JP2000501130A - 改良された染色適性を有するラッカーゼ - Google Patents
改良された染色適性を有するラッカーゼInfo
- Publication number
- JP2000501130A JP2000501130A JP9520086A JP52008697A JP2000501130A JP 2000501130 A JP2000501130 A JP 2000501130A JP 9520086 A JP9520086 A JP 9520086A JP 52008697 A JP52008697 A JP 52008697A JP 2000501130 A JP2000501130 A JP 2000501130A
- Authority
- JP
- Japan
- Prior art keywords
- laccase
- dyeing
- composition
- hair
- amino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 108010029541 Laccase Proteins 0.000 title claims abstract description 104
- 239000000203 mixture Substances 0.000 claims abstract description 102
- 238000004043 dyeing Methods 0.000 claims abstract description 89
- 210000004209 hair Anatomy 0.000 claims abstract description 68
- 239000002243 precursor Substances 0.000 claims abstract description 49
- 102000004190 Enzymes Human genes 0.000 claims abstract description 33
- 108090000790 Enzymes Proteins 0.000 claims abstract description 33
- 102000011782 Keratins Human genes 0.000 claims abstract description 30
- 108010076876 Keratins Proteins 0.000 claims abstract description 30
- 238000000034 method Methods 0.000 claims abstract description 26
- 239000003607 modifier Substances 0.000 claims abstract description 17
- 230000000813 microbial effect Effects 0.000 claims abstract description 14
- 210000002268 wool Anatomy 0.000 claims abstract description 10
- 238000010186 staining Methods 0.000 claims description 36
- 239000000835 fiber Substances 0.000 claims description 25
- 241001313536 Thermothelomyces thermophila Species 0.000 claims description 22
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 19
- -1 o-aminophenol 3,4-diaminotoluene Chemical compound 0.000 claims description 19
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 17
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 12
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 8
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 7
- DGRGLKZMKWPMOH-UHFFFAOYSA-N 4-methylbenzene-1,2-diamine Chemical compound CC1=CC=C(N)C(N)=C1 DGRGLKZMKWPMOH-UHFFFAOYSA-N 0.000 claims description 7
- 150000004985 diamines Chemical class 0.000 claims description 7
- PDGMOSZQOWALLR-UHFFFAOYSA-N 3-methoxyphenazine-2,7-diamine Chemical compound NC1=CC=C2N=C(C=C(C(OC)=C3)N)C3=NC2=C1 PDGMOSZQOWALLR-UHFFFAOYSA-N 0.000 claims description 6
- 241000233866 Fungi Species 0.000 claims description 6
- GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 claims description 6
- BAHPQISAXRFLCL-UHFFFAOYSA-N 2,4-Diaminoanisole Chemical compound COC1=CC=C(N)C=C1N BAHPQISAXRFLCL-UHFFFAOYSA-N 0.000 claims description 5
- 230000001590 oxidative effect Effects 0.000 claims description 4
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims description 4
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 claims description 3
- RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 claims description 3
- WCPGNFONICRLCL-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)ethanol Chemical compound NC1=CC=C(OCCO)C(N)=C1 WCPGNFONICRLCL-UHFFFAOYSA-N 0.000 claims description 3
- MGLZGLAFFOMWPB-UHFFFAOYSA-N 2-chloro-1,4-phenylenediamine Chemical compound NC1=CC=C(N)C(Cl)=C1 MGLZGLAFFOMWPB-UHFFFAOYSA-N 0.000 claims description 3
- HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 claims description 3
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 claims description 3
- ALYNCZNDIQEVRV-UHFFFAOYSA-M 4-aminobenzoate Chemical compound NC1=CC=C(C([O-])=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-M 0.000 claims description 3
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 claims description 3
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 claims description 3
- YOJKEVXNAVNUGW-UHFFFAOYSA-N 4-n-chlorobenzene-1,4-diamine Chemical compound NC1=CC=C(NCl)C=C1 YOJKEVXNAVNUGW-UHFFFAOYSA-N 0.000 claims description 3
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 claims description 3
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 claims description 3
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 3
- 125000005456 glyceride group Chemical group 0.000 claims description 3
- DAJJQPSBBOLGSQ-UHFFFAOYSA-N pentyl 4-(diethoxyamino)benzoate Chemical compound CCCCCOC(=O)C1=CC=C(N(OCC)OCC)C=C1 DAJJQPSBBOLGSQ-UHFFFAOYSA-N 0.000 claims description 3
- MQEHZPALNAWFGR-UHFFFAOYSA-N phenazine-1,8-dicarboxylic acid Chemical compound C1=CC=C(C(O)=O)C2=NC3=CC(C(=O)O)=CC=C3N=C21 MQEHZPALNAWFGR-UHFFFAOYSA-N 0.000 claims description 3
- ZNXLTODDKYXLAD-UHFFFAOYSA-N phenazine-2,7-diamine Chemical compound C1=C(N)C=CC2=NC3=CC(N)=CC=C3N=C21 ZNXLTODDKYXLAD-UHFFFAOYSA-N 0.000 claims description 3
- PVOLOPUMLZLTOL-UHFFFAOYSA-N phenazine-2,7-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=NC3=CC(C(=O)O)=CC=C3N=C21 PVOLOPUMLZLTOL-UHFFFAOYSA-N 0.000 claims description 3
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 claims description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 2
- KKTUQAYCCLMNOA-UHFFFAOYSA-N 2,3-diaminobenzoic acid Chemical compound NC1=CC=CC(C(O)=O)=C1N KKTUQAYCCLMNOA-UHFFFAOYSA-N 0.000 claims description 2
- QKGQHTCUNGPCIA-UHFFFAOYSA-N 2,4,5-Trihydroxytoluene Chemical compound CC1=CC(O)=C(O)C=C1O QKGQHTCUNGPCIA-UHFFFAOYSA-N 0.000 claims description 2
- BXHKFWYIKUWSEF-UHFFFAOYSA-N 2-[(8-amino-7-methoxyphenazin-2-yl)-(2-hydroxyethyl)amino]ethanol Chemical compound C1=C(N(CCO)CCO)C=C2N=C(C=C(C(OC)=C3)N)C3=NC2=C1 BXHKFWYIKUWSEF-UHFFFAOYSA-N 0.000 claims description 2
- JWGZBRAKZAULMG-UHFFFAOYSA-N 2-[(8-amino-7-methylphenazin-2-yl)-(2-hydroxyethyl)amino]ethanol Chemical compound C1=C(N(CCO)CCO)C=C2N=C(C=C(C(C)=C3)N)C3=NC2=C1 JWGZBRAKZAULMG-UHFFFAOYSA-N 0.000 claims description 2
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims description 2
- MMXGRWOPIXWDHU-UHFFFAOYSA-N 3,8-dimethoxyphenazine-2,7-diamine Chemical compound NC1=C(OC)C=C2N=C(C=C(C(OC)=C3)N)C3=NC2=C1 MMXGRWOPIXWDHU-UHFFFAOYSA-N 0.000 claims description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 2
- SHOZSPAWFLGEKI-UHFFFAOYSA-N CC1=CC2=C(C=C1)N=C3C=C(C(=CC3=N2)C)C(=O)N Chemical compound CC1=CC2=C(C=C1)N=C3C=C(C(=CC3=N2)C)C(=O)N SHOZSPAWFLGEKI-UHFFFAOYSA-N 0.000 claims description 2
- KYZHGEFMXZOSJN-UHFFFAOYSA-N benzoic acid isobutyl ester Natural products CC(C)COC(=O)C1=CC=CC=C1 KYZHGEFMXZOSJN-UHFFFAOYSA-N 0.000 claims description 2
- RUMNAEDKTMKXQP-UHFFFAOYSA-N n-[8-(diethylamino)phenazin-2-yl]methanesulfonamide Chemical compound C1=CC(NS(C)(=O)=O)=CC2=NC3=CC(N(CC)CC)=CC=C3N=C21 RUMNAEDKTMKXQP-UHFFFAOYSA-N 0.000 claims description 2
- LXTZRIBXKVRLOA-UHFFFAOYSA-N padimate a Chemical compound CCCCCOC(=O)C1=CC=C(N(C)C)C=C1 LXTZRIBXKVRLOA-UHFFFAOYSA-N 0.000 claims description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 claims 2
- OBMPCTWLIPRHDI-UHFFFAOYSA-N 2-[(8-amino-7-chlorophenazin-2-yl)-(2-hydroxyethyl)amino]ethanol Chemical compound OCCN(CCO)C1=CC=C2N=C(C=C(C(N)=C3)Cl)C3=NC2=C1 OBMPCTWLIPRHDI-UHFFFAOYSA-N 0.000 claims 1
- DWKMAFHBMADXRP-UHFFFAOYSA-N 2-[(8-amino-7-methylphenazin-2-yl)amino]ethanol Chemical compound C1=C(NCCO)C=C2N=C(C=C(C(C)=C3)N)C3=NC2=C1 DWKMAFHBMADXRP-UHFFFAOYSA-N 0.000 claims 1
- FYJOQOVUJGSARX-UHFFFAOYSA-N 2-[(8-aminophenazin-2-yl)-(2-hydroxyethyl)amino]ethanol Chemical compound C1=CC(N(CCO)CCO)=CC2=NC3=CC(N)=CC=C3N=C21 FYJOQOVUJGSARX-UHFFFAOYSA-N 0.000 claims 1
- DUAYDERMVQWIJD-UHFFFAOYSA-N 2-n,2-n,6-trimethyl-1,3,5-triazine-2,4-diamine Chemical compound CN(C)C1=NC(C)=NC(N)=N1 DUAYDERMVQWIJD-UHFFFAOYSA-N 0.000 claims 1
- GBMGXXPFNLJLMP-UHFFFAOYSA-N 3-ethoxybenzene-1,2-diamine Chemical compound CCOC1=CC=CC(N)=C1N GBMGXXPFNLJLMP-UHFFFAOYSA-N 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 230000006651 lactation Effects 0.000 claims 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 claims 1
- CCBDBWAKDHGKNI-UHFFFAOYSA-N phenazine-2,8-diamine Chemical compound C1=CC(N)=CC2=NC3=CC(N)=CC=C3N=C21 CCBDBWAKDHGKNI-UHFFFAOYSA-N 0.000 claims 1
- 150000002988 phenazines Chemical class 0.000 claims 1
- 102000004882 Lipase Human genes 0.000 abstract 1
- 108090001060 Lipase Proteins 0.000 abstract 1
- 239000004367 Lipase Substances 0.000 abstract 1
- 235000019421 lipase Nutrition 0.000 abstract 1
- 239000000975 dye Substances 0.000 description 61
- 230000000694 effects Effects 0.000 description 19
- 239000008363 phosphate buffer Substances 0.000 description 13
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 11
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- DBIJGSXWEMYQHU-UHFFFAOYSA-N benzene;benzene-1,4-diol Chemical compound C1=CC=CC=C1.OC1=CC=C(O)C=C1 DBIJGSXWEMYQHU-UHFFFAOYSA-N 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 108010037176 copper oxidase Proteins 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 239000013604 expression vector Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 150000002476 indolines Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical class C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- RXXRAXCFJOKVAC-UHFFFAOYSA-N n-(8-methoxyphenazin-2-yl)methanesulfonamide Chemical compound C1=CC(NS(C)(=O)=O)=CC2=NC3=CC(OC)=CC=C3N=C21 RXXRAXCFJOKVAC-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- XWLUFINGMMDFPD-UHFFFAOYSA-N naphthalen-1-ol Chemical compound C1=CC=C2C(O)=CC=CC2=C1.C1=CC=C2C(O)=CC=CC2=C1 XWLUFINGMMDFPD-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 229940090244 palladia Drugs 0.000 description 1
- 239000001024 permanent hair color Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002954 polymerization reaction product Substances 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 238000002741 site-directed mutagenesis Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- NZFNXWQNBYZDAQ-UHFFFAOYSA-N thioridazine hydrochloride Chemical compound Cl.C12=CC(SC)=CC=C2SC2=CC=CC=C2N1CCC1CCCCN1C NZFNXWQNBYZDAQ-UHFFFAOYSA-N 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 239000013598 vector Substances 0.000 description 1
- 210000005253 yeast cell Anatomy 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/30—Material containing basic nitrogen containing amide groups furs feathers, dead hair, furskins, pelts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/415—Aminophenols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
- A61K8/66—Enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0055—Oxidoreductases (1.) acting on diphenols and related substances as donors (1.10)
- C12N9/0057—Oxidoreductases (1.) acting on diphenols and related substances as donors (1.10) with oxygen as acceptor (1.10.3)
- C12N9/0061—Laccase (1.10.3.2)
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/0004—General aspects of dyeing
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/008—Preparing dyes in situ
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/32—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using oxidation dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/14—Wool
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/86—Products or compounds obtained by genetic engineering
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Medicinal Chemistry (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK135795 | 1995-11-30 | ||
| DK1357/95 | 1995-11-30 | ||
| PCT/DK1996/000499 WO1997019999A1 (en) | 1995-11-30 | 1996-11-29 | Laccases with improved dyeing properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000501130A true JP2000501130A (ja) | 2000-02-02 |
| JP2000501130A5 JP2000501130A5 (enExample) | 2004-10-21 |
Family
ID=8103974
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9520086A Ceased JP2000501130A (ja) | 1995-11-30 | 1996-11-29 | 改良された染色適性を有するラッカーゼ |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP0865465B1 (enExample) |
| JP (1) | JP2000501130A (enExample) |
| CN (1) | CN1084357C (enExample) |
| AU (1) | AU706338B2 (enExample) |
| CA (1) | CA2238697A1 (enExample) |
| DE (1) | DE69613143T2 (enExample) |
| ES (1) | ES2159765T3 (enExample) |
| WO (1) | WO1997019999A1 (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2265734A1 (en) | 1996-10-08 | 1998-04-16 | Novo Nordisk A/S | Diaminobenzoic acid derivatives as dye precursors |
| FR2763841B1 (fr) * | 1997-06-03 | 2000-02-11 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| FR2773474B1 (fr) * | 1998-01-13 | 2002-10-11 | Oreal | Composition tinctoriale et procedes de teinture des fibres keratiniques la mettant en oeuvre |
| FR2773475B1 (fr) * | 1998-01-13 | 2001-02-02 | Oreal | Composition tinctoriale et procedes de teinture des fibres keratiniques la mettant en oeuvre |
| FR2773473B1 (fr) * | 1998-01-13 | 2002-12-27 | Oreal | Composition tinctoriale et procedes de teinture des fibres keratiniques |
| FR2773483B1 (fr) * | 1998-01-13 | 2001-04-20 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| FR2773476B1 (fr) | 1998-01-13 | 2001-02-23 | Oreal | Composition tinctoriale et procedes de teinture des fibres keratiniques la mettant en oeuvre |
| FR2773480B1 (fr) † | 1998-01-13 | 2000-05-12 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| US7060112B2 (en) | 1998-01-13 | 2006-06-13 | L'oreal | Composition for the oxidation dyeing of keratinous fibers containing a laccase and dyeing method using this composition |
| FR2773477B1 (fr) | 1998-01-13 | 2001-02-23 | Oreal | Composition tinctoriale et procedes de teinture des fibres keratiniques la mettant en oeuvre |
| FR2773478B1 (fr) | 1998-01-13 | 2000-02-25 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| FR2773482B1 (fr) † | 1998-01-13 | 2001-04-20 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| US5899212A (en) * | 1998-05-07 | 1999-05-04 | Novo Nordisk A/S | Re-formation of keratinous fibre cross links |
| US6572843B1 (en) | 1998-12-01 | 2003-06-03 | Novozymes, A/S | Method for treating hair |
| FR2791256B1 (fr) | 1999-03-26 | 2001-08-31 | Oreal | Procede de teinture d'oxydation utilisant la n-acetylcysteine a titre d'agent reducteur et une laccase a titre d'agent oxydant |
| FR2791885B1 (fr) | 1999-04-07 | 2003-05-30 | Oreal | Procede de teinture d'oxydation utilisant un cetose a titre d'agent reducteur et une laccase a titre d'agent oxydant |
| JP4488125B2 (ja) * | 1999-06-30 | 2010-06-23 | ライオン株式会社 | 毛髪用組成物 |
| FR2798854B1 (fr) | 1999-09-24 | 2001-11-16 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| AU2001239217A1 (en) * | 2000-03-17 | 2001-09-24 | Novozymes A/S | Method for dyeing dry hair |
| FR2806908B1 (fr) | 2000-03-30 | 2002-12-20 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| FR2830193B1 (fr) * | 2001-09-28 | 2004-10-15 | Oreal | Composition tinctoriale comprenant une base d'oxydation du type diaminopyrazole et un agent oxydant de nature enzymatique |
| DE10163052A1 (de) * | 2001-12-21 | 2003-07-17 | Henkel Kgaa | Restrukturierung und Ausrüstung keratinischer Fasern |
| FR2836632B1 (fr) * | 2002-03-01 | 2006-11-03 | Oreal | Composition non colorante contenant un precurseur et un catalyseur de reaction d'oxydation |
| BRPI0503921A (pt) * | 2004-06-18 | 2006-07-18 | Oreal | composição cosmética, processos para tintura das fibras queratìnicas, processo para clareamento das fibras queratìnicas, dispositivo com múltiplos compartimentos, uso de composto hidroxialquilado e uso de uma composição de tintura |
| US7326258B2 (en) | 2004-06-18 | 2008-02-05 | L'oreal S.A. | Compositions comprising hydroxyalkyl direct dyes, implementation processes and uses thereof |
| DE102006061571A1 (de) | 2006-12-27 | 2008-07-03 | Robert Bosch Gmbh | Verfahren und Vorrichtung zum Umsetzen von Stückgütern |
| FR2978040B1 (fr) | 2011-07-22 | 2015-01-30 | Oreal | Procede de traitement de la transpiration humaine utilisant des polyphenols et un systeme catalytique d'oxydation enzymatique et/ou chimique |
| WO2015074821A1 (en) * | 2013-11-21 | 2015-05-28 | Unilever Plc | Hair colouring composition |
| US20180202011A1 (en) | 2015-09-04 | 2018-07-19 | Novozymes A/S | Methods of inhibiting aa9 lytic polysaccharide monooxygenase catalyzed inactivation of enzyme compositions |
| WO2020058253A1 (en) | 2018-09-18 | 2020-03-26 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of carbohydrate material and fermentation of sugars |
| WO2020058248A1 (en) | 2018-09-18 | 2020-03-26 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of carbohydrate material and fermentation of sugars |
| WO2020058249A1 (en) | 2018-09-18 | 2020-03-26 | Dsm Ip Assets B.V. | Process for enzymatic hydrolysis of carbohydrate material and fermentation of sugars |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3251742A (en) * | 1962-05-14 | 1966-05-17 | Revlon | Method for coloring human hair with polyhydric aromatic compound, aromatic amine andan oxidation enzyme |
| FR2673534B1 (fr) * | 1991-03-08 | 1995-03-03 | Perma | Composition pour la coloration enzymatique des fibres keratiniques, notamment des cheveux, et son application dans un procede de coloration. |
| FR2692782B1 (fr) * | 1992-06-25 | 1995-06-23 | Oreal | Procede de teinture des fibres keratiniques avec des derives indoliques ou indoliniques, du peroxyde d'hydrogene et une peroxydase. |
| DE4314317A1 (de) * | 1993-04-30 | 1994-11-03 | Henkel Kgaa | Isatinhaltige Mittel zum Färben von keratinhaltigen Fasern |
| US5480801A (en) * | 1993-09-17 | 1996-01-02 | Novo Nordisk A/S | Purified PH neutral Rhizoctonia laccases and nucleic acids encoding same |
| CN1192108C (zh) * | 1994-06-03 | 2005-03-09 | 诺沃奇梅兹生物技术有限公司 | 纯化的毁丝霉属漆酶及编码该酶的核酸 |
| WO1995033837A1 (en) * | 1994-06-03 | 1995-12-14 | Novo Nordisk Biotech, Inc. | Purified scytalidium laccases and nucleic acids encoding same |
| ATE223488T1 (de) * | 1994-06-24 | 2002-09-15 | Novozymes As | Gereinigte polyporus laccasen und dafür kodierende nukleinsäuren |
-
1996
- 1996-11-29 CA CA002238697A patent/CA2238697A1/en not_active Abandoned
- 1996-11-29 CN CN 96198697 patent/CN1084357C/zh not_active Expired - Fee Related
- 1996-11-29 DE DE69613143T patent/DE69613143T2/de not_active Expired - Fee Related
- 1996-11-29 JP JP9520086A patent/JP2000501130A/ja not_active Ceased
- 1996-11-29 EP EP96938989A patent/EP0865465B1/en not_active Expired - Lifetime
- 1996-11-29 AU AU76220/96A patent/AU706338B2/en not_active Ceased
- 1996-11-29 ES ES96938989T patent/ES2159765T3/es not_active Expired - Lifetime
- 1996-11-29 WO PCT/DK1996/000499 patent/WO1997019999A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| CA2238697A1 (en) | 1997-06-05 |
| WO1997019999A1 (en) | 1997-06-05 |
| AU7622096A (en) | 1997-06-19 |
| CN1084357C (zh) | 2002-05-08 |
| AU706338B2 (en) | 1999-06-17 |
| DE69613143D1 (de) | 2001-07-05 |
| EP0865465B1 (en) | 2001-05-30 |
| ES2159765T3 (es) | 2001-10-16 |
| EP0865465A1 (en) | 1998-09-23 |
| CN1203615A (zh) | 1998-12-30 |
| DE69613143T2 (de) | 2002-03-07 |
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