Cloning,Expression and Characterization of Clostridium cellulolyticum D-Tagatose 3-Epimerase
DOI:
CSTR:
Author:
Affiliation:

Clc Number:

Fund Project:

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    D-tagatose 3-epimerase(DTE) is the most effective enzyme for the biological production of D-psicose,a novel functional factor.In this study,a novel gene encoding DTE from Clostridium cellulolyticum H10 was cloned.pET-22b(+) was for the plasmid,E.coli BL21(DE3) acted as host cells,then the recombinant strains were constructed.The target protein was over-expressed by IPTG induction;the recombinant DTE purified to electrophoretical homogeneity with affinity chromatography was analyzed by SDS-PAGE,showing approximately 31 000 characteristic protein.The result of activity detection revealed that the recombined enzyme had a higher transforming activity.

    Reference
    Related
    Cited by
Get Citation

CHU Fei-fei, XING Qing-chao, MU Wan-meng, ZHANG Tao, MIAO Ming, JIANG Bo, ZHOU Liu-ming. Cloning, Expression and Characterization of Clostridium cellulolyticum D-Tagatose 3-Epimerase[J]. Journal of Food Science and Biotechnology,2011,30(2):283-286.

Copy
Share
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:
  • Revised:
  • Adopted:
  • Online: June 17,2014
  • Published:
Article QR Code

Copy Right:Editorial Board of Journal of Food Science and Biotechnology

Address:No. 1800, Lihu Avenue, Wuxi 214122, Jiangsu Province,China  PostCode:214122

Phone:0510-85913526  E-mail:xbbjb@jiangnan.edu.cn

Supported by:Beijing E-Tiller Technology Development Co., Ltd.

WeChat

Mobile website