2263results about "Detergent compounding agents" patented technology

A polysaccharide for a detergent formulation, wherein the polysaccharide comprises a poly saccharide backbone functionalised with carboxylic acid groups, or salts or esters thereof, and sulfur-containing groups, or salts or esters thereof.

The invention relates to application of ten antibacterial peptides in the antimicrobial field. The ten antibacterial peptides have strong antibacterial activity on multi-drug-resistant bacteria, including but not limited to gram-negative bacteria such as escherichia coli, pseudomonas aeruginosa, acinetobacter baumannii, klebsiella pneumoniae and the like, and gram-positive bacteria such as staphylococcus aureus, enterococcus faecalis and the like. Activity research proves that any one of the ten antibacterial peptides has a remarkable effect of inhibiting, killing or preventing microbial infection. Due to the strong antibacterial property of any antibacterial peptide, the antibacterial peptide has wide application potential in the aspects of preparing antibacterial drugs, preservatives, antibacterial coatings, antibacterial fibers, antibacterial packaging materials and the like. Due to the unique property of the antibacterial peptide in the aspect of antibacterial performance, a new direction is provided for the development of efficient and reliable antibacterial agents and antibacterial technologies and products in multiple fields.

The invention discloses salt-tolerant xylanase and application thereof, and relates to the technical field of biology. The amino acid sequence of the salt-tolerant xylanase is as shown in SEQ ID NO: 1. According to the invention, a new xylanase gene xynaes is separated from a metagenome of Xinjiang Aiding Lake, and the xylanase belongs to the GH10 family and has low homology with reported xylanase. The recombinant xylanase has high activity and tolerance at a high temperature, has good performance in an alkaline environment, has high tolerance to various metal ions, quickly loses activity under SDS treatment, and should be prevented from being in contact with SDS in industrial production.

Disclosed herein is a water-soluble film including pullulan, carrageenan, a plasticizer, and a cross-linker, wherein pullulan comprises from about 50 wt.% to about 75 wt.% of the film and the cross-linker, when present, comprises from about 0.001 wt.% to about 5.0 wt.% of the film, based on the total weight of the film.

To provide a novel polypeptide that degrades trans-fatty acid-containing esters, and the like.SOLUTION: The novel esterase discovered by the present inventors have activity to degrade trans-fatty acid-containing esters. The esterase disclosed herein is a polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 2, 8, 12, 16, or 22, or a polypeptide encoded by the base sequence shown in SEQ ID NO: 1, 7, 11, 15, or 21, or a polypeptide having at least 70% sequence homology thereto. This esterase has the ability to degrade esters even at low and / or high temperatures, and it was also found that it has excellent thermal stability in terms of ester decomposition ability at 65°C. The esterase disclosed herein is useful for oil treatment, for example, in wastewater treatment, detergents, and fat modification / oil production technology.SELECTED DRAWING: None

The invention provides a new energy automobile battery flexible disassembling adhesive and a preparation method thereof, and belongs to the technical field of new energy automobile batteries, the flexible disassembling adhesive comprises the following components by weight: 45-50 parts of deionized water; 8 to 10 parts of gamma-butyrolactone; 5 to 8 parts of propylene glycol methyl ether acetate; 2 to 3 parts of microencapsulated lipase; 2 to 3 parts of nano cellulose immobilized protease; 6 to 8 parts of urea peroxide; 0.5 to 1 part of nano manganese dioxide; 0.7 to 1.1 parts of a sodium citrate / sodium lactate buffer solution; 1.5 to 2.5 parts of polyvinylpyrrolidone K30; 0.8 to 1.2 parts of hydroxypropyl methyl cellulose; 0.05 to 0.1 part of a graphene oxide nanosheet; 0.5 to 0.8 part of a benzotriazole derivative; 0.1 to 0.3 part of sodium molybdate; 6 to 8 parts of sorbitol; and 5-7 parts of ascorbic acid. The flexible disassembly adhesive solves the problems of low efficiency, serious environmental pollution, high safety risk and low material recovery rate in traditional battery disassembly.

A water-soluble film comprising carrageenan and a 1-99% wt plasticiser, the film having:a. a light transmittance of greater than 20% measured with at least one wavelength in the range 400-800 nanometres; andb. a thickness from 40 to 200 micrometres.

A concentrated laundry composition premix which is dilutable in water to form a laundry liquid composition, the viscosity which when formed from a dilution of five parts by volume water to one part premix and measured at 25° C. and at 106 s−1 is from 200 to 800 mPa·s., said premix comprising at least 10% wt. water, from 0.1 to 8% wt. ethoxylated polyol ester, and comprising from 5 to 70% wt. surfactant active excluding the ethoxylated polyol ester and where the ethoxylated polyol ester is not sorbeth stearate, wherein the surfactant comprises anionic surfactant and non-ionic surfactant in a weight ratio of from 50:50 to 1:99 and wherein the composition comprises from 0 to 5% wt. alkyl ether sulphate.

The invention belongs to the field of antibacterial peptides, and particularly relates to a marine antibacterial peptide based on machine learning mining and application thereof. The invention discloses a method for mining marine antibacterial peptides based on machine learning, and 10 marine antibacterial peptides are screened, and the amino acid sequence of the marine antibacterial peptides is shown as any one of SEQ ID NO: 1-10. Wherein the Peptide 5 and the Peptide 8 have a broad-spectrum antibacterial characteristic, and the drug-resistant bacteria MIC (Minimum Inhibitory Concentration) of the Peptide 5 and the Peptide 8 is as low as 2-8 mu g / mL and is superior to that of The Peptide 2 and the Peptide 7 belong to strain specific antibacterial peptides, and are highly specific to bacillus subtilis. The antibacterial peptide has a wide application prospect in the field of preparation of antibacterial dressings and antibacterial drugs.

The present invention relates to the use of guanidine and / or at least one guanidine salt for stabilizing aqueous products, such as cosmetics and washing and cleaning products, against microbial attack.

The present invention discloses a sea dragon-derived antimicrobial peptide, SsPle, for antimicrobial applications in the complex environments of tropical islands and reefs. The amino acid sequence of this antimicrobial peptide is shown in SEQ ID NO. 3. This antimicrobial peptide, SsPle, exhibits good water solubility, broad antimicrobial activity, and highly stable antimicrobial properties under high temperature, high salt, and ultraviolet irradiation conditions. It can inhibit the release of free bacterial endotoxins and has significant application prospects as an eco-friendly antimicrobial agent in the unique environments of South China Sea islands and reefs.

To provide a cleanser for oral appliances with excellent deodorizing performance using a novel formulation technology.SOLUTION: A cleanser for oral appliances disclosed herein comprises (A) cyclodextrin, and (B) at least one selected from the group consisting of alkyl sulfates with C8-20 alkyl groups, and hydrogen carbonates.SELECTED DRAWING: None

The invention relates to a new endolysin and to its use for its anti-staphylococcal activity, in particular anti-staphylococcal activity against strains resistant to an antibiotic and / or to a phage, in particular anti-S. aureus and / or anti-S. pseudintermedius. It can therefore be used in a disinfectant or anti-biofilm solution, in food safety, in cosmetics or in therapies, for example in the treatment of pathologies caused by Staphylococcus such as skin pathologies in humans and domestic animals.

In the present invention new protease enzymes are provided. More specifically, genetically engineered protease enzymes, compositions comprising the enzymes, and methods of making and using the enzymes or compositions comprising the enzymes are provided.

A water-soluble film is provided that is excellent in film transparency and water solubility and inhibits sticking between the films. A water-soluble film includes a polyvinyl alcohol resin, wherein a crystallite size obtained from an X-ray profile obtained by wide-angle X-ray measurement is from 4.0 to 5.5 nm and a degree of crystallization obtained from the X-ray profile is from 10.0% to 25.0%, and an external haze is from 7.0% to 30.0%.

The invention provides a preparation method and application of a soapberry leaf extract, and belongs to the technical field of traditional Chinese medicine extracts.The preparation method comprises the steps that soapberry leaves, bran, cottonseed hulls, quicklime and magnesium sulfate are evenly mixed and sterilized to serve as fermentation ingredients, aspergillus niger is inoculated for solid fermentation, spores are separated after fermentation is completed, and the soapberry leaf extract is obtained; preparing spore powder and a pretreatment material; the pretreated material is subjected to countercurrent extraction, purification and concentration, and the soapberry leaf extract is obtained. The soapberry leaf extract is used as a raw material to prepare medicines, cosmetics, daily necessities or disinfection products. The solid fermentation technology is adopted for pretreatment, the production scale is large, the yield is high, other reagents do not need to be consumed, cost is low, operation is easy, and the method is suitable for industrialization.

The present invention provides a method for cleaning an object surface, the method having enzyme activity even if using high concentrations of surfactants and an enzyme together, and exhibiting excellent cleaning performance for solid fat-containing contamination adhering to the object surface of tableware or the like without being affected by the hardness of water used for cleaning (for example, 0 to 20° dH (by German hardness)).A method for cleaning an object surface including, bringing a cleaning liquid obtained by diluting a liquid cleaning agent composition with water into contact with the object surface, the liquid cleaning agent composition containing the following component (a), component (b) and component (e) and water,component (a): an alkyl sulfosuccinic acid ester having an alkyl group with 5 or more and 18 or less carbons or a salt thereof,component (b): one or more surfactants selected from semipolar surfactants and amphoteric surfactants (excluding sulfobetaines), andcomponent (e): an enzyme.

Disclosed herein are compositions that comprise at least one acrylic acid- and / or itaconic acid-polysaccharide derivative. Such a derivative can be produced by contacting acrylic acid and / or itaconic acid with a polysaccharide, wherein the acrylic acid- and / or itaconic acid-polysaccharide derivative has a degree of substitution (DoS) up to about 3.0 with at least one group formed by the acrylic acid and / or itaconic acid. Further disclosed are methods of producing acrylic acid- and / or itaconic acid-polysaccharide derivatives, as well as their use in various applications and products.

An improved polyurea and chitosan core-shell delivery particle that encapsulates a benefit agent is described. Chitosan is pre-modified with a modifying compound, which is cationic, anionic or nonionic. Alternatively, modification is completed in situ. The modifying compound is selected from the group consisting of epoxides, aldehydes or alpha, beta-unsaturated compounds and reacts with the free amine moiety of the chitosan, covalently bound to the amine moiety of the chitosan via a CN bond. The modifying compound may contain an acidic group, a hydroxyl group, and a quaternary ammonium group. The reaction product of chitosan, a modifying compound, and an electrophile, preferably a polyisocyanate, produces microcapsules that have charge, improved release properties, improved compatibility, or enhanced degradation properties (e.g., in OECD Test Method 301B).

To provide lipase with improved wash performance, reduced odor-generation and / or improved storage stability / longer shelf life / increased thermostability.SOLUTION: The present invention relates to variants of a parent lipase which has lipase activity and comprises one or more substitutions corresponding to G23S, D27N, A40I, F51I,L, E56R, D57N, V60E,K, K98I, N101D, R118F, G163S, T231R, N233R, Y220F, T244E, and P256T using SEQ ID NO: 2 for numbering. The present invention also relates to compositions or microcapsule compositions comprising a lipase variant of the invention and to liquid products comprising a microcapsule composition of the invention as well as the use of the microcapsule composition for stabilizing lipase variants of the invention.SELECTED DRAWING: None

Provided herein is a water-soluble film that includes carrageenan and 1 to 99% wt plasticiser, based on dry weight of the film. Also provided is a water-soluble capsule that includes the film.

The invention relates to a novel method for preparing microcapsule slurry. The microcapsule slurry is also an object of the invention. Perfuming compositions and consumer products, in particular perfumed consumer products in the form of home care or personal care products, comprising the microcapsule slurry are also part of the invention.

The present invention relates to detergent compositions comprising protease variants and alpha-amylases or variants thereof. Furthermore, the present invention relates to methods of using the detergent compositions.

The present invention relates to novel esterases, more particularly to esterase variants having improved activity and / or improved thermostability compared to the esterase of SEQ ID NO: 1 and the uses thereof for degrading polyester containing material, such as plastic products. The esterases of the invention are particularly suited to degrade polyethylene terephthalate, and material containing polyethylene terephthalate.

The invention provides alkali-resistant cellulase StrEgl and application thereof, and belongs to the technical field of bioengineering, the amino acid sequence of the cellulase StrEgl is as shown in SEQ ID NO.1, and the nucleotide sequence for coding the cellulase StrEgl gene is as shown in SEQ ID NO.2. The invention further provides a preparation method of the alkali-resistant cellulase StrEgl. The alkali-resistant cellulase StrEgl provided by the invention has alkali resistance and can degrade cellulose under an alkaline condition; in an environment with a pH value of 9-10, the enzymatic hydrolysate still has good enzymatic hydrolysis activity; meanwhile, the cellulase StrEgl has good tolerance to temperature, metal ions and chemical reagents, is very suitable for industrial application, and has wide application prospects in the fields of papermaking, spinning, detergents and the like.

The application relates to a modified polylactic acid oligomer and a preparation method and application thereof. The modified polylactic acid oligomer has the structure shown in the following formula (I). The modified polylactic acid oligomer obtained by copolymerization of 5-hydroxy-2-hexenoic acid and lactic acid has more excellent and stable and persistent antibacterial activity, the antibacterial efficiency is greatly improved, the sterilization rate is improved, and the sterilization time is shortened; when the modified polylactic acid oligomer is applied to various antibacterial coatings and textile finishing, the surface no longer has a wet sticky feeling, the commercialization and wide application of the material are more beneficial, and the modified polylactic acid oligomer has higher affinity to a target substrate, so that the persistence, stability and washability of a surface coating can be improved.

The invention belongs to the technical field of gene engineering and enzyme engineering, and discloses an alkaline protease mutant and application thereof. Compared with parent alkaline protease with an amino acid sequence as shown in SEQ ID NO: 1, the alkaline protease mutant has disulfide key site pair mutation, and the disulfide key site pair has the following characteristics: i, the disulfide key site pair is not in the range of an active site # imgabs0 # of the alkaline protease mutant; ii, the difference value of amino acid site numbers is greater than or equal to 10; iii, the distance between two cysteine SG atoms forming a disulfide bond is within # imgabs 1 #; iv, the angle of Chi3 is 30 degrees lt; chi3lt; chi3lt; 140 DEG or-30 DEG gt; chi3gt; chi3gt; and-140 DEG C. Compared with the parent alkaline protease, the alkaline protease mutant has the advantages that the heat resistance and / or detergent tolerance are / is obviously improved, the decontamination effect on protein dirty cloth is better, and the requirements of the daily chemical washing industry can be better met.

The invention relates to a detergent tablet comprising from 5 to 20 percent by weight citric acid or a salt thereof and from 3 to 25 percent by weight sodium benzoate and a surfactant. The invention also relates to a method of forming a wash liquor by combining a detergent tablet with water in a container. The invention also relates to the use of a detergent tablet to create a washing liquor for cleaning surfaces.

The present invention relates to mannanase variants with improved stability. The present invention also relates to polynucleotides encoding the variants; nucleic acid constructs, vectors, and host cells comprising the polynucleotides; and methods of using the variants.

To provide a detergent composition containing α-amylase that exhibits high specific activity at low temperatures.SOLUTION: A detergent composition containing one or more proteins selected from the following (A), (B), (C), and (D). (A) A protein consisting of an amino acid sequence having at least 90% identity with the amino acid sequence shown in SEQ ID NO: 2 and having α-amylase activity. (B) A protein consisting of an amino acid sequence having at least 90% identity with the amino acid sequence shown in SEQ ID NO: 4 and having α-amylase activity. (C) A protein consisting of an amino acid sequence having at least 90% identity with the amino acid sequence shown in SEQ ID NO: 6 and having α-amylase activity. (D) A protein consisting of an amino acid sequence having at least 90% identity with the amino acid sequence shown in SEQ ID NO: 8 and having α-amylase activity.SELECTED DRAWING: None