concentration
- substratum
- content
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Images
Landscapes
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Cultivation Of Plants (AREA)
Abstract
A culture medium for prevention of astragalus mongolicus test-tube sprout etiolation belongs to the technical field of plant biology. The culture medium comprises a improved MS (Murashige and Skoog) culture medium and 30 g/L sucrose, the pH value is 5.8; the boric acid content of the improved MS culture medium is increased by 1 / 3 of the original content, the ammonium nitrate content of the improved MS culture medium is reduced by 1 / 5 of the original content, and a plant growth regulator is added. By selecting of the improved MS medium, the culture medium is simple and practicable, and has obvious long-lasting effects. Only by changing the trace substance boric acid content and the large amount substance ammonium nitrate content in the improved MS culture medium, the MS minimal medium can be optimized, the purpose of overcoming etiolation can be reached, and a test tube sprout can always keep green and healthy in proliferation subculturing and rooting processes.
Description
Technical field
The present invention relates to a kind of substratum that prevents the yellow of Radix Astagali test-tube plantlet, it belongs to plant biology technical field.
Background technology
Yellow is one of Three Difficult Issues of plant tissue culture.In the group training process of Radix Astagali, etiolation is serious.Adopt traditional MS substratum as minimum medium, add the plant-growth regulator of different sorts and concentration, still cannot overcome etiolation, finally cannot seedling.The traditional method that overcomes tissue cultured seedling yellow has: improve aeration status in bottle, increase sugared consumption, increase illumination, regulate hormone ratio etc., and the sealed membrane generally using in production or bottle cap often will be taken into account isolation internal and external environment, the interior aeration status of suitably ventilative and low three conditions of cost, so its bottle is generally changeless; With the increase of sugar amount, can increase the dangerous of pollution and improve production cost; In same experimental situation, be difficult to come capable of regulating illumination intensity and light application time for the happiness photosensitiveness of each kind of plant; Therefore, only have by optimizing minimum medium MS, more suitably add conventional Hormone, could thoroughly solve the yellow problem of Radix Astagali.
Summary of the invention
In order to overcome the deficiencies in the prior art, the object of the present invention is to provide a kind of substratum that prevents the yellow of Radix Astagali test-tube plantlet, and improve the culture effect of growth coefficient and rooting rate.
The present invention is achieved through the following technical solutions:
Prevent a substratum for Radix Astagali test-tube plantlet yellow, comprise modified MS medium+30g/L sucrose, pH value is 5.8; Modified MS medium comprises large quantity of material, micro substance, molysite and organism;
Component and its corresponding concentration of large quantity of material are as follows:
Ammonium nitrate 1320 mg/L;
Saltpetre 1900 mg/L;
Potassium primary phosphate 170 mg/L;
Magnesium sulfate heptahydrate 370 mg/L;
Calcium dichloride dihydrate 440mg/L;
The component of micro substance and its corresponding concentration are as follows:
Four water manganous sulfate 22.3mg/L;
Zinc Sulphate Heptahydrate 8.6 mg/L;
Boric acid 8.3 mg/L;
Potassiumiodide 0.83 mg/L;
Sodium Molybdate Dihydrate 0.25 mg/L;
Cupric sulfate pentahydrate 0.025 mg/L;
CoCL2 6H2O 0.025 mg/L;
The component of molysite and its corresponding concentration are as follows:
Iron vitriol 27.8 mg/L;
Disodium ethylene diamine tetraacetate 37.3 mg/L;
Organic component and its corresponding concentration are as follows:
Glycine 2.0 mg/L;
Vitamin 0.1 mg/L;
Pyridoxine hydrochloride 0.5 mg/L;
Nicotinic acid 0.5 mg/L;
Inositol 100 mg/L.
Substratum also comprises plant-growth regulator, and its kind and its corresponding concentration are 6-BA0.2g/L+IBA0.05g/L.
Substratum also comprises plant-growth regulator, and its kind and its corresponding concentration are IBA2.0g/L+NAA2.0 g/L.
Boron in boric acid is the essential factor of plant cell division and Protein formation, is conducive to the formation of cell walls, affects the nitrogen metabolism in plant materials, finally has influence on growing of plant.Boron deficiency or nitrogen content be unreasonable all may cause the even yellow of test-tube plantlet spike top.Reasonably the content of boric acid and the content of ammonium nitrate are the effective measure that overcome yellow.
The invention has the beneficial effects as follows: the present invention is by selecting modified MS medium, simple successful and lasting.Only need, by changing the content of ammonium nitrate in the content of micro substance boric acid in MS substratum and large quantity of material, to optimize MS minimum medium, can reach the object that overcomes yellow, in test-tube plantlet proliferation and subculture and rooting process, remain green healthy and strong.
Accompanying drawing explanation
Fig. 1 adopts to prevent the substratum of Radix Astagali test-tube plantlet yellow and traditional MS nutrition base comparison diagram;
Fig. 2 is the cultivation effect figure that adopts the substratum that prevents the yellow of Radix Astagali test-tube plantlet;
Fig. 3 is the rooting efficiency figure that adopts the substratum that prevents the yellow of Radix Astagali test-tube plantlet.
Embodiment
Below in conjunction with specific embodiment, describe the specific embodiment of the present invention in detail:
Embodiment 1
Modified MS medium+30g/L sucrose; PH value is adjusted to 5.8, and the component of the large quantity of material of modified MS medium and its corresponding concentration are as follows:
Ammonium nitrate 1320 mg/L;
Saltpetre 1900 mg/L;
Potassium primary phosphate 170 mg/L;
Magnesium sulfate heptahydrate 370 mg/L;
Calcium dichloride dihydrate 440 mg/L;
The component of micro substance and its corresponding concentration are as follows:
Four water manganous sulfate 22.3 mg/L;
Zinc Sulphate Heptahydrate 8.6 mg/L;
Boric acid 8.3 mg/L;
Potassiumiodide 0.83 mg/L;
Sodium Molybdate Dihydrate 0.25 mg/L;
Cupric sulfate pentahydrate 0.025 mg/L;
CoCL2 6H2O 0.15 mg/L;
The component of molysite and its corresponding concentration are as follows:
Iron vitriol 27.8 mg/L;
Disodium ethylene diamine tetraacetate 37.3 mg/L;
Organic component and its corresponding concentration are as follows:
Glycine 2.0 mg/L;
Vitamin 0.1 mg/L;
Pyridoxine hydrochloride 0.5 mg/L;
Nicotinic acid 0.5 mg/L;
Inositol 100 mg/L.
Technical process:
1) get Radix Astagali test-tube plantlet;
2) wipe out the new stubble of base portion;
3) be seeded in above-mentioned substratum;
4) intensity of illumination 2000lux, photoperiod 12h/d;
Result is: after 40 days, can form green seedling clump, and effect stability, and can not return to again yellow state.
Embodiment 2
Modified MS medium+30g/L sucrose, then add plant-growth regulator, its kind and its corresponding concentration are 6-BA0.2g/L+IBA0.05g/L.
Except substratum difference, all the other adopt the technical process identical with embodiment 1.
Result is: after 40 days, can form green seedling clump, its growth coefficient is up to 5.5, and test-tube plantlet growth is healthy and strong.
Embodiment 3
Modified MS medium+30g/L sucrose, then add plant-growth regulator, its kind and its corresponding concentration are IBA2.0g/L+NAA2.0 g/L.
Except substratum difference, all the other adopt the technical process identical with embodiment 1.
Result is: rooting rate is higher, and seedling rate is high, and on the root media of screening, rooting rate reaches 85%.
The present invention optimizes MS minimum medium by the content of ammonium nitrate in the content by micro substance boric acid in change MS substratum and large quantity of material, can reach the object that overcomes yellow, in MS substratum except the content and ammonium nitrate content of boric acid, other component content is constant, and dosage of sucrose adopts conventional 30g/L.
1) content of MS substratum mesoboric acid increases 1/3 of original content.
2) in MS substratum, ammonium nitrate content reduces 1/5 of original content.
3) in test-tube plantlet propagation formula, kind and the content of plant-growth regulator is 6-BA0.2g/L+IBA0.05g/L.
4) in rooting of vitro seedling formula, the kind of plant-growth regulator and content are IBA2.0g/L+NAA2.0 g/L.
The present invention is applied on the Radix Astagali of yellow, after 40 days, can form green seedling clump, and its growth coefficient is up to 5.5, test-tube plantlet growth is healthy and strong, remains green state, can not return to yellow state again, on the root media of screening, rooting rate reaches 85%, finally seedling.With the content of boric acid and the optimization MS minimum medium of ammonium nitrate content change, the method that may alleviate etiolation with respect to other, has advantages of workable, simple.
Below with preferred embodiment, disclose the present invention, so it is not intended to limiting the invention, and all employings are equal to replaces or technical scheme that equivalent transformation mode obtains, within all dropping on protection scope of the present invention.
Claims (3)
1. a substratum that prevents the yellow of Radix Astagali test-tube plantlet, is characterized in that: comprise modified MS medium+30g/L sucrose, pH value is 5.8; Modified MS medium comprises large quantity of material, micro substance, molysite and organism;
Component and its corresponding concentration of large quantity of material are as follows:
Ammonium nitrate 1320 mg/L;
Saltpetre 1900 mg/L;
Anhydrous potassium dihydrogenphosphate 170 mg/L;
Magnesium sulfate heptahydrate 370 mg/L;
Calcium dichloride dihydrate 440mg/L;
The component of micro substance and its corresponding concentration are as follows:
Four water manganous sulfate 22.3mg/L;
Zinc Sulphate Heptahydrate 8.6 mg/L;
Boric acid 8.3 mg/L;
Potassiumiodide 0.83 mg/L;
Sodium Molybdate Dihydrate 0.25 mg/L;
Cupric sulfate pentahydrate 0.025 mg/L;
CoCL2 6H2O 0.025 mg/L;
The component of molysite and its corresponding concentration are as follows:
Iron vitriol 27.8 mg/L;
Disodium ethylene diamine tetraacetate 37.3 mg/L;
Organic component and its corresponding concentration are as follows:
Glycine 2.0 mg/L;
Vitamin 0.1 mg/L;
Pyridoxine hydrochloride 0.5 mg/L;
Nicotinic acid 0.5 mg/L;
Inositol 100 mg/L.
2. a kind of substratum that prevents the yellow of Radix Astagali test-tube plantlet according to claim 1, is characterized in that: also comprise plant-growth regulator, its kind and its corresponding concentration are 6-BA0.2g/L+IBA0.05g/L.
3. a kind of substratum that prevents the yellow of Radix Astagali test-tube plantlet according to claim 1, is characterized in that: also comprise plant-growth regulator, its kind and its corresponding concentration are IBA2.0g/L+NAA2.0 g/L.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201310593212.0A CN103641543A (en) | 2013-11-23 | 2013-11-23 | Culture medium for prevention of astragalus mongolicus test-tube sprout etiolation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201310593212.0A CN103641543A (en) | 2013-11-23 | 2013-11-23 | Culture medium for prevention of astragalus mongolicus test-tube sprout etiolation |
Publications (1)
Publication Number | Publication Date |
---|---|
CN103641543A true CN103641543A (en) | 2014-03-19 |
Family
ID=50246878
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201310593212.0A Pending CN103641543A (en) | 2013-11-23 | 2013-11-23 | Culture medium for prevention of astragalus mongolicus test-tube sprout etiolation |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103641543A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110771507A (en) * | 2019-11-26 | 2020-02-11 | 大连大学 | Preparation method of artificial astragalus membranaceus seeds |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02200194A (en) * | 1989-01-31 | 1990-08-08 | Q P Corp | Production of polysaccharides |
CN1557143A (en) * | 2004-01-13 | 2004-12-29 | 四川大学 | Polygonatum cyrtonema Hua regeneration system establishment method |
CN1653887A (en) * | 2005-03-08 | 2005-08-17 | 天津大学 | Tissue culturing method for astragalus root of Radix Astragali |
CN101874470A (en) * | 2009-11-12 | 2010-11-03 | 大连大学 | Method for improving reproduction coefficient of Phalaenopsis hybrid |
-
2013
- 2013-11-23 CN CN201310593212.0A patent/CN103641543A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02200194A (en) * | 1989-01-31 | 1990-08-08 | Q P Corp | Production of polysaccharides |
CN1557143A (en) * | 2004-01-13 | 2004-12-29 | 四川大学 | Polygonatum cyrtonema Hua regeneration system establishment method |
CN1653887A (en) * | 2005-03-08 | 2005-08-17 | 天津大学 | Tissue culturing method for astragalus root of Radix Astragali |
CN101874470A (en) * | 2009-11-12 | 2010-11-03 | 大连大学 | Method for improving reproduction coefficient of Phalaenopsis hybrid |
Non-Patent Citations (6)
Title |
---|
伍春莲: "黄芪愈伤组织的培养及其蛋白质含量的测定", 《西华师范大学学报(自然科学版)》 * |
包英华,等: "蒙古黄芪的组织培养研究", 《韶关学院学报(自然科学版)》 * |
姜存仓,等: "赣南脐橙叶片黄化及施硼效应研究", 《植物营养与肥料学报》 * |
武建林,等: "植物黄化与氮磷钾营养的关系", 《西北农业学报》 * |
邱运亮,等: "《植物组培快繁技术》", 28 February 2010, 化学工业出版社 * |
马伟明,等: "黄芪愈伤组织的诱导及分化培养", 《甘肃农业科技》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110771507A (en) * | 2019-11-26 | 2020-02-11 | 大连大学 | Preparation method of artificial astragalus membranaceus seeds |
CN110771507B (en) * | 2019-11-26 | 2022-07-01 | 大连大学 | Preparation method of artificial astragalus membranaceus seeds |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102100171B (en) | Aqueous culture method of anoectochilus | |
CN103012004A (en) | Leaf vegetable nutrient solution formula | |
CN104671881A (en) | Vegetable soilless culture nutrient solution and manufacturing method thereof | |
CN103030472A (en) | Formula of flower maintenance nutrient solution | |
CN102173906A (en) | Soilless culture nutrient solution as well as preparation method and application thereof | |
CN102531745B (en) | Special rice fertilizer for producing organic selenium-enriched rice and preparation method thereof | |
CN102126882A (en) | Preparation method of nutrient solution for culturing nutrient-deficient wheat seedling | |
CN101863705B (en) | Growth promoter for aquaculture water phytoplankton | |
CN105409740B (en) | anoectochilus roxburghii water culture method | |
CN105481608A (en) | Plant nutrient solution formula | |
CN102884981B (en) | Zanthoxylum nitidum tissue culture medium | |
CN106665044A (en) | Cultivation method of selenium-enriched tomato | |
CN102391035B (en) | Water-soluble blooming special fertilizer for substrate-cultured orchids and preparation method thereof | |
CN102668987B (en) | Multiplying culture media for strawberry | |
CN103053418A (en) | Potato microtuber manufacturing technology | |
CN101302127B (en) | Special fertilizer for M edible fungus and preparing method thereof | |
CN109020674A (en) | A kind of rice selenium-enriched foliage fertilizer | |
CN107873473A (en) | A kind of vegetable soilless-culture nutrient solution | |
CN103875532A (en) | Proliferation culture medium for tissue culture of Jietu vaccinium vitisidaea | |
CN101955391A (en) | Method for preparing nutrient solution of flowers and plants | |
CN103641543A (en) | Culture medium for prevention of astragalus mongolicus test-tube sprout etiolation | |
CN111955266A (en) | Method for strengthening and activating selenium in tea garden soil | |
CN106966795A (en) | A kind of Whole-nutrient Lycium Chinese drip irrigation special fertilizer and preparation method thereof | |
CN101381247A (en) | Sulphate-potassium magnesium fertilizer and preparation method thereof | |
CN102674966A (en) | Special culture medium for potato virus-free seedling transplanting and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C05 | Deemed withdrawal (patent law before 1993) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20140319 |