WO2014170345A2 - Method for improved utilization of the production potential of transgenic plants - Google Patents
Method for improved utilization of the production potential of transgenic plants Download PDFInfo
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- WO2014170345A2 WO2014170345A2 PCT/EP2014/057667 EP2014057667W WO2014170345A2 WO 2014170345 A2 WO2014170345 A2 WO 2014170345A2 EP 2014057667 W EP2014057667 W EP 2014057667W WO 2014170345 A2 WO2014170345 A2 WO 2014170345A2
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- SNFOMFZEJKZXTH-UHFFFAOYSA-N CC(C)(C#N)NC(c1cc(Cl)ccc1C([NH-]c1ccc(C(C(F)(F)F)(C(F)(F)F)F)cc1C)=O)=[O-] Chemical compound CC(C)(C#N)NC(c1cc(Cl)ccc1C([NH-]c1ccc(C(C(F)(F)F)(C(F)(F)F)F)cc1C)=O)=[O-] SNFOMFZEJKZXTH-UHFFFAOYSA-N 0.000 description 1
- 0 CC(C)(C=CC=C1)C=C1NC(C1=CC=CC(C)(*)C=C1C(N(*)*)=*)=* Chemical compound CC(C)(C=CC=C1)C=C1NC(C1=CC=CC(C)(*)C=C1C(N(*)*)=*)=* 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- A01N37/34—Nitriles
-
- 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
- A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/30—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the groups —CO—N< and, both being directly attached by their carbon atoms to the same carbon skeleton, e.g. H2N—NH—CO—C6H4—COOCH3; Thio-analogues 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
- 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
- A01N63/50—Isolated enzymes; Isolated proteins
Definitions
- the invention relates to a method for improving the utilization of the production potential of transgenic plants and for controlling pests such as insects and/or nematodes.
- Transgenic plants are employed mainly to utilize the production potential of respective plant varieties in the most favourable manner, at the lowest possible input of production means.
- the aim of the genetic modification of the plants is in particular the generation of resistance in the plants to certain pests or harmful organisms or else herbicides and also to abiotic stress (for example drought, heat or elevated salt levels). It is also possible to modify a plant genetically to increase certain quality or product features, such as, for example, the content of selected vitamins or oils, or to improve certain fibre properties.
- Herbicide resistance or tolerance can be achieved, for example, by incorporating genes into the useful plant for expressing enzymes to detoxify certain herbicides, so that a relatively unimpeded growth of these plants is possible even in the presence of these herbicides for controlling broad-leaved weeds and weed grasses.
- Examples which may be mentioned are cotton varieties or maize varieties which tolerate the herbicidally active compound glyphosate (Roundup®), (Roundup Ready®, Monsanto) or the herbicides glufosinate or oxynil.
- Plant parts are to be understood as meaning all above-ground and below-ground parts and organs of plants, such as shoot, leaf, flower and root, by way of example leaves, needles, stalks, stems, flowers, fruit bodies, fruits and seed, and also roots, tubers and rhizomes.
- the plant parts also include harvested material and also vegetative and generative propagation material, for example cuttings, tubers, rhizomes, slips and seed. Summary of the invention
- One aspect refers to a method for improving the utilization of the production potential of a transgenic plant and/or for controlling/combating/treating pests, characterized in that the plant is treated with an effective amount of at least one compound of the formula (I)
- A represents individually halogen, cyano, nitro, hydroxyl, amino, Ci-Cs alkyl group, substituted Ci-Cs alkyl group having at least one substituent elected from the group consisting of halogen, hydroxy, cyano, nitro, amino, halo C1-C3 alkyl group, C1-C3 alkoxy group, halo C1-C3 alkoxy group, C1-C3 alkylthio group, halo C1-C3 alkylthio group, C1-C3 alkylsulfinyl group, halo C1-C3 alkylsulfinyl group, C1-C3 alkylsulfonyl group, halo C1-C3 alkylsulfonyl group and C1-C3 alkylthio, C1-C3 alkyl group; further, an arbitrary saturated carbon atom in said optionally substituted Ci-Cs alkyl group; n represents 0, 1 , 2,
- Ri represents hydrogen, halogen, cyano Ci-Cs alkyl or Ci-Cs haloalkyl
- R2 represents hydrogen, halogen, cyano Ci-Cs alkyl or Ci-Cs haloalkyl
- R3 represents O or S
- R represents O or S
- Y represents individually hydrogen, halogen, cyano, nitro, Ci-Ce alkyl group, halo Ci-Ce alkyl group, C2-C6 alkenyl group, halo C2-C6 alkenyl group, C2-C6 alkynyl group, halo C2-C6 alkynyl group, C3-C6 cycloalkyl group, halo C3-C6 cycloalkyl group, Ci-Ce alkoxy group, halo Ci-Ce alkoxy group, Ci-Ce alkylthio group, halo Ci-Ce alkylthio group, Ci-Ce alkylsulfinyl group, halo Ci-Ce alkylsulfinyl group, Ci-Ce alkylsulfonyl group, or halo Ci-Ce alkylsulfonyl group;
- n 0, 1, 2, 3, or 4;
- X represents a Ci-Cs alkyl group or a substituted Ci-Cs alkyl group having at least one substituent selected from the group consisting of halogen, hydroxy, cyano, nitro, amino, halo C1-C3 alkyl group, C1-C3 alkoxy group, halo C1-C3 alkoxy group [0008]
- One preferred embodiment refers to the method described above, characterized in that the compound of the formula (I) is formula (1-1):
- Hal represents F, CI, I or Br
- X' represents Ci-Ce alkyl or substituted Ci-Ce alkyl having at least one substituent selected from the group consisting of halogen, hydroxy, cyano, nitro, amino, halo C1-C3 alkyl group, preferably a Ci-C6 cyanoalkyl;
- A' represents C1-C3 alkyl, C1-C3 haloalkyl, halogen, preferably methyl, halomethyl, ethyl or haloethyl, more preferably methyl or ethyl; n represents 0, 1 , 2, 3 or 4, preferably 0, 1 or 2, more preferably 1.
- One preferred embodiment refers to the method described above, characterized in that the compound of the formula (I) is selected from the group consisting of compound (1-2), (1-3), (1-4) or
- One preferred embodiment refers to the method described above, characterized in that the compound of the formula (I) is compound (1-5).
- transgenic plant contains at least one cry-gene or a cry-gene fragment coding for a Bt toxin.
- transgenic plant is a vegetable plant, maize plant, soya bean plant, cotton plant, tobacco plant, rice plant, sugar beet plant, oilseed rape plant or potato plant.
- One preferred embodiment refers to the method described above, characterized in that the use form of the compound of the formula (I) is present in a mixture with at least one mixing partner.
- One preferred embodiment refers to the method described above, characterized in that the Bt toxin of a Bt-plant is encoded by a bt-gene or fragment thereof comprising event MON87701.
- Another aspect refers to a synergistic composition
- a synergistic composition comprising a Bt toxin and a compound of formula (I) as described above.
- One preferred embodiment refers to said synergistic composition, characterized in that the Bt toxin is encoded by a cry gene or a cry-gene fragment selected from the group consisting of cryl , cry2, cry3, cry 5 and cry 9.
- One preferred embodiment refers to said synergistic composition, characterized in that the Bt toxin is encoded by a cry gene or a cry-gene fragment selected from the group consisting of especially preferred are crylAb, crylAc, cry3A, cry3B and cry9C.
- One preferred embodiment refers to said synergistic composition, characterized in that the Bt toxin is encoded by a cry gene or a cry-gene fragment selected from the subgroup cryl A, preferably cryl Aa, cryl Ab, cryl Ac or a hybrid thereof (e.g., a hybrif of cryl Ac and cryl Ab).
- One preferred embodiment refers to said synergistic composition, characterized in that the Bt toxin is encoded by a bt-gene or fragment thereof comprising event MON87701.
- a Bt plant preferably a Bt-soybean plant comprising event MON87701 or a Bt-soybean plant comprising event MON87701 and MON89788, charcterized in that at least 0.00001 g of a compound of formula (I) is attached to it.
- A represents individually halogen, cyano, nitro, hydroxyl, amino, Ci-Cs alkyl group, substituted Ci- C8 alkyl group having at least one substituent elected from the group consisting of halogen, hydroxy, cyano, nitro, amino, halo C1-C3 alkyl group, C1-C3 alkoxy group, halo C1-C3 alkoxy group, C1-C3 alkylthio group, halo C1-C3 alkylthio group, C1-C3 alkylsulfinyl group, halo C1-C3 alkylsulfinyl group, Ci- C3 alkylsulfonyl group, halo C1-C3 alkylsulfonyl group and C1-C3 alkylthio, C1-C3 alkyl group; further, an arbitrary saturated carbon atom in said optionally substituted Ci-Cs alkyl group; n represents 0, 1 , 2, 3
- Ri represents hydrogen, halogen, cyano Ci-Cs alkyl or Ci-Cs haloalkyl
- R2 represents hydrogen, halogen, cyano Ci-Cs alkyl or Ci-Cs haloalkyl
- R3 represents O or S; R represents O or S;
- X represents a Ci-Cs alkyl group or a substituted Ci-Cs alkyl group having at least one substituent selected from the group consisting of halogen, hydroxy, cyano, nitro, amino, halo C1-C3 alkyl group, Ci- C3 alkoxy group, halo C1-C3 alkoxy group and their insecticidal action are known from the prior art (see, e.g., EP 0 919 542, W0 2004/018410, W0 2010/012442 or WO 2012/034472).
- Hal represents F, CI, I or Br
- X' represents Ci-Ce alkyl or substituted Ci-Ce alkyl having at least one substituent selected from the group consisting of halogen, hydroxy, cyano, nitro, amino, halo C1-C3 alkyl group, preferably a Ci-Ce cyanoalkyl;
- A' represents C1-C3 alkyl, C1-C3 haloalkyl, halogen, preferably methyl, halomethyl, ethyl or haloethyl, more preferably methyl or ethyl; n represents 0, 1 , 2, 3 or 4, preferably 0, 1 or 2, more preferably 1.
- a composition comprises at least one compound of the general formula (I) selected from the group consisting of compound (1-2), (1-3), (1-4) or (1-5):
- a compound of formula (I) is selected from the group consisting of compound (1-2) or compound (1-5).
- the compound of formula (I) is compound (1-5).
- alkyl represents straight-chain or branched aliphatic hydrocarbons having 1 to 8, preferably 1 to 6, more preferably 1 to 3, carbon atoms. Suitable alkyl groups are, for example, methyl, ethyl, ⁇ -propyl, z ' -propyl, n-, iso-, sec- or teri-butyl, pentyl or hexyl. The alkyl group may be unsubstituted or is substituted by at least one of the substituents mentioned here.
- halogen or "Hal” represents fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine.
- haloalkyl represents alkyl groups having up to 8 carbon atoms in which at least one hydrogen atom has been replaced by a halogen.
- Suitable haloalkyl groups are, for example, CH 2 F, CHF 2 , CF 3 , CF 2 C1, CFC1 2 , CC1 3 , CF 2 Br, CF 2 CF 3 , CFHCF 3 , CH 2 CF 3 , CH 2 CH 2 F, CH 2 CHF 2 , CFC1CF 3 , CC1 2 CF 3 , CF 2 CH 3 , CF 2 CH 2 F, CF 2 CHF 2 , CF 2 CF 2 C1, CF 2 CF 2 Br, CFHCH 3 , CFHCHF 2 , CHFCF 3 , CHFCF 2 C1, CHFCF 2 Br, CFC1CF 3 , CC1 2 CF 3 , CF 2 CF 2 CF 3 , CH 2 CH 2 F,
- haloalkyl group may be unsubstituted (CH 2 CHFCH 3 , CH 2 CF 2 CF 3 , CF 2 CH 2 CF 3 , CF 2 CF 2 CH 3 , CHFCF 2 CF 3 , CF 2 CHFCF 3 , CF 2 CF 2 CHF 2 , CF 2 CF 2 CH 2 F, CF 2 CF 2 CF 2 C1, CF 2 CF 2 CF 2 Br, l,2,2,2-tetrafluoro-l-(trifluoromethyl)ethyl, 2,2,2-trifluoro- 1 -(trifluoromethyl)ethyl, pentafluoroethyl, 1 -(difluoromethyl)- 1 ,2,2,2-tetrafluoroethyl, 2-bromo- 1,2,2- trifluoro-l-(trifluoromethyl)ethyl, l-(difluoromethyl)-2,2,2-trifluoroethy
- Production potential refers to the yield of a transgenic plant under specific conditions. "Improving the utilization of the production potential of transgenic plants” thus refers to an increase of yield under unfavorable environmental conditions such as use of herbicides, drought stress, cold stress, stress induced by insects, nematodes, or fungis etc. compared to the yoeld of such plants under the same conditions without the use of the compounds of formula (I) as described herein.
- the method can also be used for an increased controll/an increased treatment of pests such as insects and/or nematodes.
- pests such as insects and/or nematodes.
- the combination of a transgenic plant such as a Bt-plant and a compound of formula (I) can show better treatment/control/combating of insects and/or nematodes compared to the expected effect.
- transgenic plants in particular useful plants, are treated with compounds of the formula (I) to increase agricultural productivity and/or to control and/or to combat pests, especially nematodes and insects.
- the invention refers to a method for combating pests by treating transgenic plants, preferably insect-resistant transgenic plant such as Bt-plants or Vip-plants with a compound of formula (I), preferably with a compound of formula (1-5).
- GMOs genetically modified organisms
- plants e.g. plants or seeds
- transgenic plants are plants of which a heterologous gene has been stably integrated into genome.
- heterologous gene essentially means a gene which is provided or assembled outside the plant and when introduced in the nuclear, chloroplastic or mitochondrial genome gives the transformed plant new or improved agronomic or other properties by expressing a protein or polypeptide of interest or by downregulating or silencing other gene(s) which are present in the plant (using for example, antisense technology, cosuppression technology, RNA interference - RNAi - technology or microRNA - miRNA - technology).
- a heterologous gene that is located in the genome is also called a transgene.
- a transgene that is defined by its particular location in the plant genome is called a transformation or transgenic event.
- the treatment according to the invention may also result in superadditive (“synergistic") effects.
- superadditive for example, reduced application rates and/or a widening of the activity spectrum and/or an increase in the activity of the active compounds and compositions which can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, bigger fruits, larger plant height, greener leaf color, earlier flowering, higher quality and/or a higher nutritional value of the harvested products, higher sugar concentration within the fruits, better storage stability, increased combating of pests, especially nematodes and insects and/or processability of the harvested products are possible, which exceed the effects which were actually to be expected.
- the active compound combinations according to the invention may also have a strengthening effect in plants. Accordingly, they are also suitable for mobilizing the defense system of the plant against attack by unwanted microorganisms. This may, if appropriate, be one of the reasons of the enhanced activity of the combinations according to the invention, for example against fungi.
- Plant-strengthening (resistance- inducing) substances are to be understood as meaning, in the present context, those substances or combinations of substances which are capable of stimulating the defense system of plants in such a way that, when subsequently inoculated with unwanted microorganisms, the treated plants display a substantial degree of resistance to these microorganisms.
- the substances according to the invention can be employed for protecting plants against attack by the abovementioned pathogens within a certain period of time after the treatment.
- the period of time within which protection is effected generally extends from 1 to 10 days, preferably 1 to 7 days, after the treatment of the plants with the active compounds.
- Plants and plant cultivars which are preferably to be treated according to the invention include all plants which have genetic modified material which impart particularly advantageous, useful traits to these plants (whether obtained by breeding and/or biotechnological means).
- Plants and plant cultivars which are also preferably to be treated according to the invention are resistant against one or more biotic stresses, i.e. said plants show a better defense against animal and microbial pests, such as against nematodes, insects, mites, phytopathogenic fungi, bacteria, viruses and/or viroids.
- Examples of nematode or insect resistant plants are described in e.g. U.S. Patent Applications 11/765,491, 11/765,494, 10/926,819, 10/782,020, 12/032,479, 10/783,417, 10/782,096, 11/657,964, 12/192,904, 11/396,808, 12/166,253, 12/166,239, 12/166,124, 12/166,209, 11/762,886, 12/364,335, 11/763,947, 12/252,453, 12/209,354, 12/491,396, 12/497,221, 12/644,632, 12/646,004, 12/701,058, 12/718,059, 12/721,595, 12/638,591, and in WO 11/002992, WO 11/014749, WO 11/103247, WO 11/103248, WO 12/135436, WO 12/135501. [0042] Examples of plants resistant to other
- Plants and plant cultivars which may also be treated according to the invention are those plants which are resistant to one or more abiotic stresses.
- Abiotic stress conditions may include, for example, drought, cold temperature exposure, heat exposure, osmotic stress, flooding, increased soil salinity, increased mineral exposure, ozone exposure, high light exposure, limited availability of nitrogen nutrients, limited availability of phosphorus nutrients, shade avoidance.
- Plants and plant cultivars which may also be treated according to the invention are those plants characterized by enhanced yield characteristics. Increased yield in said plants can be the result of, for example, improved plant physiology, growth and development, such as water use efficiency, water retention efficiency, improved nitrogen use, enhanced carbon assimilation, improved photosynthesis, increased germination efficiency, inproved combating of insects and accelerated maturation.
- Yield can furthermore be affected by improved plant architecture (under stress and non-stress conditions), including but not limited to, early flowering, flowering control for hybrid seed production, seedling vigor, plant size, internode number and distance, root growth, seed size, fruit size, pod size, pod or ear number, seed number per pod or ear, seed mass, enhanced seed filling, reduced seed dispersal, reduced pod dehiscence and lodging resistance.
- Further yield traits include seed composition, such as carbohydrate content, protein content, oil content and composition, nutritional value, reduction in anti-nutritional compounds, improved processability and better storage stability.
- ASR36 Scotts stolonifera US 2006- phosphate synthase (EPSPS) encoding gene
- EPSPS Internation synthase
- NPTII encoding gene from E. coli was L. (Tobacco)
- BT17 Bacillus thuringiensis (subsp. Tenebrionis). L. (Potato) BT18,
- PLRV virus virus
- Aventis Brassica viridochromogenes an aerobic soil bacteria.
- PPT normally acts to inhibit glutamine
- Acetylated PPT is inactive.
- AHAS acetohydroxyacid synthase
- MIR604 (OECD unique identifier: SYN-
- MIR60 Syngenta (Liberty) is derived from BT11, which Zea mays
- 4 x Seeds, Inc. contains the crylAb gene from Bacillus L. (Maize)
- PAT phosphinothricin N-acetyltransferase
- Corn rootworm-resistance is derived from
- MIR604 which contains the mcry3A gene
- glyphosate herbcicide is derived from GA21
- PAT phosphinothricin acetyltransferase
- NK603 OECD unique identifier
- MON8 Monsanto strain EG4691 Glyphosate tolerance derived Zea mays WO 8017 Company by inserting a 5-enolpyruvylshikimate-3- L. (Maize) 2009111263 phosphate synthase (EPSPS) encoding gene
- MON8 Monsanto thuringiensis providing resistance to number Zea mays WO 9034 Company of lepidopteran pests; nsect resistance L. (Maize) 2005/059103
- MON89034 (OECD identifier: MON- 89034-3) and MON88017 (OECD
- Monsanto Lepiopteran insects is derived from two Zea mays WO MON8 Company crygenes present in MON89043.
- Corn L. (Maize) 2007140256 8017 rootworm resistance is derived from a single
- cry genes and glyphosate tolerance is
- EPSPS 5-enolpyruvylshikimate-3- phosphate synthase
- insects is derived from two crygenes present
- herbcicide is derived from NK603.
- MON- Company lines NK603 (OECD identifier: MON- L. (Maize)
- Zaden BV 074492 RM3-6 the bar gene from S. hygroscopicus, which ory
- SAM S- adenosylmethionine
- CMV Cucumber mosiac virus
- WMV mosaic virus 2 resistant squash
- ALS acetolactate synthase
- ALS acetolactate synthase
- cry IF gene from Bacillus
- crylAc gene from Bacillus thuringiensis and hirsutum 1808 Inc.
- VIP3A Insect resistance
- US2009181399 hirsutum WO200403998 2 Seeds, Inc.
- Calgene (Umbellularia californica).
- MON- with MON1445 (OECD identifier: MON- 01445- 01445-2).
- GBH61 produced by inserting 2mepsps gene into WO
- JOPLI disease (fungal) resistance (trichothecene 3- WO201007621 Participati Wheat
- Kefeng NAT event containing two insect-resistant genes Oryza
- MS45 anther-specific 5126 (Zea mays)
- ZM-AAl polygalacturonase 47 (Zea mays)
- DSRED2 35S (Cauliflower Mosaic Virus)
- the aad-1 gene confers tolerance
- CRY3A metallotionin-like gene
- coding sequence modified to include a
- MON 87427 comprises the promoter
- P-e35S operably linked to
- CP4 EPSPS protein operably linked to a
- T-NOS nopaline synthase
- Agrobacterium tumefaciens Agrobacterium tumefaciens .
- Ph4a748 ABBC sequence including the
- Ph4a748 sequence
- h3At first intron of gene II of the histone
- histone H4 gene of Arabidopsis thaliana A novel aad-12 transformation event for
- pDAB4468-0416 herbicide tolerance in soybean plants - referred to herein as pDAB4468-0416.
- the invention provides DNA compositions
- the invention provides DNA compositions
- Y The invention provides plants comprising
- transgenic event MON 88302 that exhibit
- invention also provides seeds, plant parts,
- the invention also 6
- Brassica napus plant Brassica napus plant.
- soybean plants comprising a soybean
- This invention relates to soybean event
- This invention also relates in part
- the event sequence is a sequence of the event sequence
- This invention further relates in part to 9A1
- This invention relates in part to soybean
- event pDAB8264.44.06.1 includes a
- event sequence can be "stacked" with other
- the present invention provides a transgenic
- soybean comprising event MON87712 that
- probes and primers for use in a sample in a sample, probes and primers for use in a sample, probes and primers for use in a sample, probes and primers for use in a sample, probes and primers for use in a sample, probes and primers for use in
- This invention relates to soybean event
- invention includes a novel aad-12
- ENCES invention also relates in part to plant 4A2
- said event /
- polynucleotide sequence can be "stacked"
- invention provides Brassica plants having a
- chromosomal location comprises
- compositions for the identification are provided.
- invention provides Brassica plants having a
- PIONEER chromosomal location comprises
- compositions for the identification are provided.
- This invention relates in part to soybean
- event pDAB8264.44.06.1 includes a
- event sequence can be "stacked" with other
- This invention further 8A2
- This invention relates to soybean event
- This invention also relates in part
- the event sequence is a sequence of the event sequence
- This invention further relates in part to 2A2
- MON8 MONSAN The invention provides cotton event MON cotton WO2012/13480 8701 TO 88701, and plants, plant cells, seeds, plant 8A1
- LLC provides polynucleotides specific for event
- MON 88701 plants, plant cells, seeds,
- the present invention provides a transgenic alfalfa WO201300355 2 TO alfalfa event KK179-2.
- the invention also 8A1
- TECHNO provides cells, plant parts, seeds, plants,
- the invention further provides
- LLC also relates in part to methods of controlling
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- Engineering & Computer Science (AREA)
- Zoology (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Biotechnology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Microbiology (AREA)
- Virology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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Abstract
Description
Claims
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BR112015026235A BR112015026235A2 (en) | 2013-04-19 | 2014-04-15 | method for improving utilization of the potential of transgenic plant production involving the application of a phthaldiamide derivative |
| US14/784,047 US20160058001A1 (en) | 2013-04-19 | 2014-04-15 | Method for improved utilization of the production potential of transgenic plants |
| CA2909725A CA2909725A1 (en) | 2013-04-19 | 2014-04-15 | Method for improved utilization of the production potential of transgenic plants |
| CN201480034938.3A CN105555135B (en) | 2013-04-19 | 2014-04-15 | It is related to the method utilized for improvement to genetically modified plants production potential of phthaloyl amide derivatives application |
| MX2015014346A MX358633B (en) | 2013-04-19 | 2014-04-15 | Method for improved utilization of the production potential of transgenic plants involving the application of a phthaldiamide derivative. |
| ZA2015/07411A ZA201507411B (en) | 2013-04-19 | 2015-10-06 | Method for improved utilization of the production potential of transgenic plants involving the application of a phthaldiamide derivative |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13164466 | 2013-04-19 | ||
| EP13164466.8 | 2013-04-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2014170345A2 true WO2014170345A2 (en) | 2014-10-23 |
| WO2014170345A3 WO2014170345A3 (en) | 2015-01-08 |
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ID=48128208
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2014/057667 Ceased WO2014170345A2 (en) | 2013-04-19 | 2014-04-15 | Method for improved utilization of the production potential of transgenic plants |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20160058001A1 (en) |
| CN (1) | CN105555135B (en) |
| AR (1) | AR095867A1 (en) |
| BR (1) | BR112015026235A2 (en) |
| CA (1) | CA2909725A1 (en) |
| MX (1) | MX358633B (en) |
| WO (1) | WO2014170345A2 (en) |
| ZA (1) | ZA201507411B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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- 2014-04-15 AR ARP140101604A patent/AR095867A1/en unknown
- 2014-04-15 CN CN201480034938.3A patent/CN105555135B/en not_active Expired - Fee Related
- 2014-04-15 WO PCT/EP2014/057667 patent/WO2014170345A2/en not_active Ceased
- 2014-04-15 CA CA2909725A patent/CA2909725A1/en not_active Abandoned
- 2014-04-15 MX MX2015014346A patent/MX358633B/en active IP Right Grant
- 2014-04-15 US US14/784,047 patent/US20160058001A1/en not_active Abandoned
-
2015
- 2015-10-06 ZA ZA2015/07411A patent/ZA201507411B/en unknown
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| US20160058001A1 (en) | 2016-03-03 |
| MX2015014346A (en) | 2015-12-07 |
| MX358633B (en) | 2018-08-28 |
| ZA201507411B (en) | 2017-01-25 |
| CA2909725A1 (en) | 2014-10-23 |
| WO2014170345A3 (en) | 2015-01-08 |
| AR095867A1 (en) | 2015-11-18 |
| CN105555135B (en) | 2018-06-15 |
| CN105555135A (en) | 2016-05-04 |
| BR112015026235A2 (en) | 2017-10-10 |
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