IP Library Granted Patent US 10,212,942
Granted Patent B2
US 10,212,942 · App. 15/656,089 · Granted Feb 26, 2019

Combinations comprising a fungicidal strain and an active compound

Inventors: Ulrich Schoefl (Apex, NC); Maria Scherer (Landau, DE); Egon Haden (Ludwigshafen, DE)
Assignee: Bayer CropScience LP
A01N63/00A01N27/00A01N31/08A01N31/10A01N33/06A01N35/04A01N37/44A01N43/40A01N43/50A01N43/54A01N43/56A01N43/60A01N43/653A01N43/76A01N43/78A01N43/84A01N43/90A01N45/00A01N47/12A01N47/22A01N47/40A01N55/00A01N55/02A01N63/02A01N2300/00
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Quick Facts
Patent No.
US 10,212,942
App. No.
15/656,089
Granted
Feb 26, 2019
Kind
B2
Abstract

Fungicidal mixtures, comprising 1) a fungicidal strain (I) selected from a) the Bacillus substilis strain with NRRL Accession No. B-21661, and b) the Bacillus pumilus strain with NRRL Accession No. B-30087, or a mutant of these strains having all the identifying characteristics of the respective strain, or a metabolite produced by the respective strain that exhibits activity against plant pathogenic fungi, and 2) at least one chemical compound (II), selected from the active compound groups A) to F): A) azoles; B) strobilurins; C) carboxamides; D) heterocyclic compounds; E) carbamates; F) other fungicides; in a synergistically effective amount, methods for controlling harmful fungi using compositions of components 1) and 2), the use of a component 1) with a component 2) for preparing such compositions, and also fungicidal agents and seed comprising such compositions.

Claims (35)

1. A fungicidal composition for controlling phytopathogenic harmful fungi, comprising

1) Bacillus subtilis strain with NRRL Accession No. B-21661 or a mutant thereof having all the identifying characteristics of the strain, and

2) silthiofam,

in a synergistically effective amount.

2. The fungicidal composition according to claim 1 , comprising as component 1) a commercially available formulation of the Bacillus subtilis strain with NRRL Accession No. B-21661 or mutant thereof having all the identifying characteristics of the strain.

3. The fungicidal composition according to claim 1 , wherein component 1) is the Bacillus subtilis strain with NRRL Accession No. B-21661.

4. The fungicidal composition according to claim 1 , comprising an additional active compound V, selected from the groups G) to M):

G) azoles selected from the group consisting of bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole, flusilazole, flutriafol, hexaconazole, imiben-conazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, simeconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, pefurazoate, imazalil, triflumizole, cyazofamid, benomyl, carbendazim, thiabendazole, fuberidazole, ethaboxam, etridiazole and hymexazole;

H) strobilurins selected from the group consisting of azoxystrobin, dimoxy-strobin, enestroburin, fluoxastrobin, kresoxim-methyl, methominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, enestroburin, methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-[1-(6-methylpyridin-2-ylmethoxyimino)ethyl]benzyl)-carbamate and methyl 2-(ortho-(2,5-dimethylphenyloxymethylene)phenyl)-3-methoxyacrylate;

J) carboxamides selected from the group consisting of carboxin, boscalid, fenhexamid, flutolanil, furametpyr, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl, oxycarboxin, penthiopyrad, thifluzamide, tiadinil, 3,4-dichloro-N-(2-cyanophenyl)isothiazole-5-carboxamide, dimethomorph, flumorph, flumetover, fluopicolide (picobenzamid), zoxamide, carpropamid, diclocymet, mandipropamid, N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxy-phenyl)ethyl)-2-methanesulfonylamino-3-methylbutyramide, N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl)ethyl)-2-ethanesulfonyl-amino-3-methylbutyramide, methyl 3-(4-chlorophenyl)-3-(2-isopropoxy-carbonylamino-3-methylbutyrylamino)propionate, N-(4′-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4′-trifluoromethyl-biphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4′-chloro-3′-fluorobiphenyl-2-yl)-4-difluoromethyl-2-methyl-thiazole-5-carboxamide, N-(3′,4′-dichloro-4-fluorobiphenyl-2-yl)-3-difluoro-methyl-1-methylpyrazole-4-carboxamide, N-(3′,4′-dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4-carboxamide and N-(2-cyano-phenyl)-3,4-dichloro-isothiazole-5-carboxamide;

K) heterocyclic compounds selected from the group consisting of fluazinam, pyrifenox, bupirimate, cyprodinil, fenarimol, ferimzone, mepanipyrim, nuarimol, pyrimethanil, triforine, fenpiclonil, fludioxonil, aldimorph, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, procymidone, vinclozolin, famoxadone, fenamidone, octhilinone, probenazole, anilazine, diclomezine, pyroquilon, proquinazid, tricyclazole, 2-butoxy-6-iodo-3-propylchromen-4-one, acibenzolar-S-methyl, captafol, captan, dazomet, folpet, fenoxanil, quinoxyfen and N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)-[1,2,4]triazole-1-sulfonamide;

L) carbamates selected from the group consisting of mancozeb, maneb, metam, metiram, ferbam, propineb, thiram, zineb, ziram, diethofencarb, iprovalicarb, flubenthiavalicarb, propamocarb, 4-fluorophenyl N-(1-(1-(4-cyanophenyl)ethanesulfonyl)but-2-yl)carbamate, methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl-butyrylamino)propanoate and carbamate oxime ethers of the formula VI

in which Z is N or CH;

M) other fungicides selected from the group consisting of

guanidine, dodine, iminoctadine, guazatine,

antibiotics: kasugamycin, streptomycin, polyoxin, validamycin A,

nitrophenyl derivatives: binapacryl, dinocap, dinobuton,

sulfur-containing heterocyclyl compounds: dithianon, isoprothiolane,

organometallic compounds: fentin salts,

organophosphorus compounds: edifenphos, iprobenfos, fosetyl, fosetyl-aluminum, phosphorous acid and its salts, pyrazophos, tolclofos-methyl,

organochlorine compounds: chlorothalonil, dichlofluanid, flusulfamide, hexachlorobenzene, phthalide, pencycuron, quintozene, thiophanate-methyl, tolylfluanid,

inorganic active compounds: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur,

others: cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl and spiroxamine.

5. The fungicidal composition according to claim 1 , comprising the components 1) and 2) in a weight ratio of from 100:1 to 1:100.

6. A fungicidal agent, comprising at least one liquid or solid carrier and a composition according to claim 1 .

7. A seed comprising a fungicidal composition according to claim 1 .

8. A method for controlling phytopathogenic harmful fungi, wherein the fungi, their habitat or the plants to be protected against fungal attack, the soil, seed, areas, materials or spaces are/is treated with an effective amount of a fungicidal composition according to claim 1 .

9. The method according to claim 8 , wherein components 1) and 2) are applied simultaneously, that is jointly or separately, or in succession.

10. The method of claim 8 , wherein the components 1) and 2) are present in a weight ratio of from 100:1 to 1:100.

11. The method of claim 8 , wherein the composition further comprises at least one liquid or solid carrier.

12. The method of claim 8 , wherein the plants are potatoes, sugar beets, tobacco, wheat, rye, barley, oats, rice, corn, cotton, soybeans, rape, legumes, sunflowers, coffee, sugar cane, fruits, vines, ornamentals or vegetables.

13. A method for controlling harmful fungi, wherein a transgenic plant or the seed thereof is treated with a fungicidal agent suitable for controlling harmful fungi comprising a fungicidal composition according to claim 1 .

14. The method of claim 13 , wherein components 1) and 2) are applied simultaneously, that is jointly or separately, or in succession.

15. The method of claim 13 , wherein the components 1) and 2) are present in a weight ratio of from 100:1 to 1:100.

16. The method of claim 13 , wherein the composition further comprises at least one liquid or solid carrier.

Assignments (3)
CHANGE OF ADDRESS Recorded Sep 12, 2019
From: BAYER CROPSCIENCE LP
To: BAYER CROPSCIENCE LP
Reel/Frame 050370/0245 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2017
From: SCHOEFL, ULRICH; SCHERER, MARIA; HADEN, EGON
To: BASF SE
Reel/Frame 043062/0125 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2017
From: BASF SE
To: BAYER CROPSCIENCE LP
Reel/Frame 043062/0210 →
Priority Claims (1)
EP 07116844 · Sep 20, 2007 · regional
Continuity (4)
Continuation 15184691 · Jun 16, 2016
Continuation 14731791 · Jun 5, 2015
Continuation 12678543
Related Publication 20170318816A1 · Nov 9, 2017
Cited By (1)
US 12,538,926