CRCU

Chemical Research in Chinese Universities ›› 2010, Vol. 26 ›› Issue (5): 773-779.

• Articles • Previous Articles     Next Articles

Expression of CTB-human Insulin(BA) Fusion Protein in Gynostemma Pentapyhllum Makino Callus Cells and Its Hypoglycemic Effect in Mice

WANG Ya-jun1,2, QI Feng-chun2, HAO Shu-mei3, WANG Chun-yi2, SUI Bo4 and SHENG Jun1,2,5*   

  1. 1. College of Life Science, Jilin University, Changchun 130012, P. R. China;
    2. Changchun Institute of Biological Products, Changchun 130062, P. R. China;
    3. Changchun University of Science and Technology, Changchun 130022, P. R. China;
    4. Changchun Keygen Biological Products Co. Ltd., Changchun 130021, P. R. China;
    5. Yunnan Agricultural University, Kunming 650201, P. R. China
  • Received:2009-10-21 Revised:2009-12-09 Online:2010-09-25 Published:2010-11-26
  • Contact: SHENG Jun. E-mail: shengjun@ccibp.com
  • Supported by:

    Supported by the Science and Technology Development Planning Foundation of Jilin Province of China(No.20030405) and the Party and Government Administration “First-Leader-Hand” Science and Technology Project of Yunnan Province of China(No.2008QA028).

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Abstract: The plant expression vector of choleratoxin B subunit(CTB)-human insulin(BA) fusion protein pBI121/(CTB-BA) was constructed first and then the Gynostemma Pentapyhllum Makino callus cell line that could express CTB-human insulin fusion protein was constructed and its hypoglycemic effect was evaluated in mice. The plant expression vector pBI121/(CTB-BA) was digested with both BamI and SacI. Agrobacterium tumerfaciens strain LBA4404 was transformed with previously constructed recombinant plasmid pBI121/(CTB-BA) via the freeze tha- wing method, then CTB-BA gene was integrated to G Pentapyhllum Makino callus cells by co-culturing the cells with the transformed LBA4404 strain. The transformed G Pentapyhllum Makino callus cells were identified by DNA sequence assey and RT-PCR. The expressed product was identified by western-blot and its amount was tested by ELISA kit and its blood sugar decreasing effect was tested in mice．The sequences of synthetic CTB and human insulin genes(BA) were completely identical to those designed. Restriction map proved that the length of gene fragment inserted into expression vector pBI121 was consistent with that expected. The sequence of genomic DNA of expressed product was completely identical to that designed. The result of RT-PCR was consistent with that expected. The expressed product showed a specific band with a relative molecular mass of 17000 by Western-blot. The human insulin expression amount was 6.03 ?IU/mL according to the ELISA result．The animal test showed that only the G Pentapyhllum Makino callus cell line itself showed activity in decreasing the blood sugar of mice, however, the activity of the transformed G Pentapyhllum Makino callus cells was much higher. The plant expression vector pBI121/(CTB-BA) was constructed and expressed in the G Pentapyhllum Makino callus cells successfully for the first time. The transformed G Pentapyhllum Makino callus cells showed high activity in decreasing the blood sugar of mice. This study developed a new way for the development of oral administration insulin.

Key words: Human insulin peptide without C peptide, Choleratoxin B subunit, G Pentapyhllum Makino callus cells