WO2013162479A1 - Chemical hybridization of hermaphrodite plant species with easily soluble derivatives of oxanilic acid - Google Patents

Chemical hybridization of hermaphrodite plant species with easily soluble derivatives of oxanilic acid Download PDF

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WO2013162479A1
WO2013162479A1 PCT/SI2012/000031 SI2012000031W WO2013162479A1 WO 2013162479 A1 WO2013162479 A1 WO 2013162479A1 SI 2012000031 W SI2012000031 W SI 2012000031W WO 2013162479 A1 WO2013162479 A1 WO 2013162479A1
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Prior art keywords
seeds
plants
soluble
acid
water
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PCT/SI2012/000031
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French (fr)
Inventor
Primož TITAN
Jernej Iskra
Vladimir MEGLIČ
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Semenarna Ljubljana, D.D.
Institut Jožef Stefan
Kmetijski Institut Slovenije
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Publication of WO2013162479A1 publication Critical patent/WO2013162479A1/en

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01HNEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
    • A01H1/00Processes for modifying genotypes ; Plants characterised by associated natural traits
    • A01H1/02Methods or apparatus for hybridisation; Artificial pollination ; Fertility
    • A01H1/026Methods or apparatus for hybridisation; Artificial pollination ; Fertility by treatment with chemicals
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/18Biocides, 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
    • A01N37/30Biocides, 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
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/44Biocides, 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 nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/46N-acyl derivatives

Definitions

  • the present invention refers to a chemical way of exploiting a heterosis in commercially significant hermaphrodite plant species, preferably from the family of grasses (lat. Poaceae), especially common wheat (lat. Triticum aestivum L.), in which easily soluble or water-soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof or water-soluble preparations that contain them are used as an active chemical hybridization substance.
  • the invention further refers to a method for the production of hybrid seeds of Fi generation (the first filial generation) of commercially significant hermaphrodite plant species, especially common wheat, with chemical hybridization comprising:
  • the method of the invention provides for a simpler design of a seed crop for the production of hybrid seed, better spatial exploitation, better pollination of the female component (line AA) and a greater quantity of seeds of the desired F, generation based on the sown quantity of both parent components in comparison with the approaches used hitherto.
  • the invention refers to a method for the exploitation of a heterosis in plants with hermaphrodite florets (hereinafter referred to as hermaphrodites or hermaphrodite plant species), especially in common wheat, with a chemical induction of male sterility.
  • Heterosis presents superiority of the first filial generation (F] generation) over the parental generation, which is expressed for instance in a higher yield, lower mycotoxin content, more rational consumption of plant nutrients etc.
  • F first filial generation
  • Chemical hybridizing agents are efficient in inducing male sterility in the female component of the hybrid variety; however, their application in more general production of a hybrid seed is often too complicated due to a need to separate both parent components.
  • oxopyridazines with gametocidic activity are fenridazon (1- (4-chlorophenyl)- 1 ,4-dihydro-6-methyl-4-oxopyridazine-3-carboxylic acid) and clofencet (2-(4-chlorophenyl)-3-ethyl-2,5-dihydro-5-oxopyridazine-4-carboxylic acid).
  • the agent GENESIS ® (22.4 %) needs to be applied between the phenophases EC 32 and EC 39 (visible ligule of a flag leaf) in a dosage ranging from 1.4 kg to 2.7 kg of active substance per hectare.
  • the pollen grains of plants treated with the active substance clofencet have a wavy surface and the exine is by 80 % thinner.
  • the pollen grains are incapable of germination due to plasmolysis (United States - Environmental Protection Agency.
  • SC-2053 represents the active substance sintofen used as a commercial chemical hybridizing agent CROISOR ® 100.
  • a CROISOR ® 100 agent is applied when the length of a spike on the main stem is 14 mm to 18 mm long, with the dose of 13 1/ha to 15 1/ha (1.3 kg to 1.5 kg of active substance per hectare).
  • the pollen grains of treated plants have a wavy surface and degenerated cytoplasm (general retardation) (Wong et al., 1995).
  • water dispersions or emulsions can be prepared by dissolving an active ingredient in an organic solvent. This document does not discuss a preparation of water-soluble preparations containing easily soluble or water-soluble derivatives of oxanilic acid and/or the water-soluble salts thereof.
  • Modern chemical hybridizing agents are further developed, especially in direction of achieving better selectivity of gametocidic activity and reduced influence on the environment.
  • the purpose of the invention was to develop new environmentally friendly agents with gametocidic activity or chemical hybridizing agents and to reduce the introduction of volatile organic compounds into the environment and plants.
  • Oxanilic acid was found to be an interesting basis for the preparation of agents for chemical hybridization of the invention, as their synthesis is simple and economically favourable and the acid function moreover offers a possibility of a further functionalisation with the purpose of producing water-soluble active substances.
  • the present invention thus refers to a change in the structure of active substances in terms of their getting more easily-soluble and water-soluble, and to a preparation of water- soluble preparations that confer a more simple use for the application in the field in the form of water solutions.
  • the present invention refers to a chemical way of exploiting a heterosis in commercially significant hermaphrodite plant species, preferably from the family of grasses (lat. Poaceae), especially common wheat (lat. Triticum aestivum L.), in which easily soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof are used as an active chemical hybridization substance.
  • the invention further refers to a method for the production of hybrid seeds of F] generation of commercially significant hermaphrodite plant species, preferably hermaphrodite cereals from the family of grasses, more preferably common wheat, with chemical hybridization comprising:
  • X represents a halogen atom, such as fluorine, chlorine, bromine or iodine, or a -CN group or hydrogen or an alkyl or fluoroalkyl group, preferably a bromine atom or a -CN group;
  • Y represents a group selected from the group comprising -OH and/or -OM, wherein M represents a cation suitable for the formation of an agriculturally acceptable water-soluble salt, such as alkali metal cation, e. g. Na + or K + , or tetraalkylammonium ion, preferably Na + ;
  • alkali metal cation e. g. Na + or K +
  • tetraalkylammonium ion preferably Na + ;
  • the method of the invention can be used on commercially significant hermaphrodite plant species, preferably hermaphrodite cereals from the family of grasses (lat. Poaceae), especially common wheat (lat. Triticum aestivum L).
  • both parent components denotes the seeds of the female component (line AA) and the male component (line BB) of commercially significant hermaphrodite plant species, especially hermaphrodite cereals from the family of grasses, preferably common wheat. According to one aspect of the invention, they were selected in a way that the female and male components have a suitable delay in development, so that inflorescence of the male component (pollinator) becomes noticeable at the end of the premiotic phase or the beginning of the meiotic stage of organogenesis of the female component (synchronisation of flowering). It is herewith enabled that the active chemical hybridization substance, i. e.
  • the compound of general Formula (I) and/or its agriculturally acceptable water- soluble salt is applied onto plants of the female component in the period from the completion of the premeiotic phase of the plants of the female component and/or when the latter are in the meiotic stage of organogenesis.
  • the method of the invention is carried out on common wheat (lat. Triticum aestivum L.).
  • the active substance i. e. the compound of general Formula (I) and/or the water-soluble agriculturally acceptable salts thereof
  • the spikes on the main stem of the female component are 15-20 mm long
  • the spikes on the main stem of the male component are ⁇ 5 mm long.
  • genotypes (cultivars) of the common wheat selected from the group comprising Ficko, Guarni, Sana, Inoui, Marija, Bologna are especially applicable for the use of the invention.
  • the cultivar Ludwig of the common wheat (lat. Triticum aestivum L.) is suitable within the meaning of the invention.
  • hermaphrodite plant species preferably from the family of grasses (lat. Poaceae), especially preferably common wheat (lat. Triticum aestvum L.) by applying a chemical hybridizing agent, wherein the seeds of both parent components are sown in the form of a mixture
  • a chemical hybridizing agent wherein the seeds of both parent components are sown in the form of a mixture
  • such female component needs to be selected, under the consideration of already mentioned synchronisation of flowering of plants of both parent components, that has a determinant (i. e. gene) for resistance against a herbicide, preferably a non-selective herbicide.
  • N-phosphinomethy giycin glyphosate
  • gene cp4-epsps bar, gox
  • natural resistance an endogenous gene
  • Wheat resistant against non-selective herbicides and a method for the production thereof are disclosed in patent US 7,087,809 B2 (William, H. D. (2006) Natural herbicide resistance in wheat) and US patent application US 2009/0320151 (William, 2006, Kimberlee et al., 2009, Glyphosate-tolerant wheat genotypes).
  • a further aspect of the present invention is a method for producing a hybrid seed of F] generation of commercially significant hermaphrodite plant species, preferably common wheat, with chemical hybridization with an active substance of general Formula (I) and/or the agriculturally acceptable water-soluble salts thereof of the invention, wherein in the case of sowing seeds in the form of a mixture of both parent components, not only synchronisation of flowering of both parent components in order to prevent induction of a high percentage of male sterility in the pollinator in the phase of the chemical hybridization method is taken into consideration but moreover the seeds of both parent components are selected in a way that the female component expresses natural or genetically engineered resistance against a herbicide, preferably a non-selective herbicide, and the male component does not express such resistance.
  • Suitable herbicides used for the removal of the male component after the fertilisation of the female component are sulphonylurea herbicides, such as rimsulforon and nicosulfuron, imidazolinone based herbicides, such as imazamox, and organophosphorous herbicides, such as gluphosinate or glyphosate.
  • sulphonylurea herbicides such as rimsulforon and nicosulfuron
  • imidazolinone based herbicides such as imazamox
  • organophosphorous herbicides such as gluphosinate or glyphosate.
  • the non-selective herbicide such as N-phosphonomethyl glycine (glyphosate) is used.
  • a mixture of mutually mixed seeds of both parent components can contain the seeds of female component mixed with the seeds of the male component in a ratio up to about 1 : 1. Applicable and feasible ratios are known to a person skilled in the art.
  • the present invention is based on an interaction between the determinant that determines resistance to a non-selective herbicide (i. e. it either has a natural resistance to a non-selective herbicide or a gene introduced by genetic engineering), e. g. to N-phosphonomethyl glycine, and a chemical hybridizing agent based on easily soluble or water-soluble derivatives of oxanilic acid of general Formula I and/or agriculturally acceptable water-soluble salts thereof, which are a further aspect of the invention.
  • a non-selective herbicide i. e. it either has a natural resistance to a non-selective herbicide or a gene introduced by genetic engineering
  • a chemical hybridizing agent based on easily soluble or water-soluble derivatives of oxanilic acid of general Formula I and/or agriculturally acceptable water-soluble salts thereof, which are a further aspect of the invention.
  • a further purpose of the invention is also to prepare chemical hybridizing agents on the basis of easily soluble derivatives of oxanilic acid that would be simple to synthesise and apply in the field. This was achieved by a development of easily soluble solutions of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof. By changing the structure of the active ingredient in terms of its increased water solubility, it is done away with a use of volatile organic solutions, unnecessary burdening of plants and environment with volatile organic substances in their application. The synthesis of compounds of the invention is also simple and economically acceptable. As the compounds of general Formula (I) and/or the salts thereof are easily soluble or water-soluble, water-soluble preparations can be prepared that have good applicability and allow a well-homogenised application onto plants. In order to increase absorption of the active ingredient from the water solution into a plant a surfactant can be added.
  • X represents a halogen atom, such as fluorine, chlorine, bromine or iodine, or a -CN group or hydrogen or an alkyl or fluoroalkyl group, preferably a bromine atom or an iodine atom or a -CN group, more preferably a bromine atom or a -CN group;
  • Y represents a group selected from the group comprising -OH and/or -OM
  • M represents a cation suitable for the formation of an agriculturally acceptable water-soluble salt, such as alkali metal cation, e. g. Na + or K + , or tetra- alkylammonium ion, preferably Na + .
  • alkali metal cation e. g. Na + or K +
  • tetra- alkylammonium ion preferably Na + .
  • the easily soluble or water-soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof can be applied only on the plants of the female component, if the seeds of the female component were sown separately from the male component, e. g. as one or several strips of seed/plants of the female component separated from one or several strips of the seeds/plants of the male component, or on the plants that grew from a crop of a mixture of mutually mixed seeds of both parent components .
  • the method of the invention further refers to a method of producing hybrid seeds of Fi generation of commercially significant hermaphrodite plant species, especially common wheat, with chemical hybridization, wherein the seeds of a female component are sown in strips as known in the art.
  • the step of inducing male sterility in the female component (line AA) is not followed by removal of the male component (line BB) from the seed crop.
  • the compounds of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof induce male sterility in hermaphrodite plant species particularly from the family of grasses, especially common wheat, from the end of their premeiotic stages onwards and/or in their meiotic stage in the application ranging from 0.1 kg/ha to 10 kg/ha and in a concentration from 0.01 % to 1.5 %.
  • the recommended dosage of the active substance for common wheat is from 1.4 kg/hectare to 3.5 kg/hectare or until toxic concentration occurs. It should be noted that water consumption per hectare should not exceed 700 1.
  • the compounds of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof can be prepared in forms of various water-soluble preparations, e. g. water-soluble powders, water-soluble granules, water-soluble crystals or water- soluble concentrates, preferably in the form of water-soluble powders or water-soluble granules.
  • the preparation can also be in the form of a suspension concentrate, for instance in the case of reduced water consumption in the production of preparations and thus higher concentration of the active substance.
  • Water-soluble preparations can comprise one or more compounds of Formula (I) and/or agriculturally acceptable water-soluble salts thereof as the active ingredient.
  • the preparations preferably comprise as an active ingredient one or more compounds selected from the group consisting of: 4-bromooxanilic acid, 4-cianooxanilic acid, tetramethylammonium salt of 4-bromooxanilic acid, tetramethylammonium salt of 4- cianooxanilic acid and tetramethylammonium salt of 4-fluorooxanilic acid and optionally further additives known in the art, such as surfactants, e. g. non-ionic surfactants and/or defoamers.
  • surfactants e. g. non-ionic surfactants and/or defoamers.
  • ком ⁇ онент of easily soluble compounds of general Formula (I) and/or water-soluble salts thereof may require an addition of a surfactant (non-ionic surfactant) which enhances absorption of the active substance through leaf epidermis and addition of a silicon-based defoamer.
  • a surfactant non-ionic surfactant
  • the latter can be a constituent part of the preparation or can be added when preparing a water solution for application.
  • Suitable surfactants are known in the art, for instance the preparation Spartan ® (produced by Interagro (UK) Ltd) or Genapol ® UD 50 (produced by Clariant).
  • Suitable silicon-based defoamers are known to a person skilled in the art, the agent Abate (produced by Interagro (UK) Ltd) can be used for instance.
  • the conditions suitable for applying preparations based on the active substances of the invention are at temperatures above 5 °C, preferably at temperatures above 10 °C and relative humidity above 30 %, preferably above 50 %. Suitable and optimal conditions are known to a person skilled in the art.
  • the method of the invention allows for a simpler composition of a seed crop in the embodiment when sowing a mixture of mutually mixed seeds of both parent components (line AA + line BB): sowing in strips is no longer necessary, the space is better used, less time is spent for sowing, better pollination is achieved and more seeds of the desired F ! generation are produced with respect to the sown quantity of the mixture of mutually mixed seeds of both parent components.
  • treatment of plants of the female component with the chemical hybridizing agent is simpler, whereas special attention is needed when applying the agent in a crop sown in strips.
  • more seeds of the desired F) generation are obtained as there are no strips of the so-called male component (pollinator), the seeds of which can be considered to be a side product in terms of production of hybrid seeds of F) generation.
  • Example 1 Synthesis of 4-bromooxanilic acid (CHA4) and preparation of an aqueous solution for application
  • the aqueous solution for spraying was prepared by mixing 3 g of the product (I) (4- bromooxanilic acid) with 12 g of Spartan (Interagro (UK) Ltd) (agent for wetting a leaf surface). The mixture so obtained was dissolved in a corresponding quantity of water relative to the concentration and application surface (e. g. in 3 litres of water) and applied directly onto the plants in the field and their locus.
  • Example 2 Preparation of water-soluble preparations - preparation of tetramethylammonium salt of 4-bromooxanilic acid of general Formula I
  • CHA3 emulsion prepared from 3 g of CHA3/ 7.5 g of Genapol ® UD- 50/135 mL of dimethylsulfoxide
  • Example 3 Efficiency of oxanilic acid derivatives of the invention compared to the standard chemical hybridizing agent - CROISOR ® 100
  • Tested factors were: location (L) (central region, north-eastern region of Slovenia), active substance (AS): ethyl 4-bromooxanilate (CHA1), ethyl 4-cianooxanilate (CHA2), ethyl 4-fluorooxanilate (CHA3), 4-bromooxanilic acid (CHA4), 4- cianooxanilic acid (CHA5), 4-fluorooxani ic acid (CHA6), tetramethylammonium salt of 4-bromooxanilic acid (CHA7), tetramethylammonium salt of 4-cianooxanilic acid (CHA8), tetramethylammonium salt of 4-fluorooxanilic acid (CHA9) and as control Sintofen (CROISOR ® 100) (CHA10), dose (D) (Dl - 700 g/ha, D2 - 1400 g/ha, D3 - 2100 g/ha, D4 - 2800 g/ha,
  • Sowing was carried out on both locations in the first decade of October (genotype cv. Guarni - Florimond Desprez), crop's density amounted to 450 grains/m 2 , the distance between rows was 12.5 cm.
  • the trial consisted of eleven 30- metre long and 1 -metre wide strips. The first strip was for control purposes, whereas the remaining ten strips were intended for fifteen treatments.
  • the crop was supplied with nitrogen in the form of 27 % calcium ammonium nitrate (EC 13/25, 70 - 90 kg N/ ha; EC 31/32, 50 - 70 kg N/ha; EC 47/49, 70 - 90 kg N/ha), the plants were protected with a sulfonylurea herbicide (EC 13/37), strobilurin and triazole based fungicides (EC 29/37 - strobilurin; EC 51/69 - triazole) and deltametrin based insecticide.
  • the oxanilic acid derivatives and the standard chemical hybridizing agent were applied in a 0.1 % concentration. Application was performed in the morning, when relative air humidity was at least 50 % and air temperature exceeded 10 °C.
  • the nozzles Lechler 1 10 - 04 positioned 30 cm above the plant habitus were used.
  • FIG. 1 shows selectivity of activity of the standard hybridizing agent and Figure 2 shows selectivity of activity of 4- bromooxanilic acid. Table 1 : Statistically significant differences and interactions
  • the influence of the genotype on the chemical induction of male sterility was determined for the oxanilic acid derivative which reached a statistically significant highest percentage of male sterility on both locations in the season 2009/10 (compound CHA4, 4-bromooxanilic acid) and for the standard chemical hybridizing agent (CHA) - Sintofen.
  • season 2010/1 1 a field experiment with six various genotypes was carried out for this purpose in the central region.
  • the genotypes were: cv. Ficko, Guarni, Sana, Inoui, Marija, Bologna, wherein each genotype (inbred line) was sown in the shape of five consecutive plots with eight rows of 7.5 m (distance between the rows was kept at 12.5 cm).
  • the fifth plot in each cultivar was intended for control. Both active substances (sintofen and the compound CHA4) were applied in the recommended dose and under recommended conditions for the standard hybridizing agent (1400 g/ha) in the form of 0.1 % suspension. Apart from the genotype and the active substance the influence of the phenophase on the induction of male sterility and plant's height was also studied. First application was carried out when the length of the spike on the main stem reached 5 - 10 mm and the next application was carried out when said length reached to 15 - 20 mm.
  • Example 5 Influence of 4-bromooxanilic acid (CHA4) and the standard chemical hybridizing agent on the synchronisation of flowering

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Abstract

The present invention refers to a chemical way of exploiting a heterosis in commercially significant hermaphrodite plant species, especially common wheat (lat. Triticum aestivum L.), in which easily soluble or water-soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof or water-soluble preparations that contain them are used as an active chemical hybridization substance. The invention further refers to a method for the production of hybrid seeds of F1 generation of commercially significant hermaphrodite plant species, especially common wheat, with chemical hybridization with easily soluble compounds of general Formula (I) and/or the agriculturally acceptable water-soluble salts thereof, which makes it possible, unlike the ways used hithereto, a simpler design of a seed crop for the production of hybrid seeds of F1 generation, better spatial exploitation, better pollination of the female component (line AA) and a greater quantity of seeds of the desired F1 generation based on the sown quantity of both parent components.

Description

Chemical hybridization of hermaphrodite plant species with easily soluble derivatives of oxanilic acid
Subject of Invention
The present invention refers to a chemical way of exploiting a heterosis in commercially significant hermaphrodite plant species, preferably from the family of grasses (lat. Poaceae), especially common wheat (lat. Triticum aestivum L.), in which easily soluble or water-soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof or water-soluble preparations that contain them are used as an active chemical hybridization substance.
The invention further refers to a method for the production of hybrid seeds of Fi generation (the first filial generation) of commercially significant hermaphrodite plant species, especially common wheat, with chemical hybridization comprising:
selection of seeds of both parent components so that sowing of seeds of both parent components is possible in the form of separate strips or optionally in the form of a mixture of mutually mixed seeds of both parent components,
wherein in the case of sowing a mixture of seeds the female component of a hybrid variety (line AA) expresses a natural or genetically engineered resistance against a herbicide, preferably a non-selective herbicide, and the male component of a hybrid variety (line BB) does not express such resistance and wherein in the case of sowing the seeds of both parent components in the form of a mixture inflorescence of a pollinator (line BB) occurs when the end of the premeiotic stage occurs in the female component of the hybrid variety (line AA) due to flowering synchronisation of both parent components and due to prevention of induction of a high percentage of male sterility in the pollinator, induction of male sterility in the plants of the female component of the hybrid variety (line AA), wherein easily soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof are applied onto plants from the end of the premeiotic stage of the plants of the female component on and/or when the latter are in the meiotic stage, and optionally in the case of sowing seeds in the form of a mixture of both parent components, after the completed fertilisation of the plants of the female component (line AA), removing of the plants of the male component from the crop by applying a herbicide, preferably a non-selective herbicide, against which the plants of the female component express resistance, whereas the plants of the male component or pollinator do not have this resistance, onto plants and their locus.
In the case of sowing a mixture of mutually mixed seeds of both parent components of a hybrid variety the method of the invention provides for a simpler design of a seed crop for the production of hybrid seed, better spatial exploitation, better pollination of the female component (line AA) and a greater quantity of seeds of the desired F, generation based on the sown quantity of both parent components in comparison with the approaches used hitherto.
Prior Art and Technical Problem
The invention refers to a method for the exploitation of a heterosis in plants with hermaphrodite florets (hereinafter referred to as hermaphrodites or hermaphrodite plant species), especially in common wheat, with a chemical induction of male sterility. Heterosis presents superiority of the first filial generation (F] generation) over the parental generation, which is expressed for instance in a higher yield, lower mycotoxin content, more rational consumption of plant nutrients etc. For the exploitation of heterosis hybrids produced by a controlled cross between two genetically different homozygous parental components are used (cross $ line AA x $ line BB) (Blouet, A., Streiff, ., Guckert, A. (1999): Possibilities for hybrid seed production in wheat. V: Heterosis and hybrid seed production in agronomic crops. Basra A.S. (ed.). Binghamton, Food Products Press®: 81-108.)
In order to produce a hybrid seed of plant species with hermaphrodite florets an efficient system for inducing male sterility is needed. Induction of male sterility means that only the female sex starts expressing on a hermaphrodite plant species.
In the past, several genetic and transgenic approaches were suggested for the induction of male sterility in hermaphrodite plant species. Common to the systems for the induction of male sterility based on cytoplasmic-genetic male sterility, the transgene for the synthesis of cytotoxic or cytostatic polypeptides and the transgene for the formation of an exogenous double- stranded RNA for the induction of RNA interference, is the preservation of male-sterile female component with its fertile analogue (three-component system). Unlike genetic and transgenic approaches to the cultivation of hybrid variety based on three distinct lines ($ line AA, isogenous line A'A', S line BB) the chemical induction of male sterility needs only two parent components of the hybrid variety (two-component system). In addition to this, the advantage of chemical induction of male sterility is also the absence of complex genetic engineering and long-term input of a male- sterile cytoplasm with backcrossing (Wirmani et al. (2003): Two-line Hybrid Rice Breeding Manual. Hardy B. (ed.). Metro Manila, IRRI).
A relation between a selective effect of a chemical on the metabolism of a plant in the sense of induction of male sterility (gametocidic activity) and production of a hybrid seed could be traced as far back as 1957. In that year, the Method for the production of a hybrid cotton seed (lat. Gossipium hirsutum L.) by using the agent FW-450 (produced by Rohm & Haas) was described. An established term for the chemicals having a distinctive selective effect on microsporogenesis or development of viable pollen and with which chemicals it is possible to produce a hybrid seed is a chemical hybridizing agent (abbreviated CHA) (McRae, D.H. (1985): Advances in chemical hybridization. Plant breed. Review, 3: 169-191).
Chemical hybridizing agents are efficient in inducing male sterility in the female component of the hybrid variety; however, their application in more general production of a hybrid seed is often too complicated due to a need to separate both parent components.
Current approaches to a chemical exploitation of heterosis require sowing of both parent components in the form of strips. When producing a hybrid seed of common wheat (lat. Triticum aestivum L.) which is a typical hermaphrodite plant species, the strips of a female component (line AA) are normally 6 to 20 m wide and the pollinator's strips (line BB) are 1.5 to 6 m wide. Sowing of parent components in the form of strips is very demanding in practice and what's more, the central part of the strip of the female component is often poorly pollinated due to a huge distance from the location of pollen occurrence (Cisar, G., Cooper, D.B. (2002): Hybrid wheat. V: Bread wheat. Curtis B.C., Rajaram S., Gomez Macpherson H. (ed.). Rome, FAO Plant Production and Protection Series).
An important problem in chemical exploitation of heterosis is also a selection of the active substance, since most of the chemical hybridizing agents express a strong phytotoxic effect in the early stages of organogenesis (Blouet, A., Streiff, K., Guckert, A. (1999): Possibilities for hybrid seed production in wheat. V: Heterosis and hybrid seed production in agronomic crops. Basra A.S. (ed.). Binghamton, Food Products Press®: 81-108).
Consequently, the parent components cannot be sown in the form of a mixture due to flowering synchronisation, wherein the pollinator must lag behind in development. In the group of chemicals inhibiting microsporogenesis the representatives from the group of oxopyridazines and oxy- and amino-substituted cinnolines have become widely accepted as commercial agents for the chemical hybridization of common wheat (Dotlacil, L., Apltauerova, M. (1978): Pollen sterility induced by ethrel and its utilization in hybridization of wheat. Euphytica, 27: 353-360; Graham, R.D., (1986): Induction of male sterility in wheat using organic ligands with high specificity for binding copper. Euphytica, 35: 621-629; Wong, M. et al. (1995): Effectiveness of SC2053 as a chemical hybridizing agent for winter wheat. Plant Growth Regulation, 16: 243-248).
Known representatives of oxopyridazines with gametocidic activity are fenridazon (1- (4-chlorophenyl)- 1 ,4-dihydro-6-methyl-4-oxopyridazine-3-carboxylic acid) and clofencet (2-(4-chlorophenyl)-3-ethyl-2,5-dihydro-5-oxopyridazine-4-carboxylic acid). In 1970s and 1980s the company Rohm & Haas developed a series of oxopyridazines (RH-531 , RH-532, RH-2956, RH-4667, RH-5148, RH-0007), among which the active substance fenridazon (RH-0007) reached a commercial value in the form of the agent Hybrex®. Clofencet in the form of the agent GENESIS® (also MON 21200) was registered in 1997 by the company Monsanto, yet it needed to be withdrawn from use after several years due to environmental unacceptability. In order to achieve an efficient induction of male sterility the agent GENESIS® (22.4 %) needs to be applied between the phenophases EC 32 and EC 39 (visible ligule of a flag leaf) in a dosage ranging from 1.4 kg to 2.7 kg of active substance per hectare. The pollen grains of plants treated with the active substance clofencet have a wavy surface and the exine is by 80 % thinner. The pollen grains are incapable of germination due to plasmolysis (United States - Environmental Protection Agency. PESTICIDE FACT SHEET / Clofencet (1997); Bucholtz, D.L., (1988): Effect of environment and formulation on the absorption and translocation of fenridazon in wheat (Triticum aestivum L.). Plant Growth Regulation, 7: 65-73. Among substituted cinnolines the chemicals SC- 1271 (l-(4-chlorophenyl)-4-oxo-5- propoxycinnoline-3-carboxylic acid) and SC-2053 (l-(4-chlorophenyl)-4-oxo-5- (methoxyethoxy) cinnoline-3-carboxylic acid) developed by Orsan/DuPont stand out. SC-2053 represents the active substance sintofen used as a commercial chemical hybridizing agent CROISOR® 100. A CROISOR® 100 agent is applied when the length of a spike on the main stem is 14 mm to 18 mm long, with the dose of 13 1/ha to 15 1/ha (1.3 kg to 1.5 kg of active substance per hectare). The pollen grains of treated plants have a wavy surface and degenerated cytoplasm (general retardation) (Wong et al., 1995).
Use of derivatives of oxanilic acid intended for chemical hybridization is disclosed in Chakraborty, ., Devakumar, C. (2006): Ethyloxanilates as specific male gametocides for wheat (Triticum aestivum L.). Plant Breeding, 125: 441-447, wherein oxanilate ethyl esters were used as chemical hybridizing agents in the form of emulsions with an organic solvent (e. g. ethylene dichloride, methylnaphthalene, glycol ethers, cyclohexanone, anisole). Some derivatives of oxanilic acid and their use in the method for the induction of male sterility are disclosed also in GB patent No. 1 572 527 (Batch et al.). It is described therein that water dispersions or emulsions can be prepared by dissolving an active ingredient in an organic solvent. This document does not discuss a preparation of water-soluble preparations containing easily soluble or water-soluble derivatives of oxanilic acid and/or the water-soluble salts thereof.
Modern chemical hybridizing agents are further developed, especially in direction of achieving better selectivity of gametocidic activity and reduced influence on the environment. The purpose of the invention was to develop new environmentally friendly agents with gametocidic activity or chemical hybridizing agents and to reduce the introduction of volatile organic compounds into the environment and plants. Oxanilic acid was found to be an interesting basis for the preparation of agents for chemical hybridization of the invention, as their synthesis is simple and economically favourable and the acid function moreover offers a possibility of a further functionalisation with the purpose of producing water-soluble active substances. The present invention thus refers to a change in the structure of active substances in terms of their getting more easily-soluble and water-soluble, and to a preparation of water- soluble preparations that confer a more simple use for the application in the field in the form of water solutions.
Solution to the Technical Problem with Examples
The present invention refers to a chemical way of exploiting a heterosis in commercially significant hermaphrodite plant species, preferably from the family of grasses (lat. Poaceae), especially common wheat (lat. Triticum aestivum L.), in which easily soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof are used as an active chemical hybridization substance.
The invention further refers to a method for the production of hybrid seeds of F] generation of commercially significant hermaphrodite plant species, preferably hermaphrodite cereals from the family of grasses, more preferably common wheat, with chemical hybridization comprising:
selection of seeds of both parent components of a commercially significant hermaphrodite plant species so that sowing of seeds of both parent components is possible separately in the form of one or several separate strips or optionally in the form of a mixture of mutually mixed seeds of both parent components,
wherein in the case of sowing a mixture of seeds the female component of a hybrid variety (line AA) expresses a natural or genetically engineered resistance against a herbicide, preferably a non-selective herbicide, and the male component of a hybrid variety (line BB) (pollinator) does not express such resistance and wherein in the case of sowing the seeds of both parent components in the form of a mixture inflorescence of a pollinator (line BB) occurs when the end of the premeiotic stage occurs in the female component of the hybrid variety (line AA) due to flowering synchronisation of both parent components and due to prevention of induction of a high percentage of male sterility in the pollinator,
induction of male sterility in the plants of the female component of the hybrid variety (line AA), wherein easily soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof are applied as an active substance for chemical hybridization onto plants from the end of the premeiotic stage of the plants of the female component on and/or when the latter are in the meiotic stage:
Figure imgf000009_0001
(I)
wherein:
X represents a halogen atom, such as fluorine, chlorine, bromine or iodine, or a -CN group or hydrogen or an alkyl or fluoroalkyl group, preferably a bromine atom or a -CN group;
Y represents a group selected from the group comprising -OH and/or -OM, wherein M represents a cation suitable for the formation of an agriculturally acceptable water-soluble salt, such as alkali metal cation, e. g. Na+ or K+, or tetraalkylammonium ion, preferably Na+;
and optionally
in the case of sowing seeds in the form of a mixture of both parent components, after the completed fertilisation of the plants of the female component of the hybrid variety (line AA), wherein the female component expresses natural or genetically engineered resistance against herbicide, preferably a non-selective herbicide, and the male component (line BB) does not express such resistance, removing of the plants of the male component from the crop by applying a herbicide, preferably a non-selective herbicide, against which the plants of the female component express resistance, whereas the plants of the male component or pollinator do not have this resistance, onto plants and their locus.
The method of the invention can be used on commercially significant hermaphrodite plant species, preferably hermaphrodite cereals from the family of grasses (lat. Poaceae), especially common wheat (lat. Triticum aestivum L).
The expression "both parent components" as used herein denotes the seeds of the female component (line AA) and the male component (line BB) of commercially significant hermaphrodite plant species, especially hermaphrodite cereals from the family of grasses, preferably common wheat. According to one aspect of the invention, they were selected in a way that the female and male components have a suitable delay in development, so that inflorescence of the male component (pollinator) becomes noticeable at the end of the premiotic phase or the beginning of the meiotic stage of organogenesis of the female component (synchronisation of flowering). It is herewith enabled that the active chemical hybridization substance, i. e. the compound of general Formula (I) and/or its agriculturally acceptable water- soluble salt, is applied onto plants of the female component in the period from the completion of the premeiotic phase of the plants of the female component and/or when the latter are in the meiotic stage of organogenesis.
In a preferred embodiment, the method of the invention is carried out on common wheat (lat. Triticum aestivum L.). In the application phases of the active substance, i. e. the compound of general Formula (I) and/or the water-soluble agriculturally acceptable salts thereof, onto the plants, the spikes on the main stem of the female component (line AA) are 15-20 mm long, whereas the spikes on the main stem of the male component (line BB) are≤ 5 mm long. As female components (line AA), genotypes (cultivars) of the common wheat selected from the group comprising Ficko, Guarni, Sana, Inoui, Marija, Bologna are especially applicable for the use of the invention.
As the male component the cultivar Ludwig of the common wheat (lat. Triticum aestivum L.) is suitable within the meaning of the invention.
In order to exploit heterosis or production of hybrid seeds of commercially significant hermaphrodite plant species, preferably from the family of grasses (lat. Poaceae), especially preferably common wheat (lat. Triticum aestvum L.) by applying a chemical hybridizing agent, wherein the seeds of both parent components are sown in the form of a mixture, such female component needs to be selected, under the consideration of already mentioned synchronisation of flowering of plants of both parent components, that has a determinant (i. e. gene) for resistance against a herbicide, preferably a non-selective herbicide. In order to introduce resistance against N-phosphinomethy giycin (glyphosate) which is the most often used active substance in non-selective herbicides, there are various transgenic approaches known to a person skilled in the art (e. g. gene cp4-epsps, bar, gox); natural resistance (an endogenous gene) of plants is also used and it can be successfully induced by regenerating the plants on culture mediums with added said active substance - non-selective herbicide. Wheat resistant against non-selective herbicides and a method for the production thereof are disclosed in patent US 7,087,809 B2 (William, H. D. (2006) Natural herbicide resistance in wheat) and US patent application US 2009/0320151 (William, 2006, Kimberlee et al., 2009, Glyphosate-tolerant wheat genotypes).
A further aspect of the present invention is a method for producing a hybrid seed of F] generation of commercially significant hermaphrodite plant species, preferably common wheat, with chemical hybridization with an active substance of general Formula (I) and/or the agriculturally acceptable water-soluble salts thereof of the invention, wherein in the case of sowing seeds in the form of a mixture of both parent components, not only synchronisation of flowering of both parent components in order to prevent induction of a high percentage of male sterility in the pollinator in the phase of the chemical hybridization method is taken into consideration but moreover the seeds of both parent components are selected in a way that the female component expresses natural or genetically engineered resistance against a herbicide, preferably a non-selective herbicide, and the male component does not express such resistance. It is herewith achieved that after the fertilisation of the female component is completed the plants of the male component are eliminated by applying a herbicide, preferably a non-selective herbicide to obtain Fj seeds of the hybrid variety. A purer Fi generation of seeds can thus be obtained than could be if the well-known and prevailing method of sowing in strips known in the art were used, i. e. the Fj seed is obtained considerably without admixture of the BB line.
Suitable herbicides used for the removal of the male component after the fertilisation of the female component are sulphonylurea herbicides, such as rimsulforon and nicosulfuron, imidazolinone based herbicides, such as imazamox, and organophosphorous herbicides, such as gluphosinate or glyphosate. In a preferred embodiment the non-selective herbicide such as N-phosphonomethyl glycine (glyphosate) is used.
A mixture of mutually mixed seeds of both parent components can contain the seeds of female component mixed with the seeds of the male component in a ratio up to about 1 : 1. Applicable and feasible ratios are known to a person skilled in the art.
Recommended use in the production of hybrid seeds of common wheat is about 90 % of the seeds of the female component (line AA) and about 10 % of the seeds of the male component (line BB) based on the total mass of the seed mixture.
In producing hybrid barley by using cytoplasmic-genetic male sterility normally 95 % of line AA and 5 % of line BB are used. In one aspect or embodiment, the present invention is based on an interaction between the determinant that determines resistance to a non-selective herbicide (i. e. it either has a natural resistance to a non-selective herbicide or a gene introduced by genetic engineering), e. g. to N-phosphonomethyl glycine, and a chemical hybridizing agent based on easily soluble or water-soluble derivatives of oxanilic acid of general Formula I and/or agriculturally acceptable water-soluble salts thereof, which are a further aspect of the invention.
A further purpose of the invention is also to prepare chemical hybridizing agents on the basis of easily soluble derivatives of oxanilic acid that would be simple to synthesise and apply in the field. This was achieved by a development of easily soluble solutions of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof. By changing the structure of the active ingredient in terms of its increased water solubility, it is done away with a use of volatile organic solutions, unnecessary burdening of plants and environment with volatile organic substances in their application. The synthesis of compounds of the invention is also simple and economically acceptable. As the compounds of general Formula (I) and/or the salts thereof are easily soluble or water-soluble, water-soluble preparations can be prepared that have good applicability and allow a well-homogenised application onto plants. In order to increase absorption of the active ingredient from the water solution into a plant a surfactant can be added.
Easily soluble or water-soluble derivatives of oxanilic acid of the invention have a general Formula (I):
Figure imgf000013_0001
(I) wherein
X represents a halogen atom, such as fluorine, chlorine, bromine or iodine, or a -CN group or hydrogen or an alkyl or fluoroalkyl group, preferably a bromine atom or an iodine atom or a -CN group, more preferably a bromine atom or a -CN group;
Y represents a group selected from the group comprising -OH and/or -OM,
wherein M represents a cation suitable for the formation of an agriculturally acceptable water-soluble salt, such as alkali metal cation, e. g. Na+ or K+, or tetra- alkylammonium ion, preferably Na+.
With the purpose of preparing easily soluble or water-soluble compounds of general Formula (I) and the salts thereof and of checking their phytotoxicity for the use as an agent for chemical hybridization of common wheat, the following easily soluble derivatives of oxanilic acid of general Formula (I) and the water-soluble salts thereof were prepared:
Figure imgf000014_0001
(I)
wherein:
Compound No. X Y
CHA1 4-Br -OEt ethyl 4-bromooxanilate
CHA2 4-CN -OEt ethyl 4-cianooxanilate
CHA3 4-F -OEt ethyl 4-fluorooxanilate
CHA4 4-Br -OH 4-bromooxanilic acid
CHA5 4-CN -OH 4-cianooxanilic acid
CHA6 4-F -OH 4-fluorooxanilic acid
CHA7 4-Br -O' (CH3)4N+ tetramethylammonium salt of 4- bromooxanilic acid CHA8 4-CN -O" (CH3)4N+ tetramethylammonium salt of 4- cianooxanilic acid
CHA9 4-F -0" (CH3)4N+ tetramethylarnmonium salt of 4- fluorooxanilic acid
Results of tests of these compounds are presented in given examples.
A compound of general Formula (I), wherein X represents Br and Y represents an -OH group, i. e. 4-bromooxanilic acid, has been identified as particularly suitable compound for use of the invention.
The easily soluble or water-soluble derivatives of oxanilic acid of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof can be applied only on the plants of the female component, if the seeds of the female component were sown separately from the male component, e. g. as one or several strips of seed/plants of the female component separated from one or several strips of the seeds/plants of the male component, or on the plants that grew from a crop of a mixture of mutually mixed seeds of both parent components .
The method of the invention further refers to a method of producing hybrid seeds of Fi generation of commercially significant hermaphrodite plant species, especially common wheat, with chemical hybridization, wherein the seeds of a female component are sown in strips as known in the art. In this case, the step of inducing male sterility in the female component (line AA) is not followed by removal of the male component (line BB) from the seed crop.
The compounds of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof induce male sterility in hermaphrodite plant species particularly from the family of grasses, especially common wheat, from the end of their premeiotic stages onwards and/or in their meiotic stage in the application ranging from 0.1 kg/ha to 10 kg/ha and in a concentration from 0.01 % to 1.5 %.
The recommended dosage of the active substance for common wheat is from 1.4 kg/hectare to 3.5 kg/hectare or until toxic concentration occurs. It should be noted that water consumption per hectare should not exceed 700 1.
The compounds of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof can be prepared in forms of various water-soluble preparations, e. g. water-soluble powders, water-soluble granules, water-soluble crystals or water- soluble concentrates, preferably in the form of water-soluble powders or water-soluble granules.
The preparation can also be in the form of a suspension concentrate, for instance in the case of reduced water consumption in the production of preparations and thus higher concentration of the active substance.
Water-soluble preparations can comprise one or more compounds of Formula (I) and/or agriculturally acceptable water-soluble salts thereof as the active ingredient. The preparations preferably comprise as an active ingredient one or more compounds selected from the group consisting of: 4-bromooxanilic acid, 4-cianooxanilic acid, tetramethylammonium salt of 4-bromooxanilic acid, tetramethylammonium salt of 4- cianooxanilic acid and tetramethylammonium salt of 4-fluorooxanilic acid and optionally further additives known in the art, such as surfactants, e. g. non-ionic surfactants and/or defoamers.
Application of easily soluble compounds of general Formula (I) and/or water-soluble salts thereof may require an addition of a surfactant (non-ionic surfactant) which enhances absorption of the active substance through leaf epidermis and addition of a silicon-based defoamer. The latter can be a constituent part of the preparation or can be added when preparing a water solution for application.
Suitable surfactants are known in the art, for instance the preparation Spartan® (produced by Interagro (UK) Ltd) or Genapol® UD 50 (produced by Clariant).
Suitable silicon-based defoamers are known to a person skilled in the art, the agent Abate (produced by Interagro (UK) Ltd) can be used for instance.
The conditions suitable for applying preparations based on the active substances of the invention are at temperatures above 5 °C, preferably at temperatures above 10 °C and relative humidity above 30 %, preferably above 50 %. Suitable and optimal conditions are known to a person skilled in the art.
The method of the invention allows for a simpler composition of a seed crop in the embodiment when sowing a mixture of mutually mixed seeds of both parent components (line AA + line BB): sowing in strips is no longer necessary, the space is better used, less time is spent for sowing, better pollination is achieved and more seeds of the desired F! generation are produced with respect to the sown quantity of the mixture of mutually mixed seeds of both parent components. Moreover, treatment of plants of the female component with the chemical hybridizing agent is simpler, whereas special attention is needed when applying the agent in a crop sown in strips. In comparison with sowing in strips, more seeds of the desired F) generation are obtained as there are no strips of the so-called male component (pollinator), the seeds of which can be considered to be a side product in terms of production of hybrid seeds of F) generation.
Examples given in the continuation are for illustration purposes of the present invention and do not limit the scope of this invention in any way whatsoever. Unless otherwise specified, all percentages indicated in the patent application refer to mass percents.
Examples
Example 1: Synthesis of 4-bromooxanilic acid (CHA4) and preparation of an aqueous solution for application
4-bromoaniline (67.73 g; 0.394 mol) and diethyl oxalate (287.7 g; 1.969 mol) were weighted and added into a one-litre round-bottom flask and stirred for 24 hours at 1 10 °C. When the reaction was completed, the residual diethyl oxalate was partially evaporated under reduced pressure (60 mmHg). A product precipitated as a solid compound which was filtered off and washed on a suction filter with hexane. Pure ethyl 4-bromooxanilate was obtained in the form of a white powder (99.6 g, 93 mol%; lH NMR 6(ppm) 1.31 (t, 3H), 4.30 (q, 2H), 7.56 (d, 2H), 7.73 (d, 2H), 10.91 (s, 1H)).
The product was wetted with 35 mL of acetonitrile, 100 mL of water was added and 10 % water solution of NaOH was slowly added (500 mL in one hour) at a temperature of 0 °C and stirred at 20 °C for further 5 hours. The reaction mixture was neutralised with a cold 10 % aqueous solution of HC1 and the solid product was filtered off, rinsed on a suction filter with water and dried. 87.6 g (98 mol%) of the product, oxanilic acid derivative (I, X = Br, Y = -OH), 4-bromooxanilic acid (I) was obtained. 1H NMR 6(ppm) 7.53 (d, 2H), 7.75 (d, 2H), 10.84 (s, 1H)).
The aqueous solution for spraying was prepared by mixing 3 g of the product (I) (4- bromooxanilic acid) with 12 g of Spartan (Interagro (UK) Ltd) (agent for wetting a leaf surface). The mixture so obtained was dissolved in a corresponding quantity of water relative to the concentration and application surface (e. g. in 3 litres of water) and applied directly onto the plants in the field and their locus. Example 2: Preparation of water-soluble preparations - preparation of tetramethylammonium salt of 4-bromooxanilic acid of general Formula I
For the preparation of 3g of tetramethylammonium salt of 4-bromooxanilic acid 4- bromooxanilic acid (2.308 g) prepared by the method from Example 1 and tetramethylammonium hydroxide pentahydrate (1.713 g) were mixed in 200 mL of water and dissolved to the corresponding volume of the aqueous solution relative to the concentration and application surface (e. g. in 3 litres of water) and directly applied onto the plants in the field and their locus.
From the prepared compounds which were described above the following preparationswere prepared for spraying application:
Compound No. Preparation
CHA1 emulsion prepared from 3 g of CHA1/ 7.5 g of Genapol® UD 50
/24 mL of dimethylsulfoxide
CHA2 emulsion prepared from 3 g of CHA2/ 7.5 g of Genapol® UD-50
/120 mL of dimethylsulfoxide
CHA3 emulsion prepared from 3 g of CHA3/ 7.5 g of Genapol® UD- 50/135 mL of dimethylsulfoxide
CHA4 solution, 3 g of CHA4 in 12 g of Spartan® is dissolved in 3 litres of water
CHA5 solution, 3 g of CHA5 in 12 g of Spartan® is dissolved in 3 litres of water
CHA6 solution, 3 g of CHA6 in 12 g of Spartan® is dissolved in 3 litres of water
CHA7 solution, 3 g of CHA7 in 200 mL of water, 2.144 g of acid CHA3 and 2.120 g of Me4NOH x 5 H2O, pH - 9 CHA8 solution, 3 g of CHA8 in 200 mL of water, 2.308 g of acid CHA4 and 1.713 g of Me4NOH x 5 H2O, pH = 9
CHA9 solution, 3 g of CHA9 in 200 mL of water, 2.167 g of acid CHA5 and 2.064 g of Me4NOH x 5 H2O, pH = 9
CHA10- Sintofen CROISOR® 100 - following the manufacturer's control instructions
The preparations were used or applied as specified in Example 3.
Example 3: Efficiency of oxanilic acid derivatives of the invention compared to the standard chemical hybridizing agent - CROISOR® 100
The efficiency of oxanilic acid derivatives of general Formula (I) and/or the salts thereof in terms of reaching a high percentage of male sterility in common wheat (lat. Triticum aestivum L.) and their influence on the plant's height were tested in field conditions in comparison with the standard chemical hybridization agent CROISOR® 100 (active substance Sintofen, supplied by Saaten-Union Recherche S. A. R. L.). Tested factors were: location (L) (central region, north-eastern region of Slovenia), active substance (AS): ethyl 4-bromooxanilate (CHA1), ethyl 4-cianooxanilate (CHA2), ethyl 4-fluorooxanilate (CHA3), 4-bromooxanilic acid (CHA4), 4- cianooxanilic acid (CHA5), 4-fluorooxani ic acid (CHA6), tetramethylammonium salt of 4-bromooxanilic acid (CHA7), tetramethylammonium salt of 4-cianooxanilic acid (CHA8), tetramethylammonium salt of 4-fluorooxanilic acid (CHA9) and as control Sintofen (CROISOR® 100) (CHA10), dose (D) (Dl - 700 g/ha, D2 - 1400 g/ha, D3 - 2100 g/ha, D4 - 2800 g/ha, D5 - 3500 g/ha and control - 0 g/ha) and phenophase (FP) which was determined on the basis of the length of the spike (FP1 - 5 mm, FP2 - 10 mm, FP3 - 15 mm). Sowing was carried out on both locations in the first decade of October (genotype cv. Guarni - Florimond Desprez), crop's density amounted to 450 grains/m2, the distance between rows was 12.5 cm. The trial consisted of eleven 30- metre long and 1 -metre wide strips. The first strip was for control purposes, whereas the remaining ten strips were intended for fifteen treatments. During vegetation, the crop was supplied with nitrogen in the form of 27 % calcium ammonium nitrate (EC 13/25, 70 - 90 kg N/ ha; EC 31/32, 50 - 70 kg N/ha; EC 47/49, 70 - 90 kg N/ha), the plants were protected with a sulfonylurea herbicide (EC 13/37), strobilurin and triazole based fungicides (EC 29/37 - strobilurin; EC 51/69 - triazole) and deltametrin based insecticide. The oxanilic acid derivatives and the standard chemical hybridizing agent were applied in a 0.1 % concentration. Application was performed in the morning, when relative air humidity was at least 50 % and air temperature exceeded 10 °C. The nozzles Lechler 1 10 - 04 positioned 30 cm above the plant habitus were used.
Male sterility was calculated by the formula (Sc - Sf) / Sc x 100, wherein Sc is the number of seeds per spike of an untreated plant and Sf is the number of seeds per spike of a treated plant. Apart from male sterility phytotoxicity was determined as well. The indicator of phytotoxicity was the plant height. Statistically significant differences and interactions were determined by the statistical software package STATGRAPHICS Centurion XVI.
The results have shown that the compound CHA4 - i. e. 4-bromooxanilic acid - induces the highest percentage of male sterility among the tested derivatives. The results are shown in Table 1. It is of utter importance that said derivative reaches better selectivity and lower toxicity in comparison with the standard chemical hybridizing agent. This means that the efficiency of the derivative CHA4 increases with the spike getting longer and that the plant height gets lower more slowly, which is shown in Figures 1 and 2.
The figures show the interaction AS x FP x D. Figure 1 shows selectivity of activity of the standard hybridizing agent and Figure 2 shows selectivity of activity of 4- bromooxanilic acid. Table 1 : Statistically significant differences and interactions
Plant height [cm] Male sterility [%]
Location (L) ** **
Active substance (AS) ** **
Phenophase (FP) ** **
Dose (D) ** **
Statistically significant All interactions except All interactions interactions LxD
Mean values of factors [cm, %]
Location (L)
North-eastern region 62.681 ± 0.1 106b 70.8252 ± 0.34823
Central region 66.2132 ± 0.1 106a 58.2274 ± 0.3482b
Active substance (AS)
CHA1 62.3586 ± 0.2473g 76.7743 ± 0.7787d
CHA2 68.4979 ± 0.2473c 45.9719 ± 0.7787fg
CHA3 63.9412 ± 0.2473f 80.1045 ± 0.7787c
CHA4 59.891 1 ± 0.2473h 82.4494 ± 0.7787ab
CHA5 70.5985 ± 0.2473ab 50.7552 ± 0.7787e
CHA6 64.7152 ± 0.2473e 74.8315 ± 0.7787d
CHA7 66.5369 ± 0.2473d 47.3379 ± 0.7787f
CHA8 71.0378 ± 0.2473a 44.398 ± 0.7787g
CHA9 70.3285 ± 0.2473b 45.1039 ± 0.7787g
CHAIO (Standard (Sintofen)) 36.5654 ± 0.2473' 97.5362 ± 0.77873
Phenophase (FP)
FP1 65.6362 ± 0.1368a 58.7951 ± 0.4309c
FP2 64.3021 ± 0.1341b 64.8542 ± 0.4223b
FP3 63.403 ± 0.1353° 69.9296 ± 0.42623
Dose (D)
Dl 68.3425 ± 0.1747a 58.7505 ± 0.5503e D2 65.3517 ± 0.1747b 62.2927 ± 0.5503d
D3 63.92 ± 0.1747c 65.2263 ± 0.5503c
D4 63.0617 ± 0.1747d 67.2789 ± 0.5503b
D5 61.5597 ± 0.1753e 69.0831 ± 0.5521a ns No statistically significant differences at P ≥0.05
* Statistical significance defined at P < 0.05 and **P <0.01
± Standard error
Example 4: Influence of genotype on the efficiency of 4-bromooxanilic acid (CHA4) and the standard chemical hybridizing agent
The influence of the genotype on the chemical induction of male sterility was determined for the oxanilic acid derivative which reached a statistically significant highest percentage of male sterility on both locations in the season 2009/10 (compound CHA4, 4-bromooxanilic acid) and for the standard chemical hybridizing agent (CHA) - Sintofen. In the season 2010/1 1 a field experiment with six various genotypes was carried out for this purpose in the central region. The genotypes were: cv. Ficko, Guarni, Sana, Inoui, Marija, Bologna, wherein each genotype (inbred line) was sown in the shape of five consecutive plots with eight rows of 7.5 m (distance between the rows was kept at 12.5 cm). The fifth plot in each cultivar was intended for control. Both active substances (sintofen and the compound CHA4) were applied in the recommended dose and under recommended conditions for the standard hybridizing agent (1400 g/ha) in the form of 0.1 % suspension. Apart from the genotype and the active substance the influence of the phenophase on the induction of male sterility and plant's height was also studied. First application was carried out when the length of the spike on the main stem reached 5 - 10 mm and the next application was carried out when said length reached to 15 - 20 mm. Agrotechnical measures, application technique of the active substance, the method of determining the percentage of male sterility and plant's height did not differ from those in the field experiment for testing the efficiency of easily soluble oxanilic acid derivatives of the invention compared to the standard chemical hybridizing agent. The results of the experiment are gathered in Table 2.
Table 2: Influence of genotype on the efficiency of 4-bromooxanilic acid (CHA4) and the standard chemical hybridizing agent
Figure imgf000024_0001
MS - Male steri ity expressed in percents, V - plant's height expressed in centimetres
Example 5: Influence of 4-bromooxanilic acid (CHA4) and the standard chemical hybridizing agent on the synchronisation of flowering
In the field experiment carried out in order to determine the influence of a genotype on the efficiency of the CHA4 derivative and the standard chemical hybridizing agent the pollinator profile needed for the production of hybrid seeds of common winter wheat with the use of oxanilic acid derivatives was determined. Based on the date of flowering in the season 2009/10 six female components (cv. Ficko, Guarni, Sana, Inoui, Marija, Bologna) were selected out of 60 genotypes and one pollinator (cv. Ludwig). The strips of female components (9 AA) and the pollinator (<$ BB) were sown in an alternate manner, so that five consecutive plots of each female component (8 x 12,5 cm x 750 cm) were enclosed from each side by five consecutive plots of the pollinator. Flowering synchronisation was determined by the share of spikes of the female component that culminated (lemna and palea open at an angle exceeding 30 degrees) in the time when at least a half of the pollinator's spikes extrude anthers. In the case when less than 50 % of the spikes of the line AA culminate in the time when less than one half of the spikes of the line BB (visible stamina) flower, we cannot talk about a successful flowering synchronisation of both parent components of a potential hybrid variety. The results of the experiment are gathered in Table 3.
Table 3: Influence of 4-bromooxanilic acid (CHA4) and a standard chemical hybridizing agent on synchronisation of flowering
CHA4 Standard - CROISOR®100
Phenophase 1 Phenophase 2 Phenophase 1 Phenophase 2
Genotype
Culmination Culmination Culmination Culmination
[%] l%] [%] [%]
Ficko 58 53 19 47
Guarni 57 65 27 60
Sana 47 55 44 50
Inoui 43 70 29 61
Marija 48 55 22 39
Bologna 64 51 17 41

Claims

Patent claims
1. A method for the production of hybrid seeds of F) generation of commercially significant hermaphrodite plant species, preferably from the family of grasses (lat. Poaceae), especially preferably common wheat (lat. Triticum aestivum L.), with chemical hybridization comprising:
- selection of seeds of both parent components of a commercially significant hermaphrodite plant species so that sowing of seeds of both parent components is possible separately in the form of one or several separate strips or optionally in the form of a mixture of mutually mixed seeds of both parent components;
wherein in the case of sowing a mixture of seeds the female component of a hybrid variety (line AA) expresses a natural or genetically engineered resistance against a herbicide, preferably a non-selective herbicide, and the male component of a hybrid variety (line BB) does not express such resistance and wherein in the case of sowing the seeds of both parent components in the form of a mixture inflorescence of a pollinator (line BB) occurs when the end of the premeiotic stage occurs in the female component of the hybrid variety (line AA);
induction of male sterility in the plants of the female component of the hybrid variety (line AA), wherein easily soluble compounds of general Formula (I) and/or agriculturally acceptable water-soluble salts thereof are applied as an active substance for chemical hybridization onto plants from the end of the premeiotic stage of the plants of the female component on and/or when the latter are in the meiotic stage:
Figure imgf000026_0001
(I)
wherein: X represents a halogen atom, such as fluorine, chlorine, bromine or iodine, or a -CN group or hydrogen or an alkyl or fluoroalkyl group, preferably a bromine atom or a -CN group;
Y represents a group selected from the group comprising -OH and/or -OM, wherein M represents a cation suitable for the formation of an agriculturally acceptable water-soluble salt, such as alkali metal cation, e. g. Na+ or K+, or tetraalkylammonium ion, preferably Na+;
and optionally
in the case of sowing seeds in the form of a mixture of both parent components, after the completed fertilisation of the plants of the female component of the hybrid variety (line AA), removing of the plants of the male component from the crop by applying a herbicide, preferably a non-selective herbicide, against which the plants of the female component express resistance, whereas the plants of the male component or pollinator do not have this resistance, onto plants and their locus.
2. Method according to claim 1, characterised in that the seeds of commercially significant hermaphrodite plant species are selected from a group comprising hermaphrodite cereals from the family of grasses (lat. Poaceae), the preferred commercially significant hermaphrodite plant species is common wheat (lat. Triticum aestivum L.).
3. Method according to claim 1 or 2, characterised in that
the hermaphrodite plant species is common wheat (lat. Triticum aestivum L.) and that the seeds of both parent components are sown in the form of a mixture of mutually mixed seeds of both parent components, wherein the seeds of the female component of a hybrid variety (line AA) express a natural or genetically engineered resistance against a herbicide, preferably a non-selective herbicide, and the male component of a hybrid variety (line BB) does not express such resistance and wherein inflorescence of the pollinator (line BB) occurs when the end of the premeiotic stage occurs in the female component of the hybrid variety (line AA), and
- after the induction of male sterility is completed in the plants of the female component of the hybrid variety (line AA), wherein compounds of general Formula (I) and/or the agriculturally acceptable water-soluble salts thereof of claim 1 are applied as an active chemical hybridizing agent onto the plants from the end of the premeiotic stage of the plants of the female component onwards and/or when the latter are in the meiotic stage, and
- after the completed fertilisation of the plants of the female component the plants of the male component are eliminated from the crop by applying a herbicide, preferably a non-selective herbicide, more preferably glyphosate, against which the plants of the female component express resistance, whereas the plants of the male component or pollinator do not have this resistance, onto plants and their locus.
4. Method according to any of the preceding claims 1-3, characterised in that a mixture of seeds of both parent components from the family of grasses (lat. Poaceae) is sown, which seeds are selected in a way that the female component expresses natural or genetically engineered resistance against a herbicide, preferably a nonselective herbicide, whereas the male component does not express such resistance, and the seeds are in a mutual ratio up to about 1 : 1.
5. Method according to claim 4, characterised in that a mixture of seeds of common wheat (lat. Triticum aestivum L.) of both parent components is sown, wherein the female component (line AA) expresses natural or genetically engineered resistance against herbicide, preferably a non-selective herbicide, more preferably glyphosate, whereas the male component (line BB) does not express such resistance, and wherein the mixture comprises about 90 % of seeds of the female component and about 10 % of seeds of the male component (line BB) based on the total mass of the mixture of seeds.
6. Method according to claim 1 or 2, characterised in that the seeds of the female component are sown separately from the seeds of the male component in the form of one or more strips of the seeds of the female component separately from one or more strips of the seeds of the male component.
7. Method according to claim 6, characterised in that the seeds of common wheat (lat. Triticum aestivum L.) are sown.
8. Method according to claims 6 or 7, characterised in that the seeds of the female component are selected from the genotypes of common wheat (lat. Triticum aestivum L.) selected from the group comprising the genotypes Ficko, Guarni, Sana, Inoui, Marija, Bologna, whereas the seeds of the male component are selected from the genotype of the common wheat Ludwig.
9. Method according to any of preceding claims, characterised in that the active chemical hybridization substance is a compound of general Formula (I) and/or the agriculturally acceptable water-soluble salts thereof:
Figure imgf000029_0001
(I)
wherein:
X represents a bromine or iodine atom, or a -CN group or hydrogen or an alkyl or fluoroalkyl group, preferably a bromine atom or a -CN group;
Y represents a group selected from the group comprising -OH and/or -OM, wherein M represents a cation suitable for the formation of an agriculturally acceptable water-soluble salt, such as alkali metal cation, e. g. Na+ or K+, or tetraalkylammonium ion, preferably Na+.
10. Method according to any of preceding claims, characterised in that in commercially significant hermaphrodite plant species, preferably from the family of grasses, more preferably common wheat (lat. Triticum aestivum L.) a compound of general Formula (I) selected from the group comprising: 4-bromooxanilic acid, 4- cianooxanilic acid, tetramethylammonium salt of 4-bromooxanilic acid, tetramethylammonium salt of 4-cianooxanilic acid, tetramethylammonium salt of 4- fluorooxanilic acid is applied onto plants as an active chemical hybridizing agent to induce male sterility in the plants of the female component (line AA) in the period from the end of the premeiotic stage of the plants of the female component onwards and/or in their meiotic stage.
1 1. A compound for use as an active chemical hybridizing agent in the method of producing hybrid seeds of F generation of common wheat (lat. Triticum aestivum L.), characterised in that it is selected from the group comprising: 4-bromooxanilic acid, 4-cianooxanilic acid, tetramethylammonium salt of 4-bromooxanilic acid, tetramethylammonium salt of 4-cianooxanilic acid, tetramethylammonium salt of 4- fluorooxanilic acid and applied onto the plants to induce male sterility in the plants of the female component from the end of the premeiotic stage of the plants of the female component onwards and/or when the latter are in their meiotic stage.
12. A water-soluble preparation for chemical hybridization in the method of producing hybrid seeds of F] generation of common wheat (lat. Triticum aestivum L.), characterised in that it comprises one or more compounds of general Formula (I) and/or the agriculturally acceptable water-soluble salts thereof as the active chemical hybridizing agent:
Figure imgf000031_0001
(I)
wherein:
X represents a fluorine, chlorine, bromine or iodine atom, or a -CN group or hydrogen or an alkyl or fluoroalkyl group, preferably a bromine atom or a -CN group;
Y represents a group selected from the group comprising -OH and/or -OM, wherein M represents a cation suitable for the formation of an agriculturally acceptable water-soluble salt, such as alkali metal cation, e. g. Na+ or K+, or tetra- alkylammonium ion;
and optionally further additives, such as surfactants and/or defoamers.
13. Water-soluble preparation according to claim 12, characterised in that it comprises as the active chemical hybridizing agent one or more compounds selected from the group including: 4-bromooxanilic acid, 4-cianooxanilic acid, tetramethylammonium salt of 4-bromooxanilic acid, tetramethylammonium salt of 4- cianooxanilic acid and tetramethylammonium salt of 4-fluorooxanilic acid, and optionally further additives, such as surfactants and/or defoamers.
14. Water-soluble preparation according to claim 13, characterised in that it comprises as the active chemical hybridizing agent 4-bromooxanilic acid.
15. Water-soluble preparation according to any of preceding claims 12-14, characterised in that it is present in the form of a water-soluble powder, water-soluble granules, water-soluble crystals and a water-soluble concentrate, preferably in the form of a water-soluble powder or water-soluble granules.
16. Preparation for chemical hybridization in the method of producing hybrid seeds of Fj generation of common wheat, characterised in that it comprises one or more compounds according to claim 11 and is present in the form of a suspension concentrate.
17. Compounds according to claim 1 1 or preparations according to any of claims 13-15, characterised in that they are applied onto the plants of common wheat in the form of aqueous solutions in a concentration of the active substance ranging from 0.01 % to 1.5 %.
18. Compounds according to claim 1 1 or water-soluble preparations according to any of claims 13-15, characterised in that they are applied onto the plants of common wheat in the quantity of the active substance from 0.1 kg/ha to 10 kg/ha, preferably from 1.4 kg/ha to 3.5 kg/ha and in a concentration of 0.01 % to 1.5 %.
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