JPH06256105A - Plant flowering inducer - Google Patents
Plant flowering inducerInfo
- Publication number
- JPH06256105A JPH06256105A JP7999093A JP7999093A JPH06256105A JP H06256105 A JPH06256105 A JP H06256105A JP 7999093 A JP7999093 A JP 7999093A JP 7999093 A JP7999093 A JP 7999093A JP H06256105 A JPH06256105 A JP H06256105A
- Authority
- JP
- Japan
- Prior art keywords
- plant
- compound
- plant flowering
- flowering inducer
- flowering
- 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
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、植物における開花誘導
剤に関する。TECHNICAL FIELD The present invention relates to a flowering inducer in plants.
【0002】[0002]
【従来の技術】植物の花芽形成は、日長や季節変化ない
しは気温等の変化により自らの調節機構が働き、微妙に
コントロールされている。この中でも日長は最も重要な
要因で、花芽を形成する日長の長さにより、短日植物、
長日植物および中性植物に分類される。2. Description of the Related Art The flower bud formation of a plant is delicately controlled by its own regulatory mechanism that works due to changes in day length, seasonal changes, temperature, and the like. Among these, the photoperiod is the most important factor, and due to the length of photoperiod that forms flower buds,
Classified as long-day plants and neutral plants.
【0003】例えばアサガオは、熱帯アメリカあるいは
熱帯アジア原産のヒルガオ科のつる性植物で江戸時代に
育成された日本独特の園芸花卉であり、また多数の変異
品種を有し広く一般に親しまれている。しかし、アサガ
オは典型的な短日植物であり、その花芽形成には日長が
決定的な要因になる。例えばアサガオの1品種であるキ
ダチの場合、限界暗期(8時間45分)以上の連続暗期
がないと花芽が形成されない。このように、アサガオは
広く人気の高い花卉でありながらその短日性のために利
用が限定されているので、長日、貧栄養条件において開
花を誘導することができればその消費を大きく拡大でき
ることが見込まれる。For example, morning glory is a horticultural flower peculiar to Japan that was grown in the Edo era with a creeping plant belonging to the family Convolvulaceae native to tropical America or tropical Asia. However, morning glory is a typical short-day plant, and the photoperiod is a decisive factor in its flower bud formation. For example, in the case of Kuki, which is one cultivar of morning glory, flower buds are not formed unless there is a continuous dark period longer than the critical dark period (8 hours 45 minutes). As such, morning glory is a flower plant that is widely popular, but its use is limited due to its short-day nature, so if it can induce flowering in long-term, oligotrophic conditions, its consumption can be greatly expanded. Expected
【0004】また、アスパラガスは、宿根性の野菜で広
く消費されているが、雌雄が異株で、雌雄によりその品
質や収量に差がある。雌雄株を早期に区別し、雄株のみ
を栽培することができれば、生産量の向上のみならず品
質の向上をも計れることから、その開発が強く求められ
ている。しかし、アスパラガスは、自然の開花を待たい
と雌雄の判別をすることができないのが現状である。[0004] Asparagus is widely consumed in root-root vegetables, but males and females have different strains, and the quality and yield of males and females differ. If the male and female strains can be distinguished at an early stage and only the male strains can be cultivated, not only the production amount but also the quality can be improved, so that the development thereof is strongly required. However, under the present circumstances, asparagus cannot discriminate between males and females as they wait for natural flowering.
【0005】このように、自然により制御される植物の
開花を人為的に簡便に誘導することができれば、各方面
での応用が大いに期待される。As described above, if artificial flowering of plants controlled by nature can be easily induced artificially, it is expected to be applied in various fields.
【0006】篠崎らは、低温条件や根の伸長を抑制する
といった物理的ストレスを与えることによって植物の花
芽形成が誘導されるという知見を報告しているが(Me
m.Coll.Agric.Kyoto Univ.N
o.126:1−20)、化学物質により植物の花芽形
成を誘導したという報告はない。Shinozaki et al. Reported that the flower bud formation of plants was induced by physical stress such as low temperature conditions or suppression of root elongation (Me.
m. Coll. Agric. Kyoto Univ. N
o. 126: 1-20), there is no report that a chemical substance induced flower bud formation of plants.
【0007】[0007]
【発明が解決しようとする課題】本発明は、植物の花芽
形成を化学物質を用いて誘導することにより、栽培を有
利に行うことができる植物の開花誘導剤の提供を目的と
するものである。DISCLOSURE OF THE INVENTION An object of the present invention is to provide a plant flowering inducer that can be advantageously cultivated by inducing flower bud formation of a plant using a chemical substance. .
【0008】[0008]
【課題を解決するための手段】本発明者らは上記の事情
を鑑み、植物の開花誘導効果を有する薬剤を開発するこ
とを目的として鋭意検討した結果、ある種のポリアミン
類に該活性を有する化合物があることを見い出し、本発
明を完成したものである。[Means for Solving the Problems] In view of the above circumstances, the present inventors have conducted extensive studies as a result of developing a drug having an effect of inducing flowering of plants, and as a result, have the activity of certain polyamines. The present invention was completed by finding out that there are compounds.
【0009】即ち、本発明に従えば式(1): RHN−(CH2)n−NHR’ (1) (式中、R及びR’は、同一ないしは異なって水素原子
又は低級アルキル基を表し、nは2〜9までの整数を表
す)で示されるジアミン類又はその塩の少なくとも1種
を有効成分として含有する植物の開花誘導剤を提供する
ものである。That is, according to the present invention, formula (1): RHN- (CH 2 ) n -NHR '(1) (wherein R and R'are the same or different and each represents a hydrogen atom or a lower alkyl group). , N represents an integer of 2 to 9), and a plant flowering inducer containing at least one diamine represented by the formula (2) to (9) or a salt thereof as an active ingredient.
【0010】式(1)中、R及びR’で表される低級ア
ルキル基としては、炭素数1〜4の直鎖ないしは分枝鎖
のアルキル基で、例えばメチル基、エチル基、n−プロ
ピル基、イソプロピル基又はブチル基等を挙げることが
できる。また、塩としては、例えばハロゲン化水素酸
(塩酸、臭化水素酸等)、硫酸、リン酸等の無機酸の
塩、酢酸、プロピオン酸、シュウ酸、マロン酸、安息香
酸等の有機酸の塩を挙げることができる。In the formula (1), the lower alkyl group represented by R and R'is a linear or branched alkyl group having 1 to 4 carbon atoms, such as methyl group, ethyl group and n-propyl group. Group, isopropyl group, butyl group and the like. Examples of the salt include salts of inorganic acids such as hydrohalic acid (hydrochloric acid, hydrobromic acid, etc.), sulfuric acid, phosphoric acid, etc., and organic acids such as acetic acid, propionic acid, oxalic acid, malonic acid, benzoic acid, etc. Mention may be made of salt.
【0011】式(1)で示される化合物は、殆どは公知
の化合物で、試薬として市販されている物質であるが、
必要により公知の合成法(Org.Syn.,col.
vol.IV,819,1963、Ber.,18,2
956,1885等)により製造することもできる。Most of the compounds represented by the formula (1) are known compounds and are commercially available as reagents.
If necessary, a known synthesis method (Org. Syn., Col.
vol. IV, 819, 1963, Ber. , 18, 2
956, 1885, etc.).
【0012】本発明の開花誘導剤は、有効成分として前
記式(1)で表される化合物又はその塩の少なくとも一
種を含有させることにより製造することができる。即
ち、本化合物をそのまま水に溶解するか、或いは一旦適
当な溶剤に溶かした後水で希釈して用いられる。また、
所望により適当な担体、溶剤、界面活性剤等を加えて、
水和剤、乳剤等の形態に製剤して用いることもできる。The flowering inducer of the present invention can be produced by incorporating at least one compound represented by the above formula (1) or a salt thereof as an active ingredient. That is, the compound is dissolved in water as it is, or is dissolved in an appropriate solvent and then diluted with water before use. Also,
Add a suitable carrier, solvent, surfactant, etc., if desired,
It can also be used by formulating it in the form of a wettable powder, an emulsion or the like.
【0013】[0013]
【実施例】以下、試験例をもって本発明をより詳細に説
明するが、本発明はこれら試験例によって制約を受ける
ものではない。The present invention will be described in more detail below with reference to test examples, but the present invention is not limited by these test examples.
【0014】また、下記試験例において、式(1)で表
される化合物の代表例として、市販の1,3−ジアミノ
プロパン(化合物1)、プトレシン(化合物2)、カダ
ベリン(化合物3)、1,6−ジアミノヘキサン(化合
物4)、1,7−ジアミノヘプタン(化合物5)、1,
8−ジアミノオクタン(化合物6)、1,9−ジアミノ
ノナン(化合物7)及びN,N’−ジメチルエチレンジ
アミン(化合物8)を用いて試験を行った。In the following test examples, as typical examples of the compound represented by the formula (1), commercially available 1,3-diaminopropane (compound 1), putrescine (compound 2), cadaverine (compound 3), 1 , 6-diaminohexane (compound 4), 1,7-diaminoheptane (compound 5), 1,
The test was conducted using 8-diaminooctane (compound 6), 1,9-diaminononane (compound 7) and N, N'-dimethylethylenediamine (compound 8).
【0015】試験例1 アサガオ(キダチ)の花芽形成誘導試験 アサガオ種子(Pharbitis nil,cv.K
idachi)を必要数用意し、濃硫酸に50分浸し、
硬い種皮を取り除いた後1日水洗した。その後湿らせた
砂を敷いたシャーレーに種子を並べ、20℃、連続光下
(5000ルクス)に1日置いた。1日経過するとシャ
ーレーの砂上の種子は既に根を出したので、それを適度
に湿らせた砂を詰めたバットの中に埋めた。この状態で
20℃、連続光下(5000ルクス)に3日間放置し
た。この状態で殆どの種子が発芽しているので、発芽し
た種子(苗)を前記試験化合物の所定濃度の水溶液を含
む貧栄養培地に移植し、20℃、連続光下(5000ル
クス)で24日間水耕栽培した。その後栄養培地に移植
して2週間同条件下で育てた後、花芽形成の有無を顕微
鏡下で観察した。花芽形成が誘導された個体の数から誘
導率(%)を求めた。得られた結果を第1表に示す。 Test Example 1 Flower Bud Induction Test for Morning Glory (Killer ) Morning Glory Seeds (Pharbitis nil, cv. K)
Ichida) is prepared in the required number, soaked in concentrated sulfuric acid for 50 minutes,
After removing the hard seed coat, it was washed with water for 1 day. After that, the seeds were arranged on a petri dish lined with moistened sand, and placed at 20 ° C. under continuous light (5000 lux) for 1 day. After one day, the petri dish on the sand of the petri dish had already rooted, so it was buried in a vat filled with sand that had been appropriately dampened. In this state, it was left for 3 days under continuous light (5000 lux) at 20 ° C. Since most of the seeds germinated in this state, the germinated seeds (seedlings) were transplanted to a poor nutrient medium containing an aqueous solution of the test compound at a predetermined concentration, and the seeds were cultivated at 20 ° C. under continuous light (5000 lux) for 24 days. Hydroponically grown. Then, after transplanting to a nutrient medium and growing under the same conditions for 2 weeks, the presence or absence of flower bud formation was observed under a microscope. The induction rate (%) was calculated from the number of individuals in which flower bud formation was induced. The results obtained are shown in Table 1.
【表1】 [Table 1]
【0016】試験例2 アスパラガスの花芽形成誘導試験 化合物3を水で希釈して10μM濃度の溶液を作った。
アスパラガス(品種メリーワシントン)の種子を上記溶
液中に浸漬し、25℃に12日間放置した。種子を水洗
し、土に播種して25℃、12時間日長下13日間栽培
した。得られた苗について花芽形成の有無を顕微鏡下で
観察した結果、約30%の苗に花芽の形成が認められ
た。 Test Example 2 Test compound 3 for inducing flower bud formation of asparagus was diluted with water to prepare a solution having a concentration of 10 μM.
Seeds of asparagus (variety Mary Washington) were immersed in the above solution and left at 25 ° C for 12 days. The seeds were washed with water, sown in soil, and cultivated at 25 ° C. for 12 hours with a photoperiod of 13 days. The presence or absence of flower bud formation in the obtained seedlings was observed under a microscope. As a result, flower bud formation was observed in about 30% of the seedlings.
【0017】[0017]
【発明の効果】本発明の花芽形成誘導剤を使用すること
により、例えばアサガオを長日下に置いても開花させる
ことができる等、自然により制御される植物の開花を人
為的に制御することができ、栽培を極めて有利に行うこ
とができる。EFFECTS OF THE INVENTION By using the agent for inducing flower bud formation of the present invention, it is possible to artificially control flowering of a plant which is naturally controlled, for example, morning glory can be flowered even after long days. Therefore, cultivation can be performed extremely advantageously.
Claims (2)
又は低級アルキル基を表し、nは2〜9までの整数を表
す)で示されるジアミン類又はその塩の少なくとも1種
の化合物を有効成分として含有する植物の開花誘導剤。1. A formula (1): RHN- (CH 2 ) n -NHR '(1) ( wherein, R and R' are the same or different and represent a hydrogen atom or a lower alkyl group, n 2 A plant flowering inducer containing as an active ingredient at least one compound of a diamine or a salt thereof represented by an integer of up to 9).
項1記載の開花誘導剤。2. The flowering inducer according to claim 1, wherein the plant to be applied is a morning glory genus.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7999093A JPH06256105A (en) | 1993-03-02 | 1993-03-02 | Plant flowering inducer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7999093A JPH06256105A (en) | 1993-03-02 | 1993-03-02 | Plant flowering inducer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06256105A true JPH06256105A (en) | 1994-09-13 |
Family
ID=13705753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7999093A Pending JPH06256105A (en) | 1993-03-02 | 1993-03-02 | Plant flowering inducer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06256105A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0726240A1 (en) * | 1995-02-10 | 1996-08-14 | Taguidell, S.L. | Obtaining and use of diamines, polyamines and other complementary active elements from treated natural products |
-
1993
- 1993-03-02 JP JP7999093A patent/JPH06256105A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0726240A1 (en) * | 1995-02-10 | 1996-08-14 | Taguidell, S.L. | Obtaining and use of diamines, polyamines and other complementary active elements from treated natural products |
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