Immobilization of a lipoxygenase in silica gels for application in aqueous media

• Published in: Journal of molecular catalysis. B, Enzymatic Enzymatic, 2007-03, Vol.44 (3), p.117-127
• Main Authors: Karout, Ali, Chopard, Claude, Pierre, Alain C.
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Biotechnology; Catalysis; Chemical Sciences; Fundamental and applied biological sciences. Psychology; Gel; Immobilization; Immobilization of enzymes and other molecules; Immobilization techniques; Lipoxygenase; Methods. Procedures. Technologies; Silica
• ISSN: 1381-1177; 1873-3158
• DOI: 10.1016/j.molcatb.2006.09.008

The encapsulation of soybean lipoxygenase-1 (LOX-1) in silica gels and its application in an aqueous medium, were studied. The main silica precursor was tetramethoxysilane (TMOS) but the introduction of hydrophobic SiCH 3 groups brought with methyltrimethoxysilane (MTMS) was evaluated. Other sol–gel synthesis parameters investigated comprised partial or complete drying by evaporation and CO 2 supercritical drying. The influence on LOX-1 activity of the various chemicals with which the enzyme was in contact during encapsulation (acetone, methanol, polyvinyl alcohol), as well as the temperature and pH, were examined. The activity of free and encapsulated LOX-1 was assayed on the oxygenation reaction of linoleic acid by dioxygen from air dissolved in aqueous medium, in a UV–vis spectrophotometer. With free LOX-1, the reaction advancement could be followed in continuous in the spectrophotometer. With the gels, in a first approach, the conversion was simply determined after 15 min reaction after filtration of the liquid, to discriminate between active and inactive gels. For the most interesting gels, the kinetics were then assessed by continuous recording in the UV spectrophotometer, after placing a small piece of gel (≈15 mg) directly in the cell. The best gels had an activity ≈30% of free LOX. The present studies, supplemented by characterization of the gels texture and structure, respectively by nitrogen adsorption and 29Si MAS NMR, showed that drying a gel before use in aqueous media was detrimental to the activity. This effect is due to a contraction of the gel network which occurs when a dry aerogel sample is dipped in water after drying. Hence gels containing LOX-1 enzyme must not be dried but kept in water impregnated state, for optimum use.