Title of article :
Laccase Activity in CTAB-Based Water-in-Oil Microemulsions
Author/Authors :
Azimi, Maryam Department of Pharmaceutical Biotechnology - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran , Nafissi-Varcheh, Nastaran Department of Pharmaceutical Biotechnology - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran , Faramarzi, Mohammad Ali Department of Pharmaceutical Biotechnology - Faculty of Pharmacy & Biotechnology Research Center, Tehran University of Medical Sciences, Tehran , Aboofazelic, Reza Department of Pharmaceutics - School of Pharmacy & Protein Technology Research Center, Shahid Beheshti University of Medical Sciences, Tehran
Abstract :
The aim of this study was to develop a microemulsion system as a medium for laccasecatalyzed
reactions. Phase behavior studies were conducted by constructing partial pseudoternary
phase diagrams for systems comprising of cetyltrimethylammonium bromide (CTAB),
various organic solvents as the oil phase (i.e., hexane, cyclohexane, heptane, octane, isooctane,
toluene, isopropyl myristate), two co-surfactants (i.e., 1-butanol and 1-hexanol) and citrate buffer
solution, at various surfactant/co-surfactant weight ratios (Rsm). A monophasic, transparent,
non-birefringent area (designated as microemulsion domain) was seen to occur in some phase
diagrams along the surfactant/organic solvent axis, the extent of which was dependent mainly
upon the nature of co-surfactant and Rsm. On each phase diagram, three different water-inoil
(w/o) microemulsion systems with less than 50 wt% surfactant mixture and less than 20
wt% of aqueous phase were selected for laccase loading and activity measurements. Results
revealed that the catalytic activity of laccase in CTAB-based w/o microemulsions decreased
considerably, compared with its activity in the buffer solution, the extent of which depended
upon the type of component and their compositions in the microemulsions. It was suggested
that the conformational changes due to the electrostatic interactions between the cationic head
group of CTAB and the negative enzyme might be the reason for the reduction of laccase
activity, once entrapped in the microemulsion.
Keywords :
Laccase , Enzyme activity , W/o microemulsions , CTAB
Journal title :
Astroparticle Physics