EP3664612A1 - Composition a base de polyol(s) et de sterol(s) pour usage dans le domaine agricole - Google Patents
Composition a base de polyol(s) et de sterol(s) pour usage dans le domaine agricoleInfo
- Publication number
- EP3664612A1 EP3664612A1 EP18755875.4A EP18755875A EP3664612A1 EP 3664612 A1 EP3664612 A1 EP 3664612A1 EP 18755875 A EP18755875 A EP 18755875A EP 3664612 A1 EP3664612 A1 EP 3664612A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- use according
- plant
- sterol
- polyols
- nonionic surfactant
- 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.)
- Pending
Links
- 229930182558 Sterol Natural products 0.000 title claims abstract description 31
- 150000003432 sterols Chemical class 0.000 title claims abstract description 31
- 235000003702 sterols Nutrition 0.000 title claims abstract description 31
- 229920005862 polyol Polymers 0.000 title claims abstract description 24
- 150000003077 polyols Chemical class 0.000 title claims abstract description 24
- 239000000203 mixture Substances 0.000 title claims description 59
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 28
- 230000036579 abiotic stress Effects 0.000 claims abstract description 12
- 230000012010 growth Effects 0.000 claims abstract description 7
- 230000004790 biotic stress Effects 0.000 claims abstract description 6
- 230000001737 promoting effect Effects 0.000 claims abstract 2
- 241000196324 Embryophyta Species 0.000 claims description 73
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- KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 claims description 43
- SZYSLWCAWVWFLT-UTGHZIEOSA-N [(2s,3s,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)-2-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]methyl octadecanoate Chemical compound O([C@@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@]1(COC(=O)CCCCCCCCCCCCCCCCC)O[C@H](CO)[C@@H](O)[C@@H]1O SZYSLWCAWVWFLT-UTGHZIEOSA-N 0.000 claims description 40
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
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- NLQLSVXGSXCXFE-UHFFFAOYSA-N sitosterol Natural products CC=C(/CCC(C)C1CC2C3=CCC4C(C)C(O)CCC4(C)C3CCC2(C)C1)C(C)C NLQLSVXGSXCXFE-UHFFFAOYSA-N 0.000 claims description 9
- OILXMJHPFNGGTO-UHFFFAOYSA-N (22E)-(24xi)-24-methylcholesta-5,22-dien-3beta-ol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(C)C(C)C)C1(C)CC2 OILXMJHPFNGGTO-UHFFFAOYSA-N 0.000 claims description 7
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- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 6
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- DNVPQKQSNYMLRS-NXVQYWJNSA-N Ergosterol Natural products CC(C)[C@@H](C)C=C[C@H](C)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@@H]3CC[C@]12C DNVPQKQSNYMLRS-NXVQYWJNSA-N 0.000 claims description 3
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- DNVPQKQSNYMLRS-SOWFXMKYSA-N ergosterol Chemical compound C1[C@@H](O)CC[C@]2(C)[C@H](CC[C@]3([C@H]([C@H](C)/C=C/[C@@H](C)C(C)C)CC[C@H]33)C)C3=CC=C21 DNVPQKQSNYMLRS-SOWFXMKYSA-N 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 235000002378 plant sterols Nutrition 0.000 claims description 3
- 235000016831 stigmasterol Nutrition 0.000 claims description 3
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- BFDNMXAIBMJLBB-UHFFFAOYSA-N stigmasterol Natural products CCC(C=CC(C)C1CCCC2C3CC=C4CC(O)CCC4(C)C3CCC12C)C(C)C BFDNMXAIBMJLBB-UHFFFAOYSA-N 0.000 claims description 3
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- BQPPJGMMIYJVBR-UHFFFAOYSA-N (10S)-3c-Acetoxy-4.4.10r.13c.14t-pentamethyl-17c-((R)-1.5-dimethyl-hexen-(4)-yl)-(5tH)-Delta8-tetradecahydro-1H-cyclopenta[a]phenanthren Natural products CC12CCC(OC(C)=O)C(C)(C)C1CCC1=C2CCC2(C)C(C(CCC=C(C)C)C)CCC21C BQPPJGMMIYJVBR-UHFFFAOYSA-N 0.000 claims description 2
- VGSSUFQMXBFFTM-UHFFFAOYSA-N (24R)-24-ethyl-5alpha-cholestane-3beta,5,6beta-triol Natural products C1C(O)C2(O)CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 VGSSUFQMXBFFTM-UHFFFAOYSA-N 0.000 claims description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 2
- CHGIKSSZNBCNDW-UHFFFAOYSA-N (3beta,5alpha)-4,4-Dimethylcholesta-8,24-dien-3-ol Natural products CC12CCC(O)C(C)(C)C1CCC1=C2CCC2(C)C(C(CCC=C(C)C)C)CCC21 CHGIKSSZNBCNDW-UHFFFAOYSA-N 0.000 claims description 2
- XYTLYKGXLMKYMV-UHFFFAOYSA-N 14alpha-methylzymosterol Natural products CC12CCC(O)CC1CCC1=C2CCC2(C)C(C(CCC=C(C)C)C)CCC21C XYTLYKGXLMKYMV-UHFFFAOYSA-N 0.000 claims description 2
- ARYTXMNEANMLMU-UHFFFAOYSA-N 24alpha-methylcholestanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(C)C(C)C)C1(C)CC2 ARYTXMNEANMLMU-UHFFFAOYSA-N 0.000 claims description 2
- FPTJELQXIUUCEY-UHFFFAOYSA-N 3beta-Hydroxy-lanostan Natural products C1CC2C(C)(C)C(O)CCC2(C)C2C1C1(C)CCC(C(C)CCCC(C)C)C1(C)CC2 FPTJELQXIUUCEY-UHFFFAOYSA-N 0.000 claims description 2
- OILXMJHPFNGGTO-NRHJOKMGSA-N Brassicasterol Natural products O[C@@H]1CC=2[C@@](C)([C@@H]3[C@H]([C@H]4[C@](C)([C@H]([C@@H](/C=C/[C@H](C(C)C)C)C)CC4)CC3)CC=2)CC1 OILXMJHPFNGGTO-NRHJOKMGSA-N 0.000 claims description 2
- SGNBVLSWZMBQTH-FGAXOLDCSA-N Campesterol Natural products O[C@@H]1CC=2[C@@](C)([C@@H]3[C@H]([C@H]4[C@@](C)([C@H]([C@H](CC[C@H](C(C)C)C)C)CC4)CC3)CC=2)CC1 SGNBVLSWZMBQTH-FGAXOLDCSA-N 0.000 claims description 2
- BKLIAINBCQPSOV-UHFFFAOYSA-N Gluanol Natural products CC(C)CC=CC(C)C1CCC2(C)C3=C(CCC12C)C4(C)CCC(O)C(C)(C)C4CC3 BKLIAINBCQPSOV-UHFFFAOYSA-N 0.000 claims description 2
- BTEISVKTSQLKST-UHFFFAOYSA-N Haliclonasterol Natural products CC(C=CC(C)C(C)(C)C)C1CCC2C3=CC=C4CC(O)CCC4(C)C3CCC12C BTEISVKTSQLKST-UHFFFAOYSA-N 0.000 claims description 2
- LOPKHWOTGJIQLC-UHFFFAOYSA-N Lanosterol Natural products CC(CCC=C(C)C)C1CCC2(C)C3=C(CCC12C)C4(C)CCC(C)(O)C(C)(C)C4CC3 LOPKHWOTGJIQLC-UHFFFAOYSA-N 0.000 claims description 2
- 241001465754 Metazoa Species 0.000 claims description 2
- CAHGCLMLTWQZNJ-UHFFFAOYSA-N Nerifoliol Natural products CC12CCC(O)C(C)(C)C1CCC1=C2CCC2(C)C(C(CCC=C(C)C)C)CCC21C CAHGCLMLTWQZNJ-UHFFFAOYSA-N 0.000 claims description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 2
- LGJMUZUPVCAVPU-JFBKYFIKSA-N Sitostanol Natural products O[C@@H]1C[C@H]2[C@@](C)([C@@H]3[C@@H]([C@H]4[C@@](C)([C@@H]([C@@H](CC[C@H](C(C)C)CC)C)CC4)CC3)CC2)CC1 LGJMUZUPVCAVPU-JFBKYFIKSA-N 0.000 claims description 2
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- OILXMJHPFNGGTO-ZAUYPBDWSA-N brassicasterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)/C=C/[C@H](C)C(C)C)[C@@]1(C)CC2 OILXMJHPFNGGTO-ZAUYPBDWSA-N 0.000 claims description 2
- ARYTXMNEANMLMU-ATEDBJNTSA-N campestanol Chemical compound C([C@@H]1CC2)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CC[C@@H](C)C(C)C)[C@@]2(C)CC1 ARYTXMNEANMLMU-ATEDBJNTSA-N 0.000 claims description 2
- 235000000431 campesterol Nutrition 0.000 claims description 2
- SGNBVLSWZMBQTH-PODYLUTMSA-N campesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](C)C(C)C)[C@@]1(C)CC2 SGNBVLSWZMBQTH-PODYLUTMSA-N 0.000 claims description 2
- 235000013339 cereals Nutrition 0.000 claims description 2
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- QBSJHOGDIUQWTH-UHFFFAOYSA-N dihydrolanosterol Natural products CC(C)CCCC(C)C1CCC2(C)C3=C(CCC12C)C4(C)CCC(C)(O)C(C)(C)C4CC3 QBSJHOGDIUQWTH-UHFFFAOYSA-N 0.000 claims description 2
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- CAHGCLMLTWQZNJ-RGEKOYMOSA-N lanosterol Chemical compound C([C@]12C)C[C@@H](O)C(C)(C)[C@H]1CCC1=C2CC[C@]2(C)[C@H]([C@H](CCC=C(C)C)C)CC[C@@]21C CAHGCLMLTWQZNJ-RGEKOYMOSA-N 0.000 claims description 2
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- LGJMUZUPVCAVPU-HRJGVYIJSA-N stigmastanol Chemical compound C([C@@H]1CC2)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]2(C)CC1 LGJMUZUPVCAVPU-HRJGVYIJSA-N 0.000 claims description 2
- HCXVJBMSMIARIN-PHZDYDNGSA-N stigmasterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)/C=C/[C@@H](CC)C(C)C)[C@@]1(C)CC2 HCXVJBMSMIARIN-PHZDYDNGSA-N 0.000 claims description 2
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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
- A01N45/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
Definitions
- plants have intrinsic means to defend themselves.
- biotic stress denotes stress that comes from living organisms such as pathogenic microorganisms, for example fungi, bacteria, viruses, but also nematodes, insects, mites herbivores, or parasitic plants.
- the term “elicitor” denotes a substance that is recognized by plants and activates a signaling cascade that leads the plant to mobilize its defenses.
- An elicitor is a substance capable, under certain conditions, of stimulating natural defense mechanisms. These natural defenses are directed against bio-aggressors (diseases, pests).
- abiotic stress denotes stress that results from the non-living such as water stress, salt stress, flooding stress, wind, heat stress ( cold, frost, heat shock), stress due to ultraviolet (solar radiation), stress related to nutrient deficiencies, stress injury, oxidative stress, osmotic stress, chemical stress.
- bio stimulant or plant biostimulant is defined in accordance with the study commissioned by the Center for Studies and Foresight of the Ministry of Agriculture, Agri-Food and Forestry (MAAF) and financed by MAAF under Program 215 (Contract No. SSP-2013-094, Final Report - December 2014) entitled "Agricultural Stimulation Products to Improve the Biological Functionality of Soils and Plants" - Review of Available Knowledge and strategic recommendations ".
- a biostimulant is: "A material that contains a substance (s) and / or microorganism” whose function, when applied to plants or the rhizosphere, is to stimulate natural processes to improve / benefit the nutrient absorption, nutrient efficiency, tolerance to abiotic stress, and crop quality, regardless of the nutrient content of the biostimulant. ". (EBIC, 2014).
- biostimulants currently used are microorganisms, plant extracts or synthetic chemical compounds. However, the effectiveness of these biostimulants is not optimal.
- the first problem to be solved by the invention is that of developing compositions that contribute to the biostimulation of plants.
- the goal is to develop alternative compositions that are able to promote plant resistance to abiotic stress more effectively than the compounds of the prior art.
- the goal is to stimulate certain natural mechanisms to improve / benefit nutrient absorption, nutrient efficiency, tolerance to abiotic stress, and crop quality with, in the case of nutrients in particular, for direct or indirect effect, the growth of the plant, and thus the improvement of the yield.
- a second problem to be solved by the invention is that of developing compositions that are capable of stimulating certain natural mechanisms to improve tolerance to biotic stress.
- a third problem to be solved by the invention is that of developing compositions that make it possible to limit the quantity applied of plant protection products while retaining the same effect as the standard doses.
- the third objective is to develop a composition that can be used as an adjunct phytosanitary composition in particular.
- the Applicant has found that these objectives were achieved by combining a nonionic surfactant derived from polyols and a sterol hereinafter referred to as "the composition or composition of the invention".
- the invention firstly relates to the use of at least one nonionic surfactant derived from polyols and a sterol as bio stimulant of a plant hereinafter referred to as "the composition or composition of the invention ".
- the composition of the invention is used to promote germination.
- the composition of the invention is used to promote the elongation of the main roots and the multiplication and elongation of the secondary roots, in other words the growth of the main and secondary roots.
- the composition of the invention is used to promote flowering.
- the composition of the invention is used to promote the resistance of plants against abiotic stresses.
- the composition is used in particular to limit the loss of stomatal water, that is to say to allow the plant to better withstand water stress.
- the composition of the invention has a particular effect on the activation of the acquired systemic resistance system.
- the composition acts not only to stimulate natural defense mechanisms against biotic stress but also to promote resistance to abiotic stress.
- composition of the invention is not a product with specific activity makes it possible to envisage broad-spectrum use on a large number of crops, which can save minor crops for which the number of phytosanitary products available is almost -no.
- the Applicant has found that the composition of the invention makes it possible to improve the spreading of liquids on the sheet, in particular of an aqueous solution. This phenomenon results from the reduction of the surface tension of the sheet in contact with the composition of the invention. It follows that by improving the spreading of a solution containing an active product with respect to the plant, the necessary amount of product is reduced for an equivalent effect.
- the invention also relates to the use of the composition as an adjuvant of a solution containing an active product vis-à-vis the plant.
- biocontrol products are intended to prevent the action of plant pests and are chosen in particular from fungicides, fungicides, bactericides, bacteriostats, insecticides, acaricides, parasiticides, nematicides, taupicides or repellents for birds or game, one or more substances intended to destroy undesirable plants or to slow down their chosen growth, in particular among herbicides or antidicotyledons.
- composition of the invention thus constitutes an economy for the farmer that reduces the number of applications (of field trips).
- composition of the invention When used in combination with an active product vis-à-vis the plant as described above, it is simultaneously or sequentially.
- This type of synergy corresponds in all respects to the demands of society in terms of phytosanitary products:
- composition according to the invention may be applied after emergence or before emergence, on the seed, the seedling (juvenile stage prior to flowering), the plant during flowering (before, during or after pollination), the plant after fertilization, the plant being fruited, the fruit, flowers, leaves, stems, roots or soil, before or after sowing.
- composition may be in practice applied by spraying, watering, addition to a hydroponic culture medium, immersion of the seed and / or coating of the seed.
- the plant is chosen from the group comprising Dicotyledonous and Monocotyledonous plants, advantageously in the group comprising cereals, root and tuber crops, saccharifers, legumes, nut plants, oleaginous plants. or oleaginous plants, vegetable crops, fruit trees, aromatic plants and spices, flowering plants, or industrial crop plants for the production of a raw material for processing.
- the nonionic surfactant derived from polyols is chosen from the group comprising sugar and fatty acid esters, alkyl-mono- and alkyl-poly-glucosides, alkyl-aliphatic esters and mono- and alkyl-poly-glucosides and fatty acids and N-alkylglucamides, especially N-methylglucamides.
- the nonionic surfactant derived from polyols is chosen from the group comprising sucrose esters, sorbitan esters and glucose esters. According to one particular embodiment, the nonionic surfactant derived from polyols is ethoxylated or non-ethoxylated.
- the nonionic surfactant derived from polyols is sucrose stearate.
- the sterol is chosen from cholesterol, plant sterols such as campesterol, beta-sitosterol, stigmasterol, brassicasterol, campestanol, sitostanol, animal sterols such as lanosterol or sterols. yeasts or fungi such as ergosterol.
- the sterol is beta-sitosterol.
- the nonionic surfactant derived from polyols and the sterol are in solution, advantageously in the form of an aqueous solution, comprising 0.01% to 80%, preferably 0.05% to 30%, so still more preferably 0.75% to 3% by weight of the nonionic surfactant solution derived from polyols and sterol.
- the use according to the invention of at least one nonionic surfactant derived from polyols corresponding to sucrose stearate and the sterol corresponding to beta-sitosterol is advantageousously, the use according to the invention of at least one nonionic surfactant derived from polyols corresponding to sucrose stearate and the sterol corresponding to beta-sitosterol.
- the invention relates to a composition
- a composition comprising sucrose stearate as a nonionic surfactant derived from polyols and, as sterol, at least beta-sistosterol or stigmasterol or cholesterol or ergosterol or a mixture thereof.
- the beta-sistosterol is between 1 and 99% by weight of the composition and the sucrose stearate is between 99 and 1% by weight of the composition, preferably the beta-sistosterol is between 40 and 1% and the sucrose stearate is between 60 and 99% by weight of the composition.
- Figure 1 shows the comparison of the port of parsley plants after watering with water or a solution comprising the combination of sucrose stearate and beta-sitosterol according to the invention.
- FIG. 2 represents the quantification of salicylic acid in parsley plants 2, 4 or 8 hours after watering with water or a solution comprising the combination of sucrose stearate and beta-sitosterol according to the invention.
- FIGS. 3 and 4 represent the effect of a control solution (water, C) or of a solution comprising 1%, 3% or 10% of the combination of sucrose stearate and beta-sitosterol according to the invention (1 %, 3% and 10%>) on the rupture of AArabidopsis thaliana seeds seeded in stratified ( Figure 3) or non-stratified ( Figure 4).
- FIGS. 5 and 6 show the effect of a control solution (water, C) or of a solution comprising 1%, 3% or 10% of the combination of sucrose stearate and beta-sitosterol according to the invention (1 %, 3% and 10%) on the emergence of the radicle of Arabidopsis thaliana seeds grown in stratified ( Figure 5) or non-stratified ( Figure 6).
- FIGS. 5 and 6 show the effect of a control solution (water, C) or of a solution comprising 1%, 3% or 10% of the combination of sucrose stearate and beta-sitosterol according to the invention (1 %, 3% and 10%) on the emergence of the radicle of Arabidopsis thaliana seeds grown in stratified ( Figure 5) or non-stratified ( Figure 6).
- FIGS. 5 and 6 show the effect of a control solution (water, C) or of a solution comprising 1%, 3% or 10% of the combination of sucrose stearate and beta-si
- FIG. 7 and 8 show the effect of a control solution (water, C) or of a solution comprising 1%, 3% or 10% of the combination of sucrose stearate and beta-sitosterol according to the invention (1 %, 3% and 10%) on the opening of cotyledons of Arabidopsis thaliana seeds grown in stratified ( Figure 7) or non-stratified ( Figure 8).
- FIG. 9 represents the seeds of Arabidopsis thaliana germinated 120 hours after treatment with water (A), a solution comprising 1% (B) or 10% (C) of the combination of sucrose stearate and beta-sitosterol according to the invention.
- Figure 10 shows the measurement of the length of the main root of Arabidopsis thaliana plants grown in the absence of sucrose stearate and beta-sitosterol (0%) or in the presence of 10 ⁇ 5 % or 10 ⁇ 3 % of sucrose stearate and beta-sitosterol in solution.
- Figure 11 shows the evaluation of the secondary root system of Arabidopsis thaliana plants grown in the absence of sucrose stearate and beta-sitosterol (0%) or in the presence of 10 ⁇ 5 % or 10 ⁇ 3 % sucrose stearate. and beta-sitosterol in solution.
- Figure 12 shows the flowering time of Arabidopsis thaliana plants treated with solutions comprising 1, 3 and 10% of the sucrose stearate and beta-sitosterol mixture or a control solution (water; H 2 O) sprayed once (1%, 3%). % and 10%) or twice at two-day intervals (1% 2X, 3% 2X and 10% 2X).
- FIG. 13 represents the evolution of the loss in stomatal water as a function of time of plants of Arabidopsis thaliana treated with water or a solution comprising the sucrose stearate and beta-sitosterol mixture according to the invention.
- EXAMPLE 1 Preparation of Combinations of a Nonionic Surfactant and a Sterol According to the Invention and Evaluation of Their Effect on the Resistance of Parsley (Petroselinum Crispum) to Abiotic Stress
- Various combinations of the invention with a plant sterol are prepared from sucrose stearate and beta-sitosterol.
- the combinations are prepared by dry blending sucrose stearate and beta-sitosterol, with proportions varying from 0 to 100% by weight relative to the total mass of the mixture, for each of these ingredients, as indicated in the following Table 1. .
- Potted parsley plants are grown in a climatic chamber under the following conditions: 23 ° C and a photoperiod of 16h day / 8h night. Before treatment all the leaves of the parsley plants are cut. The treatment of parsley plants consists of watering the pots every three days with: - 40 ml of water (Control lot)
- sample S produces the optimal effect of resistance of the plant to abiotic stress (sample S composed of 80% sucrose stearate and 20% beta-sitosterol).
- Salicylic acid is a phenolic compound that is involved in both the establishment of local resistance and general resistance (SAR) in plants.
- the application of the solutions is done by a watering at the foot of the plant (40 ml) and a spray on the leaves.
- the tested solutions are:
- treated batch B solution composed of 97% of water and 3% of sample Y, 100% of sucrose stearate and 0% of beta-sitosterol;
- treated batch C solution composed of 97% of water and 3% of the sample S, ie 80% of sucrose stearate and 20% of beta-sitosterol.
- Each batch consists of four pots.
- sucrose stearate and beta-sitosterol induces a stimulation of salicylic acid synthesis which is greater than the addition of the effects of each individual compound (sample A: beta -sitosterol + sample Y: sucrose stearate), in response to biotic stress.
- Arabidopsis thaliana seeds are placed in a climatic chamber under a photoperiod of 16h day / 8h night at 22 ° C.
- the seeds were imbibed with water (control) or with the composition according to the invention at concentrations of 1%, 3% and 10%) in water.
- the seeds were previously stratified (that is, exposed to cold) or unstratified.
- Arabidopsis thaliana plants are cultivated on agar medium in a climatic chamber under the following conditions: 23 ° C and a photoperiod of 16h day / 8h night.
- Standard agar medium is used as a control.
- Agar media containing 10 ⁇ 5 % and 10 ⁇ 3 % of the sucrose stearate and beta-sitosterol mixture according to the sample S are used to evaluate the effect of the invention on the development of the root system.
- the length of the main root and secondary roots is measured between the 2nd and 21st day post germination.
- Figure 10 shows that the main roots of plants grown in the presence of 10 "5% and 10" 3% of the mixture according to the invention is longer than for plants grown in agar medium control.
- Figure 11 shows that plants grown in agar media containing 10 "5% and 10" 3% of the mixture according to the invention have more lateral roots that are also longer. It follows from this demonstration that the mixture sucrose stearate and beta-sitosterol allows growth of the main and secondary root system. As a result, the plant is better anchored in the soil and the penetration of nutrients into the plant is more effective due to more extensive secondary root system.
- Plants Arabidopsis thaliana potted are grown according to the conditions of Example 1.
- Solutions comprising 1, 3 and 10% of the sucrose stearate and beta-sitosterol mixture according to sample S or a control solution (water, H 2 O) are sprayed once (1%, 3% and 10%) or twice at two times. days apart (1% 2X, 3% 2X and 10%> 2X), on plants 3 weeks old.
- the number of flowering plants by modalities was measured as a function of time.
- sucrose stearate and beta-sitosterol mixture according to the invention accelerates flowering to Arabidopsis thaliana.
- Plants, 4 weeks old, are treated with a foliar spray, 4 hours before the measurements are made, with water (Control) or a solution comprising 3% of the mixture sucrose stearate and beta-sitosterol according to the sample S.
- Example 7 Evaluation of the wetting effect of a non-anionic surfactant and a sterol according to the invention on Arabidopsis thaliana
- Plants Arabidopsis thaliana potted are grown according to the conditions of Example 1.
- the leaves with Arabidopsis thaliana are treated with a foliar spray, with water (Control) or a solution comprising 3% of the sucrose stearate and beta-sitosterol mixture according to the sample S.
- the number of droplets present on the leaf surface of the plant is quantified.
- the results show a decrease in the number of droplets on the Arabidopsis thaliana leaf after application of the mixture according to the invention.
- the composition according to the invention makes it possible to reduce the surface tension of the sprayed solution on the sheets and thus allows better spreading of the droplets and better adhesion of the solution to the sheet.
- results show that there is no accumulation of the solution comprising the mixture sucrose stearate and beta-sitosterol according to the invention in the ribs and axillary buds of the plant.
- sucrose stearate and beta-sitosterol makes it possible in particular to treat grasses known to be poorly wettable.
- Another advantage is the use of this mixture as an adjuvant for products that have a contact action.
- the use of the mixture according to the invention makes it possible to increase the cover of the plant and to use less product per hectare.
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
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Application Number | Priority Date | Filing Date | Title |
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FR1757557A FR3069756B1 (fr) | 2017-08-07 | 2017-08-07 | Tensioactif non ionique comme biostimulant |
FR1757558A FR3069757B1 (fr) | 2017-08-07 | 2017-08-07 | Composition a base de sterols |
PCT/FR2018/051931 WO2019030442A1 (fr) | 2017-08-07 | 2018-07-26 | Composition a base de polyol(s) et de sterol(s) pour usage dans le domaine agricole |
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EP3664612A1 true EP3664612A1 (fr) | 2020-06-17 |
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EP18755875.4A Pending EP3664612A1 (fr) | 2017-08-07 | 2018-07-26 | Composition a base de polyol(s) et de sterol(s) pour usage dans le domaine agricole |
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US (1) | US11779019B2 (pt) |
EP (1) | EP3664612A1 (pt) |
CN (1) | CN111050561B (pt) |
BR (1) | BR112020002435B1 (pt) |
MA (1) | MA49832A (pt) |
WO (1) | WO2019030442A1 (pt) |
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MA49832A (fr) | 2017-08-07 | 2020-06-17 | Elicit Plant | Composition a base de polyol(s) et de sterol(s) pour usage dans le domaine agricole |
CN113133466B (zh) * | 2020-01-19 | 2022-03-22 | 山西嘉乐农业股份有限公司 | 豆甾醇抗逆促长剂及其制备方法 |
BR112023002066A8 (pt) * | 2020-08-06 | 2024-01-02 | Institut National De Rech Pour LAgriculture LAlimentation Et LEnvironnement | Kit para tratamento de sementes |
MX2024004204A (es) | 2021-10-08 | 2024-04-23 | Elicit Plant | Composicion agricola a base de fitosterol y su uso. |
WO2024074215A1 (en) * | 2022-10-07 | 2024-04-11 | Elicit Plant | Phytosterol-based agricultural composition and their use |
EP4445732A1 (en) * | 2023-04-13 | 2024-10-16 | Elicit Plant | A preventive treatment for preserving the yields of a cultivated crop exposed to at least a thermal stress |
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JPS5157556A (en) | 1974-11-07 | 1976-05-20 | Dai Ichi Kogyo Seiyaku Co Ltd | Inenoseiikukairyo oyobi zoshuzai |
JPS61251601A (ja) | 1985-04-02 | 1986-11-08 | Norin Suisansyo Kajiyu Shikenjo | 果樹の摘花剤 |
JPS62186936A (ja) * | 1986-02-13 | 1987-08-15 | Asahi Denka Kogyo Kk | ステリン乳化乃至可溶化組成物 |
JP3313846B2 (ja) | 1993-09-24 | 2002-08-12 | 三井農林株式会社 | 植物病害防護剤 |
GB0021498D0 (en) * | 2000-09-01 | 2000-10-18 | Novartis Nutrition Ag | New formulation |
CN1450863A (zh) * | 2000-11-03 | 2003-10-22 | 孟山都技术有限公司 | 降低胆固醇的甾醇组合物、制备和使用方法 |
EP2183959A4 (en) | 2007-08-31 | 2014-06-18 | Kao Corp | METHOD FOR EQUIPPING A PLANT WITH LOAD STRENGTH |
KR101170810B1 (ko) | 2011-09-26 | 2012-08-02 | 한국화학연구원 | 베타-시토스테롤을 유효성분으로 함유하는 식물병 방제용 조성물 및 이의 용도 |
CN103563929B (zh) | 2013-10-18 | 2015-05-13 | 陕西上格之路生物科学有限公司 | 一种含有胡萝卜苷与谷甾醇的抗病毒组合物及其抗病毒应用 |
US10993443B2 (en) * | 2013-12-04 | 2021-05-04 | Newleaf Symbiotics, Inc. | Methods and compositions for improving soybean yield |
CN115710559A (zh) | 2013-12-04 | 2023-02-24 | 新叶共生有限公司 | 用于改良玉米产量的方法和组合物 |
CN106889068A (zh) | 2017-03-03 | 2017-06-27 | 山东本源生态农业科技有限公司 | 一种促进植物生根发芽的调节剂、及其制备方法和应用 |
IT201700066508A1 (it) | 2017-06-15 | 2018-12-15 | Isagro Spa | Sospensioni concentrate di fitosteroli e relativo processo di preparazione |
MA49832A (fr) | 2017-08-07 | 2020-06-17 | Elicit Plant | Composition a base de polyol(s) et de sterol(s) pour usage dans le domaine agricole |
FR3069757B1 (fr) | 2017-08-07 | 2021-07-23 | Innovi Production | Composition a base de sterols |
FR3069756B1 (fr) | 2017-08-07 | 2020-01-10 | Innovi | Tensioactif non ionique comme biostimulant |
FR3109262B1 (fr) | 2020-04-20 | 2023-03-31 | Elicit Plant | Procede de traitement preventif d’une plante cultivee pour limiter la perte de matiere seche liee a un stress abiotique et/ou biotique |
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2018
- 2018-07-26 MA MA049832A patent/MA49832A/fr unknown
- 2018-07-26 US US16/636,346 patent/US11779019B2/en active Active
- 2018-07-26 EP EP18755875.4A patent/EP3664612A1/fr active Pending
- 2018-07-26 CN CN201880051082.9A patent/CN111050561B/zh active Active
- 2018-07-26 WO PCT/FR2018/051931 patent/WO2019030442A1/fr unknown
- 2018-07-26 BR BR112020002435-0A patent/BR112020002435B1/pt active IP Right Grant
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CN111050561B (zh) | 2022-08-12 |
US20200163338A1 (en) | 2020-05-28 |
WO2019030442A1 (fr) | 2019-02-14 |
MA49832A (fr) | 2020-06-17 |
US11779019B2 (en) | 2023-10-10 |
CN111050561A (zh) | 2020-04-21 |
BR112020002435B1 (pt) | 2023-03-21 |
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Ipc: A01P 21/00 20060101ALI20240311BHEP Ipc: A01N 43/16 20060101ALI20240311BHEP Ipc: A01N 45/00 20060101AFI20240311BHEP |