JP2001302427A - Plant growth accelerator and method for accelerating growth of plant by using the accelerator - Google Patents

Plant growth accelerator and method for accelerating growth of plant by using the accelerator

Info

Publication number
JP2001302427A
JP2001302427A JP2000123602A JP2000123602A JP2001302427A JP 2001302427 A JP2001302427 A JP 2001302427A JP 2000123602 A JP2000123602 A JP 2000123602A JP 2000123602 A JP2000123602 A JP 2000123602A JP 2001302427 A JP2001302427 A JP 2001302427A
Authority
JP
Japan
Prior art keywords
plant growth
spray
plant
promoting
accelerator
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
JP2000123602A
Other languages
Japanese (ja)
Other versions
JP2001302427A5 (en
Inventor
Takahiro Okamoto
隆廣 岡本
Hizuru Ohira
ひずる 大平
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.)
Nok Corp
Original Assignee
Nok Corp
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 Nok Corp filed Critical Nok Corp
Priority to JP2000123602A priority Critical patent/JP2001302427A/en
Publication of JP2001302427A publication Critical patent/JP2001302427A/en
Publication of JP2001302427A5 publication Critical patent/JP2001302427A5/ja
Pending legal-status Critical Current

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Classifications

    • Y02P60/216

Landscapes

  • Cultivation Of Plants (AREA)
  • Pretreatment Of Seeds And Plants (AREA)
  • Hydroponics (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a plant growth accelerator obtained by using a metabolic product of an industrially mass-culturable microbial strain as an active component. SOLUTION: The objective plant growth accelerator contains a spray-dried product of the metabolic product of Pseudomonas solanacearum (FERM P-15545) belonging to the genus Pseudomonas or Enterobacter cloacae (FERM P-8884) as an active component.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、植物生長促進剤お
よびこれを用いた植物生長促進方法に関する。更に詳し
くは、微生物の代謝産物を有効成分とする植物生長促進
剤およびこれを用いた植物生長促進方法に関するもので
ある。
[0001] The present invention relates to a plant growth promoting agent and a method for promoting plant growth using the same. More specifically, the present invention relates to a plant growth promoter containing a metabolite of a microorganism as an active ingredient and a method for promoting plant growth using the same.

【0002】[0002]

【従来の技術】植物の成長を促進させるためには、植物
ホルモンなどを植物に散布する方法がよく用いられてい
る。本出願人も先に、微生物を用いた培養液が植物の成
長促進効果を示すことを明らかとしている(特公平6-40
829号公報)。しかしながら、これらの微生物培養液に
おいては、その内部に相当量の培地成分を残しているた
め、他の雑菌による影響を受けやすく、長期にわたる保
存には向かないという問題がみられた。このための対策
としては、使用直前に調製し、一度に使い切ることが考
えられるが、抜本的な解決策とは言い難い。さらに、こ
れらの微生物培養液を散布する場合には、散水時にタン
クに相当量添加するか、別途希釈液をその都度調製して
植物体に散布しなくてはならず、取扱いが不便であっ
た。
2. Description of the Related Art In order to promote the growth of plants, a method of spraying plant hormones or the like to plants is often used. The present applicant has previously clarified that a culture solution using a microorganism exhibits a plant growth promoting effect (Japanese Patent Publication No. 6-40).
No. 829). However, these microbial cultures have a problem that they are susceptible to other germs and do not lend themselves to long-term storage because a considerable amount of the medium component remains inside. As a countermeasure for this, it is conceivable to prepare immediately before use and use up all at once, but this is not a drastic solution. Furthermore, when these microbial cultures are sprayed, a considerable amount must be added to the tank at the time of watering, or a diluent must be separately prepared and sprayed on the plant, which is inconvenient to handle. .

【0003】この解決方法として、本出願人は先に、微
生物培養液の凍結乾燥物を植物成長促進剤として用いる
ことを提案しているが(特開平2-240008号公報)、この
場合においては、処理時間が長くかつ乾燥後に粉砕を要
するなど作業が煩雑であるといった問題があった。
As a solution to this problem, the present applicant has previously proposed to use a freeze-dried product of a microorganism culture solution as a plant growth promoter (Japanese Patent Application Laid-Open No. 2-240008). In addition, there is a problem that the operation is complicated, such as a long processing time and crushing after drying.

【0004】[0004]

【発明が解決しようとする課題】本発明の目的は、工業
的に多量培養することが可能な微生物を用い、それの代
謝産物を有効成分とする植物生長促進剤を提供すること
にある。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a plant growth promoting agent which uses a microorganism which can be industrially mass-cultured and has a metabolite thereof as an active ingredient.

【0005】[0005]

【課題を解決するための手段】かかる本発明の目的は、
シユードモナス属に属する微生物Psedomonas solanacea
rum (FERM P-15545)またはEnterobacter cloacae(FERM
P−8884)の代謝産物のスプレードライ物を有効成分と
する植物生長促進剤によって達成される。
SUMMARY OF THE INVENTION The object of the present invention is as follows.
Psedomonas solanacea, a microorganism belonging to the genus Pseudomonas
rum (FERM P-15545) or Enterobacter cloacae (FERM
This is achieved by a plant growth promoter containing a spray-dried product of the metabolite of P-8884) as an active ingredient.

【0006】[0006]

【発明の実施の形態】本発明で使用される微生物Psedom
onas solanacearum (FERM P-15545)およびEnterobacter
cloacae(FERM P−8884)は、本発明者らによって発見
されたものであり、それらの詳細については、それぞれ
特開平10-28593号公報および前記特公平6-40829号公報
にそれぞれ記載されている。
BEST MODE FOR CARRYING OUT THE INVENTION The microorganism Psedom used in the present invention
onas solanacearum (FERM P-15545) and Enterobacter
Cloacae (FERM P-8888) has been discovered by the present inventors, and details thereof are described in JP-A-10-28593 and JP-B-6-40829, respectively. .

【0007】Psedomonas solanacearumおよびEnterobac
ter cloacaeの培養は、任意の培地を用い、振とう条件
下で、37〜40℃で約72〜90時間程度行われる。この際、
Psedomonas solanacearumについては、培地1L当たり約4
00〜600mg、好ましくは約480〜520mgのアデニンを、Ent
erobacter cloacaeについては培地1L当り約1〜4mg程度
のトリプトファンを添加しておくと、それから得られる
代謝産物のスプレードライ物の植物生長促進作用は一層
高められる。また、本培養に先立って、同様の培地で前
培養した物を用いることが好ましい。
[0007] Psedomonas solanacearum and Enterobac
The culture of ter cloacae is carried out at 37 to 40 ° C. for about 72 to 90 hours using an arbitrary medium under shaking conditions. On this occasion,
For Psedomonas solanacearum, about 4
00-600 mg, preferably about 480-520 mg of adenine, Ent
When about 1 to 4 mg of tryptophan is added to 1 L of the medium for erobacter cloacae, the plant growth promoting effect of a spray-dried product of a metabolite obtained therefrom is further enhanced. Further, prior to the main culture, it is preferable to use a product pre-cultured in a similar medium.

【0008】スプレードライ物は、所定時間培養した後
遠心分離して集菌し、培養液を代謝産物として得た後、
これをチヤンバー内温度約160〜190℃、好ましくは180
℃、吸引量40〜50m3/min、好ましくは45m3/min、送液量
10〜15ml、好ましくは12ml/min、出口温度70〜90℃、好
ましくは80℃の条件下でスプレードライを行うことによ
って得られる。
The spray-dried product is cultured for a predetermined time, then centrifuged to collect the cells, and a culture solution is obtained as a metabolite.
The temperature in the chamber is about 160 to 190 ° C, preferably 180
° C, suction volume 40-50 m 3 / min, preferably 45 m 3 / min
It is obtained by spray drying under the conditions of 10 to 15 ml, preferably 12 ml / min, and outlet temperature of 70 to 90 ° C, preferably 80 ° C.

【0009】スプレードライ物を用いての植物栽培は、
例えば次のような方法によって行うことができる。 (1)スプレードライ物を種子に塗布した後、土壌に播種
する方法 (2)スプレードライ物を水に溶解させ、植物の葉面に散
布するか土壌に灌注する方法 (3)スプレードライ物を混合した土壌中にに種子を播種
または苗を植え付ける方法 (4)スプレードライ物を添加した養液栽培用肥料液を用
いて、植物を養液栽培する方法 これらの各種方法において、Psedomonas solanacearum
の場合には、例えばコマツナなどの種子、カーネーショ
ン、フアレノプシスなどの苗が用いられ、Enterobacter
cloacaeの場合には、例えばレタス、キュウリ、ナス、
トマト、メロンなどの種子、キュウリ、ナス、トマト、
イネなどの苗が用いられる。
[0009] Plant cultivation using spray-dried materials
For example, it can be performed by the following method. (1) Spray-dried material is applied to seeds and then seeded on soil (2) Spray-dried material is dissolved in water and sprayed on plant leaves or drenched in soil (3) Spray-dried material Method of sowing seeds or planting seedlings in mixed soil
In the case of seeds, for example, seeds such as komatsuna, carnations, seedlings such as Phalaenopsis,
In the case of cloacae, for example, lettuce, cucumber, eggplant,
Seeds such as tomato, melon, cucumber, eggplant, tomato,
Seedlings such as rice are used.

【0010】スプレードライ物を用いる代わりに、培養
液そのものを用いたのでは種子処理自体が困難であり、
また水溶液により種子を処理すると種子の発芽率が低下
したり、種子が腐敗し易いという問題がみられる。従っ
て、養液栽培する場合にも、一旦スプレードライ物とし
た上で使用される。
[0010] If the culture solution itself is used instead of the spray-dried material, the seed treatment itself is difficult,
In addition, when seeds are treated with an aqueous solution, there are problems that the germination rate of the seeds is reduced and the seeds are easily rotted. Therefore, also in the case of nutrient cultivation, it is used after it is once spray-dried.

【0011】[0011]

【発明の効果】本発明に係る植物生長促進剤は、工業的
に多量培養可能な微生物の代謝産物のスプレードライ物
を有効成分としており、それを用いることにより植物生
長促進作用を維持しつつ、その調製および取扱いが容易
でかつ長期保存が可能であるという効果を有する。
Industrial Applicability The plant growth promoter of the present invention comprises a spray-dried product of a metabolite of a microorganism which can be industrially mass-cultured as an active ingredient. It has an effect that its preparation and handling are easy and long-term storage is possible.

【0012】[0012]

【実施例】次に、実施例について本発明を説明する。本
発明はこれらに限定されるものではない。
Next, the present invention will be described by way of examples. The present invention is not limited to these.

【0013】実施例1 トリプトン 1% 酵母エキス 0.5% NaCl 0.5% アデニン 0.05%(最終濃度) 蒸留水 残部 以上の組成を有する培地100mlを容量1Lの三角フラスコ
に添加し、121℃、1気圧、15分間の条件下で滅菌後冷却
した。それにPsedomonas solanacearum (FERMP-15545)
を上記組成の培地3mlで前培養した物を添加し、振とう
回数100rpmで振とうさせながら37℃で72時間培養した
後、遠心分離(7000rpm、10分間、4℃)して集菌した。
Example 1 Tryptone 1% Yeast extract 0.5% NaCl 0.5% Adenine 0.05% (final concentration) Distilled water Remainder 100 ml of a medium having the above composition was added to a 1 L Erlenmeyer flask, and the mixture was heated at 121 ° C, 1 atm. After sterilization under the condition of minutes, the mixture was cooled. And Psedomonas solanacearum (FERMP-15545)
Was added at 37 ° C. for 72 hours while shaking at 100 rpm, and then centrifuged (7000 rpm, 10 minutes, 4 ° C.) to collect the cells.

【0014】この培養液200mlを、チャンバー内温度180
℃、吸引量45m3/min、送液量12ml/min、出口温度80℃
の条件下でスプレードライを行い、約2.5gのスプレード
ライ物を得た。
[0014] 200 ml of this culture solution was placed in a chamber at a temperature of 180
° C, suction amount 45m 3 / min, liquid sending amount 12ml / min, outlet temperature 80 ° C
Was spray-dried under the conditions described above to obtain about 2.5 g of a spray-dried product.

【0015】スプレードライ物の中にコマツナ種子を混
ぜ、種子にスプレードライ物をまぶした。容量5Lのプラ
ンターに土壌を入れ、そこにコマツナ種子10粒または上
記スプレードライ物をまぶしたコマツナ種子10粒を播種
し、温室中で30日間栽培した。成長したコマツナの最大
葉長、葉数および乾燥重量(8株の平均)を測定する
と、コマツナ種子からのものと比較してスプレードライ
物をまぶしたものは表1に示されるように約1.1倍の生
長促進効果がみられた。 表1 無処理 スプレードライ物塗布 葉数(枚) 5.9 6.3 最大葉長(cm) 26.8 29.0 乾燥重量(g) 1.68 1.89
[0015] Komatsuna seeds were mixed into the spray-dried material, and the seeds were dusted with the spray-dried material. The soil was placed in a 5 L capacity planter, and 10 Komatsuna seeds or 10 Komatsuna seeds coated with the spray-dried material were sown and cultivated in a greenhouse for 30 days. When the maximum leaf length, the number of leaves and the dry weight (average of eight strains) of the grown Komatsuna were measured, the spray-dried ones were about 1.1 times larger than those from the Komatsuna seeds as shown in Table 1. Had the effect of promoting growth. Table 1 Number of leaves on untreated spray-dried material (sheets) 5.9 6.3 Maximum leaf length (cm) 26.8 29.0 Dry weight (g) 1.68 1.89

【0016】 実施例2 (NH4)2SO4 0.1% KH2PO4 1.0% MgSO4 0.01% クエン酸3ナトリウム 0.05% ブドウ糖 0.4% トリプトファン 3mg/ml(最終濃度) 以上の組成を有する培地100mlを容量1Lの三角フラスコ
に添加し、121℃、1気圧、15分間の条件下で滅菌後冷却
した。それに、Enterobacter cloacae(FERM P−8884)
を上記組成の培地3mlで前培養した物を添加し、振とう
回数100rpmで振とうさせながら37℃で72時間培養した
後、遠心分離(7000rpm、10分間、4℃)して集菌した。
Example 2 (NH 4 ) 2 SO 4 0.1% KH 2 PO 4 1.0% MgSO 4 0.01% Trisodium citrate 0.05% Glucose 0.4% Tryptophan 3 mg / ml (final concentration) 100 ml of a medium having the above composition was prepared. The solution was added to a 1-L Erlenmeyer flask, sterilized under the conditions of 121 ° C., 1 atm, and 15 minutes, and cooled. In addition, Enterobacter cloacae (FERM P-8844)
Was added at 37 ° C. for 72 hours while shaking at 100 rpm, and then centrifuged (7000 rpm, 10 minutes, 4 ° C.) to collect the cells.

【0017】この培養液200mlについて、実施例1と同
様の方法によりスプレードライを行い、スプレードライ
物を得た。
Spray-drying was performed on 200 ml of the culture in the same manner as in Example 1 to obtain a spray-dried product.

【0018】土壌栽培に対する効果 底に水抜き孔を設けた容量300mlのデスカップにバーミ
ュキライトを入れ、そこにレタス種子またはスプレード
ライ物をまぶしたレタス種子を播種し、温室中で30日間
成長させた。成長したレタス地上部の10個体の平均重量
を測定すると、レタス種子からのものは41gであるのに
対し、スプレードライ物をまぶしたものは62gで、約1.5
倍の生長促進効果がみられた.
Effect on Soil Cultivation Vermukilite is put into a 300 ml capacity death cup with a drain hole at the bottom, and lettuce seeds or lettuce seeds sprayed with spray-dried material are sown and grown in a greenhouse for 30 days. I let it. When the average weight of the 10 individuals on the aerial part of the grown lettuce was measured, the weight from the lettuce seeds was 41 g, while the weight of the spray-dried one was 62 g, about 1.5 g.
The growth promotion effect was doubled.

【0019】水耕栽培に対する効果 (1)レタス種子を発芽させ、ある程度の苗にしたもの
を水耕栽培したもの (2)レタス種子に上記スプレードライ物をまぶしたも
のを発芽させ、ある程度の苗にしたものを水耕栽培した
もの (3)くみあい水耕液1号および2号の水溶液の混合液1l
当り0.1gの上記スプレードライ物を添加した溶液中でレ
タス種子を生育させたもの (4)スプレードライ物を水に溶解し、発芽1週間目の
苗に対して1苗あたり2mlを葉面散布したもの 以上の条件下における30日生育後の地上部および根の16
固体の平均重量は次の表2に示される。 表2条件 地上部(g) 根(g) (1) 43.8 8.3 (2) 55.0 9.2 (3) 66.0 10.0 (4) 60.0 9.0
Effects on hydroponics (1) Lettuce seeds germinate and produce seedlings to a certain extent hydroponically cultivated (2) Lettuce seeds sprinkled with the above spray-dried material to germinate (3) Kumiai Hydroponic solution No. 1 and 1 liter of mixed solution of aqueous solution
Lettuce seeds grown in a solution to which 0.1 g of the above-mentioned spray-dried material has been added. (4) Dissolve the spray-dried material in water and spray 2 ml of the seedling on the first week of germination with 2 ml per seedling. The above-ground and root 16 after 30 days of growth under the above conditions
The average weight of the solid is shown in Table 2 below. Table 2 Conditions Aboveground part (g) Root (g) (1) 43.8 8.3 (2) 55.0 9.2 (3) 66.0 10.0 (4) 60.0 9.0

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A01G 31/00 601 A01G 31/00 601A Fターム(参考) 2B022 EA01 2B051 AB01 BA04 BB02 2B314 MA15 MA30 4H011 AB03 BA01 BB21 BC06 BC09 BC18 BC19 BC21 DA02 DC08 DD01 DD03 DH10 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) A01G 31/00 601 A01G 31/00 601A F term (Reference) 2B022 EA01 2B051 AB01 BA04 BB02 2B314 MA15 MA30 4H011 AB03 BA01 BB21 BC06 BC09 BC18 BC19 BC21 DA02 DC08 DD01 DD03 DH10

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 シユードモナス属に属する微生物Psedom
onas solanacearum(FERM P-15546)の代謝産物のスプ
レードライ物を有効成分とする植物生長促進剤。
1. A microorganism Psedom belonging to the genus Pseudomonas
A plant growth promoter comprising a spray-dried product of a metabolite of onas solanacearum (FERM P-15546) as an active ingredient.
【請求項2】 エンテロバクター属に属する微生物Ente
robacter cloacae(FERM P−8884)の代謝産物のスプレ
ードライ物を有効成分とする植物生長促進剤。
2. A microorganism Ente belonging to the genus Enterobacter.
A plant growth promoter comprising a spray-dried product of a metabolite of robacter cloacae (FERM P-8844) as an active ingredient.
【請求項3】 請求項1または2記載の植物生長促進剤
を種子に塗布した後、土壌に播種することを特徴とする
植物生長促進方法。
3. A method for promoting plant growth, comprising applying the plant growth promoting agent according to claim 1 or 2 to a seed and then sowing the seed on soil.
【請求項4】 請求項1または2記載の植物生長促進剤
を水に溶解させ、これを植物の葉面に散布しまたは土壌
に灌注することを特徴とする植物生長促進方法。
4. A method for promoting plant growth, comprising dissolving the plant growth promoter according to claim 1 or 2 in water and spraying the solution on a leaf surface of a plant or irrigating the soil.
【請求項5】 請求項1または2記載の植物生長促進剤
を混合した土壌中に種子を播種または苗を植え付けるこ
とを特徴とする植物生長促進方法。
5. A method for promoting plant growth, comprising sowing seeds or planting seedlings in soil mixed with the plant growth promoting agent according to claim 1.
【請求項6】 請求項1または2記載の植物生長促進剤
を添加した養液栽培用肥料液を用いて、植物を養液栽培
することを特徴とする植物生長促進方法。
6. A method of promoting plant growth, comprising cultivating a plant using a fertilizer solution for hydroponics to which the plant growth promoter according to claim 1 or 2 is added.
JP2000123602A 2000-04-25 2000-04-25 Plant growth accelerator and method for accelerating growth of plant by using the accelerator Pending JP2001302427A (en)

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Application Number Priority Date Filing Date Title
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JP2001302427A5 JP2001302427A5 (en) 2006-11-16

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* Cited by examiner, † Cited by third party
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CN104938089A (en) * 2015-06-27 2015-09-30 蚌埠市双墩农业生物科技开发有限责任公司 Method for improving germination rate of eggplant seeds
CN106386090A (en) * 2016-08-31 2017-02-15 马山盛世生态种养专业合作社 Planting method for lettuce
JP2019156820A (en) * 2018-03-06 2019-09-19 イビデン株式会社 Growth promoter of tomato fruit and improver of functional component content in tomato fruit, and, production method of growth promoter of tomato fruit and improver of functional component content in tomato fruit
CN111523781A (en) * 2020-04-14 2020-08-11 四川大学 Method for comprehensively evaluating growth vigor of fir regale under forest line environment
CN113929504A (en) * 2021-11-29 2022-01-14 云南大学 Fungus metabolite dry powder and fertilizer for promoting plant growth, and preparation method and application thereof

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JP2019156820A (en) * 2018-03-06 2019-09-19 イビデン株式会社 Growth promoter of tomato fruit and improver of functional component content in tomato fruit, and, production method of growth promoter of tomato fruit and improver of functional component content in tomato fruit
JP7132785B2 (en) 2018-03-06 2022-09-07 イビデン株式会社 Tomato fruit growth promoter, functional ingredient content improver in tomato fruit, and method for producing tomato fruit growth promoter and functional ingredient content improver in tomato fruit
JP7354382B2 (en) 2018-03-06 2023-10-02 イビデン株式会社 Tomato fruit growth promoter and functional component content improver in tomato fruit, and method for producing tomato fruit growth promoter and functional component content improver in tomato fruit
CN111523781A (en) * 2020-04-14 2020-08-11 四川大学 Method for comprehensively evaluating growth vigor of fir regale under forest line environment
CN111523781B (en) * 2020-04-14 2023-04-25 四川大学 Method for comprehensively evaluating growth vigor of Minjiang fir seedlings in forest environment
CN113929504A (en) * 2021-11-29 2022-01-14 云南大学 Fungus metabolite dry powder and fertilizer for promoting plant growth, and preparation method and application thereof

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