JPS60180588A - Preparation of immobilized complex of microorganism having plant pathogen-controlling activity - Google Patents
Preparation of immobilized complex of microorganism having plant pathogen-controlling activityInfo
- Publication number
- JPS60180588A JPS60180588A JP59035560A JP3556084A JPS60180588A JP S60180588 A JPS60180588 A JP S60180588A JP 59035560 A JP59035560 A JP 59035560A JP 3556084 A JP3556084 A JP 3556084A JP S60180588 A JPS60180588 A JP S60180588A
- Authority
- JP
- Japan
- Prior art keywords
- plant pathogen
- culture
- plant
- microorganism
- microorganisms
- 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.)
- Granted
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は植物病原菌防除活性のある微生物の固定化複合
体の製法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an immobilized microorganism complex having plant pathogen control activity.
近年、酵素の固定化のみならず、菌体をそのまま固定化
する方法が提案されているが、いずれも酵素反応を連続
的に行なう目的で試みがなされている。しかし、植物の
病害防除の目的でI) 試ミviまだなされていない。In recent years, methods have been proposed in which not only enzymes are immobilized, but also bacterial cells are immobilized as they are, but attempts have been made in both cases to carry out enzyme reactions continuously. However, it has not yet been tested for the purpose of controlling plant diseases.
従来菌体の固定化として(11担体結合法、(2)架橋
法、(3)包括法(「酵素工学」、福井三部ら編p15
8〜202)などが知られているが、本発明者は上記の
如き公知の固定化法を種々鋭意研究した結果、植物病原
菌に拮抗性を有する微生物(以下微生物と略称する)培
養溶液中に二価以上の金属鉱酸塩を加え、かくして得ら
れた溶液にカラギ→ンを溶解せしめ、乾燥すれば、微生
物を核として含む微小な固定化微生物とすることが出来
る。この固定化微生物は植物の疾病に対して強い防除効
果が得られ、かかる知見に基づいて本発明を完成するに
至った。Conventional immobilization of bacterial cells (11 carrier binding method, (2) cross-linking method, (3) comprehensive method ("Enzyme Engineering", edited by Fukui Sanbe et al., p. 15)
8-202), etc. However, as a result of intensive research on various known immobilization methods such as those mentioned above, the present inventors have found that microorganisms having antagonistic properties against plant pathogenic bacteria (hereinafter referred to as microorganisms) can be added to a culture solution. By adding divalent or higher metal mineral salts, dissolving carrageen in the solution thus obtained, and drying, it is possible to obtain microscopic immobilized microorganisms containing microorganisms as their core. This immobilized microorganism has a strong control effect against plant diseases, and the present invention was completed based on this knowledge.
すなわち、本発明によれば、植物病原菌防除活性のある
複合体は、微生物を常法に従い液体培地で振とう培養な
行ない、培養物は液体培地とともにミキサーで粉砕し、
その溶液中に二価以上の金含有するように添加して固定
化せしめることにより、固定化微生物を製造し、ついで
これを乾燥することにより、上記活性な有する複合体を
製造することができる。That is, according to the present invention, a complex having plant pathogen control activity is obtained by culturing microorganisms with shaking in a liquid medium according to a conventional method, and pulverizing the culture together with the liquid medium in a mixer.
By adding gold with a valence of 2 or higher to the solution and immobilizing it, an immobilized microorganism is produced, and then by drying this, the above-mentioned active composite can be produced.
本発明において使用できる微生物としては、植物病原菌
に拮抗性を有するものであれば特に制限はなく、細菌類
、放線菌類、真菌類、枯菌類、地衣類、藻類などいずれ
も使用できる。これら微生物の生菌体は勿論、凍結乾燥
したもの、凍結融解したものなどであってもよい。The microorganisms that can be used in the present invention are not particularly limited as long as they have antagonistic properties against plant pathogens, and any of bacteria, actinomycetes, fungi, subtilis, lichens, and algae can be used. These microorganisms may be living cells, or may be freeze-dried, freeze-thawed, or the like.
本発明に使用される微生物は単一種類のものでもよいが
、通用対象によっては、同種の二種類以上のものでもよ
(、史に異種間の二拌以上の微生物を同時に使用しても
よい。The microorganisms used in the present invention may be of a single type, but depending on the intended target, they may be of two or more types of the same species (in the past, two or more types of microorganisms of different species may be used at the same time). .
本発明に使用される微生物の培養は、液体振盪培養、液
体静止培養は勿論、固体培養したものであってもよい。The microorganisms used in the present invention may be cultured in liquid shaking culture, static liquid culture, or solid culture.
本発明において、カラギーナンの好適例としては、例え
ばニューゾリン(中央化成株式会社製の商品名)、デニ
ューrA/WG(コペンハーゲンペクチンファク) I
J−社製の商品名)、rニューゲルOWG (同上)な
どが挙げられる。In the present invention, suitable examples of carrageenan include Neusolin (trade name manufactured by Chuo Kasei Co., Ltd.), Denyu rA/WG (Copenhagen Pectin Fac) I
(trade name manufactured by J-Company), rNewgel OWG (same as above), and the like.
本発明に使用される二価以上の金属鉱酸塩としては、例
えば塩化カルシウム、塩化マグネシウム、塩化バリウム
、塩化第1鉄、塩化第2鉄、塩化マンガンなどが挙げら
れる。Examples of the divalent or higher-valent metal mineral salts used in the present invention include calcium chloride, magnesium chloride, barium chloride, ferrous chloride, ferric chloride, manganese chloride, and the like.
本発明方法によって得られる植物病原菌防除活性のある
複合体は、植物の疾病、特に土壌伝染性植物病原菌に対
して強力な防除効果を示しまた長時間保存しても安定で
あ、る、ので、品質管理の面でも有利である。The complex having plant pathogen control activity obtained by the method of the present invention shows a strong control effect against plant diseases, especially soil-borne plant pathogens, and is stable even when stored for a long time. It is also advantageous in terms of quality control.
以下、実施例を挙げて本発明を説明するが、本発明はこ
れら実施例によって何ら制限されるものではない。EXAMPLES The present invention will be described below with reference to Examples, but the present invention is not limited in any way by these Examples.
実施例1
ペプトン0.5%、リン酸−カリウム01.1%、硫酸
マグネシウム0.05%、砂糖1%ケ含むpH7,0の
培地10Qm11!ずつを500−坂ロフラスコに分注
し、殺菌後土壌伝染性植物病原菌フデリウム(Fuea
rium 8pp )に拮抗性を有するバチルス・ライ
ケニホルミス(Bacil’lue lichenif
ormis )を接種し、28℃にて振盪培養な行なっ
た。培養6口径塩化カルシウムを0.1Mの濃度で培養
液に加えて菌体を処理したあと、カラギーナンを5へ%
加えてよく混合させた。かくして得られた溶液な噴霧乾
燥により、乾燥固定化微生物10〜15.9を得た。Example 1 Medium 10Qm11 with pH 7.0 containing 0.5% peptone, 01.1% potassium phosphate, 0.05% magnesium sulfate, and 1% sugar! After sterilization, the soil-borne plant pathogen Fudelium (Fuea
Bacillus licheniformis (Bacillus lichenif
ormis) and cultured with shaking at 28°C. After treating the bacterial cells by adding 6-caliber calcium chloride to the culture solution at a concentration of 0.1M, carrageenan was added to 5%.
Add and mix well. By spray drying the solution thus obtained, dried immobilized microorganisms 10 to 15.9 were obtained.
実施例2
土壌伝染性植物病原菌コルチシウム・ロルフシイ(Co
rticium rolfsii )に拮抗性な有する
アスペルギルス・テルリウス(Aspergillus
terreus)。Example 2 Soil-borne plant pathogen Corticium rolfsii (Co
Aspergillus tellurium, which is antagonistic to Aspergillus rolfsii)
terreus).
トリコデルマeビリデ(Trichoderma vi
ride )4実施例1と同様にして培養した培養物ま
たは静止培養した培養物をミキサーで粉砕し、かくして
得られた培養物を実施例1と同じ方法で製造することに
より固定化微生物をそれぞれ60〜40g得た。Trichoderma vi
ride) 4 A culture cultured in the same manner as in Example 1 or a statically cultured culture is pulverized with a mixer, and the thus obtained culture is produced in the same manner as in Example 1 to obtain 60 immobilized microorganisms. ~40g obtained.
実施例ろ
実施例1及び実施例2と同様にして製造した固定化微生
物の経時的な安定性yHHべた。その結果は第1表に示
す通りである。なお、各微生物の安定性は、微生物調製
後の残存菌数2稀釈平板法で分離して算出した。Example: Stability over time of immobilized microorganisms produced in the same manner as in Examples 1 and 2. The results are shown in Table 1. The stability of each microorganism was calculated by separating the number of remaining bacteria after microorganism preparation using a 2-dilution plate method.
実施例4
実施例1と同様にして調製した固定化微生物σキュウリ
つる割病に対する防除効果を調べた。イの結果は搏2表
に示した通りである。Example 4 The effect of immobilized microorganisms prepared in the same manner as in Example 1 on controlling σ cucumber vine disease was investigated. The results of B are shown in Table 2.
すなわち1キユウリつる割病菌フずリウム・第4スボラ
ム(Fusarium oxysporum f、 s
p。Namely, the fungus Fusarium oxysporum f, s
p.
cucumerinum )ケ培養し洪積層土壌に軟土
1z当15〜6×106の菌数になるように接種し、上
記固定化微生物を直径15crnの植木鉢当り11の雲
台で混合したあとキュウリ種子を播種してつる害病の発
生に及ぼす影響を調べた。実験は1区1〔ボッ)Y用い
、1y+?ツ1トに棹子10粒すつ播種L6回反榎して
行なった。cucumerinum) and inoculated into diluvial soil at a number of 15 to 6 x 106 bacteria per 1z of soft soil.The immobilized microorganisms were mixed using 11 cloud heads per flower pot with a diameter of 15 crn, and then cucumber seeds were sown. The effect on the occurrence of vine diseases was investigated. The experiment used 1 ward 1 [boop] Y, 1y+? The cultivation was carried out by sowing 10 seeds per pot and incubating them 6 times.
発病率は萎凋枯死個体数で表わし、対照区は炉原菌を接
種した洪積層土壌である。The disease incidence is expressed as the number of wilted and dead individuals, and the control plot is diluvial soil inoculated with the furnace fungus.
防除値1−下記によって算出した。Control value 1 - Calculated as follows.
なお、表に示した数値播種後21日目に調査し人もので
ある。In addition, the numerical values shown in the table were investigated on the 21st day after seeding.
第2表 ) ン 代理人 浅 村 皓Table 2 ) hmm Agent Asamura Hajime
Claims (1)
金属鉱酸塩で処理し、ついで得られた溶液なカラギーナ
ンと反応せしめ、その反応体な乾燥することを特徴とす
る。植物病原菌防除活性を有する微生物の固定化複合体
の製造法。It is characterized by treating a solution containing microorganisms that are antagonistic to plant pathogens with a divalent or higher metal mineral salt, reacting with the resulting solution of carrageenan, and drying the reactant. A method for producing an immobilized microorganism complex having plant pathogen control activity.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59035560A JPS60180588A (en) | 1984-02-27 | 1984-02-27 | Preparation of immobilized complex of microorganism having plant pathogen-controlling activity |
| CA000461712A CA1229806A (en) | 1984-02-27 | 1984-08-24 | Process for producing immobilized microorganism- complex having controlling activity against plant pathogenic microorganism |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59035560A JPS60180588A (en) | 1984-02-27 | 1984-02-27 | Preparation of immobilized complex of microorganism having plant pathogen-controlling activity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60180588A true JPS60180588A (en) | 1985-09-14 |
| JPH0361424B2 JPH0361424B2 (en) | 1991-09-19 |
Family
ID=12445119
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59035560A Granted JPS60180588A (en) | 1984-02-27 | 1984-02-27 | Preparation of immobilized complex of microorganism having plant pathogen-controlling activity |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPS60180588A (en) |
| CA (1) | CA1229806A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4615883A (en) * | 1985-10-23 | 1986-10-07 | Plant Genetics, Inc. | Hydrogel encapsulated nematodes |
| JPS62234005A (en) * | 1986-04-02 | 1987-10-14 | Seikaken:Kk | Microbial preparation for agriculture, forestry and fishery |
| US4701326A (en) * | 1985-10-23 | 1987-10-20 | Plant Genetics, Inc. | Membrane-coated hydrogel encapsulated nematodes |
| US4753799A (en) * | 1985-10-23 | 1988-06-28 | Plant Genetics, Inc. | Production of hydrogel encapsulated nematodes |
| JPS63240726A (en) * | 1986-11-26 | 1988-10-06 | ぺんてる株式会社 | Method for forming mycorrhiza of mycorrhiza fungi |
| WO2015156274A1 (en) * | 2014-04-09 | 2015-10-15 | 株式会社エス・ディー・エス バイオテック | Microbial pesticide composition, method for manufacturing same and method for stabilizing microbial pesticide |
-
1984
- 1984-02-27 JP JP59035560A patent/JPS60180588A/en active Granted
- 1984-08-24 CA CA000461712A patent/CA1229806A/en not_active Expired
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4615883A (en) * | 1985-10-23 | 1986-10-07 | Plant Genetics, Inc. | Hydrogel encapsulated nematodes |
| US4701326A (en) * | 1985-10-23 | 1987-10-20 | Plant Genetics, Inc. | Membrane-coated hydrogel encapsulated nematodes |
| US4753799A (en) * | 1985-10-23 | 1988-06-28 | Plant Genetics, Inc. | Production of hydrogel encapsulated nematodes |
| JPS62234005A (en) * | 1986-04-02 | 1987-10-14 | Seikaken:Kk | Microbial preparation for agriculture, forestry and fishery |
| JPS63240726A (en) * | 1986-11-26 | 1988-10-06 | ぺんてる株式会社 | Method for forming mycorrhiza of mycorrhiza fungi |
| WO2015156274A1 (en) * | 2014-04-09 | 2015-10-15 | 株式会社エス・ディー・エス バイオテック | Microbial pesticide composition, method for manufacturing same and method for stabilizing microbial pesticide |
| CN106231907A (en) * | 2014-04-09 | 2016-12-14 | Sds生物技术株式会社 | Microbial pesticide composition, method for producing same, and method for stabilizing microbial pesticide |
| JPWO2015156274A1 (en) * | 2014-04-09 | 2017-04-13 | 株式会社エス・ディー・エス バイオテック | Microbial pesticide composition, method for producing the same, and method for stabilizing microbial pesticide |
| US10111423B2 (en) | 2014-04-09 | 2018-10-30 | Sds Biotech K.K. | Microbial pesticide composition of dried Bacillus |
| CN106231907B (en) * | 2014-04-09 | 2019-10-18 | Sds生物技术株式会社 | Microbial pesticide composition, method for producing same, and method for stabilizing microbial pesticide |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1229806A (en) | 1987-12-01 |
| JPH0361424B2 (en) | 1991-09-19 |
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