ES2848705T3 - Amadoriasa modificada y método para producirla, agente para mejorar la resistencia a tensioactivos de la amadoriasa y composición para medir la HbA1c usando la misma - Google Patents
Amadoriasa modificada y método para producirla, agente para mejorar la resistencia a tensioactivos de la amadoriasa y composición para medir la HbA1c usando la misma Download PDFInfo
- Publication number
- ES2848705T3 ES2848705T3 ES14834684T ES14834684T ES2848705T3 ES 2848705 T3 ES2848705 T3 ES 2848705T3 ES 14834684 T ES14834684 T ES 14834684T ES 14834684 T ES14834684 T ES 14834684T ES 2848705 T3 ES2848705 T3 ES 2848705T3
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- Prior art keywords
- amino acid
- seq
- substitution
- position corresponding
- lysine
- Prior art date
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- 108010078123 amadoriase Proteins 0.000 title claims abstract description 482
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- 239000004472 Lysine Substances 0.000 claims abstract description 189
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- 150000001413 amino acids Chemical class 0.000 claims abstract description 86
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims abstract description 57
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims abstract description 51
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- UJHVZVXYELCZLX-UHFFFAOYSA-M tributyl(dodecyl)phosphanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC UJHVZVXYELCZLX-UHFFFAOYSA-M 0.000 description 1
- RLZMYANQLOCZOB-UHFFFAOYSA-M tributyl(methyl)phosphanium;iodide Chemical compound [I-].CCCC[P+](C)(CCCC)CCCC RLZMYANQLOCZOB-UHFFFAOYSA-M 0.000 description 1
- PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 1
- SZEMGTQCPRNXEG-UHFFFAOYSA-M trimethyl(octadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C SZEMGTQCPRNXEG-UHFFFAOYSA-M 0.000 description 1
- 239000012137 tryptone Substances 0.000 description 1
- 241001515965 unidentified phage Species 0.000 description 1
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Classifications
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/26—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
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- 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.)
- C12N9/0012—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
- C12N9/0026—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on CH-NH groups of donors (1.5)
- C12N9/0032—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on CH-NH groups of donors (1.5) with oxygen as acceptor (1.5.3)
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/72—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood pigments, e.g. haemoglobin, bilirubin or other porphyrins; involving occult blood
- G01N33/721—Haemoglobin
- G01N33/723—Glycosylated haemoglobin
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y105/00—Oxidoreductases acting on the CH-NH group of donors (1.5)
- C12Y105/03—Oxidoreductases acting on the CH-NH group of donors (1.5) with oxygen as acceptor (1.5.3)
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/795—Porphyrin- or corrin-ring-containing peptides
- G01N2333/805—Haemoglobins; Myoglobins
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/90—Enzymes; Proenzymes
- G01N2333/902—Oxidoreductases (1.)
- G01N2333/906—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.7)
- G01N2333/9065—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.7) acting on CH-NH groups of donors (1.5)
- G01N2333/90672—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.7) acting on CH-NH groups of donors (1.5) with oxygen as acceptor (1.5.3) in general
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- Immunology (AREA)
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- Analytical Chemistry (AREA)
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- Cell Biology (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Food Science & Technology (AREA)
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- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013167005 | 2013-08-09 | ||
| JP2013221515 | 2013-10-24 | ||
| PCT/JP2014/071036 WO2015020200A1 (ja) | 2013-08-09 | 2014-08-08 | 改変型アマドリアーゼ及びその製造法、並びにアマドリアーゼの界面活性剤耐性向上剤及びこれを用いたHbA1c測定用組成物 |
Publications (1)
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| ES2848705T3 true ES2848705T3 (es) | 2021-08-11 |
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| US (2) | US10619183B2 (enExample) |
| EP (2) | EP3031914B1 (enExample) |
| JP (4) | JP6682268B2 (enExample) |
| CN (2) | CN105473715B (enExample) |
| ES (1) | ES2848705T3 (enExample) |
| WO (1) | WO2015020200A1 (enExample) |
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| WO2015020200A1 (ja) * | 2013-08-09 | 2015-02-12 | キッコーマン株式会社 | 改変型アマドリアーゼ及びその製造法、並びにアマドリアーゼの界面活性剤耐性向上剤及びこれを用いたHbA1c測定用組成物 |
| KR102159807B1 (ko) | 2014-10-24 | 2020-09-25 | 기꼬만 가부시키가이샤 | 디히드로게나아제 활성이 향상된 아마도리아제 |
| EP3216865B1 (en) * | 2014-11-07 | 2020-09-30 | Kikkoman Corporation | Amadoriase having enhanced anionic-surfactant tolerance |
| CN109312312B (zh) * | 2016-04-22 | 2023-06-02 | 龟甲万株式会社 | HbA1c脱氢酶 |
| JP7352838B2 (ja) * | 2018-06-27 | 2023-09-29 | 東洋紡株式会社 | フルクトシルバリルヒスチジンオキシダーゼ活性を有するタンパク質 |
| JP7540890B2 (ja) * | 2020-01-10 | 2024-08-27 | キリンホールディングス株式会社 | 低毒性のポリマー粒子の製法 |
| JP7714520B2 (ja) | 2020-02-21 | 2025-07-29 | キッコーマン株式会社 | 検体の状態を評価するためのデバイス、それを含むシステム、検体の状態を評価する方法及びそれに用いる乳酸デヒドロゲナーゼ |
| CN113773236B (zh) * | 2021-09-10 | 2023-03-14 | 上海奥威日化有限公司 | 用于制备烷基硫酸钠干燥物的前驱组合物 |
| WO2025018360A1 (ja) | 2023-07-19 | 2025-01-23 | 株式会社Provigate | フルクトシルアミノ酸オキシダーゼ、遺伝子、発現ベクター、糖化タンパク質センサ、糖化タンパク質の測定方法、及びフルクトシルアミノ酸オキシダーゼの製造方法 |
Family Cites Families (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61280297A (ja) | 1985-06-04 | 1986-12-10 | Noda Sangyo Kagaku Kenkyusho | アマドリ化合物の定量法及びその定量用試薬 |
| JPH01127895A (ja) | 1987-11-04 | 1989-05-19 | Akutoronikusu Kk | 閉ループ管型熱伝達装置 |
| EP0567642A4 (en) * | 1991-01-14 | 1994-08-17 | Bior Inc | Process for producing (r)-malic acid, microbial maleate hydratase, and process for producing said hydratase |
| GB9116315D0 (en) * | 1991-07-29 | 1991-09-11 | Genzyme Ltd | Assay |
| JP3850904B2 (ja) * | 1994-10-05 | 2006-11-29 | アークレイ株式会社 | フルクトシルアミノ酸オキシダーゼ及びその製造方法 |
| DE69635503T2 (de) * | 1995-04-11 | 2006-08-17 | Arkray, Inc. | Fructosyl-Aminosäureoxidase und Verfahren zu deren Herstellung |
| WO1997013872A1 (en) | 1995-10-12 | 1997-04-17 | Kyoto Daiichi Kagaku Co., Ltd. | Method and assaying amodori compounds |
| JP3949854B2 (ja) | 1999-10-01 | 2007-07-25 | キッコーマン株式会社 | 糖化蛋白質の測定方法 |
| EP1304385B1 (en) | 2000-07-14 | 2010-12-29 | ARKRAY, Inc. | Method of selectively determining glycated hemoglobin |
| WO2002061119A1 (fr) * | 2001-01-31 | 2002-08-08 | Asahi Kasei Kabushiki Kaisha | Compositions pour analyse de glycoproteines |
| JP4231668B2 (ja) | 2001-09-04 | 2009-03-04 | キッコーマン株式会社 | 新規なフルクトシルペプチドオキシダーゼ |
| US7291256B2 (en) * | 2002-09-12 | 2007-11-06 | Lifescan, Inc. | Mediator stabilized reagent compositions and methods for their use in electrochemical analyte detection assays |
| CN1701118A (zh) * | 2002-09-24 | 2005-11-23 | 爱科来株式会社 | 果糖基胺氧化酶 |
| JP4227820B2 (ja) | 2003-03-12 | 2009-02-18 | 旭化成ファーマ株式会社 | 新規な酵素 |
| JP4248900B2 (ja) | 2003-03-14 | 2009-04-02 | イチビキ株式会社 | 新規なフルクトシルアミンオキシダーゼをコードする遺伝子及びそれを用いての該フルクトシルアミンオキシダーゼの製造方法 |
| EP1626088B1 (en) * | 2003-05-21 | 2010-12-01 | Asahi Kasei Pharma Corporation | Method of measuring glycolated hemoglobin a1c, enzyme to be used therefor and process for producing the same |
| JPWO2005049858A1 (ja) | 2003-11-19 | 2007-11-29 | 第一化学薬品株式会社 | ヘモグロビン含有試料中の基質の測定方法 |
| ATE509119T1 (de) | 2003-11-19 | 2011-05-15 | Sekisui Medical Co Ltd | Verfahren zum testen von glykosyliertem protein |
| WO2005087946A1 (ja) | 2004-03-17 | 2005-09-22 | Daiichi Pure Chemicals Co., Ltd. | 糖化蛋白質の測定方法 |
| CN101171342B (zh) | 2005-05-06 | 2011-11-16 | 爱科来株式会社 | 蛋白质的切断方法及其用途 |
| JP4798600B2 (ja) | 2005-05-30 | 2011-10-19 | キッコーマン株式会社 | フルクトシルペプチドオキシダ−ゼの安定化方法 |
| WO2007010950A1 (ja) * | 2005-07-19 | 2007-01-25 | Kikkoman Corporation | 糖化蛋白質の測定方法および測定キット |
| CN101479383B (zh) | 2006-04-25 | 2013-10-02 | 龟甲万株式会社 | 具有优良的热稳定性的真核阿马道里酶、真核阿马道里酶的基因和重组dna,和生产具有优良的热稳定性的真核阿马道里酶的方法 |
| DE102006021401A1 (de) * | 2006-05-08 | 2007-12-13 | Henkel Kgaa | Amadoriasen in Wasch- und Reinigungsmitteln |
| ES2404059T3 (es) * | 2006-07-25 | 2013-05-23 | General Atomics | Procedimientos para analizar el porcentaje de hemoglobina glicada |
| JP4697809B2 (ja) * | 2007-02-22 | 2011-06-08 | 旭化成ファーマ株式会社 | ロイコ色素の安定化方法 |
| JP5350762B2 (ja) | 2008-08-04 | 2013-11-27 | 東洋紡株式会社 | フルクトシルアミノ酸オキシダーゼ、およびその利用法 |
| JP5243878B2 (ja) | 2008-08-04 | 2013-07-24 | 東洋紡株式会社 | フルクトシルバリルヒスチジン測定用酵素、およびその利用法 |
| CN101358229B (zh) * | 2008-09-23 | 2011-11-02 | 宁波美康生物科技有限公司 | 糖化血红蛋白酶法检测试剂盒 |
| JP5665081B2 (ja) | 2008-10-09 | 2015-02-04 | 協和メデックス株式会社 | 新規フルクトシルペプチドオキシダーゼ |
| CN102171338B (zh) * | 2008-10-10 | 2014-08-13 | 东洋纺织株式会社 | 具有果糖基缬氨酰基组氨酸氧化酶活性的蛋白质及其修饰产物以及其应用 |
| US20110251826A1 (en) * | 2008-10-14 | 2011-10-13 | Mcgoogan Gerard | Data Analyzer |
| EP2281900A1 (en) * | 2009-08-03 | 2011-02-09 | Roche Diagnostics GmbH | Fructosyl peptidyl oxidase and sensor for assaying a glycated protein |
| EP2287295A1 (en) | 2009-08-03 | 2011-02-23 | Roche Diagnostics GmbH | Mutant Fructosyl amino acid oxidase |
| JP5927771B2 (ja) | 2010-04-09 | 2016-06-01 | 東洋紡株式会社 | ヘモグロビンA1cの測定方法 |
| CN103080308B (zh) * | 2010-08-06 | 2015-08-05 | 龟甲万株式会社 | 底物特异性得到改变的阿马多里酶 |
| CA2806261A1 (en) | 2010-08-11 | 2012-02-16 | Kyowa Medex Co., Ltd. | Method for measuring glycated hemoglobin |
| JPWO2012043601A1 (ja) | 2010-09-29 | 2014-02-24 | キッコーマン株式会社 | アマドリアーゼ改変体 |
| JP6236318B2 (ja) * | 2011-06-17 | 2017-11-22 | 協和メデックス株式会社 | 糖化ヘモグロビンの測定方法、測定試薬、及び、測定キット |
| EP2705694B1 (en) * | 2011-07-12 | 2018-01-03 | Huawei Technologies Co., Ltd. | Seamless mobility schemes in named-data networking using multi-path routing and content caching |
| JP2013102736A (ja) * | 2011-11-15 | 2013-05-30 | Toyobo Co Ltd | 色素の安定性を改善した生化学分析用試験片 |
| JP6282115B2 (ja) | 2011-12-28 | 2018-02-21 | キッコーマン株式会社 | 熱安定性が向上したアマドリアーゼ、その遺伝子および組換えdnaならびに熱安定性が向上したアマドリアーゼの製造法 |
| JP5779118B2 (ja) | 2012-02-16 | 2015-09-16 | Ntn株式会社 | 転がり接触部品、転がり軸受、自在継手およびそれらの製造方法 |
| US20130269351A1 (en) | 2012-04-17 | 2013-10-17 | General Electric Company | Micromixer assembly of a turbine system and method of assembly |
| JP6401056B2 (ja) * | 2012-04-27 | 2018-10-03 | キッコーマン株式会社 | フルクトシルヘキサペプチドに作用する改変型アマドリアーゼ |
| WO2015020200A1 (ja) * | 2013-08-09 | 2015-02-12 | キッコーマン株式会社 | 改変型アマドリアーゼ及びその製造法、並びにアマドリアーゼの界面活性剤耐性向上剤及びこれを用いたHbA1c測定用組成物 |
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| US11549134B2 (en) | 2023-01-10 |
| WO2015020200A1 (ja) | 2015-02-12 |
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| US20200263228A1 (en) | 2020-08-20 |
| EP3031914A4 (en) | 2017-01-11 |
| EP3760717A1 (en) | 2021-01-06 |
| JP6682268B2 (ja) | 2020-04-15 |
| US10619183B2 (en) | 2020-04-14 |
| CN111398605B (zh) | 2024-04-05 |
| CN105473715A (zh) | 2016-04-06 |
| EP3031914B1 (en) | 2020-12-23 |
| JP2022188182A (ja) | 2022-12-20 |
| EP3031914A1 (en) | 2016-06-15 |
| JP2024170623A (ja) | 2024-12-10 |
| JPWO2015020200A1 (ja) | 2017-03-02 |
| JP2020096596A (ja) | 2020-06-25 |
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