Skip to main content
. 2011 Jul 24;2011:967239. doi: 10.4061/2011/967239

Table 2.

Immobilization parameters for Lipase G on different supports and protocols.

Immobilization protocols Support Activating agent IP (mg·g−1) HA (IU·g−1) RA (%)
Ionic adsorption MANAE-agarose* none 4.52 ± 0.18 55.6 ± 2.60 14.2 ± 0.40
covalent attachment Glyoxyl-agarose* glycidol 4.30 ± 0.20 0 0
MANAE-agarose* glutaraldehydea 4.47 ± 0.12 0 0
MANAE-agarose* glutaraldehydeb 4.52 ± 0.18 31.2 ± 4.50 8.20 ± 0.80
MANAE-agarose* glutaraldehydec 4.05 ± 0.05 0 0
MANAE-agarose* glutaraldehyded 4.09 ± 0.08 0 0
Epoxy-SiO2-PVA* epichlorohydrind 3.00 ± 0.04 9.50 ± 0.30 4.00 ± 0.20
Epoxy-SiO2-PVA** epichlorohydrin 2.50 ± 0.02 128.2 ± 8.10 60.9 ± 5.30

IP: Immobilized protein; HA: hydrolytic activity; RA: recovered activity.

*Immobilization in aqueous medium.

**Immobilization in organic medium (hexane).

aCovalent attachment in 100 mmoL·L−1 buffer phosphate at pH 7.0.

bDerivative prepared by ionic adsorption cross-linked with glutaraldehyde solution.

cCovalent attachment in 100 mmoL·L−1 buffer Tris-HCl at pH 7.0.

dCovalent attachment in 2.5 mmoL·L−1 buffer Tris-HCl at pH 7.0.