JPH02238829A - Raising seedling of dalmatian pyrethrum - Google Patents
Raising seedling of dalmatian pyrethrumInfo
- Publication number
- JPH02238829A JPH02238829A JP1056222A JP5622289A JPH02238829A JP H02238829 A JPH02238829 A JP H02238829A JP 1056222 A JP1056222 A JP 1056222A JP 5622289 A JP5622289 A JP 5622289A JP H02238829 A JPH02238829 A JP H02238829A
- Authority
- JP
- Japan
- Prior art keywords
- plant
- medium
- pyrethrum
- petals
- red
- 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
- 241000250966 Tanacetum cinerariifolium Species 0.000 title abstract description 5
- 235000017372 Piretro di Dalmazia Nutrition 0.000 title abstract 4
- 241000196324 Embryophyta Species 0.000 claims abstract description 34
- 239000004062 cytokinin Substances 0.000 claims abstract description 11
- UQHKFADEQIVWID-UHFFFAOYSA-N cytokinin Natural products C1=NC=2C(NCC=C(CO)C)=NC=NC=2N1C1CC(O)C(CO)O1 UQHKFADEQIVWID-UHFFFAOYSA-N 0.000 claims abstract description 11
- 230000008929 regeneration Effects 0.000 claims abstract description 10
- 238000011069 regeneration method Methods 0.000 claims abstract description 10
- 229930192334 Auxin Natural products 0.000 claims abstract description 9
- 239000002363 auxin Substances 0.000 claims abstract description 9
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 claims description 13
- 239000002609 medium Substances 0.000 claims description 13
- 229940015367 pyrethrum Drugs 0.000 claims description 13
- 240000004460 Tanacetum coccineum Species 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 9
- 239000001963 growth medium Substances 0.000 claims description 3
- 230000001902 propagating effect Effects 0.000 claims description 2
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 abstract description 6
- 235000013399 edible fruits Nutrition 0.000 abstract description 4
- 230000035755 proliferation Effects 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 238000012258 culturing Methods 0.000 description 4
- PRPINYUDVPFIRX-UHFFFAOYSA-N 1-naphthaleneacetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CC=CC2=C1 PRPINYUDVPFIRX-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 206010020649 Hyperkeratosis Diseases 0.000 description 2
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 239000003617 indole-3-acetic acid Substances 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- 239000006870 ms-medium Substances 0.000 description 2
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 2
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- FAIXYKHYOGVFKA-UHFFFAOYSA-N Kinetin Natural products N=1C=NC=2N=CNC=2C=1N(C)C1=CC=CO1 FAIXYKHYOGVFKA-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- QANMHLXAZMSUEX-UHFFFAOYSA-N kinetin Chemical compound N=1C=NC=2N=CNC=2C=1NCC1=CC=CO1 QANMHLXAZMSUEX-UHFFFAOYSA-N 0.000 description 1
- 229960001669 kinetin Drugs 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000003375 plant hormone Substances 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明の赤花除虫菊の育苗方法、特に花弁又は痩果を培
養することより植物体を大量に得る方法に関する.
(従来の技術)
除虫菊はその度果の部分に殺虫活性成分であるピレトリ
ンを含有しているためアフリカを中心に栽培が続けられ
ている.
除虫菊の組織培養にピレトリンを生産する試みもなされ
てはいるが、その生産量は極めて微量で工業化には至っ
ておらず、圃場での栽培が続けられている.このため、
優良品種の育苗と苗の大量生産が必要で、株分けや植物
体の成長上部を培養する方法、カルスから植物体を再生
させる方法が行われているが、花弁又は痩果から直接幼
苗を得ることは知られていない.
(発明が解決しようとする課B)
本発明の目的とするところは、除虫菊の花弁又は痩果を
用いて、除虫菊の幼苗を短期間に大量に得る方法を提供
することである.
(課題を解決するための手段)
本発明は、赤花除虫菊(Chrysanthenus+
cocci−neum)の花弁又は痩果をオーキシン
類およびサイトカイニン類を含有する植物体再生用培地
を用いて光照射下に培養し、直接植物体を再生する工程
、該再生植物体を増殖用培地を用いて培養し、多数の植
物体を増殖させる工程、を包含する赤花除虫菊の育苗方
法に関する.
本発明によれば、まず赤花除虫菊の花弁又は痩果を滅菌
し、植物体再生用培地で光照射下に培養し、カルス誘導
をせずに花弁の切片あるいは痩果の壁から直接植物体を
再生させる.
植物体再生用培地としては、植物組織堵養に通常用いら
れるムラシゲ・スクーグ(MS,表1)の培地、ホワイ
トの培地などが用いられ、これに植物体の再生を促進さ
せるためにオーキシン類およびサイトカイニン類が添加
されている.表1
ムラシゲ・スクーグ培地の成分
オーキシン類には、例えばナフタレン酢酸(NAA)、
2.4−ジクロルフェノキシ酢酸(2.4−D)インド
ール酢酸( I AA)等がある.サイトカイニン類に
は、例えばペンジルアデニン(BA)、カイネチン(K
n)等がある.オーキシン類は通常10Ilg/l以下
、好ましくは0.02〜10mg/j!の割合、特に好
ましくは0.2〜2.0 mg/ lで、サイトカイニ
ン類は通常0.02〜10mg/11,好ましくは0.
2〜lO鋼g/βの割合で培地中に含有されている.こ
れら植物ホルモンの量が過少であると、植物体が誘導さ
れにくい.培養は好気的に行われ、培養温度は15〜3
5゜C、好ましくは20〜30℃、培養pHは4〜7.
5で5.7付近が望ましい.光照度として500 〜2
0,OOO1ux ,好ましくは1.000 〜3,0
001uxで16時間照射と8時間暗黒下のサイクルで
培養を行うと、1週間から4週間後には、花弁の切り口
又は痩果の表面に植物体が形成される.植物体増殖用培
地としては、上記の植物体再生用培地が共通して用いら
れうる.増殖を促進させるために、サイトカイニン類、
例えば、BASKnが添加される.これらの濃度は通常
0.02〜10B/j!で、好ましくは2.0〜10m
g/j!で用いられる.
固体培地上で増殖した幼植物体は発根後、通常の土壌に
移植し、正常な植物体として生育させることができる.
また、この再生植物体は親植物と同程度の殺虫活性成分
を含有している.(実施例)
以下、本発明を実施例によって、さらに詳しく説明する
.
実施例l
赤花除虫菊の花弁又は痩果を70%エタノールに20秒
間浸漬し、さらに、有効塩素濃度3%のアンチホルミン
水溶液に20分間浸漬した後、滅菌水で充分に洗浄する
ことにより滅菌した.これを表1に記載した組成を有す
るMS培地にB A2.O+mg/ l、N A A
0.2mg/ lを加え1%の寒天で固化した培地に置
床し、24゜Cで16時間光照射(20001ux)、
8時間暗黒下で培養した.
1週間後から4週間以内に花弁の切り口又は痩果の表面
から直接植物体が再生される.再生された幼植物体を分
離し、表1の組成のMS培地にBA2.0mg7 Nの
みを加えた寒天培地上で培養するとさらに多数の植物体
が出現する.また、これらの幼植物体をホルモン無添加
のMS培地上で培養すると発根して完全な植物体となる
.
(発明の効果)
本発明によれば、赤花除虫菊の花弁又は痩果から直接植
物体を再生することができ、除虫菊の幼植物を大量生産
することができる.
特許出願人 農薬バイオテクノロジー開発技術研究組合DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for raising seedlings of red-flowering pyrethrum, particularly to a method for obtaining a large amount of plants by culturing petals or achenes. (Prior art) Pyrethrum continues to be cultivated mainly in Africa because its fruit contains pyrethrin, an active insecticidal ingredient. Attempts have been made to produce pyrethrin through tissue culture of pyrethrum, but the amount produced is extremely small and industrialization has not yet been achieved, and cultivation continues in the field. For this reason,
It is necessary to raise seedlings of superior varieties and mass-produce seedlings, and methods such as dividing the plant, culturing the upper part of the plant, and regenerating the plant from callus are used, but it is not possible to directly obtain seedlings from petals or achenes. unknown. (Problem B to be Solved by the Invention) An object of the present invention is to provide a method for obtaining a large amount of pyrethrum seedlings in a short period of time using the petals or achenes of pyrethrum. (Means for Solving the Problems) The present invention relates to red flowering pyrethrum (Chrysanthenus +
cocci-neum) in a plant regeneration medium containing auxins and cytokinins under light irradiation to directly regenerate the plant; This invention relates to a method for raising red-flowering pyrethrum seedlings, which includes the steps of culturing and propagating a large number of plants. According to the present invention, the petals or achenes of red-flowered pyrethrum are first sterilized, cultured in a plant regeneration medium under light irradiation, and the plants are regenerated directly from the petal sections or the walls of the achenes without inducing callus. .. As the plant regeneration medium, Murashige-Skoog (MS, Table 1) medium, White's medium, etc., which are commonly used for plant tissue nourishment, are used, and auxins and auxins are added to this to promote plant regeneration. Contains cytokinins. Table 1 Components of Murashige-Skoog medium Auxins include naphthalene acetic acid (NAA),
Examples include 2.4-dichlorophenoxyacetic acid (2.4-D) indoleacetic acid (IAA). Examples of cytokinins include penzyladenine (BA), kinetin (K
n) etc. Auxins are usually 10 Ilg/l or less, preferably 0.02 to 10 mg/j! The proportion of cytokinins is usually 0.02 to 10 mg/11, preferably 0.2 to 2.0 mg/l, particularly preferably 0.2 to 2.0 mg/l.
It is contained in the medium at a ratio of 2 to 10 g/β of steel. If the amount of these plant hormones is too low, it will be difficult to induce the plant body. Cultivation is carried out aerobically, with a culture temperature of 15-3
5°C, preferably 20-30°C, culture pH 4-7.
5 and around 5.7 is desirable. 500 to 2 as light illuminance
0,001ux, preferably 1.000 to 3,0
When culturing is carried out under a cycle of 16 hours of irradiation and 8 hours of darkness at 001 ux, plants are formed on the cut ends of petals or on the surfaces of achenes after 1 to 4 weeks. As the plant growth medium, the above-mentioned plant regeneration medium can be commonly used. To promote proliferation, cytokinins,
For example, BASKn is added. These concentrations are usually 0.02 to 10B/j! , preferably 2.0 to 10 m
g/j! Used in. After rooting, the seedlings grown on a solid medium can be transplanted into regular soil and grown as normal plants.
In addition, this regenerated plant contains the same level of insecticidal active ingredients as the parent plant. (Examples) Hereinafter, the present invention will be explained in more detail with reference to Examples. Example 1 Petals or achenes of red-flowering pyrethrum were immersed in 70% ethanol for 20 seconds, further immersed in an aqueous antiformin solution with an effective chlorine concentration of 3% for 20 minutes, and then sterilized by washing thoroughly with sterilized water. B A2. O+mg/l, N A A
Placed on a medium containing 0.2 mg/l and solidified with 1% agar, irradiated with light (20001 ux) at 24°C for 16 hours,
The cells were incubated in the dark for 8 hours. Plants are regenerated directly from the cut end of the petal or the surface of the achenes within one to four weeks. When the regenerated seedlings are separated and cultured on an agar medium prepared by adding only 2.0 mg of BA to the MS medium having the composition shown in Table 1, a larger number of plants appear. Furthermore, when these seedlings are cultured on hormone-free MS medium, they will root and become complete plants. (Effects of the Invention) According to the present invention, a plant body can be directly regenerated from the petals or achenes of red-flowering pyrethrum, and young plants of pyrethrum can be mass-produced. Patent applicant: Pesticide Biotechnology Development Technology Research Association
Claims (1)
ineum)の痩果又は花弁をオーキシン類およびサイ
トカイニン類を含有する植物体再生用培地を用いて光照
射下に培養し、直接植物体を再生する工程、 該再生植物体を増殖用培地を用いて培養し、多数の植物
体を増殖させる工程、を包含する赤花除虫菊の育苗方法
。 2、植物体再生用培地がオーキシン類を10mg/を以
下、サイトカイニン類を0.02〜10mg/lの割合
で含有する第1項に記載の方法。 3、増殖用培地がサイトカイニン類を0.02〜10m
g/l含有する第1項に記載の方法。 4、照射光が500〜20,000luxである第1項
に記載の方法。[Claims] 1. Red-flowered pyrethrum (Chrysanthemumcocc)
ineum) under light irradiation using a plant regeneration medium containing auxins and cytokinins to directly regenerate the plant; cultivating the regenerated plant using a growth medium; A method for raising red-flowering pyrethrum seedlings, which includes the steps of: and propagating a large number of plants. 2. The method according to item 1, wherein the plant regeneration medium contains auxins at a ratio of 10 mg/l or less and cytokinins at a ratio of 0.02 to 10 mg/l. 3. The growth medium contains 0.02 to 10 m of cytokinins.
The method according to paragraph 1, containing g/l. 4. The method according to item 1, wherein the irradiation light is 500 to 20,000 lux.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1056222A JPH02238829A (en) | 1989-03-10 | 1989-03-10 | Raising seedling of dalmatian pyrethrum |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1056222A JPH02238829A (en) | 1989-03-10 | 1989-03-10 | Raising seedling of dalmatian pyrethrum |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02238829A true JPH02238829A (en) | 1990-09-21 |
Family
ID=13021078
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1056222A Pending JPH02238829A (en) | 1989-03-10 | 1989-03-10 | Raising seedling of dalmatian pyrethrum |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02238829A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1076161C (en) * | 1997-10-10 | 2001-12-19 | 中国科学院昆明植物研究所 | Technology for germ plasma preservation and quick breeding by group culture of pyrethrum |
CN103828710A (en) * | 2014-03-18 | 2014-06-04 | 南京农业大学 | Efficient chrysanthemum cross-breeding method |
CN103947557A (en) * | 2014-05-13 | 2014-07-30 | 林平 | Stubble regeneration method of stevia rebaudiana rootage tissue culture seedling |
CN104285808A (en) * | 2014-10-24 | 2015-01-21 | 柳州市天姿园艺有限公司 | Special culture medium for cut chrysanthemum |
CN104304022A (en) * | 2014-10-24 | 2015-01-28 | 柳州市天姿园艺有限公司 | Special culture medium for fertilized chrysanthemum |
CN104351049A (en) * | 2014-10-24 | 2015-02-18 | 柳州市天姿园艺有限公司 | Special culture medium for cineraria |
CN109287489A (en) * | 2018-11-28 | 2019-02-01 | 云南省农业科学院花卉研究所 | A method of standardization isolated culture of pyrethrum seedling |
-
1989
- 1989-03-10 JP JP1056222A patent/JPH02238829A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1076161C (en) * | 1997-10-10 | 2001-12-19 | 中国科学院昆明植物研究所 | Technology for germ plasma preservation and quick breeding by group culture of pyrethrum |
CN103828710A (en) * | 2014-03-18 | 2014-06-04 | 南京农业大学 | Efficient chrysanthemum cross-breeding method |
CN103947557A (en) * | 2014-05-13 | 2014-07-30 | 林平 | Stubble regeneration method of stevia rebaudiana rootage tissue culture seedling |
CN104285808A (en) * | 2014-10-24 | 2015-01-21 | 柳州市天姿园艺有限公司 | Special culture medium for cut chrysanthemum |
CN104304022A (en) * | 2014-10-24 | 2015-01-28 | 柳州市天姿园艺有限公司 | Special culture medium for fertilized chrysanthemum |
CN104351049A (en) * | 2014-10-24 | 2015-02-18 | 柳州市天姿园艺有限公司 | Special culture medium for cineraria |
CN104285808B (en) * | 2014-10-24 | 2016-06-22 | 柳州市天姿园艺有限公司 | Cut Flower Chrysanthemum Morifolium special culture media |
CN109287489A (en) * | 2018-11-28 | 2019-02-01 | 云南省农业科学院花卉研究所 | A method of standardization isolated culture of pyrethrum seedling |
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