RU2010143597A - Стабилизированные жидкие ферментные композиции - Google Patents
Стабилизированные жидкие ферментные композиции Download PDFInfo
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- RU2010143597A RU2010143597A RU2010143597/04A RU2010143597A RU2010143597A RU 2010143597 A RU2010143597 A RU 2010143597A RU 2010143597/04 A RU2010143597/04 A RU 2010143597/04A RU 2010143597 A RU2010143597 A RU 2010143597A RU 2010143597 A RU2010143597 A RU 2010143597A
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- 239000007788 liquid Substances 0.000 title claims abstract 17
- 239000000203 mixture Substances 0.000 title claims abstract 17
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 19
- 108090000765 processed proteins & peptides Proteins 0.000 claims abstract 16
- 125000000539 amino acid group Chemical group 0.000 claims abstract 15
- 150000001875 compounds Chemical class 0.000 claims abstract 13
- 125000006239 protecting group Chemical group 0.000 claims abstract 13
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims abstract 8
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims abstract 8
- 125000005843 halogen group Chemical group 0.000 claims abstract 7
- 239000001257 hydrogen Substances 0.000 claims abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 7
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims abstract 7
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims abstract 5
- 125000003118 aryl group Chemical group 0.000 claims abstract 5
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims abstract 5
- -1 methoxy succinyl Chemical group 0.000 claims abstract 5
- 108090000787 Subtilisin Proteins 0.000 claims abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract 4
- COLNVLDHVKWLRT-QMMMGPOBSA-N phenylalanine group Chemical group N[C@@H](CC1=CC=CC=C1)C(=O)O COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims abstract 4
- 125000001424 substituent group Chemical group 0.000 claims abstract 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims abstract 3
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims abstract 3
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 claims abstract 3
- 125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims abstract 2
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 claims 6
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims 2
- 239000003599 detergent Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 101100006370 Arabidopsis thaliana CHX2 gene Chemical group 0.000 abstract 2
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
- C07K5/1016—Tetrapeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2/00—Peptides of undefined number of amino acids; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0806—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0815—Tripeptides with the first amino acid being basic
- C07K5/0817—Tripeptides with the first amino acid being basic the first amino acid being Arg
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
- C07K5/1005—Tetrapeptides with the first amino acid being neutral and aliphatic
- C07K5/101—Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1024—Tetrapeptides with the first amino acid being heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38663—Stabilised liquid enzyme compositions
-
- 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
- C12N9/14—Hydrolases (3)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/52—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from bacteria or Archaea
- C12N9/54—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from bacteria or Archaea bacteria being Bacillus
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/96—Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
- C12Y304/21—Serine endopeptidases (3.4.21)
- C12Y304/21062—Subtilisin (3.4.21.62)
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
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- Chemical & Material Sciences (AREA)
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- General Health & Medical Sciences (AREA)
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- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
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- Proteomics, Peptides & Aminoacids (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- General Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Detergent Compositions (AREA)
- Peptides Or Proteins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
1. Жидкая композиция, включающая субтилизин и пептидное соединение формулы B2-B1-B0-R, где ! R представляет собой водород, CH3, CX3, CHX2 или CH2X, где X представляет собой атом галогена; ! B0 представляет собой остаток фенилаланина с OH-заместителем в пара-положении и/или мета-положении; ! B1 представляет собой один аминокислотный остаток; и !B2 состоит из одного или более аминокислотных остатков, необязательно включающих N-концевую защитную группу. ! 2. Жидкая композиция по п.1, где B2 состоит из одного или двух аминокислотных остатков, включающих N-концевую защитную группу. ! 3. Жидкая композиция, включающая субтилизин и пептидное соединение формулы B2-B1-B0-R, где ! R представляет собой водород, CH3, CX3, CHX2 или CH2X, где X представляет собой атом галогена; ! B0 представляет собой один аминокислотный остаток; ! B1 представляет собой один аминокислотный остаток; и ! B2 представляет собой остаток Gly, Arg или Leu с присоединенной N-концевой защитной группой. ! 4. Жидкая композиция по п.1 или 3, где B0 представляет собой остаток тирозина. ! 5. Жидкая композиция по п.1 или 3, где B1 представляет собой остаток Ala, Cys, Gly, Pro, Ser, Thr, Val, Nva или Nle. ! 6. Жидкая композиция по п.1 или 3, где B2 содержит N-концевую защитную группу, выбранную из формильной, ацетильной, бензоильной, трифторацетильной, фторметоксикарбонильной, метоксисукцинильной, ароматической и алифатической уретановой защитных групп, бензилоксикарбонильной, трет-бутилоксикарбонильной, адамантилоксикарбонильной, пара-метоксибензилкарбонильной (MOZ), бензильной (Bn), пара-метоксибензильной (PMB) или пара-метоксифенильной (PMP) группы. ! 7. Жидкая композиция по п.1 или 3, где пептидное соединение представляет собой пептидный ал�
Claims (15)
1. Жидкая композиция, включающая субтилизин и пептидное соединение формулы B2-B1-B0-R, где
R представляет собой водород, CH3, CX3, CHX2 или CH2X, где X представляет собой атом галогена;
B0 представляет собой остаток фенилаланина с OH-заместителем в пара-положении и/или мета-положении;
B1 представляет собой один аминокислотный остаток; и
B2 состоит из одного или более аминокислотных остатков, необязательно включающих N-концевую защитную группу.
2. Жидкая композиция по п.1, где B2 состоит из одного или двух аминокислотных остатков, включающих N-концевую защитную группу.
3. Жидкая композиция, включающая субтилизин и пептидное соединение формулы B2-B1-B0-R, где
R представляет собой водород, CH3, CX3, CHX2 или CH2X, где X представляет собой атом галогена;
B0 представляет собой один аминокислотный остаток;
B1 представляет собой один аминокислотный остаток; и
B2 представляет собой остаток Gly, Arg или Leu с присоединенной N-концевой защитной группой.
4. Жидкая композиция по п.1 или 3, где B0 представляет собой остаток тирозина.
5. Жидкая композиция по п.1 или 3, где B1 представляет собой остаток Ala, Cys, Gly, Pro, Ser, Thr, Val, Nva или Nle.
6. Жидкая композиция по п.1 или 3, где B2 содержит N-концевую защитную группу, выбранную из формильной, ацетильной, бензоильной, трифторацетильной, фторметоксикарбонильной, метоксисукцинильной, ароматической и алифатической уретановой защитных групп, бензилоксикарбонильной, трет-бутилоксикарбонильной, адамантилоксикарбонильной, пара-метоксибензилкарбонильной (MOZ), бензильной (Bn), пара-метоксибензильной (PMB) или пара-метоксифенильной (PMP) группы.
7. Жидкая композиция по п.1 или 3, где пептидное соединение представляет собой пептидный альдегид Z-RAY-H, Ac-GAY-H, Z-GAY-H, Z-GAL-H, Z-GAF-H, Z-GAV-H, Z-RVY-H, Z-LVY-H, Ac-LGAY-H, Ac-FGAY-H, Ac-YGAY-H, Ac-FGVY-H или Ac-WLVY-H, где Z представляет собой бензилоксикарбонил, и Ac представляет собой ацетил.
8. Жидкая композиция по п.1 или 3, которая представляет собой жидкую композицию моющего средства, дополнительно включающую поверхностно-активное вещество.
9. Пептидное соединение формулы B2-B1-B0-R, где
R представляет собой водород, CH3, CX3, CHX2 или CH2X, где X представляет собой атом галогена;
B0 представляет собой остаток фенилаланина с OH-заместителем в пара-положении и/или мета-положении;
B1 представляет собой один аминокислотный остаток; и
B2 состоит из одного или более аминокислотных остатков с бензилоксикарбонилом в качестве N-концевой защитной группы.
10. Пептидное соединение формулы B2-B1-B0-R, где R представляет собой водород, CH3, CX3, CHX2 или CH2X, где X представляет собой атом галогена;
B0 представляет собой остаток фенилаланина с OH-заместителем в пара-положении и/или мета-положении;
B1 представляет собой один аминокислотный остаток; и
B2 представляет собой остаток Gly, Arg или Leu с присоединенной N-концевой защитной группой.
11. Пептидное соединение по п.9 или 10, где B2 включает N-концевую защитную группу, выбранную из формильной, ацетильной, бензоильной, трифторацетильной, фторметоксикарбонильной, метоксисукцинильной, ароматической и алифатической уретановой защитных групп, бензилоксикарбонильной, трет-бутилоксикарбонильной, адамантилоксикарбонильной, пара-метоксибензилкарбонильной (MOZ), бензильной (Bn), пара-метоксибензильной (PMB) или пара-метоксифенильной (PMP) группы.
12. Пептидное соединение формулы B2-B1-B0-R, где
R представляет собой водород, CH3, CX3, CHX2 или CH2X, где X представляет собой атом галогена;
B0 представляет собой один аминокислотный остаток;
B1 представляет собой небольшой аминокислотный остаток; и
B2 представляет собой остаток Gly, Arg или Leu с присоединенной ароматической N-концевой защитной группой.
13. Пептидное соединение по п.12, где B0 представляет собой остаток Tyr, Phe, Leu или Val.
14. Пептидное соединение по п.12 или 13, где ароматическая N-концевая защитная группа представляет собой бензилоксикарбонильную (Cbz), пара-метоксибензилкарбонильную (MOZ), бензильную (Bn), пара-метоксибензильную (PMB) или пара-метоксифенильную (PMP) группу.
15. Пептидное соединение по любому из пп.9, 10 и 12, которое представляет собой пептидный альдегид Z-RAY-H, Ac-GAY-H, Z-GAY-H, Z-GAL-H, Z-GAF-H, Z-GAV-H, Z-RVY-H, Z-LVY-H, Ac-LGAY-H, Ac-FGAY-H, Ac-YGAY-H, Ac-FGVY-H или Ac-WLVY-H, где Z представляет собой бензилоксикарбонил, и Ac представляет собой ацетил.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08153299 | 2008-03-26 | ||
| EP08153299.6 | 2008-03-26 | ||
| PCT/EP2009/053580 WO2009118375A2 (en) | 2008-03-26 | 2009-03-26 | Stabilized liquid enzyme compositions |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2013156600A Division RU2668563C2 (ru) | 2008-03-26 | 2013-12-19 | Стабилизированные жидкие ферментные композиции |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2010143597A true RU2010143597A (ru) | 2012-05-10 |
| RU2510662C2 RU2510662C2 (ru) | 2014-04-10 |
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Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2010143597/04A RU2510662C2 (ru) | 2008-03-26 | 2009-03-26 | Стабилизированные жидкие ферментные композиции |
| RU2013156600A RU2668563C2 (ru) | 2008-03-26 | 2013-12-19 | Стабилизированные жидкие ферментные композиции |
| RU2018131246A RU2018131246A (ru) | 2008-03-26 | 2018-08-30 | Стабилизированные жидкие ферментные композиции |
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| RU2013156600A RU2668563C2 (ru) | 2008-03-26 | 2013-12-19 | Стабилизированные жидкие ферментные композиции |
| RU2018131246A RU2018131246A (ru) | 2008-03-26 | 2018-08-30 | Стабилизированные жидкие ферментные композиции |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9181296B2 (ru) |
| EP (2) | EP3725797B1 (ru) |
| JP (2) | JP5973166B2 (ru) |
| CN (2) | CN107090014B (ru) |
| BR (1) | BRPI0909084B1 (ru) |
| ES (1) | ES2807603T3 (ru) |
| MX (1) | MX2010010348A (ru) |
| PL (1) | PL2271660T3 (ru) |
| RU (3) | RU2510662C2 (ru) |
| WO (1) | WO2009118375A2 (ru) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011076897A1 (en) | 2009-12-22 | 2011-06-30 | Novozymes A/S | Use of amylase variants at low temperature |
| EP2343310A1 (en) | 2010-01-08 | 2011-07-13 | Novozymes A/S | Serine hydrolase formulation |
| EP3404087A1 (en) | 2010-02-10 | 2018-11-21 | Novozymes A/S | Alpha-amylase variants with high stability in presence of a chelating agent |
| EP2357220A1 (en) | 2010-02-10 | 2011-08-17 | The Procter & Gamble Company | Cleaning composition comprising amylase variants with high stability in the presence of a chelating agent |
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- 2009-03-26 BR BRPI0909084-3A patent/BRPI0909084B1/pt active IP Right Grant
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Also Published As
| Publication number | Publication date |
|---|---|
| RU2668563C2 (ru) | 2018-10-02 |
| JP5973166B2 (ja) | 2016-08-23 |
| ES2807603T3 (es) | 2021-02-23 |
| WO2009118375A3 (en) | 2010-02-25 |
| JP2011515449A (ja) | 2011-05-19 |
| RU2013156600A (ru) | 2015-06-27 |
| RU2018131246A (ru) | 2020-03-02 |
| EP3725797B1 (en) | 2026-05-06 |
| US9181296B2 (en) | 2015-11-10 |
| MX2010010348A (es) | 2010-11-09 |
| JP2015180736A (ja) | 2015-10-15 |
| PL2271660T3 (pl) | 2020-11-02 |
| EP3725797A1 (en) | 2020-10-21 |
| WO2009118375A2 (en) | 2009-10-01 |
| BRPI0909084A2 (pt) | 2015-08-11 |
| US20110039752A1 (en) | 2011-02-17 |
| BRPI0909084B1 (pt) | 2020-11-03 |
| CN101981049A (zh) | 2011-02-23 |
| EP2271660A2 (en) | 2011-01-12 |
| CN101981049B (zh) | 2016-11-09 |
| RU2018131246A3 (ru) | 2021-11-12 |
| RU2510662C2 (ru) | 2014-04-10 |
| EP2271660B1 (en) | 2020-05-06 |
| CN107090014B (zh) | 2023-04-25 |
| CN107090014A (zh) | 2017-08-25 |
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