JP2018201486A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2018201486A5 JP2018201486A5 JP2017232544A JP2017232544A JP2018201486A5 JP 2018201486 A5 JP2018201486 A5 JP 2018201486A5 JP 2017232544 A JP2017232544 A JP 2017232544A JP 2017232544 A JP2017232544 A JP 2017232544A JP 2018201486 A5 JP2018201486 A5 JP 2018201486A5
- Authority
- JP
- Japan
- Prior art keywords
- amino acid
- seq
- acid sequence
- replaced
- position corresponding
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000001413 amino acids Chemical group 0.000 claims 121
- 235000001014 amino acid Nutrition 0.000 claims 54
- 229940024606 amino acid Drugs 0.000 claims 53
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Chemical group OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 claims 15
- 235000009582 asparagine Nutrition 0.000 claims 15
- 229960001230 asparagine Drugs 0.000 claims 15
- 235000004279 alanine Nutrition 0.000 claims 13
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Chemical group CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 claims 11
- 239000004473 Threonine Chemical group 0.000 claims 11
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Chemical group OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 claims 11
- 235000004554 glutamine Nutrition 0.000 claims 11
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Chemical group OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims 11
- 235000014304 histidine Nutrition 0.000 claims 11
- 235000008521 threonine Nutrition 0.000 claims 11
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 claims 10
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical group OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 claims 9
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Chemical group OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims 9
- 230000000694 effects Effects 0.000 claims 9
- 235000004400 serine Nutrition 0.000 claims 9
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical group C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims 8
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical group OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 claims 7
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical group OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims 7
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Chemical group NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims 7
- 239000004472 Lysine Chemical group 0.000 claims 7
- 235000018977 lysine Nutrition 0.000 claims 7
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical group OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims 6
- 125000000613 asparagine group Chemical group N[C@@H](CC(N)=O)C(=O)* 0.000 claims 6
- 238000010438 heat treatment Methods 0.000 claims 6
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Chemical group OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 claims 6
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims 6
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical group OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims 5
- 239000004475 Arginine Chemical group 0.000 claims 5
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 5
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical group NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims 5
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Chemical group OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims 5
- 235000009697 arginine Nutrition 0.000 claims 5
- 239000008103 glucose Substances 0.000 claims 5
- 238000006467 substitution reaction Methods 0.000 claims 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical group NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 4
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical group CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims 4
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Chemical group CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims 4
- 125000000404 glutamine group Chemical group N[C@@H](CCC(N)=O)C(=O)* 0.000 claims 4
- 125000000487 histidyl group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C([H])=N1 0.000 claims 4
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 claims 4
- 229960000310 isoleucine Drugs 0.000 claims 4
- 125000000741 isoleucyl group Chemical group [H]N([H])C(C(C([H])([H])[H])C([H])([H])C([H])([H])[H])C(=O)O* 0.000 claims 4
- 229930182817 methionine Chemical group 0.000 claims 4
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 claims 4
- 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 4
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical group SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 claims 3
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical group C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims 3
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical group NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims 3
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 claims 3
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Chemical group SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims 3
- 235000018417 cysteine Nutrition 0.000 claims 3
- 230000001419 dependent effect Effects 0.000 claims 3
- 125000001500 prolyl group Chemical group [H]N1C([H])(C(=O)[*])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 3
- 108090000623 proteins and genes Proteins 0.000 claims 3
- 125000000341 threoninyl group Chemical group [H]OC([H])(C([H])([H])[H])C([H])(N([H])[H])C(*)=O 0.000 claims 3
- 108090000790 Enzymes Proteins 0.000 claims 2
- 102000004190 Enzymes Human genes 0.000 claims 2
- 108010050375 Glucose 1-Dehydrogenase Proteins 0.000 claims 2
- 239000004471 Glycine Chemical group 0.000 claims 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical group CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 2
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical group C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 claims 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical group OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims 2
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Chemical group C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 claims 2
- 125000000637 arginyl group Chemical group N[C@@H](CCCNC(N)=N)C(=O)* 0.000 claims 2
- 235000003704 aspartic acid Nutrition 0.000 claims 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N aspartic acid group Chemical group N[C@@H](CC(=O)O)C(=O)O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 2
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims 2
- 125000001909 leucine group Chemical group [H]N(*)C(C(*)=O)C([H])([H])C(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 108010035289 Glucose Dehydrogenases Proteins 0.000 claims 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical group OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 1
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical group CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 1
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Chemical group CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 claims 1
- 238000003149 assay kit Methods 0.000 claims 1
- 239000008280 blood Substances 0.000 claims 1
- 210000004369 blood Anatomy 0.000 claims 1
- 238000012258 culturing Methods 0.000 claims 1
- 229930195712 glutamate Chemical group 0.000 claims 1
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 1
- 238000005259 measurement Methods 0.000 claims 1
- 238000000691 measurement method Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000004474 valine Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2017111101 | 2017-06-05 | ||
| JP2017111101 | 2017-06-05 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018201486A JP2018201486A (ja) | 2018-12-27 |
| JP2018201486A5 true JP2018201486A5 (enExample) | 2021-01-21 |
| JP7165493B2 JP7165493B2 (ja) | 2022-11-04 |
Family
ID=64954402
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017232544A Active JP7165493B2 (ja) | 2017-06-05 | 2017-12-04 | 保存安定性に優れたグルコースデヒドロゲナーゼ及び持続血糖測定 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP7165493B2 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113588734A (zh) * | 2021-07-17 | 2021-11-02 | 可孚医疗科技股份有限公司 | 一种电化学葡萄糖传感器及其电极制备方法 |
| EP4491619A1 (en) | 2022-03-07 | 2025-01-15 | PHC Holdings Corporation | Electron acceptor, and reagent layer and sensor each using same |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010057427A (ja) | 2008-09-04 | 2010-03-18 | Toyobo Co Ltd | グルコース脱水素酵素およびグルコースの電気化学測定法 |
| JP2011103770A (ja) | 2009-11-12 | 2011-06-02 | Toyobo Co Ltd | グルコース脱水素酵素およびグルコースの電気化学測定法 |
| JP6455134B2 (ja) | 2014-12-22 | 2019-01-23 | 東洋紡株式会社 | 新規なグルコースデヒドロゲナーゼ |
| JP7109155B2 (ja) | 2015-06-04 | 2022-07-29 | キッコーマン株式会社 | フラビン結合型グルコースデヒドロゲナーゼを用いたグルコースの測定方法 |
-
2017
- 2017-12-04 JP JP2017232544A patent/JP7165493B2/ja active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20240124855A1 (en) | Variants of a dna polymerase of the polx family | |
| CN110914417B (zh) | 一种立体选择性的转氨酶在不对称合成手性胺中的应用 | |
| JP2004267216A5 (enExample) | ||
| CN106282205B (zh) | 一种高比活l-谷氨酸氧化酶基因多位点突变体及其制备方法和应用 | |
| CN110892067A (zh) | 热稳定性提高的phi29DNA聚合酶突变体 | |
| CN103635589B (zh) | 生物体试样中的l-色氨酸分析方法以及用于该方法的试剂盒 | |
| JP2018201486A5 (enExample) | ||
| Park et al. | Isolation and characterization of transcriptional elements from Corynebacterium glutamicum | |
| JP2025106504A (ja) | 改変フェニルアラニン脱水素酵素 | |
| CN104292309B (zh) | 一种小分子多肽 | |
| CN111979163A (zh) | 一种重组罗氏真氧菌及其制备方法和应用 | |
| WO2025241381A1 (zh) | 一种能表达外源蛋白的菌株、重组人源胶原蛋白及合成方法与应用 | |
| WO2024078621A1 (zh) | 一种pht纳米孔突变体蛋白及其应用 | |
| CN116200357B (zh) | 亚胺还原酶突变体及其在合成手性四氢异喹啉中的应用 | |
| CN107164538B (zh) | 一种检测calr基因突变的内参扩增引物组合物及其扩增体系 | |
| CN105102620A (zh) | 经修饰的甘氨酸氧化酶 | |
| JP7630116B2 (ja) | 変異型ｋｌｆタンパク質、及び誘導多能性幹細胞の製造方法 | |
| CN107164473B (zh) | 一种检测calr基因1型突变的引物组合物及试剂盒 | |
| CN104610443A (zh) | 一种高稳定性重组降钙素原、制备方法及用途 | |
| WO2022071417A1 (ja) | フラビン依存性乳酸デヒドロゲナーゼを含む組成物の安定性を向上する方法 | |
| CN109337854B (zh) | 一株敲除胞外核酸酶ExeR的谷氨酸棒杆菌及其构建方法与应用 | |
| JP5821843B2 (ja) | ジアホラーゼ活性を有するタンパク質 | |
| CN105861221A (zh) | 一种基于Dal80p为靶标抑制氨基甲酸乙酯形成的黄酒酿造方法 | |
| CN111918969A (zh) | 新型水解酶和利用该酶的(1s,2s)-1-烷氧基羰基-2-乙烯基环丙烷羧酸的制造方法 | |
| Xiao et al. | DamIP: a novel method to identify DNA binding sites in vivo |