CN1864477A - Cotton leafstalk tissue cultivation and high-differentiation cotton material selective breeding method - Google Patents
Cotton leafstalk tissue cultivation and high-differentiation cotton material selective breeding method Download PDFInfo
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Abstract
The present invention discloses cotton tissue culturing process and its application in screening out high differentiation rate cotton line. The cotton tissue culturing process includes the following steps: 1. adopting sterilized leaf stem as explant and inducing callus in callus inducing culture medium; 2. completing the differentiating culture of the callus in differentiating culture medium; and 3. further culturing of the differentiated embryonic callus in embryoid germinating and seedling forming culture medium to obtain regenerated plant. The process has high differentiation rate, and may be applied in screening out high differentiation rate cotton line. In addition, the screened high differentiation rate cotton can raise the converting efficiency of agrobacterium mediating process and shorten the converting period greatly. The present invention is significant in tissue culture, selective breeding and variety improvement of cotton.
Description
Technical field
The present invention relates to a method for tissue culture that grows cotton and an application thereof, particularly relate to a method for tissue culture that grows cotton and the application in the high differentiation rate cotton strain of screening system thereof.
Background technology
Cotton somatic embryos is taken place genotype and the plant regeneration ability has decisive role.The somatic embryo that at first shows different cotton seeds in the Gossypium takes place different with the plant regeneration ability.The researcher has only upland cotton, Lei Mengdeshi cotton, Hawaii cotton energy organizator blast by a plurality of cotton seeds are compared discovery.Dong Hezhong and Chen Zhixian have compared the somatic embryo generating ability of 4 cotton culture kinds, find easily inductor blast of upland cotton, Asian cotton takes second place, sea-island cotton and african cotton relatively poor (Dong Hezhong. the research that different genotype cotton hypocotyl cultured in vitro embryoid takes place.The Laiyang Agricultural College journal, 1991,97-101 and Chen Zhixian, Li Shujun. cotton cells suspension culture embryo is taken place and some The Characteristic Study of plant regeneration. Scientia Agricultura Sinica, 1987,20 (5): 6-11).Gossypium has 50 kinds, comprise 45 wild species, 4 cultivated speciess, only cotton 8 kinds in Ke Laociji cotton, Dai Weixunshi cotton, upland cotton, sea-island cotton, Asian cotton, cotton, Lei Mengdeshi cotton and Hawaii have obtained somatic embryo up to now, and wherein upland cotton, sea-island cotton, Asian cotton, cotton and Dai Weixunshi cotton have obtained regeneration plant.
In addition, on somatic embryo generation and plant regeneration ability, also there are differences between each cotton variety.Trolinder studies 28 kinds of upland cotton, the result has only jade-like stone word 312 and T25 to have higher somatic embryo generating ability, and other kind maybe can not be carried out somatic embryo generation (Trolinder N L than difficulty, Xhixian C.Genotypespecificity of the somatic embryogenesis response in cotton.Plant Cell Rep, 1989,8:133-136).Dong Hezhong etc. are divided into four classes according to what that become embryo quantity and develop into plant with the upland cotton kind: the first kind is that the somatic cell generating ability is strong, and the kind of Yi Chengmiao is as jade-like stone word 312, jade-like stone word 201 etc.; Second class is to have certain somatic embryo generating ability, and the number of seedling amount is medium, through repeatedly obtaining more somatic embryo and partial regeneration plant after the subculture screening, as Mount Tai word 15, Mount Tai word 16 etc.; The 3rd class is that the somatic embryo generating ability is poor, and lopsided embryo is many, can obtain indivedual plant after long-time subculture screening, as cotton No. 1, No. 7 of Shandong etc.; The 4th class is that somatic cell embryonic pole difficulty maybe can not take place, like that word cotton 215, this word 506 etc.Germplasm resource for cotton is abundant, and only the jade-like stone word is cotton serial at present, and minority kinds such as middle cotton series, the cotton series in Shandong have obtained somatic embryo and regeneration plant.
Explant commonly used during cotton tissue is cultivated is all from aseptic seedling, be generally cotyledon, the hypocotyl of aseptic seedling, opened in 2002 the sea applied for the patent ([CAH01-006-113] utilizes the cotton tissue culturing method of cotyledon petiole as explant) of aseptic seedling cotyledon petiole tissue culture, Jiao in 2002 change beautiful set up aseptic seedling radicle cultivating system (Jiao Gaili, Li Junfeng. utilize new explant to set up the research of cotton transformation system of high efficiency.Cotton journal 2002,10 (1): 6-9).Under existing cultivating system, getting the individuality of being cultivated when explant carries out tissue culture will not exist, and therefore can not be used for differentiation rate genetic research and high differentiation rate material selective breeding.
Summary of the invention
The purpose of this invention is to provide the land for growing field crops petiole method for tissue culture that grows cotton.
Cotton provided by the present invention land for growing field crops petiole method for tissue culture may further comprise the steps:
(1) to be explant, is placed on evoked callus on the callus inducing medium through the ripe petiole in the land for growing field crops of sterilization; Described callus inducing medium (called after MSB1) is the MSB minimal medium (Gui Yaolin that forms by the vitamin formula of the mineral salt prescription of MS medium and B5 medium, horse is really write " Plant Tissue Breeding ", Science Press, added heteroauxin (IAA) 0.05-0.15mg/L on basis 1985:23-27), kinetin (KT) 0.05-0.15mg/L, 2,4-D 0.05-0.15mg/L, glucose 25-35g/L, gel (Gelrite) 1.5-2.5mg/L, pH 5.6-6.0;
(2) callus is placed carry out differentiation culture on the differential medium; Described differential medium (called after MSB2) is to have added heteroauxin 0.001-0.05mg/L on the basis of MSB minimal medium, kinetin 0.001-0.05mg/L, glucose 25-35g/L, gel 1.5-2.5mg/L, pH 6.5-7.0;
(3) embryo callus that differentiates is placed embryoid sprout into and carry out the cultivation of regeneration seedling on the seedling medium; It is to have added kinetin (KT) 0.001-0.05mg/L, 6-BA 0.005-0.1mg/L, sucrose 25-35g/L, gel 1.5-2.5mg/L, pH 6.5-7.0 on the basis of MSB minimal medium that described embryoid is sprouted into seedling medium (called after MSB3).
In the method for tissue culture of above-mentioned cotton, the described method that petiole is sterilized can be: it is 0.1% HgCl that petiole is immersed mass percentage concentration
2Soaked 4-5 minute in the solution, fall remaining HgCl with aseptic water washing then
2
For obtaining callus preferably, before cultivation, excise the wound part at petiole two ends earlier, again remainder is cut into the long segment of 0.4-0.6cm.
Preferred culture medium prescription is: the callus inducing medium in the step (1) is preferably and has added heteroauxin 0.1mg/L, kinetin 0.1mg/L, 2 on the basis of MSB minimal medium, 4-D 0.1mg/L, glucose 30g/L, Gelrite 2mg/L, pH 5.8; Differential medium in the step (2) is preferably and has added heteroauxin 0.005mg/L on the basis of MSB minimal medium, kinetin 0.005mg/L, and glucose 30g/L, Gelrite2mg/L, pH 6.8; Step (3) embryoid is sprouted into the seedling medium for to have added kinetin 0.01mg/L on the basis of MSB minimal medium, 6-BA 0.01mg/L, and sucrose 30g/L, Gelrite 1.5-2.5mg/L, pH 6.8.
Above-mentioned method for tissue culture all is suitable for the petiole of all cotton varieties, as middle cotton series, the cotton series of jade-like stone word or the cotton series in Shandong etc., is specially adapted to middle cotton institute 24.
Second purpose of the present invention provides a kind of method that high differentiation rate cotton strain is of screening.
The screening technique that high differentiation rate cotton strain provided by the present invention is may further comprise the steps:
1) with the petiole be explant, carry out tissue culture with said method, the selection differentiation rate reaches the high differentiation rate individual plant more than 70%, individual plant results after the selfing;
2) numerous, selfing being expanded in the individual plant plant plantation of high differentiation rate, is that explant carries out tissue culture with said method with the petiole that expands numerous plant simultaneously, and the high differentiation rate strain of selecting differentiation rate to reach more than 90% is.
The seed that the high differentiation rate strain that results obtain with above-mentioned screening technique is, with part seed plantation aseptic seedling, hypocotyl with aseptic seedling is that explant carries out tissue culture again, can do further screening to the strain system of high differentiation rate, selects the material that petiole and aseptic seedling hypocotyl all have high differentiation rate.
In addition, also can be with hybridizing, at F with the high differentiation rate individual plant of above-mentioned screening technique acquisition and the cotton of other kind
2Substitute method same as described above and select high differentiation rate strain to be, thereby be fit to the cotton material selection cross of tissue culture, expand the genotype that cotton tissue is cultivated.
The invention provides a method for tissue culture that grows cotton.This cultural method is explant with the petiole, differentiation rate height not only, and can be used for the screening of high differentiation rate cotton strain system, screening technique is simple, the cycle is short, can apply.In addition, the high differentiation rate cotton that screens can also increase substantially the transformation efficiency of agrobacterium-mediated transformation, shortens the transformation period.The present invention will play a significant role in group training, seed selection and the breed improvement thereof of cotton.
Below in conjunction with specific embodiment the present invention is described in further detail.
Embodiment
Method therefor is conventional method if no special instructions among the following embodiment.Described percentage concentration is mass percentage concentration if no special instructions.
Embodiment 1, middle cotton the screening of high differentiation rate strain system in 24
Callus inducing medium: on the basis of MSB minimal medium, added heteroauxin 0.1mg/L, kinetin 0.1mg/L, 2,4-D 0.1mg/L, glucose 30g/L, Gelrite 2mg/L, pH 5.8.
Differential medium: on the basis of MSB minimal medium, added heteroauxin 0.005mg/L, kinetin 0.005mg/L, glucose 30g/L, Gelrite 2mg/L, pH 6.8.
Embryoid is sprouted into the seedling medium: on the basis of MSB minimal medium, added kinetin 0.01mg/L, and 6-BA 0.01mg/L, sucrose 30g/L, Gelrite 1.5-2.5mg/L, pH 6.8.
Hormone in the above-mentioned medium and other component all add in the medium before sterilization, before the medium sterilization, use the 1MKOH adjust pH, then at 121 ℃, 1.1kg/cm
2Pressure under autoclave sterilization 14min.
With middle cotton institute 24 is example, and existing screening technique to the high differentiation rate cotton of the present invention strain system is elaborated, and screening process may further comprise the steps:
One, the screening of high differentiation rate individual plant
1, prepares explant
Select seedling stage 120 strain middle cotton 24 healthy individual plant, prepare explant by the following method: petiole is immersed 0.1%HgCl
2Soak in the solution and sterilized in 4-5 minute; Then with sterile purified water flushing 5 times, with the thorough HgCl that removes remnants
2The wound part at excision petiole two ends is cut into remainder the long segment of 0.5cm again and gets final product.
2, the statistics of tissue culture and differentiation rate
The explant of preparing with step 1 carries out tissue culture, adds up differentiation rate simultaneously, and method is as follows:
1) explant is placed evoked callus on the callus inducing medium, with callus same medium successive transfer culture 3 times that form;
2) callus is placed on the differential medium cultivate;
3) place embryoid to sprout on the seedling medium embryo callus that differentiates and cultivate, obtain regeneration plant.
The condition of culture of above-mentioned steps is: 28 ± 2 ℃, artificial lighting intensity 2000Lx, every day illumination cultivation 14h, secretly cultivated 10 hours.
3, the screening of high differentiation rate individual plant
Therefrom screen the individual plant of high differentiation rate, the petiole differentiation rate is greater than 70% high differentiation rate individual plant totally 14 strains (numbering W02-W15) as a result, selected 120 strain middle cotton in 24 individual plants shared ratio be 12.5%.
Two, the acquisition of high differentiation rate strain system
The differentiation rate of step 1 screening is added generation greater than 70% 15 plant height differentiation rate individual plants in Hainan, strain system results, strain system with results expands numerous again, using the method identical with step 1 then is to carry out tissue culture to expanding numerous strain, add up the differentiation rate that each individual plant expands numerous offspring, wherein the W02-W08 differentiation rate that expands numerous offspring all is higher than 80% (seeing Table 1), shows that high differentiation rate characteristic can heredity.
Differentiation rate (%) between table 1 W02-W08 individual plant different generations
| Material number | Select from generation to generation | Expand numerous generation |
| W02 | 87.2 | 94.2 |
| W03 | 85.2 | 82.1 |
| W04 | 100 | 97.6 |
| W05 | 85.2 | 94.2 |
| W06 | 84.2 | 97.2 |
| W07 | 81.7 | 83.4 |
| W08 | 85.3 | 84.1 |
Simultaneously, results Hainan adds the seed of the high differentiation rate strain system in generation, gets part seed plantation aseptic seedling, is that explant carries out tissue culture according to a conventional method with the hypocotyl of aseptic seedling, the statistics differentiation rate is to carry out the aseptic seedling hypocotyl to cultivate to the above-mentioned high differentiation rate cotton strain with the said method screening.The differentiation rate of part strain system sees Table 2, and differentiation rate has than big-difference (0-100%), and wherein differentiation rate reaches 100% material proportion up to 42.8%, shows that the cotton material with the high differentiation rate of method seed selection aseptic seedling hypocotyl of the present invention also is effective.
Table 2 screening strain is the hypocotylar differentiation rate of aseptic seedling (%)
| Strain system numbering | Differentiation rate |
| W02 | 62.5 |
| W03 | 81.3 |
| W04 | 31.3 |
| W05 | 100.0 |
| W06 | 100.0 |
| W07 | 0.0 |
| W08 | 100.0 |
| W09 | 0.0 |
| W10 | 100.0 |
| W11 | 26.7 |
| W12 | 100.0 |
| W13 | 100.0 |
| W14 | 60.0 |
| W15 | 68.8 |
Three, selection cross
With the above-mentioned middle cotton that screens the cotton variety TM-1 hybridization of the 24 high differentiation rate strains individual plant that is W10 and difficult differentiation, F
1In generation, got 40 individual plants, and each individual plant is got 30 petiole segments, and differentiation rate is 0 after tissue culture, F
2The differentiation rate statistics in generation sees Table 3, therefrom can select the individual plant of high differentiation rate, further the proof differentiation rate can be hereditary, and method of the present invention not only can be used for the high differentiation rate cotton of systematic breeding strain system, also can be used for the high differentiation rate cotton of selection cross strain system.
Table 3 middle cotton 24 * TM-1F
2For differentiation rate (%)
| The individual plant numbering | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 |
| Differentiation rate | 28.6 | 0.0 | 60.0 | 0.0 | 44.4 | 15.0 | 7.1 | 7.1 | 0.0 |
| The individual plant numbering | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 |
| Differentiation rate | 0.0 | 18.8 | 0.0 | 100.0 | 0.0 | 0.0 | 0.0 | 7.7 | 0.0 |
| The individual plant numbering | 19 | 20 | 21 | 22 | 23 | 24 | 25 | 26 | 27 |
| Differentiation rate | 88.9 | 60.0 | 100.0 | 38.9 | 64.3 | 0.0 | 33.3 | 36.8 | 11.1 |
| The individual plant numbering | 28 | 29 | 30 | 31 | 32 | 33 | 34 | 35 | 36 |
| Differentiation rate | 0.0 | 25.0 | 72.7 | 7.7 | 66.7 | 8.3 | 75.0 | 50.0 | 22.2 |
| The individual plant numbering | 37 | 38 | 39 | 40 | 41 | 42 | 43 | 44 | 45 |
| Differentiation rate | 100 | 71.4 | 7.7 | 25 | 50 | 31.6 | 0 | 36 | 63.6 |
Four, detect the genetic transformation efficiency of seed selection strain system
The differentiation rate that will select with said method is carried out agriculture bacillus mediated genetic transformation test up to 100% W10 strain system, with middle cotton institute 24 is contrast, W10 carries out genetic transformation on May 20th, 2005, used gene and carrier are provided (referring to patent of invention: coded insect-killing protein fusion and expression vector and application thereof, the patent No.: CN95119563.8) by the biological center of the Chinese Academy of Agricultural Sciences.Add up conversion ratio and grafting regeneration plant in November, 2005.Add up sterile rate in May, 2006.The conversion ratio statistics of transfer-gen plant sees Table 4, and from the resistant calli differentiation rate, the differentiation rate of W10 transfer-gen plant middle cotton 24 plant more preceding than screening have been improved 2-3 doubly, and conversion ratio has also improved 2-3 doubly.Transformation period shortened to 5-6 month by original 12 months.In addition, because the cycle of tissue culture shortens, hormone dosage reduces, the sterile rate of regeneration plant is also by original over half being reduced to about 10%.Above-mentioned experimental result shows with method of the present invention can carry out the seed selection of high differentiation rate cotton material, and the high score rate material that filters out can be used for engineered breed improvement.
The agriculture bacillus mediated genetic transformation rate of table 4 W10
| Material | Repeat | Segment number (individual) | Resistant calli (individual) | Embryo callus (individual) | Healing rate (%) | Differentiation rate (%) | Conversion ratio (%) |
| W10 | I II III IV | 136 176 160 162 | 57 120 72 68 | 26 66 48 46 | 419 68.2 45.0 42.0 | 45.6 55.0 66.7 67.6 | 19.1 37.5 30.0 28.4 |
| In 24 | I II | 140 120 | 58 52 | 13 14 | 41.4 43.3 | 22.4 26.9 | 9.3 11.7 |
Embodiment 2, in the seed selection of high differentiation rate material in 394
With the method identical with embodiment 1 394 individual plants in 150 strains are screened, more selected high differentiation rate individual plant is continued to filter out the higher strain system of differentiation rate with same procedure, the result has selected 7 differentiation rates and has been higher than 80% strain system (Z1-Z7).Added generation to Hainan in 2003, and expanded numerously in 2004 in Earthquake of Anyang station in Henan middle cotton institute experimental field, and be that explant screens with same procedure with the petiole, and it is Z3 and Z7 that the result has obtained the strain that differentiation rate reaches 90% or more, and the differentiation rate that the Z1-Z7 strain is sees Table 5.
The differentiation rate (%) of seed selection material in 394 in the table 5
| Material number | Select from generation to generation | Expand numerous generation |
| Z1 | 77.8 | 79.4 |
| Z2 | 86.7 | 76.8 |
| Z3 | 84.0 | 82.1 |
| Z4 | 81.4 | 96.7 |
| Z5 | 71.6 | 84.1 |
| Z6 | 75.6 | 83.0 |
| Z7 | 94.5 | 91.3 |
2004 is female parent with the Z7 of high differentiation rate, is that male parent is hybridized with the middle cotton institute 12 of difficulty differentiation, F
1For sending winter Hainan to add generation acquisition F
2Colony.2005, to F
2The differentiation rate of colony is added up, and the differentiation rate of 145 individual plants is normal distribution as a result, and its differentiation rate heredity shows as typical quantitative character, and the differentiation rate of part individual plant sees Table 6.
Table 6 Z6 * middle cotton 12 F
2For part individual plant differentiation rate (%)
| The individual plant numbering | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 |
| Differentiation rate | 57.1 | 50.0 | 63.6 | 11.1 | 62.5 | 20.0 | 14.3 | 0.0 | 62.5 |
| The individual plant numbering | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 |
| Differentiation rate | 50.0 | 25.0 | 0.0 | 62.5 | 60.0 | 0.0 | 22.2 | 60.0 | 37.5 |
| The individual plant numbering | 19 | 20 | 21 | 22 | 23 | 24 | 25 | 26 | 27 |
| Differentiation rate | 0.0 | 33.3 | 66.7 | 66.7 | 62.5 | 50.0 | 0.0 | 63.6 | 83.3 |
| The individual plant numbering | 28 | 29 | 30 | 31 | 32 | 33 | 34 | 35 | 36 |
| Differentiation rate | 66.7 | 33.3 | 77.8 | 0.0 | 0.0 | 62.5 | 71.4 | 0.0 | 38.5 |
| The individual plant numbering | 37 | 38 | 39 | 40 | 41 | 42 | 43 | 44 | 45 |
| Differentiation rate | 16.7 | 11.1 | 75.0 | 40.0 | 6.3 | 0.0 | 12.0 | 0.0 | 14.0 |
| The individual plant numbering | 46 | 47 | 48 | 49 | 50 | 51 | 52 | 53 | 54 |
| Differentiation rate | 62.5 | 0.0 | 55.6 | 44.4 | 63.6 | 0.0 | 40.0 | 42.9 | 0.0 |
Above-mentioned result of the test shows that cotton petiole differentiation rate shows as high heritability.Therefore, can break up forthright shape to height by selection cross and transfer in the low differentiation rate material, hang down the differentiation rate material to improve, thus the restriction of expanding cotton tissue culturing gene type.
Claims (7)
1, a method for tissue culture that grows cotton may further comprise the steps:
(1) to be explant, is placed on evoked callus on the callus inducing medium through the ripe petiole in the land for growing field crops of sterilization; Described callus inducing medium is to have added heteroauxin 0.05-0.15mg/L on the basis of the MSB minimal medium of being made up of the vitamin formula of the mineral salt prescription of MS medium and B5 medium, kinetin 0.05-0.15mg/L, 2,4-D 0.05-0.15mg/L, glucose 25-35g/L, gel 1.5-2.5mg/L, pH5.6-6.0;
(2) callus is placed carry out differentiation culture on the differential medium; Described differential medium is to have added heteroauxin 0.001-0.05mg/L on the basis of MSB minimal medium, kinetin 0.001-0.05mg/L, glucose 25-35g/L, gel 1.5-2.5mg/L, pH6.5-7.0;
(3) embryo callus that differentiates is placed embryoid sprout into and carry out the cultivation of regeneration seedling on the seedling medium; It is to have added kinetin 0.001-0.05mg/L on the basis of MSB minimal medium that described embryoid is sprouted into the seedling medium, 6-BA 0.005-0.1mg/L, sucrose 25-35g/L, gel 1.5-2.5mg/L, pH6.5-7.0.
2, method for tissue culture according to claim 1 is characterized in that: the described method that petiole is sterilized is: it is to soak 4-5 minute in 0.1% the HgCl2 solution that petiole is immersed mass percentage concentration, washes with sterile water then.
3, method for tissue culture according to claim 1 is characterized in that: excise the wound part at petiole two ends earlier before cultivation, remainder is cut into the long segment of 0.4-0.6cm as explant again.
4, according to claim 1 or 2 or 3 described method for tissue culture, it is characterized in that: the callus inducing medium in the described step (1) is for having added heteroauxin 0.1mg/L on the basis of MSB minimal medium, kinetin 0.1mg/L, 2,4-D 0.1mg/L, glucose 30g/L, gel 2mg/L, pH5.8; Differential medium in the step (2) has been for to have added heteroauxin 0.005mg/L on the basis of MSB minimal medium, kinetin 0.005mg/L, glucose 30g/L, gel 2mg/L, pH6.8; Step (3) embryoid is sprouted into the seedling medium for to have added kinetin 0.01mg/L on the basis of MSB minimal medium, 6-BA 0.01mg/L, sucrose 30g/L, gel 1.5-2.5mg/L, pH6.8.
5, a kind of method of screening high differentiation rate cotton strain system may further comprise the steps:
1) with the described method of claim 1 cotton is carried out tissue culture, the selection differentiation rate reaches the high differentiation rate individual plant more than 70%;
2) individual plant of high differentiation rate is expanded numerous, strain system results are that explant carries out tissue culture with the method for claim 1 with the petiole that expands numerous plant again, obtain the high differentiation rate strain that differentiation rate reaches more than 90% through screening to be.
6, screening technique according to claim 5, it is characterized in that: gather in the crops the seed that high differentiation rate strain is, with part seed plantation aseptic seedling, hypocotyl with aseptic seedling is that explant carries out tissue culture again, strain system to high differentiation rate does further screening, the strain system that seed selection petiole and aseptic seedling hypocotyl differentiation rate are all high.
7, according to claim 5 or 6 described screening techniques, it is characterized in that: the high differentiation rate individual plant that will obtain and the cotton of other kind hybridize, and substitute with described method at F2 and screen high differentiation rate strain system, to widen the genotype of cotton.
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| CN104004783B (en) * | 2014-05-04 | 2016-08-24 | 河北农业大学 | Method for improving cotton transgenic efficiency |
| CN104086314A (en) * | 2014-07-24 | 2014-10-08 | 中国农业科学院棉花研究所 | Culture medium for deepening color of brown cotton and culture method thereof |
| CN104086314B (en) * | 2014-07-24 | 2016-05-25 | 中国农业科学院棉花研究所 | A kind of culture medium and cultural method thereof that increases brown cotton color and luster |
| CN104109032A (en) * | 2014-07-29 | 2014-10-22 | 中国农业科学院棉花研究所 | Culture medium and culture method for increasing length of cotton fibers |
| WO2019153627A1 (en) * | 2018-02-09 | 2019-08-15 | 中国农业科学院棉花研究所 | Photoperiod sensitive genetic male sterility mutant of cotton and application thereof |
| CN108575751A (en) * | 2018-05-02 | 2018-09-28 | 中国农业科学院棉花研究所 | The cultural method of Cotton Embryogenic Callus and embryoid |
| CN108575751B (en) * | 2018-05-02 | 2021-08-20 | 中国农业科学院棉花研究所 | Method for culturing cotton embryonic callus and embryoid |
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