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JPH07112962B2 - Plant filamentous fungus control agent - Google Patents
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JPH07112962B2 - Plant filamentous fungus control agent - Google Patents

Plant filamentous fungus control agent

Info

Publication number
JPH07112962B2
JPH07112962B2 JP20419987A JP20419987A JPH07112962B2 JP H07112962 B2 JPH07112962 B2 JP H07112962B2 JP 20419987 A JP20419987 A JP 20419987A JP 20419987 A JP20419987 A JP 20419987A JP H07112962 B2 JPH07112962 B2 JP H07112962B2
Authority
JP
Japan
Prior art keywords
control agent
fusaric acid
plant
filamentous fungus
parts
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.)
Expired - Lifetime
Application number
JP20419987A
Other languages
Japanese (ja)
Other versions
JPS6447703A (en
Inventor
君子 片平
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.)
Japan Tobacco Inc
Original Assignee
Japan Tobacco Inc
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 Japan Tobacco Inc filed Critical Japan Tobacco Inc
Priority to JP20419987A priority Critical patent/JPH07112962B2/en
Publication of JPS6447703A publication Critical patent/JPS6447703A/en
Publication of JPH07112962B2 publication Critical patent/JPH07112962B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、フザリン酸を有効成分として含有する植物糸
状菌病防除剤に関する。
TECHNICAL FIELD The present invention relates to a plant filamentous fungal disease control agent containing fusaric acid as an active ingredient.

〔従来の技術〕[Conventional technology]

フザリン酸は、フザリウム・オキシスポルム(Fusarium
oxysporum)など数種の糸状菌の培養ろ液中に産出され
る坑生物質であり、酢酸ブチルを用いて抽出精製された
ものより構造は5−ブチル・ピコリン酸と決定された
(Hidakaら、1971年)。その作用機作は、カテコールア
ミン生合成阻害、すなわちドーパミンβ−水酸化酵素お
よびチロシン水酸化酵素に対する阻害であり、高血圧症
およびパーキンソン病に対する治療薬として使用されて
いる。しかし、植物病原菌に対しての抗菌活性について
は知られていない。
Fusaric acid is Fusarium oxysporum
oxysporum) is a mineral substance produced in the culture filtrate of several filamentous fungi, such as oxysporum), and the structure was determined to be 5-butylpicolinic acid from that extracted and purified using butyl acetate (Hidaka et al., 1971). Its mechanism of action is inhibition of catecholamine biosynthesis, that is, inhibition of dopamine β-hydroxylase and tyrosine hydroxylase, and it is used as a therapeutic drug for hypertension and Parkinson's disease. However, nothing is known about the antibacterial activity against plant pathogens.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

本発明は、フザリン酸が有する植物病原菌に対する予防
的、治療的な抗菌活性を利用して、優れた防除剤を提供
することを目的とする。
An object of the present invention is to provide an excellent control agent by utilizing the preventive and therapeutic antibacterial activity against phytopathogenic bacteria possessed by fusaric acid.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者は、鋭意研究の結果、フザリン酸が数種の植物
病原菌に対して予防的、治療的な殺菌活性を有すること
を見出した。これらの植物病原菌には、種々の作用の舞
病菌(Pythium aphanidermatum(edson)Fitj,P.de b
aryanum Hessl)、疫病菌(Phytophthora infestan
s)、菌核病菌(Sclerotinia sclerotiorum)、白絹病
菌(Corticium rolfsii)、腰折病もしくは紋枯病菌
(Rhizoctonia solani)、半身萎凋病菌(Verticilliu
m albo−atrum)等があり、なかでも藻菌類の舞病菌お
よび疫病菌に対して顕著な殺菌効果を示し、また担子菌
類および子のう菌類菌核形成菌に対しては菌核形成を阻
止する作用を示す(第1表および第2表)。
As a result of diligent research, the present inventor has found that fusaric acid has preventive and therapeutic bactericidal activity against several plant pathogenic fungi. These plant pathogens include Pythium aphanidermatum (edson) Fitj, P. de b
aryanum Hessl), Phytophthora infestan
s), Sclerotinia sclerotiorum, White silkworm (Corticium rolfsii), Lumbago or Bacterial wilt disease (Rhizoctonia solani), Wilt's wilt disease (Verticilliu)
, which shows a remarkable bactericidal effect against the fungal and pathogenic fungi of algae, and also inhibits the sclerotia formation against basidiomycetes and ascomycetes The action is shown (Table 1 and Table 2).

フザリン酸の添加により、菌体からニンヒドリン陽性物
質およびフェノール・硫酸陽性物質が漏出し、菌体重は
減少したことから、この薬剤は細胞膜の透過性を変化さ
せているものと推察される(第3表)。
The addition of fusaric acid leaked ninhydrin-positive substances and phenol / sulfuric acid-positive substances from the cells, and the bacterial weight was reduced. Therefore, it is speculated that this drug alters the permeability of cell membranes (No. 3). table).

フザリン酸を防除剤の有効成分として用いる場合は、他
の何らの成分も加えずそのまま用いてもよいが、通常、
固体担体、液体担体、界面活性剤、その他の製剤用補助
剤と混合して水和剤、粉剤、液剤等に製剤化する。これ
らの製剤はフザリン酸を0.1〜99.9%含む。
When using fusaric acid as an active ingredient of the control agent, it may be used as it is without adding any other ingredient, but usually,
It is mixed with a solid carrier, a liquid carrier, a surfactant, and other auxiliaries for formulation to prepare wettable powders, powders, liquids and the like. These formulations contain 0.1-99.9% fusaric acid.

固体担体としては、カオリンクレー、アッタパルジャイ
ントクレー、ベントナイト、酸性白土、バイロフィライ
ト、タルク、珪藻土、方解石、トウモロコシ穂軸粉、ク
ルミ殻粉、合成含水酸化珪素等の微粉末あるいは粒状物
を用いることができる。
As the solid carrier, kaolin clay, atta-puljain clay, bentonite, acid clay, bilophyllite, talc, diatomaceous earth, calcite, corn cob powder, walnut shell powder, fine powder or particles of synthetic hydrous silicon oxide, etc. Can be used.

液体担体としては、水等を用いることができる。Water or the like can be used as the liquid carrier.

乳化、分散、湿展等のために用いられる界面活性剤に
は、アルキル硫酸エステル塩、アルキル(アリール)ス
ルホン酸塩、ジアルキルスルホこはく酸塩、ポリオキシ
エチレンアルキルアリールエーテルりん酸エステル塩、
ナフタレンスルホン酸ホルマリン縮合物等の陰イオン界
面活性剤、ポリオキシエチレンアルキルエーテル、ポリ
オキシエチレンポリオキシプロピレンブロック共重合
体、ソルビタン脂肪酸エステル、ポリオキシエチレンソ
ルビタン脂肪酸エステル等の非イオン界面活性剤等があ
る。
Surfactants used for emulsification, dispersion, wet spreading, etc. include alkyl sulfate ester salts, alkyl (aryl) sulfonates, dialkyl sulfosuccinates, polyoxyethylene alkyl aryl ether phosphate ester salts,
Anionic surfactants such as naphthalene sulfonic acid formalin condensates, polyoxyethylene alkyl ethers, polyoxyethylene polyoxypropylene block copolymers, nonionic surfactants such as sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, etc. is there.

製剤用補助剤としては、リグニンスルホン酸塩、アルギ
ン酸塩、ポリビニルアルコール、アラビアゴム、CMC
(カルボキシメチルセルロース)、PAP(酸性りん酸イ
ソプロピル)が用いられる。
Pharmaceutical aids include lignin sulfonate, alginate, polyvinyl alcohol, gum arabic, CMC
(Carboxymethyl cellulose) and PAP (isopropyl acid phosphate) are used.

〔実施例〕〔Example〕

以下、本発明の防除剤の実施例について説明する。な
お、ここで用いる部は重量部である。
Hereinafter, examples of the control agent of the present invention will be described. The parts used here are parts by weight.

実施例1(水和剤) フザリン酸50部、珪藻土35部、ホワイトカーボン10部、
ラウリル硫酸ナトリウム3部、リグニンスルホン酸カル
シウム2部を混合粉砕することにより、フザリン酸含有
率50%の水和剤を得た。
Example 1 (wettable powder) 50 parts of fusaric acid, 35 parts of diatomaceous earth, 10 parts of white carbon,
A wettable powder having a fusaric acid content of 50% was obtained by mixing and pulverizing 3 parts of sodium lauryl sulfate and 2 parts of calcium ligninsulfonate.

実施例2(粉剤) フザリン酸1部、カオリンクレー89部、タルク10部を充
分に混合粉砕することにより、フザリン酸含有率1%の
粉剤を得た。
Example 2 (Dust) 1 part of fusaric acid, 89 parts of kaolin clay, and 10 parts of talc were thoroughly mixed and pulverized to obtain a powder having a fusaric acid content of 1%.

実施例3(液剤) フザリン酸50部、ラウリル硫酸ナトリウム2部、水48部
を混合することにより、フザリン酸含有率50%の溶剤を
得た。
Example 3 (solution) By mixing 50 parts of fusaric acid, 2 parts of sodium lauryl sulfate and 48 parts of water, a solvent having a fusaric acid content of 50% was obtained.

これらの製剤は、そのままであるいは水等で希釈し、茎
葉処理あるいは土壌処理に用いる。土壌処理に用いる場
合には、製剤を土壌表面に散布する(必要に応じ、散布
土壌と混和する)か、または土壌に潅注する。
These preparations are used as they are or diluted with water etc. for foliage treatment or soil treatment. When used for soil treatment, the formulation is applied to the surface of the soil (mixed with the applied soil, if necessary) or irrigated.

次に、本発明の防除剤の試験例について説明するが、各
例において比較対照に用いた化合物は、第4表に示した
化合物記号を用いて表わす。
Next, test examples of the control agent of the present invention will be described. The compounds used as comparative controls in each example are represented by the compound symbols shown in Table 4.

供試化合物の殺菌活性は、供試植物の病斑長を測定し、
以下の如く求めた防除価を指標として比較した。
The bactericidal activity of the test compound measures the lesion length of the test plant,
The control values obtained as described below were used as an index for comparison.

薬剤処理n日後の病斑長−薬剤処理時の病斑長=A 試験例1(タバコ舞病菌殺菌活性試験) 18〜20葉期のタバコ(品種:バーレー21)の10〜12枚目
の葉に枚病菌を針接種して30℃湿室に置き、1〜2日後
に病斑が形成された後、フザリン酸および対照化合物の
溶液を葉面に充分に薬液が付着するようにそれぞれ散布
した。散布後は30℃湿室に戻し、3日後に病斑長を測定
して防除価を求めた。その結果を第5表に示す。
Lesion length n days after drug treatment-lesion length at drug treatment = A Test Example 1 (bacterial bactericidal bactericidal activity test) 10 to 12 leaves of 18 to 20 leaf stage tobacco (variety: Burley 21) were inoculated with the fungus in a needle and placed in a humid chamber at 30 ° C. for 1 to 2 After the lesion was formed after a day, the solutions of fusaric acid and the control compound were sprayed so that the drug solution was sufficiently attached to the leaves. After spraying, it was returned to the humid chamber at 30 ° C., and after 3 days, the lesion length was measured to determine the control value. The results are shown in Table 5.

試験例2(タバコ疫病殺菌活性試験) 18〜20葉期のタバコ(品種:バーレー21)の10〜12枚目
の葉に疫病菌を針接種して20℃湿室に置き、1〜2日後
に病斑が形成された後、フザリン酸および対照化合物の
溶液を葉面に充分に薬液が付着するようにそれぞれ散布
した。散布後は20℃湿室に戻し、3〜5日後に病斑長を
測定して防除価を求めた。その結果を第6表に示す。
Test Example 2 (bacterial bactericidal bactericidal activity test) 10 to 12 leaves of 18 to 20 leaf stage tobacco (variety: Burley 21) are inoculated with the plague bacillus by needles and placed in a humid chamber at 20 ° C for 1 to 2 days After the lesions were formed later, the solutions of fusaric acid and the control compound were sprayed so that the drug solution adhered sufficiently to the leaf surface. After spraying, it was returned to a humid chamber at 20 ° C., and after 3 to 5 days, the lesion length was measured to determine the control value. The results are shown in Table 6.

これらの結果より明らかなように、フザリン酸はタバコ
疫病菌に対して顕著な殺菌活性を示し、タバコ舞病に対
しても優れた防除効果を示す。
As is clear from these results, fusaric acid has a remarkable bactericidal activity against tobacco bacillus and an excellent controlling effect against tobacco scab.

〔発明の効果〕〔The invention's effect〕

以上述べたように、フザリン酸は植物病原性糸状菌に対
する殺菌活性を有し、フザリン酸を含有する本発明の防
除剤は、植物糸状菌病に対する優れた防除効果を示す。
As described above, fusaric acid has a bactericidal activity against phytopathogenic filamentous fungi, and the control agent of the present invention containing fusaric acid exhibits an excellent control effect against plant filamentous fungal diseases.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】フザリン酸を有効成分として含有すること
を特徴とする植物糸状菌病防除剤。
1. A plant filamentous fungal disease controlling agent, which comprises fusaric acid as an active ingredient.
JP20419987A 1987-08-19 1987-08-19 Plant filamentous fungus control agent Expired - Lifetime JPH07112962B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20419987A JPH07112962B2 (en) 1987-08-19 1987-08-19 Plant filamentous fungus control agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20419987A JPH07112962B2 (en) 1987-08-19 1987-08-19 Plant filamentous fungus control agent

Publications (2)

Publication Number Publication Date
JPS6447703A JPS6447703A (en) 1989-02-22
JPH07112962B2 true JPH07112962B2 (en) 1995-12-06

Family

ID=16486472

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20419987A Expired - Lifetime JPH07112962B2 (en) 1987-08-19 1987-08-19 Plant filamentous fungus control agent

Country Status (1)

Country Link
JP (1) JPH07112962B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105638669A (en) * 2016-03-23 2016-06-08 福建省农业科学院植物保护研究所 Application of fusaric acid to inhibition of magaporthe grisea

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100743255B1 (en) * 2006-05-04 2007-07-27 한국과학기술연구원 Novel 1,3-dioxoisoindole derivatives active on T-type calcium channels

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105638669A (en) * 2016-03-23 2016-06-08 福建省农业科学院植物保护研究所 Application of fusaric acid to inhibition of magaporthe grisea

Also Published As

Publication number Publication date
JPS6447703A (en) 1989-02-22

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