Abstract: The present disclosure relates to the technical field of breeding, in particular to an environmental-friendly and efficient breeding method of high-yield and high-quality wheat cultivars. In the present disclosure, the breeding method can improve a breeding efficiency of excellent new cultivars, further realize large-scale production, and further increase a planting area of the excellent cultivars. In addition, the breeding method can increase the number of products for the new cultivars, further increase a diversity of early-generation materials, and further increase a diversity of hybrid samples through the innovation of hybridization and breeding methods. The environmental-friendly and efficient breeding method of high-yield and high-quality wheat cultivars can increase a richness of excellent characteristics of the new cultivars through high-generation materials, hybridization, and off-site identification, thereby further improving an effect of breeding.

Abstract: The present disclosure provides a blending method of high-quality and dual-purpose flour for bread and noodles, belonging to the technical field of flour processing. The method includes: selecting flour of a high-quality and dual-purpose wheat variety for bread and noodles as a high-quality basic flour for blending; according to a large gradient experimental design, selecting a gradient range ratio with a sedimentation value ?46.0 mL and a dough development time ?9.6 min, followed by subdividing for small gradient experiments; selecting a ratio with flour sedimentation value and dough development time that reach an ideal value to blend a large amount of flour; and making bread and noodles for scoring, followed by determining a blending ratio if a scoring result reaches an ideal value.

Abstract: The present invention discloses an “inferior-eliminating and superior-selecting” breeding method for synergistically improving wheat yield and quality. A method for breeding target wheat varieties with improved yield and quality is provided herein, which combines the advantages of pedigree method and hybrid method, and provides a method for selection of all generations using molecular marker in combination with phenotype identification, and for selection of each generation according to different standards. Different from the derivative system method, the method reserves the traceability of line history and genetic relationship and the characteristics of simple operation and abundant genetic diversity of the hybrid method.

Abstract: The present disclosure discloses a mutant of a lycopene epsilon cyclase (Lcye) gene crucial in a wheat carotenoid synthesis pathway and use thereof. The present disclosure provides the following proteins: (1) a protein obtained by substituting serine at position 253 of an Lcye-D1 protein with phenylalanine; (2) a derived protein that is obtained by subjecting the protein in (1) to substitution and/or deletion and/or addition of one or more amino acid residues and has the same ability as the protein in (1); (3) a protein that has a homology of more than 99%, more than 95%, more than 90%, more than 85%, or more than 80% with the amino acid sequence defined in any one of (1) and (2) and has the same function as the amino acid sequence; and (4) a fusion protein obtained by attaching a tag to N-terminus and/or C-terminus of the protein in any one of (1) to (3).

Abstract: The present disclosure discloses a mutant of a lycopene epsilon cyclase (Lcye) gene crucial in a wheat carotenoid synthesis pathway and use thereof. The present disclosure provides the following proteins: (1) a protein obtained by substituting serine at position 253 of an Lcye-D1 protein with phenylalanine; (2) a derived protein that is obtained by subjecting the protein in (1) to substitution and/or deletion and/or addition of one or more amino acid residues and has the same ability as the protein in (1); (3) a protein that has a homology of more than 99%, more than 95%, more than 90%, more than 85%, or more than 80% with the amino acid sequence defined in any one of (1) and (2) and has the same function as the amino acid sequence; and (4) a fusion protein obtained by attaching a tag to N-terminus and/or C-terminus of the protein in any one of (1) to (3).

Abstract: The present invention discloses the preparation method of cis-p-menthane-1,8-di-secondary amine compounds and their application in weed control. The preparation method is as follows: cis-p-menthane-1,8-di-Schiff base compounds are used as the raw material, and the reducing agent is added in batches into the raw material in a polar organic solvent at ?10˜50° C. to react for 1˜24 h; after the reaction is complete, the reaction solution is quenched with distilled water and extracted with dichloromethane, and the extract phase is dried with anhydrous sodium sulfate, filtered with a filter and then distilled under reduced pressure to obtain crude cis-p-menthane-1,8-di-secondary amine compounds, which are purified into the pure product through recrystallization or silica gel column chromatography.

Abstract: The present invention discloses an “inferior-eliminating and superior-selecting” breeding method for synergistically improving wheat yield and quality. A method for breeding target wheat varieties with improved yield and quality is provided herein, which combines the advantages of pedigree method and hybrid method, and provides a method for selection of all generations using molecular marker in combination with phenotype identification, and for selection of each generation according to different standards. Different from the derivative system method, the method reserves the traceability of line history and genetic relationship and the characteristics of simple operation and abundant genetic diversity of the hybrid method.

Abstract: This invention discloses a type of 1,8-bis(Schiff base)-p-menthane derivatives as well as their preparation method and applications. The reaction of 1,8-diamino-p-menthane with a substituted benzaldehyde was carried out in a polar organic solvent at 0° C.-75° C. for 1-48 h. After the completion of the reaction, part of the solvent was distilled off to perform recrystallization to get a 1,8-bis(Schiff base)-p-menthane derivative, whose pre-emergence herbicidal activity against ryegrass was determined by using the Petri dish seed germination method. The 1,8-bis(Schiff base)-p-menthane derivatives, obtained with this method in high yield and mild reaction conditions, have a good inhibitory effect on the growth of annual ryegrass, and low toxicity.

Abstract: This invention discloses a type of 1,8-bis(Schiffbase)-p-menthane derivatives as well as their preparation method and applications. The reaction of 1,8-diamino-p-menthane with a substituted benzaldehyde was carried out in a polar organic solvent at 0° C.-75° C. for 1-48 h. After the completion of the reaction, part of the solvent was distilled off to perform recrystallization to get a 1,8-bis(Schiff base)-p-menthane derivative, whose pre-emergence herbicidal activity against ryegrass was determined by using the Petri dish seed germination method. The 1,8-bis(Schiff base)-p-menthane derivatives, obtained with this method in high yield and mild reaction conditions, have a good inhibitory effect on the growth of annual ryegrass, and low toxicity.

Abstract: Disclosed is a process for preparing isopimaric acid, comprising the following steps: First step: dissolving thermally isomerized rosin in acetone, adding in drops a solution of isobutanolamine in acetone to form a precipitate, standing, filtering, washing with ethanol, and drying to obtain crude ammonium salt of isopimaric acid; recrystallizing the crude ammonium salt of isopimaric acid according to multi-recrystallization, and drying to obtain purified crystal of ammonium salt of isopimaric acid; Second step: dissolving the purified crystal of ammonium salt of isopimaric acid obtained in the first step in ether, adding hydrochloric acid in portions until the crystal of ammonium salt of isopimaric acid disappears, removing a water layer and washing the ether layer with water to neutral, evaporating the ether, dissolving the residue in acetone, adding water slowly into the solution dropwise until crystals cease to grow, then filtering and drying to obtain purified isopimaric acid.

Abstract: A method for preparing pimaric acid type resin acids includes: step (1) adding refined resin acid, turpentine, or rosin along with maleic anhydride at a mass ratio of 1:0.3-1.5 into a reaction bottle, dissolving the ingredients into a C1-C10 lower fatty acid solvent, the mass ratio of the C1-C10 low fatty acid to refined resin acid is 0.05-30:1, then carrying out additional reaction by heating directly or with assistance of a microwave, subsequently cooling, crystallizing, filtering, and washing; and step (2) combining the filtrates collected in step (1), stripping the solvent by vacuum distillation to obtain pimaric acid type resin acid coarse product, dissolving the resulting coarse product in NaOH aqueous solution to prepare aqueous solution of pimaric acid type resin acid salt, adjusting the pH to 6-14 with a mineral acid or an organic acid, and either directly purifying or acidifying followed by purifying to obtain the final product.

Abstract: A method for preparing pimaric acid type resin acids includes the following steps: step (1) adding refined resin acid, turpentine, or rosin along with maleic anhydride at a mass ratio of 1:0.3-1.5 into a reaction bottle, dissolving the ingredients into a C1-C10 lower fatty acid solvent, the mass ratio of the C1-C10 low fatty acid to refined resin acid is 0.05-30:1, then carrying out additional reaction by heating directly or with assistance of a microwave, subsequently cooling, crystallizing, filtering, and washing; and step (2) combining the filtrates collected in step (1), stripping the solvent by vacuum distillation to obtain pimaric acid type resin acid coarse product, dissolving the resulting coarse product in NaOH aqueous solution to prepare aqueous solution of pimaric acid type resin acid salt, adjusting the pH level to 6-14 with a mineral acid or an organic acid while stirring, and either directly purifying or acidifying followed by purifying, the resulting precipitation to obtain the final product.

Abstract: A method for preparing pimaric acid type resin acids includes the following steps: step (1) adding refined resin acid, turpentine, or rosin along with maleic anhydride at a mass ratio of 1:0.3-1.5 into a reaction bottle, dissolving the ingredients into a C1-C10 lower fatty acid solvent, the mass ratio of the C1-C10 low fatty acid to refined resin acid is 0.05-30:1, then carrying out additional reaction by heating directly or with assistance of a microwave, subsequently cooling, crystallizing, filtering, and washing; and step (2) combining the filtrates collected in step (1), stripping the solvent by vacuum distillation to obtain pimaric acid type resin acid coarse product, dissolving the resulting coarse product in NaOH aqueous solution to prepare aqueous solution of pimaric acid type resin acid salt, adjusting the pH level to 6-14 with a mineral acid or an organic acid while stirring, and either directly purifying or acidifying followed by purifying, the resulting precipitation to obtain the final product.

Abstract: Disclosed is a process for preparing isopimaric acid, comprising the following steps: First step: dissolving thermally isomerized rosin in acetone, adding in drops a solution of isobutanolamine in acetone to form a precipitate, standing, filtering, washing with ethanol, and drying to obtain crude ammonium salt of isopimaric acid; recrystallizing the crude ammonium salt of isopimaric acid according to multi-recrystallization, and drying to obtain purified crystal of ammonium salt of isopimaric acid; Second step: dissolving the purified crystal of ammonium salt of isopimaric acid obtained in the first step in ether, adding hydrochloric acid in portions until the crystal of ammonium salt of isopimaric acid disappears, removing a water layer and washing the ether layer with water to neutral, evaporating the ether, dissolving the residue in acetone, adding water slowly into the solution dropwise until crystals cease to grow, then filtering and drying to obtain purified isopimaric acid.

Abstract: Two-way shock proof and shock absorbing towing coupling, including two opposite planar chain holders, each holder having at least two equally spaced lugs; at least four pairs of chains, each pair having two chain sections, each chain section having a plate link and a joint connected by a pin, two ends of each pair of chains being connected with the opposite lugs on the opposite planar chain holders by pins respectively; two towing frames for connecting with two neighboring vehicles, each frame having at least two arms, each of the arms being connected pivotally with another end of each chain section in each pair of chains, at least one shock proof bearing spring provided between two planar chain holders and the spring being coaxial with the two towing frames, the two nds of the spring abutting against an inner surface of the planar chain holders respectively, and a piston sleeve.