RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      KCI등재 SCIE SCOPUS

      Improvement of the Steroid Dihydroxylation Efficiency from Dehydroepiandrosterone Using a Substrate Pre-induction Biotransformation Process

      한글로보기

      https://www.riss.kr/link?id=A103816107

      • 0

        상세조회
      • 0

        다운로드
      서지정보 열기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract)

      This study investigated the effects of hydroxylase cyptochrome P450 inducers on the efficiency of the biotransformation of dehydroepiandrosterone (DHEA) to 3β, 7α, 15α-trihydroxy-5-androsten-17-one (7α,15α-diOHDHEA)by Colletotrichum lini ST-1. Sp...

      This study investigated the effects of hydroxylase cyptochrome P450 inducers on the efficiency of the biotransformation of dehydroepiandrosterone (DHEA) to 3β, 7α, 15α-trihydroxy-5-androsten-17-one (7α,15α-diOHDHEA)by Colletotrichum lini ST-1. Special attention was given to the substrate DHEA being the best inducer and the fact that it could improve the yield of 7α, 15α-diOHDHEA.
      Based on the effects of the DHEA pre-induction phases and additional concentrations on 7α, 15α-diOHDHEA production, a substrate pre-induction process was established as follows: 2 g/L DHEA was added for the first time after 12 h of inoculation, followed by the second addition of 6 g/L DHEA after 12 h later. The results showed that this substrate pre-induction process improved the content of cytochrome P450 and that the 7α, 15α-diOH-DHEA yield reached 90.1%, which was 26.9%higher than that obtained in the original process.

      더보기

      참고문헌 (Reference)

      1 Mutafov, S., "The inducibility of 9α-steroid hydroxylating activity in resting Rhodococcus sp. cells" 32 : 585-589, 1997

      2 Romano, A., "Steroid hydroxylations with Botryodiplodia malorum and Colletotrichum lini" 71 : 429-434, 2006

      3 Marques, M. P. C., "Steroid bioconversion: Towards green processes" 88 : 12-20, 2010

      4 Lobastova, T. G., "Screening of mycelial fungi for 7α- and 7β-hydroxylase activity towards dehydroepiandrosterone" 25 : 434-442, 2007

      5 Shen, Y. J., "Progesterone hydroxylation with Colletotrichum lini AS3. 4486" 343 : 1070-1073, 2012

      6 Ahmed, E. M., "Production of 11α-hydroxyprogesterone using Aspergillus terreus immobilized on polytetrafluoroethylene" 38 : 224-229, 2007

      7 Smith, K. E., "Microbial transformations of steroids-VIII. Transformation of progesterone by whole cells and microsomes of Aspergillus fumigatus" 49 : 93-100, 1994

      8 Donova, M. V., "Microbial steroid transformations: Current state and prospects" 94 : 1423-1447, 2012

      9 Carballeira, J. D., "Microbial cells as catalysts for stereo selective redox reactions" 27 : 686-714, 2009

      10 Andryushina, V. A., "Hydroxylation of steroids by Curvularia lunata mycelium in the presence of methyl-β-cyclodextrine" 47 : 42-48, 2011

      1 Mutafov, S., "The inducibility of 9α-steroid hydroxylating activity in resting Rhodococcus sp. cells" 32 : 585-589, 1997

      2 Romano, A., "Steroid hydroxylations with Botryodiplodia malorum and Colletotrichum lini" 71 : 429-434, 2006

      3 Marques, M. P. C., "Steroid bioconversion: Towards green processes" 88 : 12-20, 2010

      4 Lobastova, T. G., "Screening of mycelial fungi for 7α- and 7β-hydroxylase activity towards dehydroepiandrosterone" 25 : 434-442, 2007

      5 Shen, Y. J., "Progesterone hydroxylation with Colletotrichum lini AS3. 4486" 343 : 1070-1073, 2012

      6 Ahmed, E. M., "Production of 11α-hydroxyprogesterone using Aspergillus terreus immobilized on polytetrafluoroethylene" 38 : 224-229, 2007

      7 Smith, K. E., "Microbial transformations of steroids-VIII. Transformation of progesterone by whole cells and microsomes of Aspergillus fumigatus" 49 : 93-100, 1994

      8 Donova, M. V., "Microbial steroid transformations: Current state and prospects" 94 : 1423-1447, 2012

      9 Carballeira, J. D., "Microbial cells as catalysts for stereo selective redox reactions" 27 : 686-714, 2009

      10 Andryushina, V. A., "Hydroxylation of steroids by Curvularia lunata mycelium in the presence of methyl-β-cyclodextrine" 47 : 42-48, 2011

      11 Kolek, T., "Hydroxylation of DHEA, androstenediol and epiandrosterone by Mortierella isabellina AM212. Evidence indicating that both constitutive and inducible hydroxylases catalyze 7α- as well as 7β-hydroxylations of 5-ene substrates" 9 : 5414-5422, 2011

      12 Mahato, S. B., "Garai(1997)Advances in microbial steroid biotransformation" 62 : 332-345, 1997

      13 Lu, W. Y., "Effect of two-steps substrate addition on steroids 11α- hydroxylation by Curvularia lunata CL-114" 32 : 233-238, 2006

      14 Bernhardt, R., "Cytochromes P450 as versatile biocatalysts" 24 : 128-145, 2006

      15 Pollard, D. J., "Biocatalysis for pharmaceutical intermediates: The future is now" 25 : 66-73, 2006

      16 Andriushina, V. G., "7α-Hydroxylation of steroid 5α-olefins by mold fungi" 46 : 69-74, 2010

      17 Chen, K. C., "11β-Hydroxylation of coxtexolone by Curvularia lunata" 12 : 305-308, 1990

      더보기

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      인용정보 인용지수 설명보기

      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2001-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      더보기

      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.14 0.13 0.75
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.57 0.46 0.239 0.02
      더보기

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼