EP3136855A1 - Utilisation d'un acide dicarboxylique pour lutter contre la croissance de plantes holoparasites ou hémiparasites - Google Patents
Utilisation d'un acide dicarboxylique pour lutter contre la croissance de plantes holoparasites ou hémiparasitesInfo
- Publication number
- EP3136855A1 EP3136855A1 EP15725815.3A EP15725815A EP3136855A1 EP 3136855 A1 EP3136855 A1 EP 3136855A1 EP 15725815 A EP15725815 A EP 15725815A EP 3136855 A1 EP3136855 A1 EP 3136855A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- plants
- dicarboxylic acid
- acid
- growth
- use according
- 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.)
- Withdrawn
Links
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 title claims abstract description 37
- 230000012010 growth Effects 0.000 title claims abstract description 34
- 241000196324 Embryophyta Species 0.000 claims abstract description 84
- 241000208000 Striga Species 0.000 claims abstract description 46
- 241000589938 Azospirillum brasilense Species 0.000 claims abstract description 31
- 241001508464 Orobanche Species 0.000 claims abstract description 27
- 244000005700 microbiome Species 0.000 claims abstract description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 11
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 23
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 21
- 235000011090 malic acid Nutrition 0.000 claims description 20
- 239000001630 malic acid Substances 0.000 claims description 17
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 12
- 230000009418 agronomic effect Effects 0.000 claims description 12
- 239000002689 soil Substances 0.000 claims description 11
- 235000011684 Sorghum saccharatum Nutrition 0.000 claims description 10
- 241000894006 Bacteria Species 0.000 claims description 9
- 230000002363 herbicidal effect Effects 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 244000000042 obligate parasite Species 0.000 claims description 6
- 244000020551 Helianthus annuus Species 0.000 claims description 5
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 5
- 235000007688 Lycopersicon esculentum Nutrition 0.000 claims description 5
- 244000061176 Nicotiana tabacum Species 0.000 claims description 5
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 5
- 240000003768 Solanum lycopersicum Species 0.000 claims description 5
- 230000007226 seed germination Effects 0.000 claims description 5
- 240000002791 Brassica napus Species 0.000 claims description 4
- 240000007594 Oryza sativa Species 0.000 claims description 4
- 235000007164 Oryza sativa Nutrition 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 240000008042 Zea mays Species 0.000 claims description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 235000006408 oxalic acid Nutrition 0.000 claims description 4
- 230000008635 plant growth Effects 0.000 claims description 4
- 235000009566 rice Nutrition 0.000 claims description 4
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 3
- 240000007087 Apium graveolens Species 0.000 claims description 3
- 235000015849 Apium graveolens Dulce Group Nutrition 0.000 claims description 3
- 235000010591 Appio Nutrition 0.000 claims description 3
- 240000007124 Brassica oleracea Species 0.000 claims description 3
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 claims description 3
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 claims description 3
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 claims description 3
- 235000004977 Brassica sinapistrum Nutrition 0.000 claims description 3
- 244000046052 Phaseolus vulgaris Species 0.000 claims description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 3
- 244000061458 Solanum melongena Species 0.000 claims description 3
- 235000021307 Triticum Nutrition 0.000 claims description 3
- 244000098338 Triticum aestivum Species 0.000 claims description 3
- 235000010726 Vigna sinensis Nutrition 0.000 claims description 3
- 244000042314 Vigna unguiculata Species 0.000 claims description 3
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 3
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 3
- YTIVTFGABIZHHX-UHFFFAOYSA-N butynedioic acid Chemical compound OC(=O)C#CC(O)=O YTIVTFGABIZHHX-UHFFFAOYSA-N 0.000 claims description 3
- -1 carboxymetyl Chemical group 0.000 claims description 3
- 235000009973 maize Nutrition 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- 239000011976 maleic acid Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims description 2
- 244000215068 Acacia senegal Species 0.000 claims description 2
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- 240000004160 Capsicum annuum Species 0.000 claims description 2
- 229920001661 Chitosan Polymers 0.000 claims description 2
- 229920000084 Gum arabic Polymers 0.000 claims description 2
- 235000002597 Solanum melongena Nutrition 0.000 claims description 2
- 244000061456 Solanum tuberosum Species 0.000 claims description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 claims description 2
- 239000000205 acacia gum Substances 0.000 claims description 2
- 235000010489 acacia gum Nutrition 0.000 claims description 2
- 229940072056 alginate Drugs 0.000 claims description 2
- 235000010443 alginic acid Nutrition 0.000 claims description 2
- 229920000615 alginic acid Polymers 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 229920005551 calcium lignosulfonate Polymers 0.000 claims description 2
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 claims description 2
- 239000004927 clay Substances 0.000 claims description 2
- 239000000470 constituent Substances 0.000 claims description 2
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 235000013305 food Nutrition 0.000 claims description 2
- 238000011065 in-situ storage Methods 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003415 peat Substances 0.000 claims description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- 240000003829 Sorghum propinquum Species 0.000 claims 2
- 235000002566 Capsicum Nutrition 0.000 claims 1
- 244000070406 Malus silvestris Species 0.000 claims 1
- 239000006002 Pepper Substances 0.000 claims 1
- 235000016761 Piper aduncum Nutrition 0.000 claims 1
- 240000003889 Piper guineense Species 0.000 claims 1
- 235000017804 Piper guineense Nutrition 0.000 claims 1
- 235000008184 Piper nigrum Nutrition 0.000 claims 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- 235000005822 corn Nutrition 0.000 claims 1
- 235000019362 perlite Nutrition 0.000 claims 1
- 239000010451 perlite Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 18
- 230000001747 exhibiting effect Effects 0.000 abstract description 2
- 230000003071 parasitic effect Effects 0.000 description 20
- 229940099690 malic acid Drugs 0.000 description 13
- 239000012228 culture supernatant Substances 0.000 description 12
- 230000035784 germination Effects 0.000 description 12
- 241000207832 Lamiales Species 0.000 description 9
- 244000062793 Sorghum vulgare Species 0.000 description 9
- 150000001991 dicarboxylic acids Chemical class 0.000 description 9
- 230000001580 bacterial effect Effects 0.000 description 8
- 230000002401 inhibitory effect Effects 0.000 description 8
- 239000006228 supernatant Substances 0.000 description 8
- 241000201310 Phelipanche ramosa Species 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- 235000013339 cereals Nutrition 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 5
- 239000008363 phosphate buffer Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- LINOMUASTDIRTM-QGRHZQQGSA-N deoxynivalenol Chemical compound C([C@@]12[C@@]3(C[C@@H](O)[C@H]1O[C@@H]1C=C(C([C@@H](O)[C@@]13CO)=O)C)C)O2 LINOMUASTDIRTM-QGRHZQQGSA-N 0.000 description 3
- 229930002954 deoxynivalenol Natural products 0.000 description 3
- 239000001963 growth medium Substances 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 238000011534 incubation Methods 0.000 description 3
- 229940116298 l- malic acid Drugs 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- LINOMUASTDIRTM-UHFFFAOYSA-N vomitoxin hydrate Natural products OCC12C(O)C(=O)C(C)=CC1OC1C(O)CC2(C)C11CO1 LINOMUASTDIRTM-UHFFFAOYSA-N 0.000 description 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 2
- XHSDUVBUZOUAOQ-WJQMYRPNSA-N (3e,3ar,8bs)-3-[[(2r)-4-methyl-5-oxo-2h-furan-2-yl]oxymethylidene]-4,8b-dihydro-3ah-indeno[1,2-b]furan-2-one Chemical compound O1C(=O)C(C)=C[C@@H]1O\C=C/1C(=O)O[C@@H]2C3=CC=CC=C3C[C@@H]2\1 XHSDUVBUZOUAOQ-WJQMYRPNSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- DGMPVYSXXIOGJY-UHFFFAOYSA-N Fusaric acid Chemical compound CCCCC1=CC=C(C(O)=O)N=C1 DGMPVYSXXIOGJY-UHFFFAOYSA-N 0.000 description 2
- 241000223221 Fusarium oxysporum Species 0.000 description 2
- 231100000678 Mycotoxin Toxicity 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003124 biologic agent Substances 0.000 description 2
- 229940041514 candida albicans extract Drugs 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 238000004949 mass spectrometry Methods 0.000 description 2
- 239000002207 metabolite Substances 0.000 description 2
- 239000002636 mycotoxin Substances 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000012138 yeast extract Substances 0.000 description 2
- LMSDCGXQALIMLM-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid;iron Chemical compound [Fe].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O LMSDCGXQALIMLM-UHFFFAOYSA-N 0.000 description 1
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
- 241000208838 Asteraceae Species 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 235000006008 Brassica napus var napus Nutrition 0.000 description 1
- 241000219193 Brassicaceae Species 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 241001268643 Eulocastra Species 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000223218 Fusarium Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241001446276 Helia <angisperm> Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 244000088959 Ochrosia oppositifolia Species 0.000 description 1
- 102000015636 Oligopeptides Human genes 0.000 description 1
- 108010038807 Oligopeptides Proteins 0.000 description 1
- 241000308150 Orobanchaceae Species 0.000 description 1
- 241000453615 Phytomyza orobanchia Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 241000013557 Plantaginaceae Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 241000208292 Solanaceae Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 238000004166 bioassay Methods 0.000 description 1
- 230000000443 biocontrol Effects 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 235000020958 biotin Nutrition 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- 229940046414 biotin 1 mg Drugs 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000002983 circular dichroism Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000005712 elicitor Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000002031 ethanolic fraction Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000003008 fumonisin Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000007952 growth promoter Substances 0.000 description 1
- 230000005802 health problem Effects 0.000 description 1
- 208000006278 hypochromic anemia Diseases 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000000411 inducer Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- 238000009329 organic farming Methods 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 229930195732 phytohormone Natural products 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000001228 trophic effect Effects 0.000 description 1
- 239000012137 tryptone Substances 0.000 description 1
Classifications
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
- A01N37/04—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof polybasic
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/06—Unsaturated carboxylic acids or thio analogues thereof; Derivatives thereof
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
-
- 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
-
- 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
- A01N63/10—Animals; 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
- 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
- A01N63/20—Bacteria; Substances produced thereby or obtained therefrom
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
- C12N1/205—Bacterial isolates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
Definitions
- the present invention relates to the technical field of the protection of agricultural crops (poaceae, solanaceae, brassicaceae, asteraceae) vis-à-vis holoparasites plants and epirhized hemiparasites (that is to say that develop on the roots of their plant host), of the order Scrophulariales, and in particular Striga and Orobanche. More specifically, the invention relates to the use of a dicarboxylic acid having 2 to 5 carbon atoms or a strain Azospirillum brasilense L4 deposited under the number 1-4830 with the CNCM to fight against the growth of holo plants or hemiparasites.
- Holoparasite plants are non-chlorophyllian parasitic plants in nature and therefore need to take their organic matter from a host plant.
- the hemiparasitic plants are chlorophyllian parasitic plants that provide only part of the synthesis of the carbonaceous substances necessary for their development. These parasitic plants develop at the expense of their host by becoming attached to their roots via the formation of a haustorium (sucker ) which results in the establishment of a connection between the xylem conducting vessels of the host plant and the parasitic plant (Bouwmeester et al., 2003, Curr Opin Plant Plant, 6: 358-364).
- parasitic plants will pump sap from the host plant, slow down the development of aerial parts, induce chlorosis and reduce photosynthesis (Ejeta and Butler, 2000. Parasitic plants, Irr RA Frederiksen and GN Odvody (eds) Compendium of Sorghum Diseases, 2nd Edition, APS Press, The American Phytopathological Society, pp. 53-56). To survive, these parasitic plants must produce a large amount of seeds. Thus, as soon as the aerial parts emerge, the parasitic plant flowers and produces enormous quantities of seeds that may remain viable in the soil for several years (Haussmann et al., 2000, Reld Crop Res., 66: 195-211). .
- the plants of the Striga and Orobanche genera belong to the same order, that of the Scrophulariales, but do not belong to the same family (the plants of the genus Striga belong to the family Scrophulariaceae and are hemiparasites, while plants of the genus Orobanche belong to the family Orobanchaceae and are holoparasites). These plants have many points in common: small seeds facilitating their dissemination, germination dependent on the presence of strigolactone elicitors, trophic spoliation of the host plant via the development of a haustorium.
- Striga in all tropical and subtropical regions of the world and in particular in sub-Saharan Africa and Orobanche, mainly in the temperate countries of Asia and Central Europe and in particular around the Mediterranean. They affect the growth of a very wide variety of plants of agronomic interest (maize, rice, sorghum, millet, sunflower, rapeseed, tobacco, tomato, etc.), whether in temperate (Orobanche), or tropical (Striga ). They cause significant yield losses on a large number of crops.
- the seeds of these parasitic plants are of very small size which favors their propagation over long distances by the wind, the animals, or by contaminated agricultural machinery.
- the transport of seed from infected host plants is also a source of dissemination.
- crop protection against Orobanche or Striga plants involves the use of non-selective herbicides, coupled with the use of cereal varieties resistant to these herbicides (De Groote et al., 2008, Agric. System 97: 83-94).
- These chemical control means in addition to their toxicity to the environment, are expensive.
- the use of plant protection products including herbicides will be greatly reduced.
- Strigae or Fusarium art rosporioides that produce mycotoxins (ie fusaric acid, fumonisins, and deoxynivalenol (DON)) (Amsellem et al., 2001, BioControl 46: 211-228, Abuelgasim and roschel, 2003, FAO plant production and protection. Paper IMo.120. Addendum 1, 109-144; Lendzemo et al. 2004 Field Crop es. 91: 51-61; Venne et al., 2009, PesL Manag. Sci. 65: 572-580).
- Mycotoxins are able to inhibit the germination of Striga and Orobanche seeds, but they can trigger health problems in mammals. In particular, they represent a risk for cattle and human food and therefore can not be considered as completely harmless substances.
- the present invention proposes to use a dicarboxylic acid containing from 2 to 5 carbon atoms to combat growth of holo plants or hemiparasites, and in particular to control the growth of plants of the genus Striga and / or plants of the genus Orobanche. It is also possible to use combinations of several dicarboxylic acids, having 2 to 5 carbon atoms, to control the growth of holo plants or hemiparasites, to obtain the desired effect.
- the active agents proposed for inhibiting the development of holo or hemiparasite plants are chosen from dicarboxylic acids (hereinafter also called diacids) comprising from 2 to 5 atoms. of carbon.
- diacids comprise two carboxylic acid functions that are directly linked together, in the case of oxalic acid, or linked by a saturated or unsaturated carbon chain comprising 1, 2 or 3 carbon atoms.
- This carbon chain is preferably linear and may be unsubstituted or substituted with one or more substituents, in particular of OH, OCH 3 and CH 2 OCH 3 type .
- oxalic acid By way of example of such diacids, mention may be made of oxalic acid, malonic acid, maleic acid, malic acid, glutaric acid, and acetylene dicarboxylic acid.
- L-form malic acid which has been shown to be particularly active in inhibiting the growth of Striga or Orobanche plants, is preferred.
- Malic acid in L form could be isolated, by the inventors, from culture supernatant of a bacterial strain, Azospirillum brasilense L4, deposited, in accordance with the Budapest Treaty of 1977, under the number 1-4830, the December 18, 2013, at the CNCM, National Collection of Cultures of Microorganisms, Institut Pasteur, 25 rue Dondel Roux, 75724 Paris Cedex 15, FRANCE. This strain was isolated in 1995 from a sorghum field infested with a Striga parasitic plant in Mali.
- the Azospirillum brasilense strain L4 that has been reported as having the ability to inhibit in vitro the growth of Striga hermonù AC and Orobanche ramosa and in soil microcosms, protect vis-a-vis sorghum and Striga to stimulate the growth of the cereal (Bouillant et al., 1997, CR Acad III Life Sci 320: 159-162, Miche et al., 2000, Eur J. Plant Pathol. 106: 347-351) has now been filed under the number 1-4830 with the CNCM (National Collection of Cultures of Microorganisms, France).
- This strain produces in culture very specific metabolites, compared with other strains of Azospirillum brasilense (and especially with respect to that reported by Dadon et al., 2004: Isr. J. Plant Sci. 52: 83-86). .
- the inventors have analyzed the culture supernatant of the strain Azospirillum brasilense L4, deposited under the number 1-4830, with the CNCM (National Collection of Cultures of Microorganisms, France) and have was able to demonstrate that malic acid in L form is responsible for the herbicidal activity observed with holo or hemiparasite plants.
- the malic acid in L form is not the major component present in the culture supernatant of the bacterial strain, Azospirillum brasilense L4, deposited under the number 1-4830 with the CNCM (National Collection of Cultures of Microorganisms, France).
- the inventors have also demonstrated that this herbicidal activity observed with respect to holo or hemiparasite plants is generalizable to the chemical class of dicarboxylic acids comprising from 2 to 5 carbon atoms.
- the invention therefore proposes using active agents of natural origin, with a low environmental impact, to limit, inhibit the growth of parasitic plants.
- dicarboxylic acids comprising from 2 to 5 carbon atoms are also capable of inhibiting the elongation of procaulomas or radicles. from germinated seeds of the parasitic plant, and, therefore, to block the growth of the parasitic plant, as is apparent in particular from the data presented in Table 1 below.
- the dicarboxylic acid may be brought into contact with at least one holo plant seed or hemiparasite to be eradicated.
- the dicarboxylic acid will be used in sufficient quantity to obtain the desired effect, and in particular to block the seed germination and / or to inhibit the elongation of procaulomas or radicles from seeds germinated holo plants or hemiparasites, the Scrophulariales, and in particular Striga and / or Orobanche.
- from 30 to 300 kg of dicarboxylic acid per hectare of treated soil may be used.
- a solution comprising from 1 to 20 g of dicarboxylic acid per liter of solution may be used.
- the dicarboxylic acid can be applied to seeds and / or plant plants or crops to be protected.
- the herbicidal compositions containing a dicarboxylic acid according to the invention may in particular be in the form of aqueous solutions or granules. These compositions may contain, in addition to the active dicarboxylic acid, ions derived from K 2 HPO 4 or KH 2 PO 4 , one or more fillers such as silica, clay, kaolin or talc and one or more surfactants. such as dodecylbenzene or calcium lignosulfonate.
- malic acid in L form the latter may be produced by chemical synthesis or directly by the bacterial strain, Azospirillum brasilense L4, deposited under number 1-4830 with the CM (National Collection of Cultures of France). Microorganisms, France).
- the acid may be isolated or the herbicidal composition may directly contain the culture supernatant of the bacteria.
- the culture supernatant can be obtained by placing the bacteria in any suitable culture medium.
- the growth conditions of Azospirillum brasilense bacteria known to those skilled in the art and especially described in (Nelson and Knowles, 1978, Can J. Microbiol24: 1395-1403) may be used. In particular, the growth will be carried out at a temperature of 26 to 32.degree.
- Buffered aqueous medium containing salts, nutrients and a source of carbon for the growth of the bacteria.
- salts include NaCl, 2 ⁇ O 4, H 2 PO 4, MgSO 4, NaCl, CaCl 2, NH 4 Cl.
- nutrients mention may be made of Na 2 MoO 4 , MnSO 4 , H 3 BO 3 , CuSO 4 , ZnSO 4 , FeEDTA, yeast extract, and biotin.
- carbon sources mention may be made of glucose, malate and fructose in particular. Examples of such media include Nfb and Nfb * media described in particular Nelson and Knowles, 1978, Can. J. Microbiol. 24: 1395-1403 and Vial et al., 2006, J. Bacteriol. 188: 5364-5373.
- the Azospirillum brasilense strain deposited under the number I-4830, with the CNCM (National Collection of Cultures of Microorganisms, France) and used in the context of the invention to inhibit the growth of holo or hemiparasitic plants, the order of the Scrophulariales, and in particular Striga and / or Orobanche, presents another advantage for crop improvement, since it is also capable of stimulating plant growth, and is capable of producing a phytostimulatory agent for with respect to plants of agronomic interest (Bouillant et al., 1997, CR Acad Sci 320: 159-162).
- the invention proposes to use bacteria of the strain Azospirillum brasilense L4, deposited under the number 1-4830, with the CNCM (National Collection of Cultures of Microorganisms, France) also to produce a phytostimulatory agent vis-à-vis -vis agricultural crops or plants of agronomic interest to protect against the growth of holo plants or hemiparasites.
- phytostimulatory agent is meant a growth promoter of the plants of interest.
- bacteria of the strain Azospirillum brasilense deposited under the number 1-4830, with the CNCM (National Collection of Cultures of Microorganisms, France) can be used to coat seeds of such agricultural crops or plants of interest agronomic.
- the bacteria are incorporated in a matrix constituting a coating of the seeds of agricultural crops or plants of agronomic interest.
- This coating may contain one or more constituents such as peat, periite, gum arabic, carboxymethyl cellulose, polyvinylpyrrolidone, chitosan or alginate.
- the bacteria will be used in sufficient quantity to obtain the desired effect, and in particular to block the germination of seeds of holo plants or hemiparasites, of the order of Scrophulariales, and in particular of Striga and / or Orobanche, and / or to to inhibit the elongation of procaulomas or radicles from germinated seeds of holo or hemiparasite plants, of the order Scrophulariales, and in particular of Striga and / or Orobanche, and / or to stimulate the growth of agricultural crops or plant species; agronomic interest.
- 3 ⁇ 10 7 bacterial cells per gram of seed of agricultural crops or plants of agronomic interest to be protected and / or phytostimulated will be used.
- the dicarboxylic acids comprising from 2 to 5 carbon atoms proposed in the context of the invention for combating the growth of holo or hemiparasite plants, of the order of Scrophulariales, and in particular of Striga and / or Orobanche can therefore be used , by seed companies, to coat their seeds, but also by companies Phytopharmacy, both in the field of conventional agriculture (synthesis of dicarboxylic acids comprising from 2 to 5 carbon atoms by chemical processes) and in the field of organic farming (production of active agents by living organisms, in the case of malic acid in L form, in particular).
- FIG. 1 presents representative photographs of the effect obtained on the growth of Striga hermontica, in a microtiter box, in the presence of the supernatant of A. brasilense strain L4 grown in Nfb * medium and L-malic acid at 2mg / mL in 50mM phosphate buffer.
- Figure 2 shows the effect of the A. brasilense L4 supernatant on the seed germination percentage of Striga hermontica and Orobanche ramosa (A) and on the length of procauloma of the seeds of Striga hermontica and Orobanche ramosa (B).
- the activity of diacids on Striga and Orobanche parasitic plants was tested by preparing solutions of the selected diacid in water or in 50 mM phosphate buffer pH 7 at concentrations of 1 to 20 mg / ml.
- filter papers (Whatmann 3) are placed at the bottom of the wells and soaked with sterile water. Thirty sterilized seeds (rinsing with 70% ethanol, then Ca (CIO) 21 % (m / v) and Tween® 20, then with plenty of water) of the holo or hemipasite plants are arranged, in each well, on the surface of the filter papers. After 10 days of incubation at 30 ° C. and in the dark, increasing doses of a diacid or culture supernatant are added, in the presence of a germination inducer, GR24.
- Figure 1 shows the representative photographs of the effects obtained on the growth of Striga hermontica in a microtiter box in the presence of the supernatant of the Nfb * cultured L4 brasilense strain L-malic acid at 2 mg / ml in phosphate buffer and highlights their inhibitory effect on the growth of procululi of holo or hemiparasitic plants.
- Figure 2 shows the impact of the A. brasilense L4 supernatant on the seed germination percentage of Striga hermontica and Orobanche ramosa (A) and the length of the procauloma of the seeds of Striga hermontica and Orobanche ramosa (B ).
- Striga and Orobanche in vitro (microtiter box bioassays, Figures 1 and 2) and to inhibit Striga growth in sorghum cultures in microcosms under controlled conditions ((Bouillant et al., 1997, CR Acad Sci 320
- the molecules involved in this effect have been isolated by an appropriate chromatographic method and then identified by mass spectrometry compared to chemical standards.It has also been shown that different dicarboxylic acids are effective, to control the growth of holo or hemiparasite plants of the order Scrophulariales, and in particular Striga and / or Orobanche (T ableau 1).
- Striga plants The emergence of Striga plants is visually estimated after 2 months of incubation. Phytotoxicity is estimated by comparison with a control without malic acid or culture supernatant. A 22% reduction in the number of Striga plants that emerged compared to the control condition, is observed in the presence of malic acid 2 g / L and 90% in the presence of malic acid 20 g / L In the presence of the supernatant bacterial, a 58% decrease in the number of Striga compared to the control condition was observed.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- Biotechnology (AREA)
- Chemical & Material Sciences (AREA)
- Virology (AREA)
- Microbiology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Tropical Medicine & Parasitology (AREA)
- Biomedical Technology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cultivation Of Plants (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1453891A FR3020241B1 (fr) | 2014-04-29 | 2014-04-29 | Utilisation d'un acide dicarboxylique pour lutter contre la croissance de plantes holoparasites ou hemiparasites |
PCT/FR2015/051150 WO2015166184A1 (fr) | 2014-04-29 | 2015-04-28 | Utilisation d'un acide dicarboxylique pour lutter contre la croissance de plantes holoparasites ou hémiparasites |
Publications (1)
Publication Number | Publication Date |
---|---|
EP3136855A1 true EP3136855A1 (fr) | 2017-03-08 |
Family
ID=51518911
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP15725815.3A Withdrawn EP3136855A1 (fr) | 2014-04-29 | 2015-04-28 | Utilisation d'un acide dicarboxylique pour lutter contre la croissance de plantes holoparasites ou hémiparasites |
Country Status (11)
Country | Link |
---|---|
US (1) | US20170042148A1 (pt) |
EP (1) | EP3136855A1 (pt) |
CN (1) | CN106455558A (pt) |
AP (1) | AP2016009528A0 (pt) |
AU (1) | AU2015255102A1 (pt) |
BR (1) | BR112016024674A2 (pt) |
CA (1) | CA2945919A1 (pt) |
FR (1) | FR3020241B1 (pt) |
MA (1) | MA39892A (pt) |
WO (1) | WO2015166184A1 (pt) |
ZA (1) | ZA201608218B (pt) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3644739A1 (en) | 2017-06-26 | 2020-05-06 | King Abdullah University Of Science And Technology | Plant growth promoter with strigolactones regulation activities |
GB2586014A (en) * | 2019-07-24 | 2021-02-03 | Arthur Maine Robins Ronald | Broad-spectrum herbicide |
-
2014
- 2014-04-29 FR FR1453891A patent/FR3020241B1/fr active Active
-
2015
- 2015-04-28 CA CA2945919A patent/CA2945919A1/fr not_active Abandoned
- 2015-04-28 AU AU2015255102A patent/AU2015255102A1/en not_active Abandoned
- 2015-04-28 WO PCT/FR2015/051150 patent/WO2015166184A1/fr active Application Filing
- 2015-04-28 BR BR112016024674A patent/BR112016024674A2/pt not_active Application Discontinuation
- 2015-04-28 US US15/305,673 patent/US20170042148A1/en not_active Abandoned
- 2015-04-28 CN CN201580023801.2A patent/CN106455558A/zh active Pending
- 2015-04-28 EP EP15725815.3A patent/EP3136855A1/fr not_active Withdrawn
- 2015-04-28 AP AP2016009528A patent/AP2016009528A0/en unknown
- 2015-04-28 MA MA039892A patent/MA39892A/fr unknown
-
2016
- 2016-11-28 ZA ZA2016/08218A patent/ZA201608218B/en unknown
Non-Patent Citations (2)
Title |
---|
None * |
See also references of WO2015166184A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2015166184A1 (fr) | 2015-11-05 |
CA2945919A1 (fr) | 2015-11-05 |
BR112016024674A2 (pt) | 2017-08-15 |
US20170042148A1 (en) | 2017-02-16 |
FR3020241A1 (fr) | 2015-10-30 |
MA39892A (fr) | 2017-03-08 |
AP2016009528A0 (en) | 2016-10-31 |
AU2015255102A1 (en) | 2016-11-17 |
FR3020241B1 (fr) | 2020-02-21 |
CN106455558A (zh) | 2017-02-22 |
ZA201608218B (en) | 2018-05-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Mwakinyali et al. | Recent development of aflatoxin contamination biocontrol in agricultural products | |
Toghueo et al. | Biocontrol and growth enhancement potential of two endophytic Trichoderma spp. from Terminalia catappa against the causative agent of Common Bean Root Rot (Fusarium solani) | |
Tagele et al. | Effectiveness of multi-trait Burkholderia contaminans KNU17BI1 in growth promotion and management of banded leaf and sheath blight in maize seedling | |
EP1876232B1 (fr) | Nouvelle souche de trichoderma atroviride, un milieu de culture la contenant, ainsi que l'utilisation de ladite souche notamment comme stimulant de la germination et/ou de la croissance des plantes | |
CA2838231C (fr) | Utilisation des ulvanes comme activateurs des reactions de defense des plantes et de resistance contre des contraintes biotiques ou abiotiques | |
Joseph et al. | Effectiveness of Pseudomonas species in the management of tomato early blight pathogen Alternaria solani | |
EP3013147B1 (en) | Compositions comprising pesticide precursors and methods of making and use | |
Álvarez et al. | Plant fungal disease management using nanobiotechnology as a tool | |
EP3136855A1 (fr) | Utilisation d'un acide dicarboxylique pour lutter contre la croissance de plantes holoparasites ou hémiparasites | |
Kiptoo et al. | Rhizoctonia solani of potato and its management: a review | |
OA18998A (en) | Utilisation d'un acide dicarboxylique pour lutter contre la croissance de plantes holoparasites ou hémiparasites | |
EP2914113B1 (fr) | Composition à base de bactéries pour améliorer la croissance des plantes | |
KR20220159058A (ko) | 담수에서 분리한 항균력 및 식물생장촉진능을 가지는 아크레모니움 투바키 nnibrfg2982 균주 및 이의 용도 | |
Navi et al. | Use of Trichoderma in the management of diseases in North American row crops | |
Nurhaida et al. | Isolation and screening of endophytic fungi isolated from Annona muricata leaves for antimicrobial activity | |
Al-Askar et al. | Improving growth and productivity as well as controlling Sclerotium rolfsii in Jerusalem Artichoke using biotic and abiotic agents | |
CA3106569A1 (fr) | Methode de biocontrole de la fusariose des cereales | |
JP5198015B2 (ja) | Herbaspirillum属細菌の新規用途 | |
WO2008012400A1 (fr) | Utilisation d'inocula fongiques pour l'amelioration de la production maraichere | |
FR2700542A1 (fr) | Champignons Trichoderma produisant des alkyl-6-delta-lactones capables à la fois de stimuler la croissance des plantes et d'exercer une activité antifongique. | |
EP4262398A1 (fr) | Nouvel agent de biocontrole et son utilisation pour la lutte contre des maladies fongiques de plantes | |
Alamene | Effects of plant essential oils and biocontrol agents on the growth of and mycotoxin production by Aspergillus spp. on groundnut | |
WO2022195230A1 (fr) | Utilisation d'un extrait d'algue rouge comme agent nematostatique et/ou nematicide | |
Pratap et al. | Effect of Different Concentrations of Nano-Fungicides on Mycelial Radial Growth of Phytophthora infestans | |
EP4117439A1 (fr) | Composition phytosanitaire comprenant des ulvanes et du silicium |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20161121 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: ANDRIANJAKA-CAMPS, ZO-NOROSOA Inventor name: WISNIEWSKI-DYE, FLORENCE Inventor name: MICHE, LUCIE Inventor name: BELLVERT, FLORIANT Inventor name: COMTE, GILLES Inventor name: DUPONNOIS, ROBIN Inventor name: PRIGENT-COMBARET, CLAIRE Inventor name: BALLY, RENE Inventor name: BERTRAND, CEDRIC Inventor name: BERNILLON, JACQUES |
|
DAX | Request for extension of the european patent (deleted) | ||
PUAG | Search results despatched under rule 164(2) epc together with communication from examining division |
Free format text: ORIGINAL CODE: 0009017 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20180301 |
|
B565 | Issuance of search results under rule 164(2) epc |
Effective date: 20180301 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: A01N 37/36 20060101ALI20180226BHEP Ipc: A01N 63/00 20060101ALI20180226BHEP Ipc: C12N 1/20 20060101ALI20180226BHEP Ipc: C12R 1/01 20060101ALI20180226BHEP Ipc: A01N 63/02 20060101ALI20180226BHEP Ipc: A01P 21/00 20060101ALI20180226BHEP Ipc: A01N 37/06 20060101ALI20180226BHEP Ipc: A01N 37/04 20060101AFI20180226BHEP Ipc: A01P 13/02 20060101ALI20180226BHEP |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: INSTITUT DE RECHERCHE POUR LE DEVELOPPEMENT (IRD) Owner name: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE Owner name: INSTITUT ENSEIGNEMENT SUPERIEUR ET RECHERCHE EN AL Owner name: UNIVERSITE CLAUDE BERNARD LYON I |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20180912 |