US 5,885,304 AGrant
Enhancement of Laccase Reactions
Issue Date:1999-03-23
•24 Claims
•7 Drawing Sheets
Abstract
The present invention relates to a detergent composition, detergent additive as well as a method of oxidizing a substrate which comprises contacting the substrate with a composition which includes an enzyme selected from the group consisting of laccase, catechl oxidase, monophenol monooxygenase, and bilirubin oxidase and an enhancing agent.
Metadata
Assignee
- Novo Nordisk A/S
Inventors
- Palle Schneider
- Anders Hjelholt Pedersen
Application Information
Application Number:US 8435340
Filing Date:1997-04-16
Priority Date:1993-06-29
Art Unit:171
Classifications
IPC:
C11D 3396C11D 3395D06L 302
Field of Search:
5104352108302;303;300;305;312;313;367;374;375;376;392;530192632137;401
Patent Drawings (7 sheets)
Description
Technical Field
This invention relates to activation of enzymes. More specifically, the invention relates to agents capable of enhancing the activity of laccases and related enzymes.
The invention also relates to methods of oxidizing a substrate in the presence of a laccase enzyme, and an enhancing agent. More specifically, the invention relates to a method of bleaching of dye in solutions, to a method of inhibiting the transfer of a textile dye from a dyed fabric to another fabric when said fabrics are washed together in a wash liquor, to a method of bleaching lignin-containing material, in particular bleaching of pulp for paper production, to a method of treatment of waste water from pulp manufacturing, and to a method of enzymatic polymerization and/or modification of lignin or lignin containing material.
Background Art
Laccases (E.C. 1.10.3.2) are enzymes that catalyse the oxidation of a substrate (an electron or hydrogen donor) with oxygen. Such enzymes are known from microbial, plant and animal origins, e.g. from fungi. They are typically copper proteins, i.e. they contain a copper atom or atoms as a prosthetic group.
Use of laccases has been suggested e.g. in bleaching of pulp for paper production, in treatment of waste water from pulp production, for improved bleaching in laundry detergents, for dye transfer inhibition during laundering, and for lignin modification, e.g. in particle board production.
The compound 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate), ABTS, supplied by Boehringer Mannheim, is a chromogenic substrate, and a common peroxidase and phenol oxidase assay agent. These enzymes catalyse the oxidation of ABTS by hydrogen peroxide and dioxygen, respectively, producing a greenish-blue colour, which process may be monitored photometrically.
ABTS has been found to form a stable radical cation when oxidized by a laccase enzyme (polyphenol oxidase, EC 1.10.3.2), and has been proposed to act as a redox mediator for oxidation of non-phenolic lignin model compounds Bourbonnais R., Paice M. G.; FEBS Lett (1990) 267 99-102!.
Studies on demthylation and delignification of kraft pulp by a laccase enzyme in the presence of ABTS showed that the extent of partial demethylation by laccase was increased in the presence of ABTS Bourbonnais, R. and Paice, M. G.; Appl. Microbiol. Biotechnol. (1992) 36 823-827!.
Certain oxidizable substrates e.g. metal ions and phenolic compounds such as 7-hydroxycoumarin (7 HCm), vanillin (VAN), and p-hydroxybenzenesulfonate (pHBS), have been described as accelerators or enhancers, able to enhance bleaching reactions (cf. e.g. WO 92/18683, WO 92/18687, and Kato M. and Shimizu S., Plant Cell Physiol. 1985 26 (7), pp. 1291-1301 (cf. Table 1 particular), or Saunders B. C. et al., Peroxidase, London, 1964, p. 141 ff).
Summary of the Invention
It has now surprisingly been found that organic chemical compounds consisting of at least two aromatic rings, of which aromatic rings at least one ring is substituted with one or more of the following atoms: nitrogen, oxygen, and sulfur, and which aromatic rings may furthermore be fused rings, are capable of enhancing the activity of laccase enzymes.
Accordingly, in its first aspect, the invention provides an agent for enhancing the activity of laccase enzymes, which agent is an organic chemical compound consisting of at least two aromatic rings, of which aromatic rings at least one ring is substituted with one or more of the following atoms: nitrogen, oxygen, and sulfur; and which aromatic rings may furthermore be fused rings.
In a more specific aspect, the invention provides an agent for enhancing the activity of laccase enzymes, which agent is an organic chemical compound of the general formula I: ##STR1##
in which general formula A represents a single bond, or one of the following groups: (--CR.sup.11 .dbd.CR.sup.15 --).sub.n, (--CR.sup.11 .dbd.N--N.dbd.CR.sup.15 --), (--NR.sup.11 --), (--CR.sup.12 .dbd.N--).sub.n, (--NR.sup.11 --CR.sup.12 .dbd.N--N.dbd.CR.sup.15 --), (--NR.sup.11 --CR.sup.12 .dbd.N--).sub.n, (--CR.sup.12 .dbd.N--NR.sup.11 --), (--NR.sup.11 --CR.sup.12 .dbd.CR.sup.13 --), (--N.dbd.N--), in which groups n represents an integer of from 1 to 6; or A represents carbon, carbonyl, nitrogen, sulfur, oxygen, selenium, or phosphor, which carbon, phosphor and nitrogen may be unsubstituted or substituted with a substituent group R.sup.11 ;
and in which general formula the substituent groups R.sup.1 -R.sup.13 and R.sup.15, which may be identical or different, independent represents any of the following radicals: hydrogen, hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, phospho, phosphono, phosponooxy, sulfandiyl, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with a substituent group R.sup.14 ; and which phenyl may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.14 ; and which C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.14 ;
which substituent group R.sup.14 represents any of the following radicals: hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, aminoalkyl, piperidino, piperazinyl, pyrrolidino, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; and which phenyl may be furthermore be substituted with one or ore of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl; and which C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy groups may furthermore be saturated or unsaturated, branched or unbranched, and may furthermore be substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl;
or in which general formula R.sup.5 and R.sup.6 may together form a group --B--, in which B represents a single bond, the group (--CH.dbd.CH--).sub.n, or the group (--CH.dbd.N--).sub.n, in which groups n represents an integer of from 1 to 6; or B represents carbon, nitrogen, sulfur, oxygen, selenium, or tellurium, which carbon and nitrogen may be unsubstituted or substituted with a substituent group R.sup.14 as defined above;
or in which general formula two of the substituent groups R.sup.1 -R.sup.10 may together form a group --C--, in which C represents any of the following groups: (--CHR.sup.11 --N.dbd.N--), (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n, in which groups n represents an integer of from 2 to 4, and in which groups R.sup.11 is a substituent group as defined above;
or in which general formula R.sup.5 and R.sup.12, and/or R.sup.6 and R.sup.13, when n in the above formula being 1, may together form a group --D--, in which D represents the groups: (--CH.sup.11 --), (--NR.sup.11 --), (--CR.sup.11 .dbd.CR.sup.15 --), (--CR.sup.11 .dbd.N--), (--N.dbd.CH.sup.11 --), (--O--), (>C.dbd.O) or (--S--), and in which groups R.sup.11 and R.sup.15 are substituent groups as defined above.
In another specific aspect, the invention provides an agent for enhancing the activity of a laccase enzyme, which agent is an organic chemical compound of the general formula II: ##STR2##
in which the substituent groups R.sup.1 -R.sup.8, which may be identical or different, independently represents any of the following radicals: hydrogen, hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with a substituent group R.sup.9 ; and which phenyl may further be substituted or substituted with one or more substituent groups R.sup.9 ; and which C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.9 ;
which substituent group R.sup.9 represents any of the following radicals: hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy; and which phenyl may furthermore be substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl; and which C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy groups may furthermore be saturated or unsaturated branched or unbranched, and may furthermore be substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy, and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl;
or in which general formula two of the substituent groups R.sup.1 -R.sup.8 may together from a group --B--, in which B represents any of the following groups: (--N.dbd.N--), (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n, (--N.dbd.CR.sup.9 --NR.sup.10 --) or (--N.dbd.N--CR.sup.9 --), in which groups n represents an integer of from 1 to 3, R.sup.9 is a substituent group as defined above and R.sup.10 is defined as R.sup.9.
In another aspect, the invention provides a method for oxidizing a substrate with a laccase or a laccase related enzyme, in the presence of oxygen and in the presence of an enhancing agent of the invention.
In a more specific aspect, the invention provides a method for bleaching dye in solutions by treatment with a laccase or a laccase related enzyme in the presence of oxygen in the presence of an enhancing agent of the invention.
In another specific aspect, the invention provides a method of inhibiting the transfer of a textile dye from a dyed fabric to another fabric when said fabrics are washed together in a wash liquor, the method comprising treatment of the wash liquor, with a laccase or a laccase related enzyme in the presence of oxygen and in the presence of an enhancing agent of the invention.
In another aspect, the invention provides a method of bleaching lignin-containing material, in particular bleaching of pulp for paper production, the method comprising treatment of the lignin or lignin containing material with a laccase or a laccase related enzyme in the presence of a source of oxygen and in the presence of an enhancing agent of the invention.
In a further aspect, the invention provides a method of enzymatic polymerization and/or modification of lignin or lignin containing material, the method comprising treatment of the lignin or lignin containing material with a laccase or a laccase related enzyme in the presence of a source of oxygen and in the presence of an enhancing agent of the invention.
In a yet further aspect, the invention provides a method of treatment of waster water, in particular waste water from pharmaceutical or chemical industry, e.g. waste water from dye manufacturing, from textile industry, or from pulp manufacturing, the method comprising treatment of the waste water with a laccase or a laccase related enzyme in the presence of a source of oxygen and in the presence of an enhancing agent of the invention.
In a particular aspect, the invention provides a detergent additive capable of inhabiting the transfer of a textile dye from a dyed fabric to another fabric when said fabrics are washed together in a wash liquor, the detergent additive comprising an enzyme exhibiting laccase activity and oxygen and an enhancing agent of the invention.
In other aspects, the invention provides detergent additives and detergent compositions capable of inhibiting the transfer of a textile dye from a dyed fabric to another fabric when said fabrics are washed together in a wash liquor, the detergent composition comprising an enzyme exhibiting laccase activity and oxygen and an enhancing agent of the invention.
Brief Description of Drawings
The present invention is further illustrated by reference to the accompanying drawings, in which:
FIG. 1 shows the specific formulas of some enhancing agents of the invention (I) 6-hydroxy-2-naphtoic acid; (II) 7-methoxy-2-naphtol; (III) 7-amino-2-naphthalene sulfonic acid; (IV) 5-amino-2-naphthalene sulfonic acid; (V) 1,5-diaminonaphthalene; (VI) 7-hydroxy-1,2-naphthimidazole; (VII) 10-methylphenothiazine; (VIII) 10-phenothiazine-propionic acid; (IX) N-hydroxysuccinimide-10-phenothiazine-propionate; (X) benzidine; (XI) 3,3'-dimethylbenzidine; (XII) 3,3'-dimethoxybenzidine; (XIII) 3,3',5,5'-tetramethylbenzidine; (XIV) 4'-hydroxy-4-biphenylcarboxylic acid; (XV) 4-amino-4'-methoxystilbene; (XVI) 4,4'-diaminostilbene-2,2'-disulfonic acid; (XVII) 4,4'-diaminodiphenylamine; (XVIII) 2,7-diaminofluorene; (XIX) 4,4'-dihydroxy-biphenylene; (XX) triphenylamine; (XXI) 10-ethyl-4-ethyl-4-phenothiazinecarboxylic acid; (XXII) 10-ethylphenothiazine; (XXIII) 10-propylphenothiazine; (XXIV) 10-isopropylphenothiazine; (XXV) methyl-10-phenothiazinepropionate; (XXVI) 10-phenylphenothiazine; (XXVII) 10-allylphenothiazine; (XXVIII) 10-phenoxazinepropionic acid; (XXIX) 10-(3-(4-methyl-1-piperazinyl)propyl)phenothizine; (XXX) 10-(2-pyrrolidinoethyl)phenothiazine; (XXXI) 10-methylphenoxazine; (XXXII) iminostilbene; (XXXIII) 2-(p-aminophenyl)-6-methylbenzothiazole-7-sulfonic acid; (XXXIV) N-benzylidene-4-biphenylamine; (XXXV) 5-amino-2-naphthalenesulfonic acid; (XXXVI) 7-methoxy-2-naphtol; (XXXVII) 4,4'-dihydroxybenzophenone; (XXXVIII) N-(4-(dimethylamino)benzylidene)-p-anisidine; (XXXIX) 3-methyl-2-benzothiazolinone(4-(dimethylamino)benzylidene)hydrazone; (XL) 2-acethyl-10-methylphenothiazine; (XLI) 10-(2-hydroxyethyl)phenothiazine; (XLII) 10-(2-hydroxyethyl)phenoxazine; (XLIII) 10-(3-hydroxypropyl)phenothiazine; (XLIV) 4,4'-dimethoxy-N-methyl-diphenylamine; (XLV) vanillin azine.
FIG. 2 shows the bleaching of Direct Blue 1 with bilirubin oxidase and 10-methylphenothiazine (MPT) (.quadrature. 0 .mu.M MPT; .diamond-solid. 2.5 .mu.M MPT; .box-solid. 5.0 .mu.M MPT; .diamond. 10.0 .mu.M MPT).
Detailed Disclosure of the Invention
The Enhancing Agent
The present invention relates to the use of the chemical compounds for enhancing the activity of laccase enzymes. Accordingly, the invention provides an agent capable of enhancing the effect of a laccase enzyme in the following termed enhancing agent.
The enhancing agent of the invention is an organic chemical compound consisting of at least two aromatic rings, of which aromatic rings at least one ring is substituted with one or more nitrogen, oxygen, and/or sulfur atoms, and which aromatic rings may furthermore be fused rings.
In a more preferred embodiment, the enhancing agent of the invention is an organic chemical compound of the general formula I: ##STR3##
in which general formula A represents a single bond, or one of the following groups: (--CR.sup.11 .dbd.CR.sup.15 --).sub.n, (--CR.sup.11 .dbd.N--N.dbd.CR.sup.15 --), (--nR.sup.11 --), (--CR.sup.13 .dbd.N--).sub.n, (--NR.sup.11 --CR.sup.12 .dbd.N--N.dbd.CR.sup.15 --), (--NR.sup.11 --CR.sup.12 .dbd.N--).sub.n, (--CR.sup.12 .dbd.N--NR.sup.11 --), (--NR.sup.11 --CR.sup.12 .dbd.CR.sup.13 --), (--N.dbd.N--), in which groups n represents an integer of from 1 to 6; or A represents carbon, carbonyl, nitrogen, sulfur, oxygen, selenium, or phosphor, which carbon, phosphor and nitrogen may be unsubstituted or substituted with a substituent group R.sup.11 ;
and in which general formula the substituent groups R.sup.1 -R.sup.13 and R.sup.15, which may be identical or different, independently represents any of the following radicals: hydrogen, hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, phospho, phosphono, phosphonooxy, sulfandiyl, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with a substituent group R.sup.14 ; and which phenyl may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.14 ; and which C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.14 ;
which substituent group R.sup.14 represents any of the following radicals: hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, aminoalkyl, piperidino, piperazinyl, pyrrolidino, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; and which phenyl may furthermore be substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl; and which C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy groups may furthermore be saturated or unsaturated, branched or unbranched, and may furthermore be substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl;
or in which general formula R.sup.5 and R.sup.6 may together form a group --B--, in which B represents a single bond, the group (--CH.dbd.CH--).sub.n, or the group (--CH.dbd.N--).sub.n, in which groups n represents an integer of from 1 to 6; or B represents carbon, nitrogen, sulfur, oxygen, selenium, or tellurium, which carbon and nitrogen may be unsubstituted or substituted with a substituent group R.sup.14 as defined above;
or in which general formula two of the substituent groups R.sup.1 -R.sup.10 may together form a group --C--, in which C represents any of the following groups: (--CHR.sup.11 --N.dbd.N--), (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n, in which groups n represents an integer of from 2 to 4, and in which groups R.sup.11 is a substituent group as defined above;
or in which general formula R.sup.5 and R.sup.12, and/or R.sup.6 and R.sup.13, when n in the above formula being 1, may together form a group --D--, in which D represents the groups: (--CHR.sup.11), (--NR.sup.11 --), (--CR.sup.11 .dbd.CR.sup.15 --), (--CR.sup.11 .dbd.N--), (--N.dbd.CR.sup.11 --), (--O--), (>C.dbd.O) or (--S--), and in which groups R.sup.11 and R.sup.15 are substituent groups as defined above.
In particular embodiments, the enhancing agent is 2-(p-aminophenyl)-6-methylbenzothiazole-7-sulfonic acid, N-(4-(dimethylamino)benzylidene)-p-anisidine, 3-methyl-2-benzothiazolinone(4-(dimethylamino)benzylidene)hydrazone, vanillin azine.
In another preferred embodiment, the enhancing agent of the invention is an organic chemical compound of the general formula II: ##STR4##
in which the substituent groups R.sup.1 -R.sup.8, which may be identical or different, independently represents any of the following radicals: hydrogen, hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 - alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with a substituent group R.sup.9 ; and which phenyl may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.9 ; and which C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.9 ;
which substituent groups R.sup.9 represents any of the following radicals: hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy; and which phenyl may furthermore be substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl; and which C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy groups may furthermore be saturated or unsaturated, branched or unbranched, and may furthermore be substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl;
or in which general formula two of the substituent groups R.sup.1 -R.sup.8 may together form a group --B--, in which B represents any of the following groups: (--N.dbd.N--), (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n, (--N.dbd.CR.sup.9 --NR.sup.10 --) or (--N.dbd.N--CR.sup.9 --), in which groups n represents an integer of from 1 to 3, R.sup.9 is a substituent group as defined above and R.sup.10 is defined as R.sup.9.
In a more specific embodiment, the enhancing agent of the invention is an organic chemical compound of the following formula: ##STR5##
in which formula E represents a single bond, a carbonyl group or one of the following groups: (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n or (--NR.sup.11 --), in which n represents an integer from 1 to 2. The substituents groups R.sup.1 -R.sup.11 may be identical or different, independently being one of the following radicals: hydrogen, hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with a substituent group R.sup.14 ; and which phenyl may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.14 ; and which C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.14 ;
which substituent group R.sup.14 represents any of the following radicals: hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy; and which phenyl may furthermore be substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl; and which C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy groups may furthermore be saturated or unsaturated, branched or unbranched, and may furthermore be substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy, and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl;
or in which specific formula two of the substituent groups R.sup.5 and R.sup.6 may together form a group --B--, in which B represents the groups: ('CH.dbd.N--).sub.n, (--CH.dbd.CH--) or (--CHR.sup.14 --) in which groups n represents an integer of from 1 to 2 and R.sup.14 is a substituent group as defined above.
In particular embodiments, the enhancing agent is 4-amino-4'-methoxystilbene, 4,4'-diaminostilbene-2,2'-disulfonic acid, iminostilbene, 4,4'-dihydroxybenzophenone, N-benzylidene-4-biphenylamine, 4,4'-diaminodiphenylamine, 4,4'-dimethoxy-N-methyl-diphenylamine, 2,7-diaminofluorene, triphenylamine.
In another specific embodiment, the enhancing agent may be described by the following formula: ##STR6##
in which formula X represents one of the following groups: (--O--), (13 S--), (--NR.sup.15 --), (--CHR.sup.15 --), (>C.dbd.O), (--CH.dbd.CH--), (--CH.dbd.N--) and the substituent groups R.sup.1 -R.sup.9 and R.sup.15, which may be identical or different, independently represents any of the following radicals: hydrogen, hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl; C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with a substituent group R.sup.10 ; and which one or more substituent groups R.sup.10 ; and which C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.10 ;
which substituent group R.sup.10 represents any of the following radicals: hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, aminoalkyl, piperidino, piperazinyl, pyrrolidino, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 alkoxy; and which phenyl may furthermore be substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl; and which C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy groups may furthermore be saturated or unsaturated, branched or unbranched, and may furthermore be substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl;
or in which general formula tow of the substituent groups R.sup.1 -R.sup.8 may together form a group --B--, in which B represents any of the following the groups: (--CHR.sup.10 --N.dbd.N--), (--CH.dbd.CH--).sub.n, ('CH.dbd.N--).sub.n or (--N.dbd.CR.sup.10 --NR.sup.11 --), in which groups n represents an integer of from 1 to 3, R.sup.10 is a substituent group as defined above and R.sup.11 is defined as R.sup.10.
In particular embodiments, the enhancing agent is 10-methylphenothiazine, 10-phenothiazine-propionic acid, N-hydroxysuccinimide-10-phenothiazine-propionate or 10-ethyl-4phenothiazine-carboxylic acid, 10-ethylphenothiazine, 10-propylphenothiazine, 10-isopropylphenothiazine, methyl-10phenothiazinepropionate, 10-phenylphenothiazine, 10-allylphenothiazine, 10-(3-(4-methyl-1-piperazinyl)propyl)phenothiazine, (10-(2-pyrrolidinoethyl)phenothiazine, 2-acetyl-10-methyl-phenothiazine, 4-carboxy-10-phenothiazine, 10-methyl-phenoxazine, 10-ethylphenoxazine, 10-phenoxazine-propionic acid, 4-carboxy-10-phenoxazine-propionic acid, 10-(2-hydroxyethyl)phenothiazine, 10-(2-hydroxyethyl)phenoxazine or 10-(3-hydroxypropyl)phenothiazine.
In another specific embodiment, enhancing agent is biphenyl derivative of the following formula: ##STR7##
in which the substituent groups R.sup.1 -R.sup.10, which may be identical or different, independently represents any of the following radicals: hydrogen, hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with a substituent group R.sup.11 ; and which phenyl may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.11 ; and which C.sub.1 -C.sub.14 alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 alkyl groups may be saturated or unsaturated, branched or unbranched, and may be furthermore be unsubstituted or substituted with one or more substituent groups R.sup.11 ;
which substituent group R.sup.11 represents any of the following radicals: hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy; and which phenyl may furthermore be substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl; and which C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy groups may furthermore be saturated or unsaturated, branched or unbranched, and may furthermore be substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl,
In particular embodiments, the enhancing agent is benzidine, 3,3'-dimethylbenzidine, 3,3'-dimethoxybenzidine, 3,3',5,5'-tetramethylbenzidine, 4'-hydroxy-4-biphenylcarboxylic acid, or 4,4'-dihydroxybiphenylene.
In another specific embodiment, the enhancing agent is a naphthalene derivative of the following formula: ##STR8##
in which the substituent groups R.sup.1 -R.sup.8, which may be identical or different, independently represents any of the following radicals: hydrogen, hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with a substituent group R.sup.9 ; and which phenyl may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.9 ; and which C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and may furthermore be unsubstituted or substituted with one or more substituent groups R.sup.9 ;
which substituent group R.sup.9 represents any of the following radicals: hydroxy, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, sulfamoyl, nitro, amino, phenyl, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; which carbamoyl, sulfamoyl, and amino groups may furthermore be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy; and which phenyl may furthermore be substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl, and which C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy groups may furthermore be saturated or unsaturated, branched or unbranched, and may furthermore be substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy and esters and salts hereof, carbamoyl, sulfo and esters and salts hereof, and sulfamoyl;
or in which general formula two of the substituent groups R.sup.1 -R.sup.8 may together form a group --B--, in which B represents any of the following groups: (--N.dbd.N--), (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n, (--N.dbd.CR.sup.9 --NR.sup.10 --) or (--N.dbd.N--CR.sup.9 --), in which groups n represents an integer of from 1 to 3, R.sup.9 is substituent group as defined above and R.sup.10 is defined as R.sup.9.
In particular embodiments, the enhancing agent is 6-hydroxy-2-naphtoic acid, 7-methoxy-2-naphtol, 7-amino-2-naphthalene sulfonic acid, 5-amino-2-naphthalene sulfonic acid, 1,5-diaminonaphthalene, 7-hydroxy-1,2-naphthimidazole, 5-amino-2-naphthalenesulfonic acid, or 7-methoxy-2-naphtol.
The enhancing agent of the invention may be in free form or in the form of an addition salt.
Methods of Oxidizing a Substrate
In another aspect, the invention provides a method of oxidizing a substrate with a laccase enzyme and in the presence of an enhancing agent.
The enhancing agent may be present in free form or in the form of an addition salt.
The enhancing agent may be present in concentrations of from 0.01 to 500 .mu.M, more preferred 0.1 to 250 .mu.M, most preferred 0.5 to 100 .mu.M.
Molecular oxygen from the atmosphere will usually be present in sufficient quantity.
Laccase and Related Enzymes
The enhancing agents of the invention are agents capable of enhancing the activity of laccases and laccase related enzymes. In the context of this invention, laccases and laccase related enzymes contemplate any laccase enzyme comprised by the enzyme classification EC 1.10.3.2, any chatechol oxidase enzyme comprised by the enzyme classification EC 1.10.3.1, any bilirubin oxidase enzyme comprised by the enzyme classification EC 1.3.3.5 or any monophenol monooxygenase enzyme comprised by the enzyme classification EC 1.14.99.1.
Preferably, the laccase employed in the method of the invention is derived from a fungi such as Trametes, e.g. T. villosa or T. versicolor, Collybia, Fomes, Lentinus, Pleurotous, Rhizoctonia, e.g. R. solani, Aspergillus, Neurospora, Podospora, Phlebia, e.g. P. radiata (WO 92/01046), Coriolus, e.g. C. hirsitus (JP 2-238885), Myceliophthora, e.g. M. thermophila or Botrytis. Bilirubin oxidase may preferably be derived from Myrothecium, e.g. M. verrucaria.
The laccase or the laccase related enzyme may furthermore be one which is producible by a method comprising cultivating a host cell transformed with a recombinant DNA vector which carries a DNA sequence encoding said laccase as well as DNA sequences encoding functions permitting the expression of the DNA sequence encoding the laccase, in a culture medium under conditions permitting the expression of the laccase enzyme, and recovering the laccase from the culture.
Determination of Laccase Activity (LACU)
Laccase activity is determined from the oxidation of syringaldazin under aerobic conditions. The violet colour produced is photometered at 530 nm. The analytical conditions are 19 .mu.M syringaldazin, 23.2 mM acetate buffer, pH 5.5, 30.degree. C., 1 min. reaction time.
1 laccase unit (LACU) is the amount of enzyme that catalyses the conversion of 1.0 .mu.mole syringaldazin per minute at those conditions.
Determination of Bilirubin Oxidase Activity (Sigma Units)
1 bilirubin oxidase Sigma unit is the amount of enzyme that will oxidize 1.0 .mu.mole of bilirubin per minute at pH 8.4 and 30.degree. C.
Industrial Applications
In a preferred embodiment, the method of the invention finds application for bleaching of dye in solutions.
In another embodiment, the method of the invention finds application for dye transfer inhibition, e.g. for treatment of dyed textiles (cf. e.g. WO 92/18687) or during laundering (cf. e.g. WO 91/05839).
Accordingly, in a specific embodiment, the invention provides a method inhibiting the transfer of a textile dye from a dyed fabric to another fabric when said fabrics are washed together in a wash liquor, the method comprising treatment of the wash liquor with a laccase or a laccase related enzyme in the presence of an enhancing agent. The textile dye may be a synthetic dye such as an azo dye, or a natural or nature-identical dye.
In a third embodiment, the method of the invention finds application in bleaching of pulp for paper production.
Accordingly, the invention provides a method for bleaching of lignin-containing material, in particular bleaching of pulp for paper production, which method comprises treatment of the lignin or lignin containing material with a laccase or a laccase related enzyme in the presence of an enhancing agent of the invention.
In a fourth embodiment, the method of the invention finds application for lignin modification, e.g. in the manufacture of wood composites, e.g. wood fibre materials such as chipboards, fibre boards, or particle boards, or in the manufacture of laminated wood products, such as laminated beams and plywood.
Accordingly, the invention provides a method for enzymatic polymerization and/or modification of lignin or lignin containing material, which method comprises treatment of the lignin or lignin containing material with a laccase or a laccase related enzyme in the presence of an enhancing agent of the invention.
In a fifth embodiment, the method of the invention finds application in treatment of waste water e.g. waste water from the chemical or pharmaceutical industry, from dye manufacturing, from dye-works, from the textile industry, or from pulp production (cf. e.g. U.S. Pat. No. 4,623,465, or JP-A-2-31887).
In a more specific aspect, the invention provides a method for treatment of waste water from dye manufacturing, from dye-works, from textile industry, or from pulp manufacturing, the method comprising treatment of the waste water with a laccase or a laccase related enzyme in the presence of an enhancing agent of the invention.
Detergent Compositions
According to the invention, the enhancing agent may be added as a component of a detergent composition. As such, it may be included in the detergent composition in the form of a detergent additive. The detergent composition as well as the detergent additive may additionally comprise one or more other enzymes conventionally used in detergents, such as proteases, lipases, amylases, cutinases, cellulases and peroxidases.
In a specific aspect, the invention provides a detergent additive. The enzymes may be included in a detergent composition by adding separate additives containing one or more enzymes, or by adding a combined additive comprising all of these enzymes. A detergent additive of the invention, i.e. a separated additive or a combined additive, can be formulated e.g. as granulates, liquids, slurries, etc. Preferred detergent additive formulations are granulates, in particular non-dusting granulates, liquids, in particular stabilized liquids, slurries, or protected enzymes.
Non-dusting granulates may be produced, e.g., as disclosed in U.S. Pat. Nos. 4,106,991 and 4,661,452 (both to Novo Industri A/S) an may optionally be coated by methods known in the art. Examples of waxy coating materials are poly(ethylene oxide) products (polyethyleneglycol, PEG) with means molar weights of 1000 to 20000; ethoxylated nonylphenols having from 16 to 50 ethylene oxide units; ethoxylated fatty alcohols in which the alcohol contains from 12 to 20 carbon atoms and in which there are 15 to 80 ethylene oxide units; fatty alcohols; fatty acids; and mono- and di- and triglycerides of fatty acids. Examples of film-forming coating materials suitable for application by fluid bed techniques are given in patent GB 1483591. Liquid enzyme preparations may, for instance, be stabilized by adding a polyol such as propylene glycol, a sugar or sugar alcohol, lactic acid or boric acid according to established methods. Other enzyme stabilizers are well known in the art. Protected enzymes may be prepared according to the method disclosed in EP 238,216.
The detergent composition of the invention may be in any convenient form, e.g. as powder, granules, paste or liquid. A liquid detergent may be aqueous, typically containing up to 70% water and 0-30% organic solvent, or nonaqueous.
The detergent composition comprises one or more surfactants, each of which may be anionic, nonionic, cationic, or zwitterionic. The detergent will usually contain 0-50% of anionic surfactant such as linear alkylbenzenesulfonate (LAS), alpha-olefinsulfonate (AOS), alkyl sulfate (fatty alcohol sulfate) (AS), alcohol ethoxysulfate (AEOS or AES), secondary alkanesulfonates (SAS), alpha-sulfo fatty acid methyl esters, alkyl- or alkenylsuccinic acid or soap. It may also contain 0-40% of nonionic surfactant such as alcohol ethoxylate (AEO or AE), carboxylated alcohol ethoxylates, nonylphenol ethoxylate, alkylpolyglycoside, alkyldimethylamineoxide, ethoxylated fatty acid monoethanolamide, fatty acid monoethanolamide, or polyhydroxy alkyl fatty acid amide (e.g. as described in WO 92/06154).
The detergent composition may additionally comprise one or more older enzymes, such as amylase, lipases, cutinases, proteases, cellulases an peroxidases.
The detergent may contain 1-65% of a detergent builder or complexing agent such as zeolite, diphosphate, triphosphate, phosphonate, citrate, nitrilotriacetic acid (NTA), ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTMPA), alkyl- or alkenylsuccinic acid, soluble silicates or layered silicates (e.g. SKS-6 from Hoechst). The detergent may also be unbuilt, i.e. essentially free of detergent builder.
The detergent may comprise one or more polymers. Examples are carboxymethylcellulose (CMC), poly(vinylpyrrolidone) (PVP), olyethyleneglycol (PEG), poly(vinyl alcohol) PVA), polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers and lauryl methacrylate/acrylic acid copolymers.
The detergent may contain a bleaching system which may comprise a H.sub.2 O.sub.2 source such as perborate or pecarbonate which may be combined with a peracid-forming bleach activator such as teraacetylethylenediamine (TAED) or nonnoyloxybenzenesulfonate (NOBS). Alternatively, the bleaching system may comprise peroxyacids of e.g. the amide, imide, or sulfone type.
The enzymes of the detergent composition of the invention may be stabilized using conventional stabilizing agents, e.g. a polyol such as propylene glycol or glycerol, a sugar or sugar alcohol, lactic acid, boric acid, or a boric acid derivative as e.g. an aromatic borate ester, and the composition may be formulated as described in e.g. WO 92/19709 and WO 92/19708.
The detergent may also contain other conventional detergent ingredients such as e.g. fabric conditioners including clays, foam boosters, suds suppressors, anti-corrosion agents, soil-suspending agents, anti-soil redeposition agents, dyes, bactericides, optical brighteners, or perfume.
The pH (measured in aqueous solution at use concentration) will usually be neutral or alkaline, e.g. 7-11.
Particular forms of detergent compositions within the scope of the invention include:
1) A detergent composition formulated as a granulate having a bulk density of at least 600 g/l comprising
2) A detergent composition formulated as a granulate having a bulk density of at least 600 g/l comprising
3) A detergent composition formulated as a granulate having a bulk density of at least 600 g/l comprising
4) A detergent composition formulated as a granulate having a bulk density of at least 600 g/l comprising
5) An aqueous liquid detergent composition comprising
6) An aqueous structured liquid detergent composition comprising
7) A detergent composition formulated as a granulate having a bulk density of at least 600 g/l comprising
8) A detergent composition formulated as a granulate comprising
9) A detergent composition formulated as a granulate comprising
10) An aqueous liquid detergent composition comprising
11) An aqueous liquid detergent composition comprising
12) A detergent composition formulated as a granulate having a bulk density of at least 600 g/l comprising
13) Detergent formulations as described in 1)-12) where the content of linear alkylbenzenesulfonate--or a part of it--is substituted by alkyl sulfate (C.sub.12 -C.sub.18).
14) Detergent formulations as described in 1)-13) which contain a stabilized or encapsulated peracid either as an additional component or as a substitute for already specified bleach systems.
15) Detergent compositions as described in 3), 7), 9) and 12) where the content of perborate is substituted with percarbonate.
16) Detergent composition formulated as a nonaqueous detergent liquid comprising a liquid nonionic surfactant as e.g. linear alkoxylated primary alcohol, a builder system (e.g. phosphate), enzyme and alkali. The detergent may also comprise anionic surfactant and/or a bleach system.
The following examples further illustrate the present invention, and they are not intended to be in any way limiting to the scope of the invention as claimed.
Example 1
Bleaching of Direct Blue 1 with Bilirubin Oxidase and 10-Methylphenothiazine
The bleaching of Direct Blue 1 (DB1) by bilirubin oxidase obtained from Sigma with and without 10-methyl-phenothiazine (MPT) is presented in the attached FIG. 2.
The following conditions were used:
The experiment was started by the addition of enzyme, and the absorbance at 605 nm was monitored for 5 minutes. The temperature was 25.degree. C.
No attempt to maintain a constant concentration of dissolved oxygen was made.
As evidenced by FIG. 2, bleaching is enhanced by increasing concentrations of the enhancer of the invention.
Example 2
Bleaching of Direct Blue 1
Bilirubin Oxidase
Myrothecium verrucaria bilirubin oxidase was purchased from Sigma (B-0390). A stock solution was made containing 27 Sigma units/ml, which was stored in the freezer until use.
Laccase Obtained from Trametes villosa
800 ml culture broth of Trametes villosa, CBS 678.70, was filtered with filter aid to give a clear filtrate, which was concentrated and washed by ultrafiltration on a membrane with a cut-off of 6-8 kDa. One ml samples of concentrated preparation was applied onto a Q-Sepharose HP column (Pharmacia, Sweden) equilibrated with 0.1M fosfate pH 7, and the laccase was eluted with a flat NaCl gradient around 0.25M. Fractions with laccase activity from 10 runs were pooled and concentrated by ultrafiltration to an activity of 500 LACU/ml.
Enhancers
Chemicals were obtained from Sigma-Aldrich, Janssen Chimica, Kodak, Tokyo Kasai Organic Chemicals or Daiichi Pure Chemicals Co. N-methylated derivatives of phenothiazine and phenoxazine were made by methylation with methyliodide as described by Cornel Bodea and Ioan Silberg in "Recent Advances in the Chemistry of Phenothiazines"(Advances in heterocyclic chemistry, 1968, Vol. 9, pp. 321-460); B. Cardillo & G. Casnati in Tetrahedron, 1967, Vol. 23, p. 3771. Phenothiazine and phenoxazine propionic acids may be prepared as described in J. Org. Chem. 15, 1950, pp. 1125-1130. Hydroxyethyl and hydroxypropyl derivatives of phenothiazine and phenoxazine may be prepared as described by G. Cauquil in Bullentin de la Society Chemique de France, 1960, p. 1049.
Due to low solubility some of the enhancers were dissolved in a small volume of ethanol before dilution in water.
The following conditions were used:
Reagents were mixed in a 1 cm thermostated cuvette at 30.degree. C. and the bleaching was started by addition of enzyme.
The bleaching was detected spectrophotometrically at 610 nm, which is the absorption peak of DB1. After 5 sec. bleaching was followed for 4 minutes.
From the results presented in Table 1-2, below, it appears that adding enhancers of the invention a much faster bleaching of the dye can be obtained compared to the experiment without enhancer. Enzyme dosages given are in the final incubation mixture.
Claims
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The claims shown below may not include correction changes. Use the corrected PDF for authoritative text.
What is claimed:
1. A method of oxidizing a substrate, comprising treating the substrate with an enzyme selected from the group consisting of laccase, catechol oxidase, monophenol monooxygenase and bilirubin oxidase and an enhancing agent of the following formula: ##STR9## wherein E is a single bond, a carbonyl group or one of the following groups: (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n or (--NR.sup.11 --), in which n represents an integer from 1 to 2; and R.sup.1 -R.sup.11 may be identical or different and independently are one of the following radicals: hydrogen, hydroxy, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, sulfamoyl, phospho, phosphono, phosphonooxy or an ester or salt thereof, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 - alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; wherein the carbamoyl, sulfamoyl, and amino groups may be unsubstituted or substituted once or twice with a substituent group R.sup.14 ; the phenyl group may be unsubstituted or substituted with one or more substituent groups R.sup.14 ; and the C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and unsubstituted or substituted with one or more substituent groups R.sup.14 ; wherein R.sup.14 is any of the following radicals; hydroxy, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, sulfamoyl, phospho, phosphono, phosphonooxy or an ester or salt thereof, nitro, amino, phenyl, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; wherein the carbamoyl, sulfamoyl, and amino groups may be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy; the phenyl group may be unsubstituted or substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, or sulfamoyl; and the C.sub.1 -C.sub.5 -alkyl and C.sub.1 -C.sub.5 -alkoxy groups may be saturated or unsaturated, branched or unbranched, and unsubstituted or substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, or sulfamoyl; or in which R.sup.5 and R.sup.6 together form a group --B--, in which B is (--CH.dbd.N--).sub.m, (--CH.dbd.CH--) or (--CHR.sup.14 --) in which m is 1 or 2 and R.sup.14 is as defined above.
2. The method according to claim 1, in which the enzyme is a laccase.
3. The method according to claim 1, in which the enhancing agent is 4-amino-4'-methoxystilbene, 4,4'-diaminostilbene-2,2'-disulfonic acid, iminostilbene, 4,4'-dihydroxybenzophenone, N-benzylidene-4-biphenylamine,4,4'-diaminodiphenylamine,4,4'-dimethoxy-N-m ethyl-diphenylamine, 2,7-diaminofluorene or triphenylamine.
4. The method according to claim 2, in which the enhancing agent is 4-amino-4'-methoxystilbene, 4,4'-diaminostilbene-2,2'-disulfonic acid, iminostilbene, 4,4'-dihydroxybenzophenone, N-benzylidene-4-biphenylamine, 4,4'-diaminodiphenylamine, 4,4'-dimethoxy-N-methyl-diphenylamine, 2,7-diaminofluorene or triphenylamine.
5. A detergent additive comprising an enzyme exhibiting laccase activity and an enhancing agent of the following formula; ##STR10## wherein E is a single bond, a carbonyl group or one of the following groups: (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n or (--NR.sup.11 --) in which n represents an integer from 1 to 2; and R.sup.1 -R.sup.11 may be identical or different and independently are one of the following radicals: hydrogen, hydroxy, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, sulfamoyl, phospho, phosphono, phosphonooxy or an ester or salt thereof, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 - alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; wherein the carbamoyl, sulfamoyl, and amino groups may be unsubstituted or substituted once or twice with a substituent group R.sup.14 ; the phenyl group may be unsubstituted or substituted with one or more substituent groups R.sup.14 ; and the C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and unsubstituted or substituted with one or more substituent groups R.sup.14 ; wherein R.sup.14 is any of the following radicals; hydroxy, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, sulfamoyl, phospho, phosphono, phosphonooxy or an ester or salt thereof, nitro, amino, phenyl, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; wherein the carbamoyl, sulfamoyl, and amino groups may be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy; the phenyl group may be unsubstituted or substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, or sulfamoyl; and the C.sub.1 -C.sub.5 -alkyl and C.sub.1 -C.sub.5 -alkoxy groups may be saturated or unsaturated, branched or unbranched, and unsubstituted or substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, or sulfamoyl; or in which R.sup.5 and R.sup.6 together form a group --B--, in which B is (--CH.dbd.N--).sub.m, (--CH.dbd.CH--) or (--CHR.sup.14 --) in which m is 1 or 2 and R.sup.14 is as defined above.
6. The detergent additive according to claim 4, in which the enhancing agent is 4-amino-4'-methoxystilbene.
7. The detergent additive according to claim 4, in which the enhancing agent is 4,4'-diaminostilbene-2,2'-disulfonic acid.
8. The detergent additive according to claim 4, in which the enhancing agent is iminostilbene.
9. The detergent additive according to claim 4, in which the enhancing agent is 4,4'-dihydroxybenzophenone.
10. The detergent additive according to claim 4, in which the enhancing agent is N-benzylidene-4-biphenylamine.
11. The detergent additive according to claim 4, in which the enhancing agent is 4,4'-diaminodiphenylamine.
12. The detergent additive according to claim 4, in which the enhancing agent is 4,4'-dimethoxy-N-methyl-diphenylamine.
13. The detergent additive according to claim 4, in which the enhancing agent is 2,7-diaminofluorene.
14. The detergent additive according to claim 5, in which the enhancing agent is triphenylamine.
15. A detergent composition comprising a detergent additive according to claim 4 and a surfactant.
16. The detergent composition according to claim 15, in which the enhancing agent is 4-amino-4'-methoxystilbene, 4,4'-diaminostilbene-2,2'-disulfonic acid, iminostilbene, 4,4'-dihydroxybenzophenone, N-benzylidene-4-biphenylamine, 4,4'-diaminodiphenylamine, 4,4'-dimethoxy-N-methyl-diphenylamine, 2,7-diaminofluorene or triphenylamine.
17. A method of bleaching of lignin-containing material, comprising treating the material with an enzyme selected from the group consisting of laccase, catechol oxidase, monophenol monooxygenase and bilirubin oxidase and an enhancing agent of the following formula: ##STR11## wherein E is a single bond, a carbonyl group or one of the following groups: (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n or (--NR.sup.11 --), in which n represents an integer from 1 to 2; and R.sup.1 -R.sup.11 may be identical or different and independently are one of the following radicals: hydrogen, hydroxy, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, sulfamoyl, phospho, phosphono, phosphonooxy or an ester or salt thereof, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 - alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, aryl-C.sub.1 -C.sub.5 -alkyl; wherein the carbamoyl, sulfamoyl, and amino groups may be unsubstituted or substituted once or twice with a substituent group R.sup.14 ; the phenyl group may be unsubstituted or substituted with one or more substituent groups R.sup.14 ; and the C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and unsubstituted or substituted with one or more substituent groups R.sup.14 ; wherein R.sup.14 is any of the following radicals; hydroxy, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, sulfamoyl, phospho, phosphono, phosphonooxy or an ester or salt thereof, nitro, amino, phenyl, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -alkoxy; wherein the carbamoyl, sulfamoyl, and amino groups may be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy; the phenyl group may be unsubstituted or substituted with one or more of the following radicals: hydroxy, amino, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, or sulfamoyl; and the C.sub.1 -C.sub.5 -alkyl and C.sub.1 -C.sub.5 -alkoxy groups may be saturated or unsaturated, branched or unbranched, and unsubstituted or substituted once or twice with any of the following radicals: hydroxy, amino, formyl, carboxy or an ester or salt thereof, carbamoyl, sulfo or an ester or salt thereof, or sulfamoyl; or in which R.sup.5 and R.sup.6 together form a group --B--, in which B is (--CH.dbd.N--).sub.m, (--CH.dbd.CH--) or (--CHR.sup.14 --) in which m is 1 or 2 and R.sup.14 is as defined above.
18. The method according to claim 17, in which the enzyme is a laccase.
19. The method according to claim 17, in which the enhancing agent is 4-amino-4'-methoxystilbene, 4,4'-diaminostilbene-2,2'-disulfonic acid, iminostilbene, 4,4'-dihydroxybenzophenone, N-benzylidene-4-biphenylamine, 4,4'-diaminodiphenylamine, 4,4'-dimethoxy-N-methyl-diphenylamine, 2,7-diaminofluorene or triphenylamine.
20. The method according to claim 18, in which the enhancing agent is 4-amino-4'-methoxystilbene, 4,4'-diaminostilbene-2,2'-disulfonic acid, iminostilbene, 4,4'-dihydroxybenzophenone, N-benzylidene-4-biphenylamine, 4,4'-diaminodiphenylamine, 4,4'-dimethoxy-N-methyl-diphenylamine, 2,7-diaminofluorene or triphenylamine.
21. A method of bleaching a lignin-containing material, comprising treating the material with an enzyme selected from the group consisting of laccase, catechol oxidase, monophenol monooxygenase and bilirubin oxidase and an enhancing agent of the following formula: ##STR12## in which X is (--O--), (--S--), (--NR.sup.15 --), (--CHR.sup.15 --) (>C.dbd.O), (--CH.dbd.CH--), (--CH.dbd.N--), or (--N.dbd.N--); and R.sup.1 -R.sup.9 and R.sup.15, which may be identical or different, independently are a radical selected from the group consisting of: hydrogen, hydroxy, formyl, carboxy and esters and salts thereof, carbamoyl, sulfo and esters and salts thereof, sulfamoyl, phospho, phosphono, phosphonooxy and esters and salts thereof, nitro, amino, phenyl, C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 alkyl; in which the carbamoyl, sulfamoyl, and amino groups may be unsubstituted or substituted once or twice with a substituent group R.sup.10 ; in which phenyl may be unsubstituted or substituted with one or more substituent groups R.sup.10 ; and in which C.sub.1 -C.sub.14 -alkyl, C.sub.1 -C.sub.5 -alkoxy, carbonyl-C.sub.1 -C.sub.5 -alkyl, and aryl-C.sub.1 -C.sub.5 -alkyl groups may be saturated or unsaturated, branched or unbranched, and may be unsubstituted or substituted with one or more substituent groups R.sup.10 ; in which R.sup.10 independently represents a radical selected from the group consisting of hydroxy, formyl, carboxy and esters and salts thereof, carbamoyl, sulfo and esters thereof, nitro, amino, phenyl, aminoalkyl, piperidino, piperazinyl, pyrrolidino, C.sub.1 -C.sub.5 -alkyl, and C.sub.1 -C.sub.5 -alkoxy; in which the carbamoyl, sulfamoyl, and amino groups may be unsubstituted or substituted once or twice with hydroxy, C.sub.1 -C.sub.5 -alkyl, or C.sub.1 -C.sub.5 -alkoxy; in which phenyl may be substituted with one or more radicals selected from the group consisting of hydroxy, amino, formyl, carboxy and esters and salts thereof, carbamoyl, sulfo and esters and salts thereof, and sulfamoyl; and in which C.sub.1 -C.sub.5 -alkyl and C.sub.1 -C.sub.5 -alkoxy groups may be saturated or unsaturated, branched or unbranched, and unsubstituted or substituted once or twice with any radicals selected from the group consisting of hydroxy, amino, formyl, carboxy and esters and salts thereof, carbamoyl, sulfo and esters and salts thereof, and sulfamoyl; or in which two of R.sup.1 -R.sup.8 may together form a group --B-- which is selected from the group consisting of (--CHR.sup.10 --N.dbd.N--), (--CH.dbd.CH--).sub.n, (--CH.dbd.N--).sub.n and (--N.dbd.CR.sup.10 --NR.sup.11 --), in which n is an integer of from 1 to 3, R.sup.10 is a substituent group as defined above and R.sup.11 is defined as R.sup.10.
22. The method according to claim 21, in which the enzyme is a laccase.
23. The method according to claim 22, in which X is (--O--) or (--S--) and R.sup.5 is an alkyl group which may be further substituted.
24. The method according to claim 22, in which enhancing agent is 10-methylphenothiazine, 10-phenothiazine-propionic acid, N-hydroxysuccinimide-10-phenothiazine-propionate, 10-ethyl-4-phenothiazine-carboxylic acid, 10-ethylphenothiazine, 10-propylphenothiazine, 10-isopropylphenothiazine, methyl-10-phenothiazinepropionate, 10-phenylphenothiazine, 10-allylphenothiazine, 10-(3-(4-methyl-1-piperazinyl)propyl)phenothiazine, 10-(2-pyrrolidinoethyl)phenothiazine, 2-acetyl-10-methylphenothiazine, 4-carboxy-10-phenothiazine-propionic acid, 10-methylphenoxazine, 10-ethylphenoxazine, 10-phenoxazine-propionic acid, 4-carboxy-10-phenoxazine-propionic acid, 10-(2-hydroxyethyl)phenothiazine, 10-(2-hydroxyethyl)phenoxazine or 10-(3-hydroxypropyl)phenothiazine.