US20030094251A1 - Enhancing laccase activity using pro-oxidants and pro-degradants - Google Patents
Enhancing laccase activity using pro-oxidants and pro-degradants Download PDFInfo
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- US20030094251A1 US20030094251A1 US10/027,165 US2716501A US2003094251A1 US 20030094251 A1 US20030094251 A1 US 20030094251A1 US 2716501 A US2716501 A US 2716501A US 2003094251 A1 US2003094251 A1 US 2003094251A1
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- acid
- oxidant
- degradant
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- 230000003244 pro-oxidative effect Effects 0.000 title claims abstract description 39
- 108010029541 Laccase Proteins 0.000 title claims abstract description 38
- 239000008380 degradant Substances 0.000 title claims abstract description 32
- 230000000694 effects Effects 0.000 title description 11
- 230000002708 enhancing effect Effects 0.000 title description 4
- 102000004190 Enzymes Human genes 0.000 claims abstract description 37
- 108090000790 Enzymes Proteins 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 36
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 34
- 239000000203 mixture Substances 0.000 claims abstract description 32
- 230000008569 process Effects 0.000 claims abstract description 32
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 29
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims abstract description 22
- 230000001590 oxidative effect Effects 0.000 claims abstract description 22
- 235000010323 ascorbic acid Nutrition 0.000 claims abstract description 17
- 239000011668 ascorbic acid Substances 0.000 claims abstract description 17
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims abstract description 14
- 238000004061 bleaching Methods 0.000 claims abstract description 14
- 235000001968 nicotinic acid Nutrition 0.000 claims abstract description 14
- 239000011664 nicotinic acid Substances 0.000 claims abstract description 14
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000004202 carbamide Substances 0.000 claims abstract description 11
- 239000000758 substrate Substances 0.000 claims abstract description 11
- 229940072107 ascorbate Drugs 0.000 claims abstract description 9
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 8
- 229960003512 nicotinic acid Drugs 0.000 claims abstract description 8
- 239000011122 softwood Substances 0.000 claims abstract description 8
- 229920001732 Lignosulfonate Polymers 0.000 claims abstract description 7
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims abstract description 7
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000011121 hardwood Substances 0.000 claims abstract description 7
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 claims abstract description 7
- WVYADZUPLLSGPU-UHFFFAOYSA-N salsalate Chemical compound OC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1O WVYADZUPLLSGPU-UHFFFAOYSA-N 0.000 claims abstract description 7
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 claims abstract description 7
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229920005610 lignin Polymers 0.000 claims description 15
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 13
- 239000007800 oxidant agent Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 108010015428 Bilirubin oxidase Proteins 0.000 claims description 7
- 108010031396 Catechol oxidase Proteins 0.000 claims description 7
- 102000030523 Catechol oxidase Human genes 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 229920001131 Pulp (paper) Polymers 0.000 claims description 6
- 102000003425 Tyrosinase Human genes 0.000 claims description 6
- 108060008724 Tyrosinase Proteins 0.000 claims description 6
- 239000003570 air Substances 0.000 claims description 6
- 101710121765 Endo-1,4-beta-xylanase Proteins 0.000 claims description 4
- 229920002678 cellulose Polymers 0.000 claims 2
- 239000001913 cellulose Substances 0.000 claims 2
- 239000002994 raw material Substances 0.000 claims 1
- 238000004076 pulp bleaching Methods 0.000 description 9
- OHDRQQURAXLVGJ-HLVWOLMTSA-N azane;(2e)-3-ethyl-2-[(e)-(3-ethyl-6-sulfo-1,3-benzothiazol-2-ylidene)hydrazinylidene]-1,3-benzothiazole-6-sulfonic acid Chemical compound [NH4+].[NH4+].S/1C2=CC(S([O-])(=O)=O)=CC=C2N(CC)C\1=N/N=C1/SC2=CC(S([O-])(=O)=O)=CC=C2N1CC OHDRQQURAXLVGJ-HLVWOLMTSA-N 0.000 description 7
- 239000003599 detergent Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000002835 absorbance Methods 0.000 description 4
- 239000007844 bleaching agent Substances 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 108091028043 Nucleic acid sequence Proteins 0.000 description 3
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- YARKTHNUMGKMGS-LQGKIZFRSA-N chembl3193980 Chemical compound COC1=C(O)C(OC)=CC(\C=N\N=C\C=2C=C(OC)C(O)=C(OC)C=2)=C1 YARKTHNUMGKMGS-LQGKIZFRSA-N 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 2
- 229940124530 sulfonamide Drugs 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
- QGXCOCVWIKYPKW-UHFFFAOYSA-N 3-ethyl-2h-1,3-benzothiazole-6-sulfinic acid Chemical compound OS(=O)C1=CC=C2N(CC)CSC2=C1 QGXCOCVWIKYPKW-UHFFFAOYSA-N 0.000 description 1
- HJBLUNHMOKFZQX-UHFFFAOYSA-N 3-hydroxy-1,2,3-benzotriazin-4-one Chemical compound C1=CC=C2C(=O)N(O)N=NC2=C1 HJBLUNHMOKFZQX-UHFFFAOYSA-N 0.000 description 1
- HRRVLSKRYVIEPR-UHFFFAOYSA-N 6-hydroxy-5-nitroso-1H-pyrimidine-2,4-dione Chemical compound OC1=NC(O)=C(N=O)C(O)=N1 HRRVLSKRYVIEPR-UHFFFAOYSA-N 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 108010054320 Lignin peroxidase Proteins 0.000 description 1
- 108010059896 Manganese peroxidase Proteins 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 102100038277 Prostaglandin G/H synthase 1 Human genes 0.000 description 1
- 108090000459 Prostaglandin-endoperoxide synthases Proteins 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- BPHHNXJPFPEJOF-UHFFFAOYSA-J chembl296966 Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC(S([O-])(=O)=O)=C(N)C2=C(O)C(N=NC3=CC=C(C=C3OC)C=3C=C(C(=CC=3)N=NC=3C(=C4C(N)=C(C=C(C4=CC=3)S([O-])(=O)=O)S([O-])(=O)=O)O)OC)=CC=C21 BPHHNXJPFPEJOF-UHFFFAOYSA-J 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000001952 enzyme assay Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- GMJUGPZVHVVVCG-UHFFFAOYSA-N n-hydroxy-n-phenylacetamide Chemical compound CC(=O)N(O)C1=CC=CC=C1 GMJUGPZVHVVVCG-UHFFFAOYSA-N 0.000 description 1
- -1 nicoliante Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000008057 potassium phosphate buffer Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010188 recombinant method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y110/00—Oxidoreductases acting on diphenols and related substances as donors (1.10)
- C12Y110/03—Oxidoreductases acting on diphenols and related substances as donors (1.10) with an oxygen as acceptor (1.10.3)
- C12Y110/03002—Laccase (1.10.3.2)
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C5/00—Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
- D21C5/005—Treatment of cellulose-containing material with microorganisms or enzymes
-
- 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
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
Definitions
- the present invention relates to the enhancement of enzyme activity. More specifically, the present invention relates to pro-oxidants and pro-degradants that, in combination, are useful in enhancing the activity of enzymes having laccase activity, especially in the field of pulp bleaching.
- Paper pulp is typically processed from wood through the Kraft (and other) processes.
- the process produces a pulp with a dark brown color, mostly due to the presence of lignin and lignin derivatives.
- the lignin has to be removed by a process known in the art as “bleaching.” This is typically done commercially in several stages in pulp mills, wherein lignin is first oxidized and then removed from the pulp.
- Bio-bleaching is a methodology whereby an enzyme is used to decrease the optical brightness and/or lignin content of pulp or paper.
- the standard measure of bleaching efficiency is “Kappa number.”
- Enzymes that have most commonly been used include laccase, lignin peroxidase, and manganese peroxidase.
- An enzyme group that has received particular attention is the laccase family of enzymes, which are copper-containing enzymes that are known to be good oxidizing agents in the presence of oxygen. Laccases are found in microbes, fungi, and higher organisms.
- oxidizing efficiency of a laccase can be improved through the use of a mediator, also known as an enhancing agent.
- a mediator also known as an enhancing agent.
- Systems that include a laccase and a mediator are known in the art as laccase-mediator systems (LMS).
- LMS laccase-mediator systems
- mediators for use in a laccase-mediator system.
- HBT 1-hydroxybenzotriazole
- ABTS 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfinic acid)
- NHA N-hydroxyacetinilide
- NHAA N-acetyl-N-phenylhydroxylamine
- HBTO HBTO (3-hydroxy-1,2,3-benzotriazin-4(3H)-one
- VIO violuric acid
- the present invention provides two-component mediators, wherein one component serves as a pro-oxidant and the other component serves as a pro-degradant and booster.
- the two-component mediators enhance the bleaching of pulp.
- the invention provides a two-component mediator for use in a laccase-mediator system, the two-component mediator comprising (i) a pro-oxidant and (ii) a pro-degradant.
- the invention also provides a composition comprising an oxidative enzyme, a pro-oxidant, and a pro-degradant
- the invention also provides a process for oxidizing a substrate that comprises treating the substrate with an oxidizing enzyme, a pro-oxidant, and a pro-degradant.
- the invention provides a process for bleaching a lignin-containing material that comprises treating the material with an oxidative enzyme, a pro-oxidant, and a pro-degradant.
- the process of the invention can further include the step of adding an oxidizing agent.
- the oxidizing agent is at least one of air, oxygen, and hydrogen peroxide.
- the pro-oxidant is ascorbic acid, ascorbate, salicylic acid, salicylate, nicotinic acid, nicotinate, a hardwood black liquor, a softwood black liquor, ligno-organosolv, lignin sulfonate, or a mixture thereof.
- the pro-degradant is urea, thiourea, sulfamic acid, sulfamide, guanidine, methylsulfonic acid, or a mixture thereof.
- the present invention discloses the novel use of two components as mediators to enhance the bleach efficiency of an enzyme exhibiting laccase activity. It has been discovered that, although the use of a pro-oxidant or a pro-degradant alone as described herein is not necessarily useful as a mediator, the combination of a pro-oxidant or a pro-degradant together exert synergistic effects and produce better bleach efficiency for paper pulp.
- pro-oxidant For ease of reference and without loss of generality, one component is called a “pro-oxidant.”
- the pro-oxidant include ascorbic acid, ascorbate, salicylic acid, salicylate, nicotinic acid, nicoliante, hardwood black liquor, softwood black liquor, ligno-organosolv, lignin sulfonate, and mixtures thereof. Compounds with related structures or structural analogs may also be used.
- the pro-oxidants are active mediators in the discoloration of a dye, e.g., Chicago Blue. However, these may or may not have efficiency as mediators for pulp bleaching.
- the second component is called a “pro-degradant.”
- the pro-degradant include urea, thiourea, sulfamic acid, sulfamide, and guanidine. Compounds with related structures or structural analogs may also be used.
- the pro-degradants are often not active mediators, even in the discoloration of a dye, e.g., Chicago Blue. In pulp bleaching tests with laccase, they show either negative results or slightly positive results.
- the enzymes exhibiting laccase activity include the laccase enzymes of enzyme classification EC 1.10.3.2, the catechol oxidase enzymes of enzyme classification EC 1.10.3.1, the monophenol monooxygenase enzymes of enzyme classification EC 1.14.99.1, and the bilirubin oxidase enzymes of enzyme classification EC 1.3.3.5.
- the EC (Enzyme Commission) number is based upon the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology (IUBMB).
- the laccase of this invention may be derived from microbial, fungal, or other sources. It may furthermore be produced by a recombinant method, such as cultivating a host cell transformed with a recombinant DNA vector which includes a DNA sequence encoding the laccase (and DNA sequences encoding functions that permit the expression of laccase DNA sequence) in a culture medium under conditions that permit the expression of the laccase, and recovering the enzyme from the culture.
- mediators are developed specifically for pulp bleaching
- the same mediator mixtures and laccase enzyme(s) can be used for other applications, including treatment of pulp waste water, de-inking, industrial color removal, bleach for laundry detergents, oral care teeth whiteners, and as catalysts or facilitators for polymerization and oxidation reactions.
- Another aspect of the invention provides a process for oxidizing a substrate that comprises treating the substrate with a composition comprising an oxidizing enzyme and a pro-oxidant and a pro-detergent.
- the pro-oxidant and pro-detergent can be selected from the above described pro-oxidants and pro-detergents.
- the oxidative enzyme is a laccase, a catechol oxidase, a monophenol monooxygenase, a bilirubin oxidase, or a mixture thereof.
- the process further comprises adding a hydrolase, such as xylanase.
- the pro-oxidants and pro-detergents may each be individually present in concentrations of from about 0.01 micromolar to 1000 micromolar, more preferably from about 0.1 micromolar to about 250 micromolar and most preferably from about 0.5 to about 100 micromolar.
- the enzyme is used in amounts of from about 0.1 to 400 units (defined in Examples using ABTS as substrate) for 1 g dry pulp, more preferably from 1 to 200 units and even more preferably from about 10 to 100 units and most preferably from 20 to ⁇ 50 units.
- the process of the invention can further include the step of adding an oxidizing agent, such as at least one of air, oxygen, and hydrogen peroxide.
- an oxidizing agent such as at least one of air, oxygen, and hydrogen peroxide.
- One embodiment of the invention provides a process for bleaching a lignin-containing material that comprises treating the material with an oxidative enzyme and a pro-oxidant and a pro-detergent.
- the a pro-oxidant and a pro-detergent may each be separately present in an amount of from about 0.1% to about 15% based on the weight of the dry lignin containing material, more preferably from about 0.1% to about 10% and even more preferably from about 0.5% to about 5% and most preferably from about 1% to about 4%.
- the oxidative enzyme is a laccase, a catechol oxidase, a monophenol monooxygenase, a bilirubin oxidase, or a mixture thereof.
- the process further comprises adding a hydrolase, such as xylanase.
- a lignin containing material is wood pulp.
- the process for bleaching a lignin-containing material can further include the step of adding an oxidizing agent, such as at least one of air, oxygen, and hydrogen peroxide.
- the specific activity was determined using ABTS (0.5 mM) as substrate.
- One unit of activity is equal to the umol of the oxidized product from ABTS per min per mg protein at pH 6.0 at 23° C.
- the activity of laccase was determined using syringaldazine as substrate.
- one unit of activity is equal to the change of 0.001 UV absorbance at A530 nm per minute per ug protein in 2 ml of 100 mM, pH 5.5 potassium phosphate buffer, and 0.5 ml of 0.25 mM syringaldazine in methanol at 23° C.
- the dried pulp was added to 80 ml of 50 mM phosphate, pH 5.5, and disintegrated in a blender. The pulp was then transferred to a 500-ml conical flask and the blender was washed with 20 ml of the same buffer. The washed buffer and the pulp were combined. The mediator was added at 1-4% (w/w, based on the dry pulp) followed by the addition of the laccase. The pH of the pulp mixture was adjusted to 5.5 if needed. The flask was covered with an aluminum foil with holes punched through and incubated at 50° C. for 16 hrs on a rotary shaker at 200 rpm.
- the filtered pulp was repulped in the alkaline solution and incubated at 70° C. for 3 hrs.
- the pH of the pulp mixture should be between 11.7-12.00 during the entire treatment. After the treatment, the pulp mixture was filtered through a Buchner funnel and the pulp was washed with water extensively and then dried in a hood overnight.
- the pro-oxidants and pro-degradants were tested individually as mediators to enhance laccase-catalyzed bleaching of Chicago Blue in solution.
- the Chicago Blue Dye also known as Direct Blue 1 or DB1
- DB1 Direct Blue 1
- the Chicago Blue Dye is fully described by Schneider et al. in U.S. Pat. No. 5,885,304, which is hereby incorporated by reference.
- Each of the compounds i.e., potential mediators
- a phosphate buffer and a Chicago Blue solution A solution of a laccase was added to make up 1 ml of the final solution, containing 20 uM mediator, 20 mM buffer at pH 5.5 or 7.0, 0.1-1% laccase (v/v) and Chicago Blue solution, with absorbance at A610 nm between 0.6 to 0.8.
- the change in the absorbance at A610 nm was measured immediately using a UV-VIS spectrophotometer (UV-1201, Shimadzu Scientific Instruments) after the enzyme was added. The decrease in absorbance was recorded at 30-second intervals for 5 minutes and was used to estimate the efficiency of the mediator.
- Example laccase mediator 1 mediator 2 pulp Decrease in Kappa 2 0 0 0 2 g 0 3 100 ul 0 0 2 g 2.6 4 100 ul urea, 87 mg 0 2 g 2.6 5 100 ul 0 ascorbate, 20 mg 2 g 4.8 6 100 ul urea, 88 mg ascorbate, 79 mg 2 g 7.1
- mediators of the invention also include mediators which are functionally equivalent to the mediators specifically recited herein, such equivalents having minor structural variations such as the addition of a methyl or ethyl substituent or the formation of a methyl ester from a carboxylic acid. Accordingly, this invention is not to be regarded as limited to the embodiments disclosed herein.
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Abstract
Description
- This application claims the benefit of U.S. Provisional Application No. 60/318,294, filed on Sep. 10, 2001.
- The present invention relates to the enhancement of enzyme activity. More specifically, the present invention relates to pro-oxidants and pro-degradants that, in combination, are useful in enhancing the activity of enzymes having laccase activity, especially in the field of pulp bleaching.
- Paper pulp is typically processed from wood through the Kraft (and other) processes. The process produces a pulp with a dark brown color, mostly due to the presence of lignin and lignin derivatives. For many applications, the lignin has to be removed by a process known in the art as “bleaching.” This is typically done commercially in several stages in pulp mills, wherein lignin is first oxidized and then removed from the pulp.
- Recently, several research groups have been working with enzymes to biologically bleach pulp, referred to as “bio-bleaching.” Bio-bleaching is a methodology whereby an enzyme is used to decrease the optical brightness and/or lignin content of pulp or paper. The standard measure of bleaching efficiency is “Kappa number.” Enzymes that have most commonly been used include laccase, lignin peroxidase, and manganese peroxidase. An enzyme group that has received particular attention is the laccase family of enzymes, which are copper-containing enzymes that are known to be good oxidizing agents in the presence of oxygen. Laccases are found in microbes, fungi, and higher organisms.
- For many applications, the oxidizing efficiency of a laccase can be improved through the use of a mediator, also known as an enhancing agent. Systems that include a laccase and a mediator are known in the art as laccase-mediator systems (LMS). There are several known mediators for use in a laccase-mediator system. These include HBT (1-hydroxybenzotriazole), ABTS [2,2′-azinobis(3-ethylbenzothiazoline-6-sulfinic acid)], NHA (N-hydroxyacetinilide), NHAA (N-acetyl-N-phenylhydroxylamine), HBTO (3-hydroxy-1,2,3-benzotriazin-4(3H)-one), and VIO (violuric acid). In addition, there are several compounds containing NH—OH or N—O that have been found to be useful as mediators.
- A major limitation of this methodology in the commercial context is the cost and the efficiency of the mediators used. It is critical therefore to discover additional mediators.
- The present invention provides two-component mediators, wherein one component serves as a pro-oxidant and the other component serves as a pro-degradant and booster. When used in combination with a laccase, the two-component mediators enhance the bleaching of pulp. Thus, the invention provides a two-component mediator for use in a laccase-mediator system, the two-component mediator comprising (i) a pro-oxidant and (ii) a pro-degradant.
- The invention also provides a composition comprising an oxidative enzyme, a pro-oxidant, and a pro-degradant The invention also provides a process for oxidizing a substrate that comprises treating the substrate with an oxidizing enzyme, a pro-oxidant, and a pro-degradant. Further, the invention provides a process for bleaching a lignin-containing material that comprises treating the material with an oxidative enzyme, a pro-oxidant, and a pro-degradant.
- The process of the invention can further include the step of adding an oxidizing agent. In one embodiment, the oxidizing agent is at least one of air, oxygen, and hydrogen peroxide.
- In one embodiment, the pro-oxidant is ascorbic acid, ascorbate, salicylic acid, salicylate, nicotinic acid, nicotinate, a hardwood black liquor, a softwood black liquor, ligno-organosolv, lignin sulfonate, or a mixture thereof. In another embodiment, the pro-degradant is urea, thiourea, sulfamic acid, sulfamide, guanidine, methylsulfonic acid, or a mixture thereof.
- The present invention discloses the novel use of two components as mediators to enhance the bleach efficiency of an enzyme exhibiting laccase activity. It has been discovered that, although the use of a pro-oxidant or a pro-degradant alone as described herein is not necessarily useful as a mediator, the combination of a pro-oxidant or a pro-degradant together exert synergistic effects and produce better bleach efficiency for paper pulp.
- For ease of reference and without loss of generality, one component is called a “pro-oxidant.” Examples of the pro-oxidant include ascorbic acid, ascorbate, salicylic acid, salicylate, nicotinic acid, nicoliante, hardwood black liquor, softwood black liquor, ligno-organosolv, lignin sulfonate, and mixtures thereof. Compounds with related structures or structural analogs may also be used. The pro-oxidants are active mediators in the discoloration of a dye, e.g., Chicago Blue. However, these may or may not have efficiency as mediators for pulp bleaching.
- For ease of reference and without loss of generality, the second component is called a “pro-degradant.” Examples of the pro-degradant include urea, thiourea, sulfamic acid, sulfamide, and guanidine. Compounds with related structures or structural analogs may also be used. The pro-degradants are often not active mediators, even in the discoloration of a dye, e.g., Chicago Blue. In pulp bleaching tests with laccase, they show either negative results or slightly positive results.
- It has been discovered that when a pro-oxidant and a pro-degradant are added together with a laccase enzyme, some combinations are capable of a large decrease in the Kappa number. The enzymes exhibiting laccase activity include the laccase enzymes of enzyme classification EC 1.10.3.2, the catechol oxidase enzymes of enzyme classification EC 1.10.3.1, the monophenol monooxygenase enzymes of enzyme classification EC 1.14.99.1, and the bilirubin oxidase enzymes of enzyme classification EC 1.3.3.5. The EC (Enzyme Commission) number is based upon the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology (IUBMB).
- The laccase of this invention may be derived from microbial, fungal, or other sources. It may furthermore be produced by a recombinant method, such as cultivating a host cell transformed with a recombinant DNA vector which includes a DNA sequence encoding the laccase (and DNA sequences encoding functions that permit the expression of laccase DNA sequence) in a culture medium under conditions that permit the expression of the laccase, and recovering the enzyme from the culture.
- While the mediators are developed specifically for pulp bleaching, the same mediator mixtures and laccase enzyme(s) can be used for other applications, including treatment of pulp waste water, de-inking, industrial color removal, bleach for laundry detergents, oral care teeth whiteners, and as catalysts or facilitators for polymerization and oxidation reactions.
- Another aspect of the invention provides a process for oxidizing a substrate that comprises treating the substrate with a composition comprising an oxidizing enzyme and a pro-oxidant and a pro-detergent. The pro-oxidant and pro-detergent can be selected from the above described pro-oxidants and pro-detergents.
- The oxidative enzyme is a laccase, a catechol oxidase, a monophenol monooxygenase, a bilirubin oxidase, or a mixture thereof. The process further comprises adding a hydrolase, such as xylanase.
- The pro-oxidants and pro-detergents may each be individually present in concentrations of from about 0.01 micromolar to 1000 micromolar, more preferably from about 0.1 micromolar to about 250 micromolar and most preferably from about 0.5 to about 100 micromolar.
- The enzyme is used in amounts of from about 0.1 to 400 units (defined in Examples using ABTS as substrate) for 1 g dry pulp, more preferably from 1 to 200 units and even more preferably from about 10 to 100 units and most preferably from 20 to −50 units.
- The process of the invention can further include the step of adding an oxidizing agent, such as at least one of air, oxygen, and hydrogen peroxide.
- One embodiment of the invention provides a process for bleaching a lignin-containing material that comprises treating the material with an oxidative enzyme and a pro-oxidant and a pro-detergent. In this aspect of the invention, the a pro-oxidant and a pro-detergent may each be separately present in an amount of from about 0.1% to about 15% based on the weight of the dry lignin containing material, more preferably from about 0.1% to about 10% and even more preferably from about 0.5% to about 5% and most preferably from about 1% to about 4%. The oxidative enzyme is a laccase, a catechol oxidase, a monophenol monooxygenase, a bilirubin oxidase, or a mixture thereof. In another embodiment, the process further comprises adding a hydrolase, such as xylanase.
- One example of a lignin containing material is wood pulp. The process for bleaching a lignin-containing material can further include the step of adding an oxidizing agent, such as at least one of air, oxygen, and hydrogen peroxide.
- Laccase Enzyme Assay
- In the examples, two Aspergillus laccases have been used, both from Novozymes A/S (Denmark). NovoSample 51002 works best at pH 4-5 while NovoSample 51003 works best at pH 5-6. Enzyme dosage has been found to have an effect on bio-bleaching. For example, 0.1 ml of the 51003 laccase gives a modest Kappa number reduction when HBT is used, and a huge reduction when ABTS is used.
- The specific activity was determined using ABTS (0.5 mM) as substrate. One unit of activity is equal to the umol of the oxidized product from ABTS per min per mg protein at pH 6.0 at 23° C. The extinction coefficient of the oxidized ABTS is: ε(max) at 420 nm=36,000M-1 cm-1.)
- Alternatively, the activity of laccase (NS51003) was determined using syringaldazine as substrate. In this case, one unit of activity is equal to the change of 0.001 UV absorbance at A530 nm per minute per ug protein in 2 ml of 100 mM, pH 5.5 potassium phosphate buffer, and 0.5 ml of 0.25 mM syringaldazine in methanol at 23° C.
- Kappa Number
- Delignification of the pulp was measured as the change in Kappa number according to TAPPI method T236 cm-85. Briefly, a known mass of paper pulp (containing lignin) was reacted with an excess of potassium permanganate in acid solution for a specified period of time to oxidize the lignin. After the reaction, the residual permanganate was determined by titration. The Kappa number was defined as the volume (ml) of 0.1N potassium permanganate consumed by 1 g of moisture-free pulp in 0.5N sulfuric acid after a ten-minute reaction time at 25° C. under conditions such that one-half of the permanganate remains unreacted. A linear relationship with the lignin content of the pulp and the measurement of the Kappa number has been done on samples as low as 300 mg of pulp.
- Pulp Bleaching
- A softwood Kraft pulp, Kappa number 31.0, was treated with a laccase (NS51003) under the following conditions:
Enzyme dosage 45 units/g pulp pH 5.5 Temperature 50° C. Reaction time 16 hours Pulp consistency 2% - The dried pulp was added to 80 ml of 50 mM phosphate, pH 5.5, and disintegrated in a blender. The pulp was then transferred to a 500-ml conical flask and the blender was washed with 20 ml of the same buffer. The washed buffer and the pulp were combined. The mediator was added at 1-4% (w/w, based on the dry pulp) followed by the addition of the laccase. The pH of the pulp mixture was adjusted to 5.5 if needed. The flask was covered with an aluminum foil with holes punched through and incubated at 50° C. for 16 hrs on a rotary shaker at 200 rpm.
- After the enzymatic treatment, the pulp mixture was filtered through a Buchner funnel and the pulp was washed with water. The pulp from the control experiment was treated under the same pH and temperature conditions as described above. The washed pulp was then treated with an alkaline solution under the following conditions:
Pulp 2 g Water 200 ml NaOH 240 mg H2O2 (30%) 400 ul Temperature 70° C. Reaction time 3 hours - The filtered pulp was repulped in the alkaline solution and incubated at 70° C. for 3 hrs. The pH of the pulp mixture should be between 11.7-12.00 during the entire treatment. After the treatment, the pulp mixture was filtered through a Buchner funnel and the pulp was washed with water extensively and then dried in a hood overnight.
- The delignification of the pulp was measured as the change in the Kappa number according to TAPPI method T236 cm-85.
- The following examples are illustrative of the present invention, and are not intended to be construed in any way as limiting the scope of the invention.
- In this example, the pro-oxidants and pro-degradants were tested individually as mediators to enhance laccase-catalyzed bleaching of Chicago Blue in solution. The Chicago Blue Dye, also known as Direct Blue 1 or DB1, is a commonly used assay for the oxidative efficiency of laccase. The Chicago Blue Dye is fully described by Schneider et al. in U.S. Pat. No. 5,885,304, which is hereby incorporated by reference.
- Each of the compounds (i.e., potential mediators) was dissolved in water, or in ethanol if the potential mediator was not water soluble, and then mixed with a phosphate buffer and a Chicago Blue solution. A solution of a laccase was added to make up 1 ml of the final solution, containing 20 uM mediator, 20 mM buffer at pH 5.5 or 7.0, 0.1-1% laccase (v/v) and Chicago Blue solution, with absorbance at A610 nm between 0.6 to 0.8. The change in the absorbance at A610 nm was measured immediately using a UV-VIS spectrophotometer (UV-1201, Shimadzu Scientific Instruments) after the enzyme was added. The decrease in absorbance was recorded at 30-second intervals for 5 minutes and was used to estimate the efficiency of the mediator.
- The following are the results from the bleaching experiments of Chicago Blue:
ΔmA610 Usage ΔmA610 (3 min) Mediator (0.1 umole/ml) (ugram) (3 min) at pH 5.5 at pH 7.0 none 0 0 ABTS 10 445 341 Lignin organosolv 20 ug/ml 390 265 Ascorbic acid 20 ug/ml 6 2 Nicotinic acid 20 ug/ml 0 0 Urea 20 ug/ml 1 0 Pine black liquor 100 (14%) 26 18 Lignosulfonic acid 25 ug/ml 24 — Salicylic acid 20 ug/ml 11 — - In these examples, we used the pulp bleaching as described above, laccase as the oxidative enzyme, a pro-oxidant (as mediator 2), and a pro-degradant (as mediator 1).
Example laccase mediator 1 mediator 2 pulp Decrease in Kappa 2 0 0 0 2 g 0 3 100 ul 0 0 2 g 2.6 4 100 ul urea, 87 mg 0 2 g 2.6 5 100 ul 0 ascorbate, 20 mg 2 g 4.8 6 100 ul urea, 88 mg ascorbate, 79 mg 2 g 7.1 - The data above clearly indicate that urea is barely active in enhancing bleaching. However, in the presence of a pro-oxidant, a noticeable decrease in Kappa number was obtained.
- In these further examples, we used the pulp bleaching as described above, laccase as the enzyme, a pro-oxidant (as mediator 2), and a pro-degradant (as mediator 1). In the following table, SA=salicylic acid, AA=ascorbic acid. The decrease in Kappa number is the difference in the Kappa numbers of the corresponding experiments with and without mediators under the same experimental conditions used for the pulp tests.
Laccase Pulp Decrease in Kappa Example (ml) Mediator 1 Mediator 2 (g) number 7 0.1 SA, 80 mg Dicyandiamide, 80 mg 2 −4.7 8 0.1 SA, 80 mg Melamine, 80 mg 2 −5.9 9 0.2 SA, 80 mg sulfanilic acid, 80 mg 2 −4.0 10 0.15 SA, 80 mg Sulfanilamide, 80 mg 2 −3.3 11 0.2 AA, 80 mg Sulfanilamide, 80 mg 2 −4.1 12 0.1 AA, 80 mg Melamine, 80 mg 2 −6.1 13 0.1 AA, 80 mg Dicyandiamide, 80 mg 2 −6.1 - It is to be understood that the above described embodiments are illustrative only and that modification throughout may occur to one skilled in the art. For example, a person of skill in the art will recognize that the mediators of the invention also include mediators which are functionally equivalent to the mediators specifically recited herein, such equivalents having minor structural variations such as the addition of a methyl or ethyl substituent or the formation of a methyl ester from a carboxylic acid. Accordingly, this invention is not to be regarded as limited to the embodiments disclosed herein.
Claims (26)
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US10/027,165 US20030094251A1 (en) | 2001-09-10 | 2001-12-20 | Enhancing laccase activity using pro-oxidants and pro-degradants |
PCT/US2002/026758 WO2003023142A1 (en) | 2001-09-10 | 2002-08-21 | Enhancing laccase activity using pro-oxidants and pro-degradants |
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US9663899B2 (en) * | 2015-08-26 | 2017-05-30 | Solenis Technologies, L.P. | Method for making lignocellulosic paper and paper product |
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ES2372379B1 (en) * | 2010-06-28 | 2012-11-27 | Instituto Nacional De Investigacion Y Tecnologia Agraria Y Alimentaria (Inia) | PROCEDURE FOR DELIGNIFICATION OF LIGNOCELLULOSICAL MATERIALS. |
CN103859579A (en) * | 2014-04-01 | 2014-06-18 | 吉林烟草工业有限责任公司 | Method for degrading lignin in tobacco stems |
CN106120432B (en) * | 2016-06-29 | 2018-08-17 | 江汉大学 | The method for manufacturing paper pulp using corn leafage one kettle way |
WO2021156342A1 (en) * | 2020-02-04 | 2021-08-12 | Novozymes A/S | Solid stabilized laccase compositions |
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US5246543A (en) * | 1989-08-18 | 1993-09-21 | Degussa Corporation | Process for bleaching and delignification of lignocellulosic materials |
US5885304A (en) * | 1993-06-29 | 1999-03-23 | Novo Nordisk A/S | Enhancement of laccase reactions |
US6103059A (en) * | 1993-06-16 | 2000-08-15 | Lignozym Gmbh | Process for delignification of a lignin containing pulp |
US6242245B1 (en) * | 1997-09-26 | 2001-06-05 | Consortium für elektrochemische Industrie GmbH | Multicomponent system for modifying, degrading or bleaching lignin or lignin-containing materials, and processes for its use |
-
2001
- 2001-12-20 US US10/027,165 patent/US20030094251A1/en not_active Abandoned
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- 2002-08-21 WO PCT/US2002/026758 patent/WO2003023142A1/en not_active Application Discontinuation
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5246543A (en) * | 1989-08-18 | 1993-09-21 | Degussa Corporation | Process for bleaching and delignification of lignocellulosic materials |
US6103059A (en) * | 1993-06-16 | 2000-08-15 | Lignozym Gmbh | Process for delignification of a lignin containing pulp |
US6358904B1 (en) * | 1993-06-16 | 2002-03-19 | Hans-Peter Call | Multicomponent bleaching system |
US5885304A (en) * | 1993-06-29 | 1999-03-23 | Novo Nordisk A/S | Enhancement of laccase reactions |
US6242245B1 (en) * | 1997-09-26 | 2001-06-05 | Consortium für elektrochemische Industrie GmbH | Multicomponent system for modifying, degrading or bleaching lignin or lignin-containing materials, and processes for its use |
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US9663899B2 (en) * | 2015-08-26 | 2017-05-30 | Solenis Technologies, L.P. | Method for making lignocellulosic paper and paper product |
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