jamshid Raheb - National Institute of Genetics and Biotechnology Engineering, Research Institute of Medical Biotechnology, Department of Molecular Medicine
seyed abolghassem mohammadi bondarkhilli - National Institute of Genetics and Biotechnology Engineering, Research Institute of Medical Biotechnology, Department of Molecular Medicine
Mehdi MohMMADI - Natinal Institute of Genetic Engineering and Biotechnology
Kambiz Akbari - Natinal Institute of Genetic Engineering and Biotechnology
Hossein Shahbani - National Institute of Genetic Engineering and Biotechnology
Arefeh Alipour - National Institute of Genetic Rngineering and Biotechnology

Today, efforts go towards the replacement of chemical surfactants by natural biological biosurfactants (biosurfactant), as these materials are not carcinogenic and highly compatibile with the environment. One of the main classes of biosurfactants is rhamnose containing glycolipid biosurfactant (rhamnolipids). This type of biosurfactants can be applied in many industries such as oil industry, pharmaceutical industry, food industry and esc. In the present study, with elimination of regulatory elements of monorhamnolipid operon, the suitable construct was made and transformed to E. coli BL۱۲ and E. coli DH۵α competent cells. Then the production of monorhamnolipid in recombinant E. coli BL۱۲ harboring pET ۱۲a vector and mono and di-rhamnolipid biosurfactant in recombinant E. coli DH۵α harboring pTrc ۹۹A evaluated by CTAB plate and thin layer chromatography (TLC). The relative production of mono and dirhamnolipid biosurfactant was determined by oil spreading method. Finally, the efficiency of the extracted biosurfactant was verified by E۱۲ method in different salinity and pH conditions.

Biosurfactant, Rhamnolipid, E. coli BL۱۲, E. coli DH۵α, transformation