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      In situ esterification and extractive fermentation for butyl butyrate production with Clostridium tyrobutyricum

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      https://www.riss.kr/link?id=O120630853

      • 저자
      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2017년

      • 작성언어

        -

      • Print ISSN

        0006-3592

      • Online ISSN

        1097-0290

      • 등재정보

        SCI;SCIE;SCOPUS

      • 자료형태

        학술저널

      • 수록면

        1428-1437   [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]

      • 소장기관
      • 구독기관
        • 전북대학교 중앙도서관  
        • 성균관대학교 중앙학술정보관  
        • 부산대학교 중앙도서관  
        • 전남대학교 중앙도서관  
        • 제주대학교 중앙도서관  
        • 중앙대학교 서울캠퍼스 중앙도서관  
        • 인천대학교 학산도서관  
        • 숙명여자대학교 중앙도서관  
        • 서강대학교 로욜라중앙도서관  
        • 계명대학교 동산도서관  
        • 충남대학교 중앙도서관  
        • 한양대학교 백남학술정보관  
        • 이화여자대학교 중앙도서관  
        • 고려대학교 도서관  
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      다국어 초록 (Multilingual Abstract)

      Butyl butyrate (BB) is a valuable chemical that can be used as flavor, fragrance, extractant, and so on in various industries. Meanwhile, BB can also be used as a fuel source with excellent compatibility as gasoline, aviation kerosene, and diesel components. The conventional industrial production of BB is highly energy‐consuming and generates various environmental pollutants. Recently, there have been tremendous interests in producing BB from renewable resources through biological routes. In this study, based on the fermentation using the hyper‐butyrate producing strain Clostridium tyrobutyricum ATCC 25755, efficient BB production through in situ esterification was achieved by supplementation of lipase and butanol into the fermentation. Three commercially available lipases were assessed and the one from Candida sp. (recombinant, expressed in Aspergillus niger) was identified with highest catalytic activity for BB production. Various conditions that might affect BB production in the fermentation have been further evaluated, including the extractant type, enzyme loading, agitation, pH, and butanol supplementation strategy. Under the optimized conditions (5.0 g L−1 of enzyme loading, pH at 5.5, butanol kept at 10.0 g L−1), 34.7 g L−1 BB was obtained with complete consumption of 50 g L−1 glucose as the starting substrate. To our best knowledge, the BB production achieved in this study is the highest among the ever reported from the batch fermentation process. Our results demonstrated an excellent biological platform for renewable BB production from low‐value carbon sources. Biotechnol. Bioeng. 2017;114: 1428–1437. © 2017 Wiley Periodicals, Inc.
      A systematic optimization combining in situ enzymatic catalysis with Clostridium tyrobutyricum fermentation for butyl butyrate production was performed. In this study, different exogenous lipases and fermentation conditions were examined, providing potential reference to other bio‐ester producing fermentations.
      번역하기

      Butyl butyrate (BB) is a valuable chemical that can be used as flavor, fragrance, extractant, and so on in various industries. Meanwhile, BB can also be used as a fuel source with excellent compatibility as gasoline, aviation kerosene, and diesel comp...

      Butyl butyrate (BB) is a valuable chemical that can be used as flavor, fragrance, extractant, and so on in various industries. Meanwhile, BB can also be used as a fuel source with excellent compatibility as gasoline, aviation kerosene, and diesel components. The conventional industrial production of BB is highly energy‐consuming and generates various environmental pollutants. Recently, there have been tremendous interests in producing BB from renewable resources through biological routes. In this study, based on the fermentation using the hyper‐butyrate producing strain Clostridium tyrobutyricum ATCC 25755, efficient BB production through in situ esterification was achieved by supplementation of lipase and butanol into the fermentation. Three commercially available lipases were assessed and the one from Candida sp. (recombinant, expressed in Aspergillus niger) was identified with highest catalytic activity for BB production. Various conditions that might affect BB production in the fermentation have been further evaluated, including the extractant type, enzyme loading, agitation, pH, and butanol supplementation strategy. Under the optimized conditions (5.0 g L−1 of enzyme loading, pH at 5.5, butanol kept at 10.0 g L−1), 34.7 g L−1 BB was obtained with complete consumption of 50 g L−1 glucose as the starting substrate. To our best knowledge, the BB production achieved in this study is the highest among the ever reported from the batch fermentation process. Our results demonstrated an excellent biological platform for renewable BB production from low‐value carbon sources. Biotechnol. Bioeng. 2017;114: 1428–1437. © 2017 Wiley Periodicals, Inc.
      A systematic optimization combining in situ enzymatic catalysis with Clostridium tyrobutyricum fermentation for butyl butyrate production was performed. In this study, different exogenous lipases and fermentation conditions were examined, providing potential reference to other bio‐ester producing fermentations.

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