KR910001042A - 에폭시-활성화된 비이드상에 고정된 폴리뉴클레오티드 포스포릴라제 - Google Patents
에폭시-활성화된 비이드상에 고정된 폴리뉴클레오티드 포스포릴라제 Download PDFInfo
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- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/08—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer
- C12N11/082—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C12N11/084—Polymers containing vinyl alcohol units
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- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/26—Preparation of nitrogen-containing carbohydrates
- C12P19/28—N-glycosides
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- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/08—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer
- C12N11/082—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds
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- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/08—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer
- C12N11/089—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
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Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 폴리뉴클레오티드 포스포릴라제 (PNP아제) 고정반응에서의 pH의 효과를 나타낸 것이고,
제2도는 폴리뉴클레오티드 생성물의 분자량에 대한 지지체 공극크기 및 반응시간의 효과를 나타낸 것이다.
Claims (19)
- 고체의 수불성인, 에폭시-활성화된 유기 중합체의 입자에 공유결합에 의해 고정된 풀리-뉴클레오티드포스포릴라제.
- 제1항에 있어서, 중합체가 에폭시-활성화된 다당체, 폴리(메트) 아크릴레이트, 폴리(메트)아크릴 아미드, 폴리비닐아세테이트 또는 폴리비닐알코올인 폴리뉴클레오티드 포스포릴라제.
- 제2항에 있어서, 중합체가 옥시란 아크릴성 단일중합체 또는 공중합체이고 입자의 평균직경이 약 1 내지 1,000㎛이며 입자 공극의 평균직경이 약 0.01 내지 1㎛일 폴리뉴클레오티드 포스포릴라제.
- 제3항에 있어서, 입자의 평균 직경이 약 10내지 500㎛이고 입자 공극의 평균직경이 약 0.02 내지 0.5㎛인 폴리뉴클레오티드 포스포릴라제.
- 제4항에 있어서, 중합체가 (A) 글리시딜 그룹을 지닌 에틸렌성 불포화 단량체, (B) 2개 이상의 라디칼 중합가능한 이중결합을 지닌 공단량체 및 (C) 라디칼-중합가능한 수용성 공단량체의 공중합체인 폴리뉴클레오티드 포스포릴라제.
- 제5항에 있어서, 중합체가 (A)글리시딜 메타크릴레이트 및/또는 알릴 글리시딜 에테르, (B) N.N'-메틸렌-비스-메타크릴아미드 및 (C) 메타크릴아미드의 공중합체인 폴리뉴클레오티드 포스포릴라제.
- 제6항에 있어서, 입자의 직경이 약 100 내지 300㎛이고 입자 공극의 직경이 약 0.02 내지 0.2㎛인 폴리뉴클레오티드 포스포릴라제.
- 제3항에 있어서, 중합체가 에폭시-활성화된 폴리비닐알코올인 폴리뉴클레오티드 포스포릴라제.
- 폴리뉴클레오티드 포스포릴라제를 pH 4내지 6범위에서 수용액중에 고체의 수-불용성인, 에폭시-활성화된 유기 중합체와 반응시킴을 특징으로 하여, 폴리뉴클레오티드 포스포릴라제를 고정시키는 방법.
- 제9항에 있어서, 반응을 4-모르폴린에탄설폰산 완충액 중에서 수행하는 방법.
- 제10항에 있어서, 중합체가 옥시란 아크릴성 또는 에폭시-활성화된 폴리비닐 알코올이며 입자의 평균 직경이 약 100 내지 300㎛이고 입자 공극의 평균 직경이 약 0.02 내지 0.2㎛인 방법.
- 고정된 폴리뉴클레오티드 포스포릴라제 존재하에 폴리리보뉴클레오티드를 뉴클레오시드 디포스페이트로 부터 합성하는 방법에 있어서, 고체의 수-불용성인, 에폭시-활성화된 유기중합체의 입자에 공유결합에 의해 고정된 폴리뉴클레오티드 포스포릴라제를 사용함을 특징으로 하는 방법.
- 제12항에 있어서, 중합체가 에폭시-활성화된 다당체, 폴리(메트)아크릴레이트, 폴리(메트)아크릴아미드, 폴리비닐아세테이트 또는 폴리비닐 알코올인 방법.
- 제13항에 있어서, 중합체가 옥시란 아크릴성 단일중합체 또는 공중합체이고 입자의 평균직경이 약 1 내지 1,000㎛이며 입자 공극의 평균직경이 약 0.01 내지 1㎛인 방법.
- 제14항에 있어서, 입자의 평균 직경이 약 10 내지 500㎛이고 입자 공극의 평균직경이 약 0.02 내지 0.5㎛인 방법.
- 제15항에 있어서, 중합체가 (A) 글리시딜 그룹을 지닌 에틸렌성 불포화 단량체, (B) 2개 이상의 라디칼 중합가능한 이중결합을 지닌 공단량체 및 (C) 라디칼-중합가능한 수용성 공단량체의 공중합체인 방법.
- 제16항에 있어서, 중합체가 (A)글리시딜 메타크릴레이트 및/또는 알릴 글리시딜 에테르, (B) N,N'-메틸렌-비스-메타크릴아미드 및 (C) 메타크릴 아미드의 공중합체인 방법.
- 제17항에 있어서, 입자의 직경이 약 100 내지 300㎛이고 입자의 공극 직경이 약 0.02 내지 0.2㎛인 방법.
- 고정된 폴리뉴클레오티드 포스포릴라제 존재하에 폴리뉴클레오티드의 탈인산화에 의해 리보뉴클레오시드 디포스페이트를 생성시키는 방법에 있어서, 고체의 수-불용성인, 에폭시-활성화된 유기 중합체의 입자에 공유결합에 의해 고정된 폴리뉴클레오티드 포스포릴라제를 사용함을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US20819488A | 1988-06-16 | 1988-06-16 | |
US208,194 | 1988-06-16 | ||
US208194 | 1988-06-16 |
Publications (2)
Publication Number | Publication Date |
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KR910001042A true KR910001042A (ko) | 1991-01-30 |
KR910005628B1 KR910005628B1 (ko) | 1991-08-01 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019890008296A KR910005628B1 (ko) | 1988-06-16 | 1989-06-16 | 에폭시-활성화된 비이드상에 고정된 폴리뉴클레오티드 포스포릴라제 |
Country Status (11)
Country | Link |
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EP (1) | EP0346865A3 (ko) |
JP (1) | JPH02109979A (ko) |
KR (1) | KR910005628B1 (ko) |
AU (1) | AU3653789A (ko) |
DK (1) | DK296089A (ko) |
FI (1) | FI892939A (ko) |
HU (1) | HUT50865A (ko) |
IL (1) | IL90600A0 (ko) |
NO (1) | NO892497L (ko) |
PT (1) | PT90886A (ko) |
ZA (1) | ZA894605B (ko) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991000346A1 (en) * | 1989-07-03 | 1991-01-10 | E.I. Du Pont De Nemours And Company | Polynucleotide phosphorylase immobilized on tris(hydroxymethyl)methylacrylamide polymer beads |
EP0562373A3 (en) * | 1992-03-23 | 1994-05-25 | Siemens Ag | Immobilisation of biochemical substances |
DE4333674A1 (de) * | 1993-10-02 | 1995-04-06 | Merck Patent Gmbh | Nukleotidhaltiges Sorbens für die Affinitätschromatographie |
DE19653730C2 (de) * | 1996-12-11 | 1999-06-24 | Schering Ag | Immobilisierte Proteine aus Rohextrakt und deren Verwendung zur Umsetzung von Estern |
US5905024A (en) * | 1996-12-17 | 1999-05-18 | University Of Chicago | Method for performing site-specific affinity fractionation for use in DNA sequencing |
KR20010101092A (ko) * | 1998-12-10 | 2001-11-14 | 오미야 히사시 | 운반체상에 dna를 고정화시키는 방법 |
DE60315790T2 (de) * | 2003-01-16 | 2008-06-05 | Adorkem Technology S.P.A., Costa Volpino | Immobilisierte Biokatalysatoren für die Herstellung von natürlichen Nukleosiden und modifizierten Analogen durch enzymatische Transglykosylierungsreaktionen |
BR112023001947A2 (pt) * | 2020-08-05 | 2023-04-11 | Oncovir Inc | Produção escalonável de polirribonucleotídeos de tamanho controlado |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US4210723A (en) * | 1976-07-23 | 1980-07-01 | The Dow Chemical Company | Method of coupling a protein to an epoxylated latex |
US4208309A (en) * | 1977-05-20 | 1980-06-17 | Rohm Gmbh | Pearl polymer containing hollow pearls |
DE3136940A1 (de) * | 1981-09-17 | 1983-03-31 | Hoechst Ag, 6230 Frankfurt | "verfahren zur herstellung von 5'-ribonucleotiden" |
US4582860A (en) * | 1983-12-15 | 1986-04-15 | Rohm And Haas Company | Oxirane resins for enzyme immobilization |
-
1989
- 1989-06-13 IL IL90600A patent/IL90600A0/xx unknown
- 1989-06-14 EP EP19890110788 patent/EP0346865A3/en not_active Withdrawn
- 1989-06-15 NO NO89892497A patent/NO892497L/no unknown
- 1989-06-15 FI FI892939A patent/FI892939A/fi not_active Application Discontinuation
- 1989-06-15 DK DK296089A patent/DK296089A/da not_active Application Discontinuation
- 1989-06-16 ZA ZA894605A patent/ZA894605B/xx unknown
- 1989-06-16 PT PT90886A patent/PT90886A/pt not_active Application Discontinuation
- 1989-06-16 AU AU36537/89A patent/AU3653789A/en not_active Abandoned
- 1989-06-16 HU HU893131A patent/HUT50865A/hu unknown
- 1989-06-16 JP JP1152454A patent/JPH02109979A/ja active Pending
- 1989-06-16 KR KR1019890008296A patent/KR910005628B1/ko active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
HUT50865A (en) | 1990-03-28 |
DK296089D0 (da) | 1989-06-15 |
NO892497L (no) | 1989-12-18 |
IL90600A0 (en) | 1990-01-18 |
PT90886A (pt) | 1989-12-29 |
ZA894605B (en) | 1991-02-27 |
JPH02109979A (ja) | 1990-04-23 |
FI892939A (fi) | 1989-12-17 |
FI892939A0 (fi) | 1989-06-15 |
DK296089A (da) | 1989-12-17 |
EP0346865A3 (en) | 1990-09-12 |
KR910005628B1 (ko) | 1991-08-01 |
NO892497D0 (no) | 1989-06-15 |
AU3653789A (en) | 1989-12-21 |
EP0346865A2 (en) | 1989-12-20 |
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