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Microarray analysis of an antibiotic over-production mutant(△wblA△SCO1712) and additional deletion of a carbon flux-regulatingSCO5426 in Streptomyces coelicolor

첫 페이지 보기
  • 발행기관
    한국생물공학회 바로가기
  • 간행물
    한국생물공학회 학술대회 바로가기
  • 통권
    2010 추계학술대회 및 국제심포지움 (2010.10)바로가기
  • 페이지
    pp.192-192
  • 저자
    Seon-Hye KIM, Hye-Jin KIM, Han-Na LEE, Eung-Soo KIM
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A129368

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원문정보

초록

영어
In previous study, we successfully utilized Streptomyces interspecies DNA microarray analysis system to identify novel regulatory genes associated with secondary metabolite overproduction in S. peucetius Doxorubicin (DXR) overproducing industrial strain [1]. Especially wblA, a whiB-like putative transcription factor gene, and SCO1712, a tetR-family transcriptional regulatory gene, were identified as strong antibiotic biosynthetic down-regulators in both S. coelicolor as well as S. peucetius species. Moreover, these two strong antibiotic down-regulators were specifically deleted in the S. coelicolor wild-type chromosome, resulting S. coelicolor △wblA△SCO1712 double knock-out (KO) mutant which shown significantly higher actinorhodin (Act) productions [2]. To further increase our understanding about the genetic nature of Streptomyces antibiotic overproduction, a comparative transcriptome analysis was conducted again using S. coelicolor whole genome chip between S. coelicolor wild-type and a S. coelicolor △wblA△SCO1712 double KO mutant. As a result, the double KO strain was found to express the Act biosynthetic cluster genes stronger than the wild-type. Also, various gene expression signatures were obtained by deletion of wblA and SCO1712. 875 genes showed a two-fold or greater change in expression at two or more time points and 14 genes showed non-change in expression pattern at most of time points. First, in case of putative wblA &SCO1712 dependent genes, expression pattern was confirmed in wild-type and double KO mutant using RT-PCR. And these genes were individually over-expression into S. coelicolor to verity the biological functions of these putative targets, so we selected some putative effective antibiotics-relating regulators in M145 wild-type. Second, SCO5426 relating regulation of carbon flux was found among wblA & SCO1712 independent genes [3]. So SCO5426 was disrupted in S. coelicolor △wblA△SCO1712 double KO mutant additionally and Act productivity was increased than double KO mutant. This additional transcriptomics-driven approach in a double KO mutant led to the identification of previously-unidentified novel wblA &SCO1712 dependent or independent regulatory genes related to secondary metabolite overproduction.

키워드

Streptomyces wblA SCO1712 SCO5426 Microarray

저자

  • Seon-Hye KIM [ Dept. of Biological Engineering, Inha University, Incheon, 402-751. ]
  • Hye-Jin KIM [ Dept. of Biological Engineering, Inha University, Incheon, 402-751. ]
  • Han-Na LEE [ Dept. of Biological Engineering, Inha University, Incheon, 402-751. ]
  • Eung-Soo KIM [ Dept. of Biological Engineering, Inha University, Incheon, 402-751. ]

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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