KR920000931A - 아스코르빈산-2-인산의 제조법 - Google Patents

아스코르빈산-2-인산의 제조법 Download PDF

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KR920000931A
KR920000931A KR1019910010222A KR910010222A KR920000931A KR 920000931 A KR920000931 A KR 920000931A KR 1019910010222 A KR1019910010222 A KR 1019910010222A KR 910010222 A KR910010222 A KR 910010222A KR 920000931 A KR920000931 A KR 920000931A
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dna
cells
phosphate
ascorbic acid
treated
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KR1019910010222A
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KR940005598B1 (ko
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다쓰로 후지오
사다오 데시바
아끼히꼬 마루야마
사또시 고이즈미
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가또 미끼오
교오와학꼬고오교 가부시끼가이샤
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/52—Genes encoding for enzymes or proenzymes
    • 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
    • C12N9/10—Transferases (2.)
    • C12N9/12—Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02—Oxygen as only ring hetero atoms
    • C12P17/04—Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
    • 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
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    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/822—Microorganisms using bacteria or actinomycetales
    • Y10S435/874—Pseudomonas

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Abstract

내용 없음.

Description

아스코르빈산-2-인산의 제조법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 플라스미드 pSK1의 제한 효소지도를 나타낸다.
제2도, 제3도 및 제4도는 각각 플라스미드 pSK7, pSK8 및 pSK14의 제작공정을 나타낸다.

Claims (11)

  1. i) 에스케리키아 속에 속하고, 하기 SEQ ID : 1의 서열로 정의되는 DNA로 구성된 군에서 선택된 DNA 및 이 DNA에 하이브리드화하며 아스코르빈산 인산화 효소을 코딩하는 DNA를 함유하는 재조합 DNA를 보유하는 미생물의 세포 ,처리 세포, 배양 브로쓰 또는 처리 배양 브로쓰의 존재하에 아스코르빈산을 수성매체 중에서 인산기 공여체와 반응시키고, (ii) 아스코르빈산-2-인산을 회수함을 특징으로 하는 아스코르빈산 -2-인산의 제조방법.
    SEQ ID : 1
  2. 제1항에 있어서, 인산기 공여체가 아데노신 트리포스페이트(ATP), p-니트로페닐 포스페이트, 아세틸 포스페이트, 피로인산, 트리폴리인산, 테트라폴리인산 및 폴리인산으로 구성된 군에서 선택된 방법.
  3. 제1항에 있어서, 처리 세포가 건조세포, 아세톤-처리세포, 계면활성제-및/ 또는 유기용매-처리세포, 용균효소-처리세포, 고정세포 또는 세포유래추출효소 제제로 구성된 군에서 선택되고, 처리 배양 브로쓰가 배양 브로쓰, 건조배양 브로쓰, 계면활성제-및/ 또는 유기용매-처리 배양 브로쓰 및 아세톤-처리배양 브로쓰로 구성된 군에서 선택된 방법.
  4. 제1항 내지 제3항중 어느 한 항에 있어서, DNA가 슈도모나스 아조토콜리간스 ATCC 12417에서 단리된 방법.
  5. 제1 항내지 제3항중 어느 한 항에 있어서, 에스케리키아 속 미생물이 에스케리키아 콜리 FERM BP-2970인 방법.
  6. 아스코르빈산 인산화 효소를 코딩하고 하기 SEQ ID : 1로 서열로 표시되는 누클레오티드 서열을 갖는 DNA.
    SEQ ID : 1
  7. 제6항에 있어서, 유전자가 슈도모나스 아조토콜리간스 ATCC 12417에서 단리된 DNA.
  8. 제6항 또는 제7항에서 정의된 DNA를 함유하는 재조합 DNA.
  9. 제8항에 있어서, 에스케리키아 콜리 FERM BP-2970에 의해 보유되는 pSK 14로 명명된 재조합 DNA.
  10. 에스케리키아 콜리 FERM BP-2970의 생물학적으로 순수한 배양물.
  11. 에스케리키아 콜리 FERM BP-2970을 배지에서 배양하고, 배양물에서 균세포를 수거하고, 세포내에 축적된 아스코르빈산 인산화 효소를 회수함을 특징으로 하는 아스코르빈산 인산화 효소의 제조방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개되는 것임.
KR1019910010222A 1990-06-21 1991-06-19 아스코르빈산-2-인산의 제조법 KR940005598B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP163877/90 1990-06-21
JP(A)90-163877 1990-06-21
JP02163877A JP3122663B2 (ja) 1990-06-21 1990-06-21 アスコルビン酸―２―リン酸の製造法

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KR920000931A true KR920000931A (ko) 1992-01-29
KR940005598B1 KR940005598B1 (ko) 1994-06-21

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US (1) US5250425A (ko)
EP (1) EP0462833B1 (ko)
JP (1) JP3122663B2 (ko)
KR (1) KR940005598B1 (ko)
AT (1) ATE142698T1 (ko)
CA (1) CA2044911C (ko)
DE (1) DE69121983T2 (ko)
ES (1) ES2093079T3 (ko)

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DE69841217D1 (de) * 1997-01-13 2009-11-19 Univ Emory Glutathion zur behandlung von influenzainfektionen
US6733996B2 (en) * 2002-08-26 2004-05-11 Trustees Of Dartmouth College Methods for regulating gene expression using light
US9376661B2 (en) 2010-02-05 2016-06-28 Cornea Regeneration Institute Co., Ltd. Method for culture of corneal endothelial cells, process for production of corneal endothelial cell sheet for transplantation purposes, and culture kit for corneal endothelial cells
JP6088176B2 (ja) * 2012-08-16 2017-03-01 株式会社耐熱性酵素研究所 アスコルビン酸リン酸化酵素改変体
JP6534612B2 (ja) * 2013-02-19 2019-06-26 株式会社耐熱性酵素研究所 グリセロールのリン酸化物の製造方法
CN106282081B (zh) * 2016-08-31 2020-02-11 江南大学 一种高产维生素c-2-磷酸酯的方法

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DE3784655T2 (de) * 1986-12-18 1993-07-15 Kyowa Hakko Kogyo Kk Verfahren zur herstellung von ascorbinsaeure-2-phosphat.
JP2695180B2 (ja) * 1987-10-08 1997-12-24 協和醗酵工業株式会社 アスコルビン酸−２−リン酸の製造法

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EP0462833B1 (en) 1996-09-11
DE69121983T2 (de) 1997-02-27
EP0462833A3 (en) 1992-04-29
KR940005598B1 (ko) 1994-06-21
CA2044911A1 (en) 1991-12-22
EP0462833A2 (en) 1991-12-27
DE69121983D1 (de) 1996-10-17
JP3122663B2 (ja) 2001-01-09
JPH0453494A (ja) 1992-02-21
ATE142698T1 (de) 1996-09-15
ES2093079T3 (es) 1996-12-16
US5250425A (en) 1993-10-05
CA2044911C (en) 1998-04-21

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