JPS63216804A - Growth control of plant - Google Patents

Growth control of plant

Info

Publication number
JPS63216804A
JPS63216804A JP4878787A JP4878787A JPS63216804A JP S63216804 A JPS63216804 A JP S63216804A JP 4878787 A JP4878787 A JP 4878787A JP 4878787 A JP4878787 A JP 4878787A JP S63216804 A JPS63216804 A JP S63216804A
Authority
JP
Japan
Prior art keywords
chitosan
plants
oligosaccharide
growth
added
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
Application number
JP4878787A
Other languages
Japanese (ja)
Inventor
Takashi Adachi
足立 堯
Takafumi Ishii
隆文 石井
Hidemasa Hidaka
日高 秀昌
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Meiji Seika Kaisha Ltd
Original Assignee
Meiji Seika Kaisha Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Meiji Seika Kaisha Ltd filed Critical Meiji Seika Kaisha Ltd
Priority to JP4878787A priority Critical patent/JPS63216804A/en
Publication of JPS63216804A publication Critical patent/JPS63216804A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To control growth plants, particularly agricultural crops, enable productive regulation thereof and promote stabilization of price, by using a chitosan oligosaccharide. CONSTITUTION:A chitosan oligosaccharide (oligosaccharide or composition thereof containing glutamine or a derivative thereof as a constituent saccharide and having 2-10 polymerization degree) obtained by hydrolyzing chitin or a chitosan derivative, such as N-acetylchitosan, N-propionylchitosan or sulfated carboxymethylchitosan with an acid or chitosanase as an aqueous solution in 0.25-0.0025% concentration is added to soil, sprayed or added and mixed with a liquid fertilizer for nutriculture and applied to plants. Thereby the growth of plants is controlled to regulate production of agricultural crops, such as vegetables, with particularly remarkable fluctuation of prices and reduce oversupply in the market. The price is safely and lightly stabilized.

Description

【発明の詳細な説明】 し産業上の利用分野] 本発明はキトサンオリゴ糖を植物または土壌等に施用す
ることにより植物の生長を制御し、価格変動の著しい野
菜等の農作物の生産分野で価格安定を図ることを可能に
する方法に関するものである。
[Detailed Description of the Invention] Industrial Application Fields] The present invention controls the growth of plants by applying chitosan oligosaccharides to plants or soil, thereby reducing the price in the field of producing agricultural products such as vegetables whose prices fluctuate significantly. It concerns methods that make it possible to achieve stability.

[従来の技術とその問題点] 農作物の生長を制御し、価格変動の著しい野菜等の生産
分野で価格安定を図ることは農業生産上重要な課題であ
る。
[Conventional techniques and their problems] Controlling the growth of agricultural crops and stabilizing prices in the production field of vegetables and other crops, where prices fluctuate significantly, is an important issue in agricultural production.

植物の生長促進物質としては従来からジベレリン、オー
キシン等の植物ホルモンが報告されており、また植物の
生長抑制物質としてはアブシジン酸などが知られている
が、これらの植物ホルモンの作用は多面的であり、植物
に対して同時に多くの作用をもたらすことからある作用
が有益であっても、別の作用はむしろ有害な場合もあり
実用的には用途が限定されている。
Plant hormones such as gibberellin and auxin have been reported as plant growth-promoting substances, and abscisic acid and other substances are known as plant growth-inhibiting substances, but the actions of these plant hormones are multifaceted. They have many effects on plants at the same time, so even if some effects are beneficial, others may be harmful, so their practical use is limited.

一方近年になって、植物体の細胞壁を構成する多糖体の
分解によって得られるオリゴ環が植物自体の生体防御反
応や分化誘導などの調節物質として重要な役割を持って
いることが報告されるようになってきた0例えば植物細
胞壁から調製されたオリゴガラクツロン酸はダイズに作
用させると、ある種の抗菌物質(ファイトアレキシン)
の合成を促進し、病原菌に対する抵抗性が増強されるし
、カエデの細胞壁から調整されたオリゴ環(キシロオリ
ゴ1)は、エントウの芽生えに対するオーキシンの生長
促進作用を逆に抑制する効果のあることが報告されてい
る。このような芽すゴ糖の作用は植物ホルモンとは異な
り、その作用は多面的であるというよりは、むしろ特異
的であるとされている。
On the other hand, in recent years, it has been reported that oligo rings obtained by the decomposition of polysaccharides that constitute the cell walls of plants play an important role as regulators of the plant's own biological defense response and induction of differentiation. For example, when oligogalacturonic acid prepared from plant cell walls acts on soybeans, it produces a type of antibacterial substance (phytoalexin).
The oligo ring (xylo-oligo 1) prepared from the cell wall of maple has the effect of suppressing the growth-promoting effect of auxin on the budding of Japanese maple. It has been reported. The action of this kind of gosaccharide is different from that of plant hormones, and its action is said to be specific rather than pleiotropic.

[問題点を解決するための手段] 本発明の目的は種々のオリゴ糖の中から植物の生長を抑
制する作用を有する糖を見出し、このオリゴ糖を農業生
産に応用し、農作物の価格安定を図ることにある。本発
明者らは、上記目的を達成させるため、植物の生長を抑
制する作用を有するオリゴ糖について広く検索し、キト
サンを分解して得られるオリゴm<以下、キトサンオリ
ゴ環と称する。)に植物の根および地上部の生育を抑制
する作用があることを新たに見出し、本発明を完成した
。すなわち本発明は、キトサンオリゴ環を用いることを
特徴とする植物の生長制御方法である。
[Means for Solving the Problems] The purpose of the present invention is to discover sugars that have the effect of inhibiting plant growth from among various oligosaccharides, apply this oligosaccharide to agricultural production, and stabilize the prices of agricultural products. It's about trying. In order to achieve the above object, the present inventors extensively searched for oligosaccharides that have the effect of inhibiting plant growth, and found oligosaccharides obtained by decomposing chitosan (hereinafter referred to as chitosan oligo rings). ) has the effect of suppressing the growth of roots and above-ground parts of plants, and have completed the present invention. That is, the present invention is a method for controlling plant growth, which is characterized by using chitosan oligo rings.

本発明に適する植物としては様々なものがあるが、特に
農作物、たとえばかいわれ大根、大根。
There are various plants that are suitable for the present invention, but in particular agricultural products such as daikon radish and daikon radish.

はうれん草、レタス、キャベツ、サトイモなどの野菜類
をあげることができる。
You can feed vegetables such as spinach, lettuce, cabbage, and taro.

キトサンとは節足動物、甲殻類の殻、昆虫の表皮のほか
糸状菌、酵母等の微生物の細胞壁な″どに含まれるキチ
ンを脱アセチル化して得られる多糖体である。本発明に
係るキトサンオリゴ環とは以下のように定義される。キ
トサンまたはキトサンを化学修飾して得られるN−アセ
チルキトサン。
Chitosan is a polysaccharide obtained by deacetylating chitin contained in the shells of arthropods, crustaceans, the epidermis of insects, and the cell walls of microorganisms such as filamentous fungi and yeast.Chitosan according to the present invention The oligo ring is defined as follows: chitosan or N-acetyl chitosan obtained by chemically modifying chitosan.

N−プロピオニルキトサン、硫酸化カルボキシメチルキ
トサンなどのキトサン誘導体を酸またはキトサナーゼで
分解して得られる分解物またはその主成分であるオリゴ
糖で、その構成糖成分はグルコサミンまたはその誘導体
であり、その重合度が2〜10のオリゴ糖またはその組
成物をいう。
A decomposition product obtained by decomposing chitosan derivatives such as N-propionyl chitosan and sulfated carboxymethyl chitosan with acid or chitosanase, or its main component oligosaccharide, whose constituent sugar component is glucosamine or its derivative, and its polymerization An oligosaccharide having a degree of 2 to 10 or a composition thereof.

このようなキトサンオリゴ環は例えば以下のごとくして
調製される。キトサン1部に対し20部の1ON塩酸を
添加し、溶解した後、53℃で48時間処理したのち不
溶物をン戸通して除き、ろ液を陽イオン交換樹脂でオリ
ゴ糖を分画する。さらに陰イオン交換樹脂で脱塩、中和
を行い、これを濃縮し、必要により乾燥すればキトサン
オリゴ環が得られる。
Such a chitosan oligo ring is prepared, for example, as follows. After dissolving 20 parts of 1ON hydrochloric acid per 1 part of chitosan and treating the mixture at 53° C. for 48 hours, insoluble materials are removed by passing through a door, and oligosaccharides are fractionated from the filtrate using a cation exchange resin. Furthermore, by desalting and neutralizing with an anion exchange resin, concentrating this, and drying if necessary, a chitosan oligo ring can be obtained.

このようにして得られたキトサンオリゴ環は0.25〜
0.0025%の水溶液として土壌中に添加したり、葉
面散布を行ったり、さらに養液栽培用液体肥料中に添加
混合するなどして植物に施用すると、植物の生長を抑制
し、本発明の目的を達することができる。
The chitosan oligo ring thus obtained is 0.25~
When applied to plants by adding it to soil as a 0.0025% aqueous solution, spraying it on the leaves, or adding it to liquid fertilizer for hydroponic cultivation, it suppresses the growth of plants, and the present invention suppresses plant growth. can reach the purpose of

[実施例コ 次に、本発明を実施例により詳しく説明する。[Example code] Next, the present invention will be explained in detail with reference to examples.

実施例1 キトサン20gに対し4001のION塩酸溶液を添加
し、53℃で48時間反応させた。反応終了後、水を加
えて12とし清適した後、反応液を陽イオン交換樹脂(
BIO−RAD AG−5W) 200m1!を充填し
たカラムに通液し、0.6N〜3Nの塩酸溶液で溶出さ
せ、重合度2〜10のオリゴ糖両分を得た。収量は4g
であった。
Example 1 A 4001 ION hydrochloric acid solution was added to 20 g of chitosan, and the mixture was reacted at 53° C. for 48 hours. After the reaction is complete, water is added to make the solution 12, and the reaction solution is poured into a cation exchange resin (
BIO-RAD AG-5W) 200m1! The solution was passed through a column packed with , and eluted with a 0.6N to 3N hydrochloric acid solution to obtain both oligosaccharides with a degree of polymerization of 2 to 10. Yield is 4g
Met.

このようにして得られたキトサンオリゴ環を用いて、そ
の植物生育抑制作用をかいわれ大根を用いて調べた。す
なわち、かいわれ大根の種子36粒を合成樹脂製クール
マットをセットしたガラス容器に播種し、水道水70m
Rを添加して23℃で4日間は暗所で、続く2日間は5
000ルツクスの照射条件下で栽培した。キトサンオリ
ゴ環は対水道水当り0.25〜0.00025%の割合
で添加した。結果を第1表に示す。
Using the chitosan oligo ring thus obtained, its plant growth inhibitory effect was investigated using radish. In other words, 36 Kaiware radish seeds were sown in a glass container set with a synthetic resin cool mat, and then soaked in 70 m of tap water.
After adding R, at 23°C for 4 days in the dark, and for the following 2 days at 23°C.
Cultivated under irradiation conditions of 000 lux. The chitosan oligo ring was added at a rate of 0.25 to 0.00025% based on tap water. The results are shown in Table 1.

第  1  表 なお、第1表中の数値はキトサンオリゴ糖無添加の条件
下で栽培したかいわれ大根の茎葉長(co+) 、根長
(cm)の平均値を100とした場合の指数で示した。
Table 1 The values in Table 1 are expressed as an index based on the average value of the stem and leaf length (co+) and root length (cm) of Kaiwara radish grown under conditions without the addition of chitosan oligosaccharide as 100. .

表より明らかなように、キトサンオリゴ環には0.25
〜0.0025%の添加量で生長抑制作用が認められた
As is clear from the table, the chitosan oligo ring has 0.25
A growth inhibitory effect was observed at an addition amount of ~0.0025%.

実施例2 かいわれ大根の種子36粒を合成樹脂製ウールマットを
セットした容器中に播種し、液体肥料70mRを添加し
て23℃で栽培した。実験区は以下に示す通りである。
Example 2 Thirty-six seeds of Kaiware radish were sown in a container set with a synthetic resin wool mat, and 70 mR of liquid fertilizer was added thereto, and the seeds were cultivated at 23°C. The experimental areas are as shown below.

対照区:液体肥料中で6日間栽培。Control plot: Cultivated in liquid fertilizer for 6 days.

キトサンオリゴ糖処理区: キトサンオリゴ糖無添加の状態で3日 間栽培し、栽培3日目にキトサンオリ ゴ糖を250γ/mj!の割合で添加し、2日間栽培し
た後、かいわれ大根の生 育しているウールマットをキトサンオ リゴ糖無添加の液体肥料中に移しかえ てさらに3日間栽培。
Chitosan oligosaccharide treated area: Cultivated for 3 days without adding chitosan oligosaccharide, and on the third day of cultivation, chitosan oligosaccharide was added at 250γ/mj! After cultivating for 2 days, the wool mat on which Kaiware radish was growing was transferred to liquid fertilizer without chitosan oligosaccharides and cultivated for another 3 days.

かいわれ大根の茎葉長(cm)の変化を第1図に示す。Figure 1 shows changes in stem and leaf length (cm) of Kaiware radish.

図面より明らかなように、キトサンオリゴ糖処理区では
処理期間中かいわれ大根の生育は停止しているが、栽培
開始後5日目に再びキトサンオリゴ糖を含まない液体肥
料中で栽培すると、再び生長が開始された。
As is clear from the drawing, the growth of daikon radish in the chitosan-oligosaccharide treatment area stopped during the treatment period, but when it was grown again in liquid fertilizer that did not contain chitosan-oligosaccharide on the fifth day after the start of cultivation, it began to grow again. has been started.

[発明の効果] 本発明の方法によれば、植物、特に農作物の生産調整が
可能であるので、市場における農作物のダブつきを少な
くし、価格の安定を安全、かつ手軽に行うことができる
[Effects of the Invention] According to the method of the present invention, it is possible to adjust the production of plants, especially agricultural products, so that it is possible to reduce duplication of agricultural products in the market and stabilize prices safely and easily.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はかいわれ大根の茎葉長の変化を示すグラフであ
る。
FIG. 1 is a graph showing changes in stem and leaf length of Kaiware radish.

Claims (1)

【特許請求の範囲】[Claims] キトサンオリゴ糖を用いることを特徴とする植物の生長
制御方法。
A method for controlling plant growth, characterized by using chitosan oligosaccharide.
JP4878787A 1987-03-05 1987-03-05 Growth control of plant Pending JPS63216804A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4878787A JPS63216804A (en) 1987-03-05 1987-03-05 Growth control of plant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4878787A JPS63216804A (en) 1987-03-05 1987-03-05 Growth control of plant

Publications (1)

Publication Number Publication Date
JPS63216804A true JPS63216804A (en) 1988-09-09

Family

ID=12812943

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4878787A Pending JPS63216804A (en) 1987-03-05 1987-03-05 Growth control of plant

Country Status (1)

Country Link
JP (1) JPS63216804A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998032335A1 (en) * 1997-01-23 1998-07-30 Dcv, Inc. Method for treating cotyledonous plants
WO1998034464A3 (en) * 1997-02-12 1999-01-21 Dcv Inc Method for treating cotyledonous plants
WO1999040790A1 (en) * 1998-02-12 1999-08-19 Dcv, Inc. Method for treating cotyledonous plants
KR20020016708A (en) * 2000-08-26 2002-03-06 강두환 Cultivation Method of Hallabong at a hightemperture by using the lowmolecular Chitosan oligosaccharide
CN1316882C (en) * 2003-01-30 2007-05-23 中国科学院上海生命科学研究院 Chitosan oligosaccharide containging pesticide composition and its application
JP2008189593A (en) * 2007-02-05 2008-08-21 Yaizu Suisankagaku Industry Co Ltd Defloration agent and defloration method
CN102835402A (en) * 2012-05-29 2012-12-26 陕西西大华特科技实业有限公司 Bactericidal composition containing benziothiazolinone and chitosan oligosaccharide
CN104705323A (en) * 2015-03-13 2015-06-17 黄业新 Sterilizing composition containing thiodiazole copper and zineb
CN104705324A (en) * 2015-03-13 2015-06-17 黄业新 Sterilizing composition containing zhongshengmycin and chitosan oligosaccharide

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998032335A1 (en) * 1997-01-23 1998-07-30 Dcv, Inc. Method for treating cotyledonous plants
WO1998034464A3 (en) * 1997-02-12 1999-01-21 Dcv Inc Method for treating cotyledonous plants
WO1999040790A1 (en) * 1998-02-12 1999-08-19 Dcv, Inc. Method for treating cotyledonous plants
KR20020016708A (en) * 2000-08-26 2002-03-06 강두환 Cultivation Method of Hallabong at a hightemperture by using the lowmolecular Chitosan oligosaccharide
CN1316882C (en) * 2003-01-30 2007-05-23 中国科学院上海生命科学研究院 Chitosan oligosaccharide containging pesticide composition and its application
JP2008189593A (en) * 2007-02-05 2008-08-21 Yaizu Suisankagaku Industry Co Ltd Defloration agent and defloration method
CN102835402A (en) * 2012-05-29 2012-12-26 陕西西大华特科技实业有限公司 Bactericidal composition containing benziothiazolinone and chitosan oligosaccharide
CN104705323A (en) * 2015-03-13 2015-06-17 黄业新 Sterilizing composition containing thiodiazole copper and zineb
CN104705324A (en) * 2015-03-13 2015-06-17 黄业新 Sterilizing composition containing zhongshengmycin and chitosan oligosaccharide

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