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American Scientific Research Journal for Engineering, Technology, and Sciences (ASRJETS)
ISSN (Print) 2313-4410, ISSN (Online) 2313-4402
© Global Society of Scientific Research and Researchers
http://asrjetsjournal.org/
Cloning, Expression of Hirudin Gene from Leech (Hirudo
orientalis) in BL21(DE3) Strain
Adnan Al-Badran
a
, Sabaa Al-Fadal
b*
a
University of Basrah, College of Science, Biology department, Basra, Iraq
b
University of Basrah, College of Pharmacy, Pharmacognosay department, Basra, Iraq
a
Email: aalbadran@yahoo.com
b
Email: sabaaal.fadal@gmail.com
Abstract
The use of leeches in bloodletting therapy is one of the most important techniques in ancient medicine from
Greek time up to now. Leeches saliva contain anticoagulant hirudin which facilitate blood flow, this is one
reason for using leeches to save thousands of severed fingers, noses and ears in recent years. In this study,
hirudin gene successfully cloning and expressed in BL21(DE3) strain. Leech type was detected as H. orientalis
by using two types of genes 18SrDNA and CO-I genes, Hirudin gene was amplified by specific primers from H.
orientalis cDNA. Furthermore, Hirudin gene was expressed in BL21(DE3) strain under the control of T7
promoter in pET-16b vector, constructed vector pET-16-HR vector was extracted and used to amplify hirudin
gene by specific primers, then hirudin gene band was appeared after digestion of extracted plasmid with Hind III
and NdeI restriction enzyme. Hirudin expression was established by Real-time PCR. Production of hirudin
established in LB medium and purified by IMAC column, DEAE Sepharose and SP Sepharose. Concentration
of produced hirudin within its solution was measured by ELISA kit which reached to 1.35ng, thrombin titration
method was used to determine hirudin activity which showed Hirudin protein required 360μl from thrombin for
clot formation.
Keyword: Hirudin; Hirudo orientalis; Real-Time PCR; DEAE Sepharose; SP Sepharose.
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* Corresponding author.