Author/Authors :
Fathi-Roudsari, Mehrnoosh National Institute of Genetic Engineering and Biotechnology - Tehran, Iran , Salmanian, Ali-Hatef National Institute of Genetic Engineering and Biotechnology - Tehran, Iran , Behmanesh, Mehrdad Department of Genetics - Faculty of Biological Sciences - Tarbiat Modares University - Tehran, Iran , Sadeghizadeh, Majid Department of Genetics - Faculty of Biological Sciences - Tarbiat Modares University - Tehran, Iran , Khajeh, Khosro Department of Biochemistry - Faculty of Biological Sciences - Tarbiat Modares University - Tehran, Iran
Abstract :
Phenolic compounds, which are produced routinely by industrial and urban activities, possess
dangers to live organisms and environment. Laccases are oxidoreductase enzymes with the ability of remediating
a wide variety of phenolic compounds to more benign molecules. The purpose of the present research is surface
display of a laccase enzyme with adhesin involved in diffuse adhesion (AIDA-I) autotransporter system on the
surface of Escherichia coli cells for bioremediation of phenolic compounds. Methods: The expression of laccase
was regulated by a phenol-responsive promoter (a σ54 promoter). The constitutively-expressed CapR transcription
activator was able to induce laccase expression in the presence of phenolic compounds. Results: Western blot
analysis showed the expression and correct transfer of the enzyme to the outer membrane of E. coli cells in the
presence of phenol. Activity assay confirmed the correct folding of the enzyme after translocation through the
autotransporter system. HPLC analysis of residual phenol in culture medium showed a significant reduction of
phenol concentration in the presence of cells displaying laccase on the surface. Conclusion: Our findings confirm
that autodisplay enables functional surface display of laccase for direct substrate-enzyme availability by
overcoming membrane hindrance.