CN1653889A - Method for preserving germplasm for Atractylis lancea tissue culture propagation - Google Patents
Method for preserving germplasm for Atractylis lancea tissue culture propagation Download PDFInfo
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- CN1653889A CN1653889A CN 200510037859 CN200510037859A CN1653889A CN 1653889 A CN1653889 A CN 1653889A CN 200510037859 CN200510037859 CN 200510037859 CN 200510037859 A CN200510037859 A CN 200510037859A CN 1653889 A CN1653889 A CN 1653889A
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Abstract
The germ plasm maintaining technology for the tissue culture propagation of atractylodes includes selecting excellent clone rhizome as explant, inducing germination directly in MS culture medium with added hormones in different kinds and concentration, proliferation, secondary culture, rooting, and test seedling transplanting to complete the maintenance of excellent germ plasm resource. The technology of the present invention is stable, reliable, repeatable and long in germ plasm maintaining period, and can culture seedling of atractylodes superior to that obtained through seed culture.
Description
Technical field
The present invention relates to the quality saving method of plant, refer in particular to the quality saving technology of Atractylis lancea tissue culture propagation.
Technical background
Atractylis lancea (Atractylodes lancea (thunb.) DC) is a feverfew, is herbaceos perennial.Atractylis lancea is the genuine traditional Chinese medicine material, can be used for treating diseases such as indigestion, stomachache and nyctotyphlosis, the scientific research human pharmacology understanding to it of just enriching constantly.Now people also utilize on its preventing cold and SARS, treatment nodal tachycardia, diabetes, the bacillary dysentery etc.
But because the destruction of ecotope and rob excavating of formula in the past, the resource of wild Atractylis lancea is day by day rare, has been in Critical Condition.Atractylis lancea is out of stock in spite of rising price on the medicinal material market.At present, the whole nation is Atractylis chinensis on each big medicinal material market, and its quality and curative effect all are inferior to Atractylis lancea.Except the habitat of protection Atractylis lancea, domestication and cultivation just become the important means of rescue Atractylis lancea resource.Present discovers that wild Atractylis lancea has polytype, and various types of yield and qualities have bigger difference, therefore cultivates the key that the high-quality Atractylis lancea becomes the high yield and high quality cultivation.And the selection choiceness, preserving high-quality germ plasm resource is again the key of cultivation high-quality Atractylis lancea.
The breeding of Atractylis lancea is mainly by two kinds of approach: the one, and sexual propagation is promptly multiplied seedling of future generation by seed; Because wild Atractylis lancea has polytype, long-term companion planting will cause the natural hybrization between the dissimilar Atractylis lanceas, and germ plasm resource is degenerated rapidly.Another kind of breeding approach is vegetative propagation, promptly by the method for root division, this class propagation method is subjected to the restriction of seasonality and natural conditions, in case maternal plant has infected damage by disease and insect etc. simultaneously, cause germ to spread soon by vegetative propagation, also will make the output of Atractylis lancea and quality be subjected to very big influence.Therefore, the necessary quality saving problem of utilizing tissue culture technique to solve the Atractylis lancea high-quality resource.But the report that the quality saving success of Atractylis lancea high-quality resource is not arranged so far.
Summary of the invention
The objective of the invention is at problems of the prior art, a kind of Atractylis lancea quality saving technology is provided, this technology is not subjected to the restriction of natural conditions or regional disparity, the long preservation that helps germplasm, the seedling of high-quality purifying can be provided at any time, and the growth of seedling of preserving the back cultivation is fast, can make Atractylis lancea reach good quality and high output.
In order to realize above-mentioned purpose of the present invention, the invention provides following technical scheme:
The quality saving method of Atractylis lancea tissue culture propagation, comprise that selecting clonal rhizome for use is explant, on the MS medium of additional hormone, directly induce and sprout, bud through propagation, subculture, take root, test-tube seedling transplanting, finish the quality saving process of high-quality resource, minimal medium is selected MS additional saccharose 3%, agar 0.8% for use; Bud is induced with proliferated culture medium and is selected MS+6-BA 2.0～3.0mg/l+NAA0.1～0.2mg/l for use; Subculture medium is selected MS+6-BA 1.0mg/l+NAA0.05～0.1mg/l for use; Root media is 1/2MS+NAA0.2mg/l or 1/2MS+IBA1.0mg/l, pH5.4～5.8, conventional autoclaving; The test-tube plantlet condition of culture selects 20 ± 2 ℃; Illumination 12h/d, intensity of illumination 1500～2000Lux.
It is explant that said method can be selected the rhizome of reproductive stage for use.
Select that into people's reproductive growth phase, plant begin solid season the period of drawing materials of said method rhizome.
The said method explant is selected the rhizome of 0.5-1.5 centimetre of length.
Said method can carry out successive transfer culture as required, and regular situation should be every 1-2 month successive transfer culture once.
After the transplanting of test-tube plantlet is chosen in culture of rootage 10-15 days, in the time of the long 4-6 of seedling cauline leaf centimetre, before transplanting, opened bottle cap in 2-3 days, treat the intensification of leaf look, be transplanted to the greenhouse again, begin to make in a week humidity to remain on more than 90%, humidity is remained on about 75%, plant open country after 10-15 days, again through field planting field in January.
Compare with conventional method, the invention has the advantages that:
1, compare with the method for carrying out quality saving with seed, the present invention is not subjected to the restriction of natural conditions or regional disparity.Seminal propagation is subjected to the weather of location and the restriction of geographical conditions, and the present invention obtains seedling by trophosome being carried out tissue culture, be not subjected to the restriction of weather conditions, because tissue cultivating seedling can be cultivated preservation by long-term subculture, therefore in case need seedling can be provided at any time.
2, the cultivation after convenient the preservation: because tissue cultivating seedling reproduction coefficient height, speed is fast, and the high-quality seedling can be provided rapidly, and the fast growth of the seedling after the transplanting helps large-scale cultivation.
3, reduce the land used of conventional clone quality saving: conventional clone is preserved germplasm need take certain soil, and easily infected virus, disease cause germ plasm resource to degenerate.Utilize the technology of the present invention, can reduce land used, simultaneously can to a little less than grow, severe infections clone viral, disease carries out the detoxification cultivation on medium, make clone rejuvenation, purifying, reaches the purpose of germplasm long preservation.
4, the technology of the present invention is reliable and stable, and is repeatable strong, can satisfy not only to expand numerous but also preserve the purpose of germ plasm resource.
5, the germ plasm resource that provides of the technology of the present invention is transplanted to neat, the robust growth of seedling behind the field, and resistance, growth potential are better than the seedling of cultivating seeds and can keep the preceding clonal merit of cultivation.
Description of drawings
Fig. 1 is the tissue cultivating seedling of successive transfer culture 9 times
Embodiment
Further specify essentiality content of the present invention with embodiment below, but content of the present invention is not limited thereto.
Embodiment one:
The rhizome of selecting the Atractylis lancea choiceness for use is an explant, is selected in October then the period of drawing materials of rhizome, and explant is selected the rhizome of 0.5 centimetre of length.On the MS medium of additional variety classes and concentration hormone, directly induce and sprout, then by propagation, subculture, take root and finish the quality saving process to the test-tube seedling transplanting training;
The medium of above-mentioned breeding is selected MS additional saccharose 3%, agar 0.8% for use, and bud is induced with proliferated culture medium and selected MS+6-BA2.0mg/l+NAA0.1mg/l for use; Subculture medium is selected MS+6-BA 1.0mg/l+NAA0.05mg/l for use; Root media is 1/2MS+NAA0.2mg/l, and pH is 5.5, conventional autoclaving; The test-tube plantlet condition of culture selects 20 ± 2 ℃; Illumination 12h/d, intensity of illumination is 1500Lux, successive transfer culture 1 time.
The transplanting of test-tube plantlet was chosen in culture of rootage after 10 days, when the seedling cauline leaf is grown 4 centimetres, opened bottle cap in preceding 2 days in transplanting, treat the intensification of leaf look, be transplanted to the greenhouse again, begin to make in a week humidity to remain on more than 90%, humidity is remained on about 75%, plant open country after 10 days, again through field planting field in January.
Tissue cultivating seedling robust growth after the field planting is neat, by a series of biological character investigation and statistics, group training seedling shows and the great uniformity of previous generation maternal plant, and the clonal field plant growing way in same source is neat, still keeps the obvious characteristic of original strain between each clone.
Embodiment two:
The rhizome of selecting the Atractylis lancea choiceness for use is an explant, is selected in December then the period of drawing materials of rhizome, and explant is selected the rhizome of 1.0 centimetres of length.On the MS medium of additional variety classes and concentration hormone, directly induce and sprout, then by propagation, subculture, take root and finish the quality saving process to the test-tube seedling transplanting training;
The medium of above-mentioned breeding is selected MS additional saccharose 3%, agar 0.8% for use, and bud is induced with proliferated culture medium and selected MS+6-BA3.0mg/l+NAA0.2mg/l for use; Subculture medium is selected MS+6-BA 1.0mg/l+NAA0.1mg/l for use; Root media is 1/2MS+IBA1.0mg/l, and pH is 5.6, conventional autoclaving; The test-tube plantlet condition of culture selects 20 ± 2 ℃; Illumination 12h/d, intensity of illumination is 1800Lux, successive transfer culture 1 time.
The transplanting of test-tube plantlet was chosen in culture of rootage after 12 days, when the seedling cauline leaf is grown 5 centimetres, opened bottle cap in preceding 3 days in transplanting, treat the intensification of leaf look, be transplanted to the greenhouse again, begin to make in a week humidity to remain on more than 90%, humidity is remained on about 75%, plant open country after 12 days, again through field planting field in January.
Tissue cultivating seedling robust growth after the field planting is neat, by a series of biological character investigation and statistics, group training seedling shows and the great uniformity of previous generation maternal plant, and the clonal field plant growing way in same source is neat, still keeps the obvious characteristic of original strain between each clone.
Embodiment three:
The rhizome of selecting the Atractylis lancea choiceness for use is an explant, is selected in back in February, 1 period of drawing materials of rhizome, and explant is selected the rhizome of 1.5 centimetres of length.On the MS medium of additional variety classes and concentration hormone, directly induce and sprout, then by propagation, subculture, take root and finish the quality saving process to the test-tube seedling transplanting training;
The medium of above-mentioned breeding is selected MS additional saccharose 3%, agar 0.8% for use, and bud is induced with proliferated culture medium and selected MS+6-BA2.0mg/l+NAA0.1mg/l for use; Subculture medium is selected MS+6-BA 1.0mg/l+NAA0.05mg/l for use; Root media is 1/2MS+NAA0.2mg/l, and pH is 5.8, conventional autoclaving; The test-tube plantlet condition of culture selects 20 ± 2 ℃; Illumination 12h/d, intensity of illumination is 2000Lux, successive transfer culture 1 time.
The transplanting of test-tube plantlet was chosen in culture of rootage after 15 days, when the seedling cauline leaf is grown 6 centimetres, opened bottle cap in preceding 2 days in transplanting, treat the intensification of leaf look, be transplanted to the greenhouse again, begin to make in a week humidity to remain on more than 90%, humidity is remained on about 75%, plant open country after 15 days, again through field planting field in January.
Tissue cultivating seedling robust growth after the field planting is neat, by a series of biological character investigation and statistics, group training seedling shows and the great uniformity of previous generation maternal plant, and the clonal field plant growing way in same source is neat, still keeps the obvious characteristic of original strain between each clone.
Embodiment four:
Drawn material is the tissue cultivating seedling of successive transfer culture 1 time among the embodiment one, continue successive transfer culture, take root again after 8 times and the transplanting of test-tube plantlet, as shown in Figure 1, find that by investigation of field biological character and statistics the test-tube plantlet after preserving by more than 300 days subcultures still keeps good vitality, the clone plant in same source, the field growing gesture is neat, still keeps original clonal obvious characteristic.This shows that the present invention shows obvious effects to the preservation of Atractylis lancea germplasm.
Claims (5)
1, a kind of quality saving method of Atractylis lancea tissue culture propagation, it is characterized in that: the quality saving process is an explant for selecting clonal rhizome for use, on the MS medium of additional hormone, directly induce and sprout, bud through propagation, subculture, take root, test-tube seedling transplanting, wherein minimal medium is selected MS additional saccharose 3%, agar 0.8% for use, and bud is induced with proliferated culture medium and selected MS+6-BA 2.0～3.0mg/l+NAA0.1～0.2mg/l for use; Subculture medium is selected MS+6-BA 1.0mg/l+NAA0.05～0.1mg/l for use; Root media is 1/2MS+NAA0.2mg/l or 1/2MS+IBA1.0mg/l, pH5.4～5.8, conventional autoclaving; The test-tube plantlet condition of culture selects 20 ± 2 ℃; Illumination 12h/d, intensity of illumination 1500～2000Lux.
2, the quality saving method of a kind of Atractylis lancea tissue culture propagation according to claim 1 is characterized in that selecting the rhizome of reproductive stage for use is explant.
3, the quality saving method of a kind of Atractylis lancea tissue culture propagation according to claim 2 is characterized in that selecting the rhizome of 0.5～1.5 centimetre of length as explant.
4, the quality saving method of a kind of Atractylis lancea tissue culture propagation according to claim 1, it is characterized in that can be every 1-2 month successive transfer culture once.
5, the quality saving method of a kind of Atractylis lancea tissue culture propagation according to claim 1, the transplanting that it is characterized in that test-tube plantlet was chosen in culture of rootage after 10～15 days, when the seedling cauline leaf is grown 4～6 centimetres, before transplanting, open bottle cap in 2～3 days, treat the intensification of leaf look, be transplanted to the greenhouse again, begin to make in a week humidity to remain on more than 90%, humidity is remained on about 75%, plant open country after 10～15 days, again through field planting field in January.
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102726293A (en) * | 2012-06-27 | 2012-10-17 | 中国热带农业科学院椰子研究所 | Method for in vitro preservation of betel nut genetic resources |
| CN102763591A (en) * | 2012-07-05 | 2012-11-07 | 中国农业科学院作物科学研究所 | Atrac tylodes macrocephala koidz conservation method and re-cultivating method |
| CN102061334B (en) * | 2010-02-05 | 2012-11-28 | 南京中医药大学 | Specific DNA molecular markers for identifying genuine medicinal material of swordlike atractylodes rhizome as well as preparation method and application thereof |
| CN103960129A (en) * | 2014-04-24 | 2014-08-06 | 江苏农林职业技术学院 | Atractylis lancea tissue culturing and rapid propagating method |
| CN104982336A (en) * | 2015-07-28 | 2015-10-21 | 江苏大学 | Manufacturing method for artificial atractylis lancea seed |
| CN105993956A (en) * | 2016-06-14 | 2016-10-12 | 江苏茅山地道中药材种植有限公司 | Fast propagating method for atractylis lancea |
| CN108575749A (en) * | 2018-04-24 | 2018-09-28 | 镇江市德尔生物制品研究所有限公司 | Atractylis lancea Aseptic seedling culture base and apply its Atractylis lancea Aseptic seedling culture technique |
| CN115281085A (en) * | 2022-07-08 | 2022-11-04 | 内蒙古民族大学 | Tissue culture propagation method of rhizoma atractylodis macrocephalae |
| CN115362937A (en) * | 2022-08-26 | 2022-11-22 | 中国中医科学院中药研究所 | Rhizoma atractylodis test-tube plantlet and culture method thereof, and method for transplanting rhizoma atractylodis test-tube plantlet |
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2005
- 2005-02-25 CN CNB2005100378590A patent/CN1307867C/en not_active Expired - Fee Related
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102061334B (en) * | 2010-02-05 | 2012-11-28 | 南京中医药大学 | Specific DNA molecular markers for identifying genuine medicinal material of swordlike atractylodes rhizome as well as preparation method and application thereof |
| CN102726293A (en) * | 2012-06-27 | 2012-10-17 | 中国热带农业科学院椰子研究所 | Method for in vitro preservation of betel nut genetic resources |
| CN102763591A (en) * | 2012-07-05 | 2012-11-07 | 中国农业科学院作物科学研究所 | Atrac tylodes macrocephala koidz conservation method and re-cultivating method |
| CN102763591B (en) * | 2012-07-05 | 2013-11-13 | 中国农业科学院作物科学研究所 | Atrac tylodes macrocephala koidz conservation method and re-cultivating method |
| CN103960129A (en) * | 2014-04-24 | 2014-08-06 | 江苏农林职业技术学院 | Atractylis lancea tissue culturing and rapid propagating method |
| CN104982336A (en) * | 2015-07-28 | 2015-10-21 | 江苏大学 | Manufacturing method for artificial atractylis lancea seed |
| CN105993956A (en) * | 2016-06-14 | 2016-10-12 | 江苏茅山地道中药材种植有限公司 | Fast propagating method for atractylis lancea |
| CN108575749A (en) * | 2018-04-24 | 2018-09-28 | 镇江市德尔生物制品研究所有限公司 | Atractylis lancea Aseptic seedling culture base and apply its Atractylis lancea Aseptic seedling culture technique |
| CN115281085A (en) * | 2022-07-08 | 2022-11-04 | 内蒙古民族大学 | Tissue culture propagation method of rhizoma atractylodis macrocephalae |
| CN115362937A (en) * | 2022-08-26 | 2022-11-22 | 中国中医科学院中药研究所 | Rhizoma atractylodis test-tube plantlet and culture method thereof, and method for transplanting rhizoma atractylodis test-tube plantlet |
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