Biotechnology and Bioprocess Engineering

, Volume 16, Issue 2, pp 352–359 | Cite as

Cloning and overexpression of aprE3-17 encoding the major fibrinolytic protease of Bacillus licheniformis CH 3-17

  • Hyeon-Deok Jo
  • Gun-Hee Kwon
  • Jae-Yong Park
  • Jaeho Cha
  • Young-Sun Song
  • Jeong Hwan Kim
Research Paper

Abstract

Bacillus licheniformis (B. licheniformis) CH3-17, an isolate from cheonggukjang, a traditional Korean fermented soyfood, secretes several fibrinolytic enzymes into the culture medium, showing strong fibrinolytic activity. A gene homologous to aprE of Bacillus subtilis (B. subtilis), aprE3-17, was cloned by PCR. DNA sequencing showed that aprE3-17 encodes a prepro-type serine protease consisting of 382 amino acids. The mature enzyme was 27 kDa in size. The aprE3-17 gene was overexpressed in B. subtilis WB600 using pHY300PLK, an Escherichia coli (E. coli)-Bacillus shuttle vector, and the 27 kDa enzyme was purified from the culture supernatant. The optimum pH for activity was 6.0. Purified enzyme quickly degraded the Aα and Bβ chains of fibrinogen but could not degrade the γ-chain.

Keywords

fibrinolytic enzyme bacilli gene expression Bacillus licheniformis fermented soyfood 

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Copyright information

© The Korean Society for Biotechnology and Bioengineering and Springer-Verlag Berlin Heidelberg 2011

Authors and Affiliations

  • Hyeon-Deok Jo
    • 1
  • Gun-Hee Kwon
    • 2
  • Jae-Yong Park
    • 3
  • Jaeho Cha
    • 4
  • Young-Sun Song
    • 5
  • Jeong Hwan Kim
    • 1
    • 2
  1. 1.Division of Applied Life Science (BK21), Graduate SchoolGyeongsang National UniversityJinjuKorea
  2. 2.Institute of Agriculture & Life ScienceGyeongsang National UniversityJinjuKorea
  3. 3.Department of Food Science and NutritionCatholic University of DaeguGyeongsanKorea
  4. 4.Department of MicrobiologyPusan National UniversityBusanKorea
  5. 5.School of Food and Life ScienceInje UniversityGimhaeKorea

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