KR920019942A - 폴리-β-하이드록시 알카노에이트 (PHA) 공중합체 및 그 제조방법, 이를 생산하는 미생물과 PHA 공중합체의고분자 블렌드 - Google Patents

폴리-β-하이드록시 알카노에이트 (PHA) 공중합체 및 그 제조방법, 이를 생산하는 미생물과 PHA 공중합체의고분자 블렌드 Download PDF

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Publication number
KR920019942A
KR920019942A KR1019910005607A KR910005607A KR920019942A KR 920019942 A KR920019942 A KR 920019942A KR 1019910005607 A KR1019910005607 A KR 1019910005607A KR 910005607 A KR910005607 A KR 910005607A KR 920019942 A KR920019942 A KR 920019942A
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South Korea
Prior art keywords
hydroxy
pha
copolymer
pha copolymer
polymer blend
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KR1019910005607A
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English (en)
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KR100189468B1 (ko
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이양걸
임건빈
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이상운
고려합섬 주식회사
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Priority to KR1019910005607A priority Critical patent/KR100189468B1/ko
Priority to DE69126444T priority patent/DE69126444T2/de
Priority to AT91916731T priority patent/ATE154048T1/de
Priority to JP3515824A priority patent/JPH07500615A/ja
Priority to PCT/KR1991/000019 priority patent/WO1992018553A1/en
Priority to EP91916731A priority patent/EP0582567B1/en
Priority to US08/122,590 priority patent/US5395919A/en
Priority to AU86121/91A priority patent/AU8612191A/en
Publication of KR920019942A publication Critical patent/KR920019942A/ko
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Publication of KR100189468B1 publication Critical patent/KR100189468B1/ko

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/24Preparation of oxygen-containing organic compounds containing a carbonyl group
    • C12P7/26Ketones
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/62Carboxylic acid esters
    • C12P7/625Polyesters of hydroxy carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/06Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/8215Microorganisms
    • Y10S435/822Microorganisms using bacteria or actinomycetales
    • Y10S435/874Pseudomonas

Abstract

내용 없음

Description

폴리-β-하이드록시 알카노에이트(PHA) 공중합체 및 그 제조방법, 이를 생산하는 미생물과 PHA 공중합체의 고분자 블렌드
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제 1도는 PHA 공중합체의 정량을 위한 PHB 표준정량 직선이다. PHA의 정량을 위해 PHB를 표준 시료로 하여, CC 스펙트럼을 분석, 면적을 비교, 계산함으로서 PHA의 양을 계산한다.
제 2도는 PHA 공중합체의 GC 스펙트럼이다. PHA를 메틸 에스테르화 하여 GC를 분석한 결과 각 피이크는 PHA를 구성하는 모너머들의 메틸 에스테르 분자이다.
제 3도는 GC 스펙트럼 상에서 PHA 공중합 고분자의 각 모노머의 보지시간(Retention Time)의 Log 값과 탄소수와의 관계를 나타낸다. 탄소수에 비례하여 Log(RT)값이 증가함을 보여준다.

Claims (12)

  1. 하기 구조식(Ⅰ)의 모노머와 구조식(Ⅱ)의 모노머로 구성된 평균 분자량 10,000 이상의 폴리-β-하이드록시 알카노에이트(PHA)의 공중합체.
    (n=2, 4, 6, 8, 10 및 m=0, 2, 4, 6, 8)
  2. 제 1항에 있어서, 하기와 같은 모노머의 중량함량 범위의 조성을 가짐을 특징으로 하는 PHA 공중합체. 3-하이드록시 부티레이트 ; 0.0-0.5wt%, 3-하이드록시 헥사노에이트 ; 1.0-5.0wt%, 3-하이드록시-4-헥세노에이트 ; 0.0-1.0wt%, 3-하이드록시 옥타노에이트 ; 5.0-15.0wt%, 3-하이드록시-6-옥테노에이트 ; 0.0-5.0wt%, 3-하이드록시 데카노에이트 ; 40.0-60.0wt%, 3-하이드록시-8-데케노에이트 ; 0.0-10.0wt%, 3-하이드록시 운데카노에이트 ; 10.0-20.0wt%, 3-하이드록시-10-운데케노에이트 ; 0.0-20.0wt%, 3-하이드록시 테트라데카노에이트 ; 0.0-5.0wt%, 3-하이드록시-12-테트라데케노에이트 ; 0.0-5.0wt%.
  3. 제 1항의 PHA 공중합체를 생산하는 슈도모나스 속의 세파시아종(KCCM 10004) 및 그 변종.
  4. 탄소원, 질소원, 기타 영양원으로 포함하는 배양액에서 슈도모나스속 세파시아종(KCCM 10004) 및 그 변종을 배양한 후 질소원 및 기타 영양원을 제한하여 균체에서 PHA 공중합체를 생산하는 방법.
  5. 제 4항에 있어서, 탄소원은 포도당, 과당, 말토스, 당밀, 어유임을 특징으로 하는 방법.
  6. 제 4항에 있어서, 탄소원은 아세테이트, 프로피오네이트, 부티레이트, 발레레이트, 락테이트, 시트레이트 등의 유기산을 사용함을 특징으로 하는 방법.
  7. 제 4항에 있어서, 탄소원은 에탄올, 글리세롤, n-프로판올, n-부탄올, 프로필렌글리콜 등의 알콜을 사용함을 특징으로 하는 방법.
  8. 제 4항에 있어서, 질소원은 암모늄 이온염 또는 요소를 사용하여 균체를 증식한 후 배양액 중의 암모늄 이온 농도를 0.03g/L 이하로 제한하여 PHA 공중합체를 생산함을 특징으로 하는 방법.
  9. 제 4항에 있어서, 황산 마그네슘의 농도는 0.2-0.4g/L 임을 특징으로 하는 방법.
  10. 제 4항에 있어서, 미량 원소용액의 농도는 0.5-1㎖/L 임을 특징으로 하는 방법.
  11. 제 1항의 PHA 공중합체 0.5-99.5wt%와 PHB 99.5-0.5wt%로 구성된 분자량 1만 이상의 고분자 블렌드.
  12. 제 2항의 PHA 공중합체 0.5-99.5wt%와 PHB 99.5-0.5wt%로 구성된 분자량 1만 이상의 고분자 블렌드.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019910005607A 1991-04-09 1991-04-09 폴리-베타-하이드록시알카노에이트(pha)공중합체및그제조방법,이를생산하는미생물과pha공중합체의고분자블렌드 KR100189468B1 (ko)

Priority Applications (8)

Application Number Priority Date Filing Date Title
KR1019910005607A KR100189468B1 (ko) 1991-04-09 1991-04-09 폴리-베타-하이드록시알카노에이트(pha)공중합체및그제조방법,이를생산하는미생물과pha공중합체의고분자블렌드
DE69126444T DE69126444T2 (de) 1991-04-09 1991-09-16 Poly-g(b)-hydroxyalkanoat (pha) copolymer, verfahren zu seiner herstellung, die es produzierende mikrobe, und pha-copolymermischung
AT91916731T ATE154048T1 (de) 1991-04-09 1991-09-16 Poly-g(b)-hydroxyalkanoat (pha) copolymer, verfahren zu seiner herstellung, die es produzierende mikrobe, und pha-copolymermischung
JP3515824A JPH07500615A (ja) 1991-04-09 1991-09-16 ポリ−β−ヒドロキシアルカノエート(PHA)共重合体およびその製造方法、これを生産する微生物とPHA共重合体の高分子ブレンド
PCT/KR1991/000019 WO1992018553A1 (en) 1991-04-09 1991-09-16 POLY-β-HYDROXY ALKANOATE (PHA) COPOLYMER, METHOD OF ITS PRODUCTION, THE MICROBE WHICH PRODUCES IT, AND PHA COPOLYMER BLEND
EP91916731A EP0582567B1 (en) 1991-04-09 1991-09-16 POLY-$g(b)-HYDROXY ALKANOATE (PHA) COPOLYMER, METHOD OF ITS PRODUCTION, THE MICROBE WHICH PRODUCES IT, AND PHA COPOLYMER BLEND
US08/122,590 US5395919A (en) 1991-04-09 1991-09-16 Poly-β-hydroxy alkanoate (PHA) copolymer, method of its production, the microbe which produces it, and PHA copolymer blend
AU86121/91A AU8612191A (en) 1991-04-09 1991-09-16 Poly-beta-hydroxy alkanoate (pha) copolymer, method of its production, the microbe which produces it, and pha copolymer blend

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019910005607A KR100189468B1 (ko) 1991-04-09 1991-04-09 폴리-베타-하이드록시알카노에이트(pha)공중합체및그제조방법,이를생산하는미생물과pha공중합체의고분자블렌드

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KR920019942A true KR920019942A (ko) 1992-11-20
KR100189468B1 KR100189468B1 (ko) 1999-06-01

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US (1) US5395919A (ko)
EP (1) EP0582567B1 (ko)
JP (1) JPH07500615A (ko)
KR (1) KR100189468B1 (ko)
AT (1) ATE154048T1 (ko)
AU (1) AU8612191A (ko)
DE (1) DE69126444T2 (ko)
WO (1) WO1992018553A1 (ko)

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Publication number Publication date
KR100189468B1 (ko) 1999-06-01
DE69126444D1 (de) 1997-07-10
EP0582567A1 (en) 1994-02-16
ATE154048T1 (de) 1997-06-15
WO1992018553A1 (en) 1992-10-29
US5395919A (en) 1995-03-07
EP0582567B1 (en) 1997-06-04
AU8612191A (en) 1992-11-17
JPH07500615A (ja) 1995-01-19
DE69126444T2 (de) 1997-09-25

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