Laboratory Medicine ›› 2017, Vol. 32 ›› Issue (4): 338-342.DOI: 10.3969/j.issn.1673-8640.2017.04.021

• Orginal Article • Previous Articles     Next Articles

Identification of fibrinolytic enzyme-producing strain and optimization of producing enzyme conditions

LI Lizhuo1, HUANG Huanjing2, LI Zhuowei3, ZHENG Mei4   

  1. 1. Department of Cardiology,the First Hospital of Hebei Medical University,Shijiazhuang 050031,Hebei,China
    2. NCPC GeneTech Biotechnology Co.,Ltd.,Shijiazhuang 050035,Hebei,China
    3. Hebei Yuanzheng Pharmaceutical Co.,Ltd.,Shijiazhuang 050041,China
    4. Department 3 of Cardiology,the First Hospital of Shijiazhuang,Shijiazhuang 050011,Hebei,China
  • Online:2017-04-20 Published:2017-05-01

Abstract:

Objective To identify fibrinolytic enzyme-producing strain (LZ-01) and optimize producing enzyme conditions. Methods The morphological characteristics of LZ-01 were observed. Physiological and biochemical tests and the sequence similarity analysis of phoR gene were adopted to determine the strain. Through single factor experiment,the influence of carbon source and nitrogen source on enzyme activity was investigated,and the optimal conditions of enzyme production were determined by orthogonal experiment. Results After the identification,the similarity of this strain and Bacillus amyloliquefaciens standard strain FZ42 was 99.78%. So,the strain was identified as Bacillus amyloliquefaciens. After optimizing,the producing enzyme activity increased by 3.63 times. Conclusions This study provides a theoretical basis for the further development of fibrinolytic drugs.

Key words: Fibrinolytic enzyme, Identification, Bacillus amyloliquefaciens, Optimization, Single factor experiment, Orthogonal experiment

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