JP2012530742A - 殺真菌活性を有する酵母および殺真菌剤の組み合わせ - Google Patents
殺真菌活性を有する酵母および殺真菌剤の組み合わせ Download PDFInfo
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- JP2012530742A JP2012530742A JP2012516576A JP2012516576A JP2012530742A JP 2012530742 A JP2012530742 A JP 2012530742A JP 2012516576 A JP2012516576 A JP 2012516576A JP 2012516576 A JP2012516576 A JP 2012516576A JP 2012530742 A JP2012530742 A JP 2012530742A
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- methyl
- phenyl
- carboxamide
- ethyl
- inhibitors
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- 238000000034 method Methods 0.000 claims abstract description 15
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- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims description 5
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- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 description 1
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- 239000011733 molybdenum Substances 0.000 description 1
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- 150000003904 phospholipids Chemical class 0.000 description 1
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- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
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- 229920001184 polypeptide Polymers 0.000 description 1
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- 229920002689 polyvinyl acetate Polymers 0.000 description 1
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- 238000012794 pre-harvesting Methods 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
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- 229920005989 resin Polymers 0.000 description 1
- 230000007226 seed germination Effects 0.000 description 1
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- 238000013268 sustained release Methods 0.000 description 1
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- 230000009261 transgenic effect Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
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- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/30—Microbial fungi; Substances produced thereby or obtained therefrom
- A01N63/32—Yeast
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/30—Microbial fungi; Substances produced thereby or obtained therefrom
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Mycology (AREA)
- Biotechnology (AREA)
- Virology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
a)化学殺真菌剤を用いた段階、および
b)酵母を用いた段階
で行われ、2つの施用a)およびb)の間の時間間隔は以下の通りとする。
フェンヘキサミド、テブコナゾール、フルキンコナゾール、トリアジメノール、トリアジメホン、ジフェンコナゾール、エポキシコナゾール、ペンコナゾール、ビテルタノール、プロピコナゾール、ミクロブタニル、イマザリル、プロクロラズ、スピロキサミン、トリデモルフ、フェンプロピモルフ、フェンプロピジン、トリフロキシストロビン、アゾキシストロビン、クレソキシム−メチル、ピラクロストロビン、フェナミドン、フェノキサドン、ピリメタニル、シプロジニル、メパニピリム、ジカルボキシアミド類、イプロジオン、プロピネブ、マンコゼブ、ホセチル−アルミニウム、ジメトモルフ、フルアジナム、イプロバリカルブ、カルベンダジム、チオファネートメチル、チアベンダゾール、フルオピコリド、メタラキシル、メタラキシル−M、フルオピラム、ビキサフェン、ボスカリド、イソピラザム、ペンチオピラドおよびジチオカルバメートから選択される。
フェンヘキサミド、テブコナゾール、フルキンコナゾール、トリアジメノール、トリアジメホン、ジフェンコナゾール、エポキシコナゾール、ペンコナゾール、ビテルタノール、プロピコナゾール、ミクロブタニル、イマザリル、プロクロラズ、スピロキサミン、トリデモルフ、フェンプロピモルフ、フェンプロピジン、トリフロキシストロビン、アゾキシストロビン、クレソキシム−メチル、ピラクロストロビン、フェナミドン、フェノキサドン、ピリメタニル、シプロジニル、メパニピリム、ジカルボキシアミド類、イプロジオン、プロピネブ、マンコゼブ、ホセチル−アルミニウム、ジメトモルフ、フルアジナム、イプロバリカルブ、カルベンダジム、チオファネートメチル、チアベンダゾール、フルオピコリド、メタラキシル、メタラキシル−M、フルオピラム、ビキサフェン、ボスカリド、イソピラザム、ペンチオピラドおよびジチオカルバメート。
Claims (9)
- a)メチニコビア・フルクチコラ(Metschnikowia fructicola)の生物学的に純粋な培養物、および
b)(F1)核酸合成阻害剤、例えば、ベナラキシル、ベナラキシル−M、ブピリメート、クロジラコン、ジメチリモール、エチリモール、フララキシル、ヒメキサゾール、メタラキシル、メタラキシル−M、オフラセ、オキサジキシルおよびオキソリン酸;
(F2)有糸分裂および細胞分裂の阻害剤、例えば、ベノミル、クロルフェナゾール、ジエトフェンカルブ、エタボキサム、フベリダゾール、ペンシクロン、チオファネート、チオファネート−メチルおよびゾキサミド;
(F3)呼吸阻害剤、例えば、CI呼吸阻害剤としてジフルメトリム、CII呼吸阻害剤として、ビキサフェン、ボスカリド、カルボキシン、フェンフラム、フルトラニル、フルオピラム、フラメトピル、フルメシクロックス、イソピラザム(9R成分)、イソピラザム(9S成分)、メプロニル、オキシカルボキシン、ペンチオピラドおよびチフルザミド、CIII呼吸阻害剤として、アミスルブロム、アゾキシストロビン、シアゾファミド、ジモキシストロビン、エネストロブリン、ファモキサドン、フェナミドン、フルオキサストロビン、クレソキシム−メチル、メトミノストロビン、オリサストロビン、ピコキシストロビン、ピラクロストロビン、ピリベンカルブおよびトリフロキシストロビン;
(F4)例えば、ビナパクリル、ジノカップ、フルアジナムおよびメプチルジノカップのような脱共役剤として作用することができる化合物;
(F5)ATP産生阻害剤、例えば、酢酸フェンチン、塩化フェンチン、水酸化フェンチンおよびシルチオファム;
(F6)アミノ酸および/またはタンパク質生合成阻害剤、例えば、アンドプリム、ブラストサイジン−S、カスガマイシン、カスガマイシン塩酸塩水和物およびメパニピリム;
(F7)シグナル伝達阻害剤、例えば、フェンピクロニルおよびキノキシフェン;
(F8)脂質および膜合成阻害剤、例えば、ビフェニル、クロゾリネート、エディフェンホス、エトリジアゾール、ヨードカルブ、イプロベンホス、イソプロチオラン、プロシミドン、プロパモカルブ、プロパモカルブ塩酸塩、ピラゾホス、トルクロホス−メチルおよびビンクロゾリン;
(F9)エルゴステロール生合成阻害剤、例えば、アルジモルフ、アザコナゾール、ビテルタノール、ブロムコナゾール、シプロコナゾール、ジクロブトラゾール、ジフェノコナゾール、ジニコナゾール、ジニコナゾール−M、ドデモルフ、酢酸ドデモルフ、エポキシコナゾール、エタコナゾール、フェナリモル、フェンブコナゾール、フェンヘキサミド、フェンプロピジン、フェンプロピモルフ、フルキンコナゾール、フルルプリミドール、フルシラゾール、フルトリアホール、フルコナゾール、ファーコナゾール−シス、ヘキサコナゾール、イミベンコナゾール、イプコナゾール、メトコナゾール、ミクロブタニル、ナフチフィン、ヌアリモール、オキスポコナゾール、パクロブトラゾール、ペフラゾエート、ペンコナゾール、ピペラリン、プロクロラズ、プロピコナゾール、プロチオコナゾール、ピリブチカルブ、ピリフェノックス、キンコナゾール、シメコナゾール、スピロキサミン、テブコナゾール、テルビナフィン、テトラコナゾール、トリアジメホン、トリアジメノール、トリデモルフ、トリフルミゾール、トリホリン、トリチコナゾール、ウニコナゾール、ビニコナゾールおよびボリコナゾール;
(F10)細胞壁合成阻害剤、例えば、ベンチアバリカルブ、ジメトモルフ、フルモルフ、イプロバリカルブ、マンジプロパミド、ポリオキシン、ポリオキソリム、プロチオカルブ、バリダマイシンAおよびバリフェナール;
(F11)メラニン生合成阻害剤、例えば、カルプロパミド、ジクロシメット、フェノキサニル、フタリド、ピロキロンおよびトリシクラゾール;
(F12)例えば、アシベンゾラル−S−メチル、プロベナゾールおよびチアジニルのような、宿主の防御を誘起することができる化合物;
(F13)例えば、ボルドー液、カプタホール、キャプタン、クロロタロニル、ナフテン酸銅、酸化銅、塩基性塩化銅、水酸化銅等の銅調製物、硫酸銅、ジクロフルアニド、ジチアノン、ドジン、ドジン遊離塩基、ファーバム、フルオロホルペット、ホルペット、グアザチン、酢酸グアザチン、イミノクタジン、イミノクタジンアルベシル酸塩、イミノクタジン三酢酸塩、マンカッパー、マンコゼブ、マンネブ、メチラム、メチラム亜鉛、オキシン銅、プロパミジン、プロピネブ、多硫化カルシウムを含む硫黄および硫黄調製物、チラム、トリルフルアニド、ジネブおよびジラムのような多部位作用を有することができる化合物;
(F14)さらに、例えば、2,3−ジブチル−6−クロロチエノ[2,3−d]ピリミジン−4(3H)−オン、エチル(2Z)−3−アミノ−2−シアノ−3−フェニルプロパ−2−エノエート、ペンフルフェン(N−[2−(1,3−ジメチルブチル)フェニル]−5−フルオロ−1,3−ジメチル−1H−ピラゾール−4−カルボキサミド)、N−{2−[1,1’−ビ(シクロプロピル)−2−イル]フェニル}−3−(ジフルオロメチル)−1−メチル−1H−ピラゾール−4−カルボキサミド、3−(ジフルオロメチル)−1−メチル−N−(3’,4’,5’−トリフルオロビフェニル−2−イル)−1H−ピラゾール−4−カルボキサミド、3−(ジフルオロメチル)−N−[4−フルオロ−2−(1,1,2,3,3,3−ヘキサフルオロプロポキシ)フェニル]−1−メチル−1H−ピラゾール−4−カルボキサミド、(2E)−2−(2−{[6−(3−クロロ−2−メチルフェノキシ)−5−フルオロピリミジン−4−イル]オキシ}フェニル)−2−(メトキシイミノ)−N−メチルエタンアミド、(2E)−2−{2−[({[(2E,3E)−4−(2,6−ジクロロフェニル)ブタ−3−エン−2−イリデン]アミノ}−オキシ)メチル]フェニル}−2−(メトキシイミノ)−N−メチルエタンアミド、2−クロロ−N−(1,1,3−トリメチル−2,3−ジヒドロ−1H−インデン−4−イル)ピリジン−3−カルボキサミド、N−(3−エチル−3,5,5−トリメチルシクロヘキシル)−3−(ホルミルアミノ)−2−ヒドロキシベンズアミド、5−メトキシ−2−メチル−4−(2−{[({(1E)−1−[3−(トリフルオロメチル)フェニル]エチリデン}アミノ)オキシ]メチル}フェニル)−2,4−ジヒドロ−3H−1,2,4−トリアゾール−3−オン、(2E)−2−(メトキシイミノ)−N−メチル−2−(2−{[({(1E)−1−[3−(トリフルオロメチル)フェニル]エチリデン}アミノ)オキシ]メチル}フェニル)エタンアミド、(2E)−2−(メトキシイミノ)−N−メチル−2−{2−[(E)−({1−[3(トリフルオロメチル)フェニル]エトキシ}イミノ)メチル]フェニル}エタンアミド、(2E)−2−{2−[({[(1E)−1−(3−{[(E)−1−フルオロ−2−フェニルエテニル]オキシ}フェニル)エチリデン]アミノ}オキシ)メチル]フェニル}−2−(メトキシイミノ)−N−メチルエタンアミド、1−(4−クロロフェニル)−2−(1H−1,2,4−トリアゾール−1−イル)シクロヘプタノール、メチル1−(2,2−ジメチル−2,3−ジヒドロ−1H−インデン−1−イル)−1H−イミダゾール−5−カルボキシレート、N−エチル−N−メチル−N’−{2−メチル−5−(トリフルオロメチル)−4−[3−(トリメチルシリル)プロポキシ]フェニル}イミドホルムアミド、N’−{5−(ジフルオロメチル)−2−メチル−4−[3−(トリメチルシリル)プロポキシ]フェニル}−N−エチル−N−メチルイミドホルムアミド、O−{1−[(4−メトキシフェノキシ)メチル]−2,2−ジメチルプロピル}1H−イミダゾール−1−カルボチオエート、N−[2−(4−{[3−(4−クロロフェニル)プロパ−2−イン−1−イル]オキシ}−3−メトキシフェニル)エチル]−N2−(メチルスルホニル)バリンアミド、5−クロロ−7−(4−メチルピペリジン−1−イル)−6−(2,4,6−トリフルオロフェニル)[1,2,4]トリアゾロ[1,5−a]ピリミジン、5−アミノ−1,3,4−チアジアゾール−2−チオール、プロパモカルブ−ホセチル、1−[(4−メトキシフェノキシ)メチル]−2,2−ジメチルプロピル1H−イミダゾール−1−カルボキシレート、1−メチル−N−[2−(1,1,2,2−テトラフルオロエトキシ)フェニル]−3−(トリフルオロメチル)−1H−ピラゾール−4−カルボキサミド、2,3,5,6−テトラクロロ−4−(メチルスルホニル)ピリジン、2−ブトキシ−6−ヨード−3−プロピル−4H−クロメン−4−オン、2−フェニルフェノールおよび塩、3−(ジフルオロメチル)−1−メチル−N−[2−(1,1,2,2−テトラフルオロエトキシ)フェニル]−1H−ピラゾール−4−カルボキシアミド、3,4,5−トリクロロピリジン−2,6−ジカルボニトリル、3−[5−(4−クロロフェニル)−2,3−ジメチルイソオキサゾリジン−3−イル]ピリジン、3−クロロ−5−(4−クロロフェニル)−4−(2,6−ジフルオロフェニル)−6−メチルピリダジン、4−(4−クロロフェニル)−5−(2,6−ジフルオロフェニル)−3,6−ジメチルピリダジン、キノリン−8−オール、キノリン−8−オール硫酸塩(2:1)(塩)、5−メチル−6−オクチル−3,7−ジヒドロ[1,2,4]トリアゾロ[1,5−a]ピリミジン−7−アミン、5−エチル−6−オクチル−3,7−ジヒドロ[1,2,4]トリアゾロ[1,5−a]ピリミジン−7−アミン、ベンチアゾール、ベトキサジン、カプシマイシン、カルボン、キノメチオナート、クロロネブ、クフラネブ、シフルフェナミド、シモキサニル、シプロスルファミド、ダゾメット、デバカルブ、ジクロロフェン、ジクロメジン、ジクロラン、ジフェンゾコート、ジフェンゾコートメチルサルフェート、ジフェニルアミン、エコメイト、フェリムゾン、フルメトベル、フルオピコリド、フルオロイミド、フルスルファミド、フルチアニル、ホセチル−アルミニウム、ホセチル−カルシウム、ホセチル−ナトリウム、ヘキサクロロベンゼン、イルママイシン、イソチアニル、メタスルホカルブ、メチル(2E)−2−{2−[({シクロプロピル[(4−メトキシフェニル)イミノ]メチル}チオ)メチル]フェニル}−3−メトキシアクリレート、メチルイソチオシアネート、メトラフェノン、(5−ブロモ−2−メトキシ−4−メチルピリジン−3−イル)(2,3,4−トリメトキシ−6−メチルフェニル)−メタノン、ミルディオマイシン、トルニファニド、N−(4−クロロベンジル)−3−[3−メトキシ−4−(プロパ−2−イン−1−イルオキシ)フェニル]プロパンアミド、N−[(4−クロロフェニル)(シアノ)メチル]−3−[3−メトキシ−4−(プロパ−2−イン−1−イルオキシ)フェニル]プロパンアミド、N−[(5−ブロモ−3−クロロピリジン−2−イル)メチル]−2,4−ジクロロピリジン−3−カルボキシアミド、N−[1−(5−ブロモ−3−クロロピリジン−2−イル)エチル]−2,4−ジクロロピリジン−3−カルボキシアミド、N−[1−(5−ブロモ−3−クロロピリジン−2−イル)エチル]−2−フルオロ−4−ヨードピリジン−3−カルボキシアミド、N−{(Z)−[(シクロプロピルメトキシ)イミノ][6−(ジフルオロメトキシ)−2,3−ジフルオロフェニル]メチル}−2−フェニルアセトアミド、N−{(E)−[(シクロプロピルメトキシ)イミノ][6−(ジフルオロメトキシ)−2,3−ジフルオロフェニル]メチル}−2−フェニルアセトアミド、ナタマイシン、ニッケルジメチルジチオカルバメート、ニトロタール−イソプロピル、オクチリノン、オキサモカルブ、オキシフェンチイン、ペンタクロロフェノールおよび塩、フェナジン−1−カルボン酸、フェノトリン、亜リン酸およびこの塩、プロパモカルブホセチレート、プロパノシン−ナトリウム、プロキナジド、ピロールニトリン、キントゼン、S−プロパ−2−エン−1−イル5−アミノ−2−(1−メチルエチル)−4−(2−メチルフェニル)−3−オキソ−2,3−ジヒドロ−1H−ピラゾール−1−カルボチオエート、テクロフタラム、テクナゼン、トリアゾキシド、トリクラミド、5−クロロ−N’−フェニル−N’−プロパ−2−イン−1−イルチオフェン−2−スルホノヒドラジドおよびザリラミドのような化合物;
から選択される少なくとも一つの殺真菌剤
を含む組成物。 - 成分a)がメチニコビア・フルクチコラ(Metschnikowia fructicola)NRRL Y−30752株またはこの変異株の生物学的に純粋な培養物である、請求項1に記載の組成物。
- 殺真菌剤が、メタラキシル、メタラキシル−M、ボスカリド、フルオピラム、ビキサフェン、ペンチオピラド、アゾキシストロビン、ファモキサドン、フェナミドン、クレソキシム−メチル、ピラクロストロビン、トリフロキシストロビンから選択される、請求項1または2に記載の組成物。
- 殺真菌剤が、メタラキシル、フルオピラム、トリフロキシストロビンから選択される、請求項1または2に記載の組成物。
- 植物または植物部分に対して望ましくない微生物を防除するための、請求項1から4のいずれかに記載の組成物の使用。
- 植物または植物部分に対する家畜害虫を防除するための、請求項1から4のいずれかに記載の組成物の使用。
- 植物または植物部分に対して望ましくない微生物を防除するための、請求項1から4のいずれかに記載の組成物の使用であって、望ましくない微生物が
ボトリチス・シネレア(Botrytis cinerea)、アスぺルギルス・ニガー(Aspergillus niger)、ペニシリウム・ディギタータム(Penicillium digitatum)、ペニシリウム・エクスパンザム(Penicillium expansum)、ゲオトリクム・カンディダム(Geotrichum candidum)、リゾプス・ストロニファー(Rhizopus stolonifer)、フザリウム属種(Fusarium spp.)およびモリニリア属種(Molinilia spp.)
から選択される、使用。 - 望ましくない微生物に対して植物または植物部分を保護するための方法であって、
a)化学殺真菌剤を用いた植物または植物部分の処理、および
b)酵母を用いた植物または植物部分の処理
の段階を含み、
段階a)は、核果およびイチゴについては収穫前60日から7日に、または仁果については収穫前100日から14日に行い、段階b)は、収穫前14日から1日に行う、方法。 - 段階a)の化学殺真菌剤は、フェンヘキサミド、テブコナゾール、フルキンコナゾール、トリアジメノール、トリアジメホン、ジフェンコナゾール、エポキシコナゾール、ペンコナゾール、ビテルタノール、プロピコナゾール、ミクロブタニル、イマザリル、プロクロラズ、スピロキサミン、トリデモルフ、フェンプロピモルフ、フェンプロピジン、トリフロキシストロビン、アゾキシストロビン、クレソキシム−メチル、ピラクロストロビン、フェナミドン、フェノキサドン、ピリメタニル、シプロジニル、メパニピリム、ジカルボキシアミド類、イプロジオン、プロピネブ、マンコゼブ、ホセチル−アルミニウム、ジメトモルフ、フルアジナム、イプロバリカルブ、カルベンダジム、チオファネートメチル、チアベンダゾール、フルオピコリド、メタラキシル、メタラキシル−M、フルオピラム、ビキサフェン、ボスカリド、イソピラザム、ペンチオピラド、ジチオカルバメートから選択され、
段階b)の処理は、メチニコビア・フルクチコラ(Metschnikowia fructicola)NRRL Y−30752株またはこの変異株の生物学的に純粋な培養物を含む、請求項8に記載の方法。
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Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19716257A1 (de) | 1997-04-18 | 1998-10-22 | Bayer Ag | Fungizide Wirkstoffkombination |
DE10341945A1 (de) * | 2003-09-11 | 2005-04-21 | Bayer Cropscience Ag | Verwendung von fungiziden Mitteln zur Beizung von Saatgut |
DE10347090A1 (de) | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
EP1606999A1 (de) * | 2004-06-18 | 2005-12-21 | Bayer CropScience AG | Saatgutbehandlungsmittel für Soja |
DE102004049041A1 (de) | 2004-10-08 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
DE102004049761A1 (de) * | 2004-10-12 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
DE102005023835A1 (de) * | 2005-05-24 | 2006-12-07 | Bayer Cropscience Ag | Fungizide Wirkstoffkombination |
UA90171C2 (ru) * | 2005-09-09 | 2010-04-12 | Байер Кропсайенс Акциенгезельшафт | Фунгицидная композиция и способ ее получения |
EP2070413A1 (en) | 2007-12-11 | 2009-06-17 | Bayer CropScience AG | Active compound combinations |
AU2010272872B2 (en) * | 2009-07-16 | 2014-08-28 | Bayer Intellectual Property Gmbh | Synergistic active substance combinations containing phenyl triazoles |
BR112012026211A2 (pt) | 2010-04-14 | 2015-09-15 | Bayer Ip Gmbh | combinações de composto ativo |
PL2597951T3 (pl) | 2010-07-26 | 2017-06-30 | Bayer Intellectual Property Gmbh | Wykorzystanie inhibitora dehydrogenazy bursztynianowej i inhibitora kompleksu III łańcucha oddechowego do poprawy stosunku mikroorganizmów szkodliwych do mikroorganizmów pożytecznych |
NZ587490A (en) * | 2010-08-20 | 2013-03-28 | Greentide Ltd | Anti-Microbial Compounds containing compounds with a sugar substituent |
EP2460407A1 (de) * | 2010-12-01 | 2012-06-06 | Bayer CropScience AG | Wirkstoffkombinationen umfassend Pyridylethylbenzamide und weitere Wirkstoffe |
CN102258047B (zh) * | 2011-05-25 | 2013-07-10 | 江苏龙灯化学有限公司 | 杀菌剂组合物 |
WO2012171914A1 (en) * | 2011-06-14 | 2012-12-20 | Bayer Intellectual Property Gmbh | Use of an enaminocarbonyl compound in combination with a biological control agent |
CN104507318B (zh) * | 2012-05-30 | 2018-12-25 | 拜尔农作物科学股份公司 | 包括生物防治剂和来自呼吸链复合体iii抑制剂的杀真菌剂的组合物 |
CN103535365A (zh) * | 2012-07-11 | 2014-01-29 | 陕西美邦农药有限公司 | 一种杀菌组合物 |
CN102907435A (zh) * | 2012-10-27 | 2013-02-06 | 刘善勇 | 一种抑制草坪草生长的复配植物生长调节剂 |
CN103271044B (zh) * | 2013-06-24 | 2015-02-11 | 杭州宇龙化工有限公司 | 一种含有噻酰菌胺与噻呋酰胺的杀菌组合物 |
CN103636627B (zh) * | 2013-11-19 | 2015-04-01 | 广西田园生化股份有限公司 | 含噻呋酰胺与吗啉类杀菌剂的超低容量液剂 |
CN103749493B (zh) * | 2014-02-14 | 2016-01-27 | 南京南农农药科技发展有限公司 | 一种含有井冈霉素a和噻呋酰胺的复配杀菌剂的悬浮剂及其制备方法 |
CN104012579B (zh) * | 2014-06-23 | 2017-01-04 | 联保作物科技有限公司 | 一种杀菌组合物及其应用 |
CN104285989B (zh) * | 2014-09-10 | 2017-06-23 | 广东中迅农科股份有限公司 | 一种含有吡唑醚菌酯和丙烷脒的农药组合物 |
CN104686529B (zh) * | 2015-03-16 | 2016-11-02 | 四川农业大学 | 一种用于防治小麦赤霉病的药剂组合及其应用 |
CN104738035A (zh) * | 2015-03-25 | 2015-07-01 | 安徽省农业科学院植物保护与农产品质量安全研究所 | 一种含灭锈胺和井冈霉素的杀菌组合物 |
CN106035379A (zh) * | 2016-06-27 | 2016-10-26 | 中国烟草总公司郑州烟草研究院 | 含苯基酰胺类、苯甲酰胺类杀菌剂和生防菌的菌药组合物、制剂及应用 |
CN105941422B (zh) * | 2016-07-13 | 2018-10-30 | 南京吉星生物技术开发有限公司 | 一种含啶酰菌胺的杀菌组合物及其应用 |
CN107904180A (zh) * | 2017-12-15 | 2018-04-13 | 北京工商大学 | 一株用于果蔬采后病害防治的核果梅奇酵母及其制备与使用方法 |
CN108522528A (zh) * | 2018-05-29 | 2018-09-14 | 青岛农业大学 | 一种新型水稻专用叶面喷施药肥 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004528030A (ja) * | 2001-03-14 | 2004-09-16 | イスラエル国 | 農産物の損傷を制御するのに有用な新規の拮抗酵母、その使用方法及びそれを含む組成物 |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0650325T3 (da) * | 1992-07-17 | 1997-06-16 | Zeneca Ltd | Pesticide midler |
CN1089552C (zh) * | 1993-01-12 | 2002-08-28 | 诺瓦蒂斯有限公司 | 控制葱属植物白腐小核菌感染的方法 |
DE19716257A1 (de) * | 1997-04-18 | 1998-10-22 | Bayer Ag | Fungizide Wirkstoffkombination |
DE19857963A1 (de) * | 1998-12-16 | 2000-06-21 | Bayer Ag | Agrochemische Formulierungen |
DE10228103A1 (de) * | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
DE10228102A1 (de) * | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
DE10228104A1 (de) * | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombination |
WO2005009474A1 (ja) | 2003-07-24 | 2005-02-03 | Shionogi & Co., Ltd. | 難水溶性薬物を含むドライシロップ剤 |
DE10335183A1 (de) * | 2003-07-30 | 2005-02-24 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
DE10341945A1 (de) * | 2003-09-11 | 2005-04-21 | Bayer Cropscience Ag | Verwendung von fungiziden Mitteln zur Beizung von Saatgut |
DE10347090A1 (de) * | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
DE102004020840A1 (de) * | 2004-04-27 | 2005-11-24 | Bayer Cropscience Ag | Verwendung von Alkylcarbonsäureamiden als Penetrationsförderer |
DE102004045242A1 (de) * | 2004-09-17 | 2006-03-23 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
DE102004049041A1 (de) * | 2004-10-08 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
DE102004049761A1 (de) * | 2004-10-12 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
DE102005023835A1 (de) * | 2005-05-24 | 2006-12-07 | Bayer Cropscience Ag | Fungizide Wirkstoffkombination |
DE102005035300A1 (de) * | 2005-07-28 | 2007-02-01 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
UA90171C2 (ru) * | 2005-09-09 | 2010-04-12 | Байер Кропсайенс Акциенгезельшафт | Фунгицидная композиция и способ ее получения |
EP1982717A1 (de) * | 2007-04-20 | 2008-10-22 | Bayer CropScience AG | Verwendung von Fungiziden zur Behandlung von Fischmykosen |
MX2010002423A (es) * | 2007-09-20 | 2010-03-30 | Basf Se | Combinaciones que comprenden una cepa fungicida y un compuesto activo. |
CL2008003422A1 (es) * | 2007-11-29 | 2009-08-07 | Bayer Cropscience Ag | Procedimiento para reducir la contaminacion por aflatoxinas y ocratoxinas que afecten a plantas de cereales, frutos secos, frutas y/o especias y/o material vegetal, mediante el uso de uno o mas compuestos fungicidas seleccionado entre 29 compuestos fungicidas distintos. |
EP2070414A1 (en) * | 2007-12-11 | 2009-06-17 | Bayer CropScience AG | Active compound combinations |
EP2105049A1 (en) * | 2008-03-28 | 2009-09-30 | Bayer CropScience AG | Method of plant growth promotion using amide compounds |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004528030A (ja) * | 2001-03-14 | 2004-09-16 | イスラエル国 | 農産物の損傷を制御するのに有用な新規の拮抗酵母、その使用方法及びそれを含む組成物 |
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KR20170096227A (ko) | 2017-08-23 |
CR20110700A (es) | 2012-05-10 |
KR101769537B1 (ko) | 2017-08-18 |
EP2269454A1 (en) | 2011-01-05 |
EP3266305A1 (en) | 2018-01-10 |
AR077183A1 (es) | 2011-08-10 |
EA201290010A1 (ru) | 2012-07-30 |
EP2445348A1 (en) | 2012-05-02 |
MX2011013933A (es) | 2012-04-30 |
ZA201109367B (en) | 2013-02-27 |
WO2010149369A1 (en) | 2010-12-29 |
TW201105242A (en) | 2011-02-16 |
CN102480965B (zh) | 2014-07-16 |
CA2766325A1 (en) | 2010-12-29 |
PT2445348E (pt) | 2014-10-29 |
EP2445348B1 (en) | 2014-08-20 |
KR20120040158A (ko) | 2012-04-26 |
AU2015213382B2 (en) | 2017-03-02 |
CN102480965A (zh) | 2012-05-30 |
AU2015213382A1 (en) | 2015-09-03 |
US20140205580A1 (en) | 2014-07-24 |
EP3266305B1 (en) | 2020-01-29 |
CL2011003270A1 (es) | 2012-07-13 |
BRPI1013498A2 (pt) | 2015-08-25 |
JP5676591B2 (ja) | 2015-02-25 |
ES2519168T3 (es) | 2014-11-06 |
PL2445348T3 (pl) | 2015-01-30 |
CA2766325C (en) | 2018-07-31 |
ES2784427T3 (es) | 2020-09-25 |
AU2010265093A1 (en) | 2012-01-19 |
EP2737797A1 (en) | 2014-06-04 |
US20110033433A1 (en) | 2011-02-10 |
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