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Hydroxylation of Flavonoid compounds, Phloretin and chrysin, using Streptomyces species.

첫 페이지 보기
  • 발행기관
    한국생물공학회 바로가기
  • 간행물
    한국생물공학회 학술대회 바로가기
  • 통권
    2009 추계학술대회 및 국제심포지움 (2009.11)바로가기
  • 페이지
    pp.159-159
  • 저자
    Woo-il KIM, Jongki LEE, Jiwon ROH, Chang-Ju JEON, KwonYoung CHOI, TaeJin KIM, Byung-Gee KIM, June-Hyung KIM
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A114619

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원문정보

초록

영어
Flavonoids are classified as Chalcone, Flavone, Flavanon and etc. Phloretin is a kind of chalcone compounds, and Apigenin and Chrysin are a flavone that are known for their
antitumor, antioxidant, antiarthritic, anti-amyloid and anti-inflammatory properties. However,
very poor oral bioavailability makes them largely ineffective in vivo. In previous studies, Omethylated
or hydroxylated flavonoid compounds are certificated more effective absorption in
vivo than flavonoid compounds. Twelve microorganisms were initially screened for their
abilities to catalyze biotransformation of chrysin and phloretin. Chrysin was orthohydroxylated
by Streptomyces ceolicolor to produce baicalein (5,6,7-tetrahydroxyflavone), which was confirmed using authentic baicalein with mass analysis. Maximum conversion was 12 %, which was achieved for 4 hours of reaction, and the substrate (chrysin) and reaction product (baicalein) was completely metabolized after 6 hours of reaction. Three kinds of Cytochrome P450 inhibitor, Coumarin, Erythromycin and Quinidine was added with 0.5mM final concentration. Coumarin had no effect on the bioconversion of chrysin and Quinidine inhibited conversion of chrysin into baicalein about 45 ~ 70 %, and Erythromycin completely blocked the bioconversion, which suggest bioconversion of chrysin was mediated through P450 system of Streptomyces Ceolicolor. Addition of different kinds of detergent (Triton X- 100, Tween 80, Brij 35) into reaction mixture, was not effective for the enhancement of bioconversion using Streptomyces Ceolicolor.In the biotransformation phloretin using Streptomyces avermitilis, two main products were identified in GC/MS analysis. They were interpreted as hydroxylated products of phloretin in A-ring at different position.

키워드

Flavonoid Biotransformation Hydroxylation Phloletin Chrysin

저자

  • Woo-il KIM [ Department of Chemical Engineering, Dong-A University ]
  • Jongki LEE [ Department of Chemical Engineering, Dong-A University ]
  • Jiwon ROH [ Department of Chemical Engineering, Dong-A University ]
  • Chang-Ju JEON [ Department of Chemical Engineering, Dong-A University ]
  • KwonYoung CHOI [ School of Chemical and Biological Engineering, Seoul National University ]
  • TaeJin KIM [ School of Chemical and Biological Engineering, Seoul National University ]
  • Byung-Gee KIM [ School of Chemical and Biological Engineering, Seoul National University ]
  • June-Hyung KIM [ Department of Chemical Engineering, Dong-A University ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국생물공학회 [The Korean Society for Biotechnology and Bioengineering]
  • 설립연도
    1984
  • 분야
    공학>생물공학
  • 소개
    이 법인은 생물 공학의 발전과 보급에 이바지하고, 회원 상호 간의 연구 협력과 친목을 도모함을 목적으로 한다 1. 생물공학 분야의 발전을 위한 연구 협력 2. 생물공학의 실용화를 촉진시키기 위한 산학 협동 3. 학술연구 발표회, 강연회, 연수회 등 학술활동의 개최 4. 국,영문 학술지,소식지,학술회의 Proceedings 및 학술도서의 발간 5. 생물공학 발전을 위한 정책 건의 6. 기타 국제 교류 등 본 학회의 목적 달성을 위한 제반 활동

간행물

  • 간행물명
    한국생물공학회 학술대회
  • 간기
    반년간
  • 수록기간
    1985~2013
  • 십진분류
    KDC 476 DDC 576

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