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. 2017 Jan 30;22(2):212. doi: 10.3390/molecules22020212

Table 1.

Catalytic properties of the biocatalysts prepared by immobilization of PFL and TLL on mono and heterofunctional silica particles.

Protein Loading = 1 mg/g of Support
Support TLL PFL
IY d (%) RA e (%) HA f (IU/g) IY d (%) RA e (%) HA f (IU/g)
OS a 88.6 ± 1.0 110.4 ± 0.4 104.7 ± 0.3 92.0 ± 1.8 208.1 ± 4.1 20.3 ± 0.7
OSGlu a 89.2 ± 1.6 36.9 ± 1.3 35.2 ± 1.1 87.5 ± 0.6 110.3 ± 5.7 9.8 ± 0.5
OSEpx b 84.3 ± 0.1 58.6 ± 1.3 75.5 ± 0.8 80.4 ± 3.6 157.1 ± 7.0 13.4 ± 0.9
OSGlx c 86.9 ± 0.4 50.5 ± 3.5 43.8 ± 2.6 90.0 ± 1.5 139.7 ± 2.4 13.3 ± 1.1
Protein Loading = 10 mg/g of Support
Support TLL PFL
IY d (%) RA e (%) HA f (IU/g) IY d (%) RA e (%) HA f (IU/g)
OS a 96.9 ± 0.3 93.3 ± 0.1 169.1 ± 9.2 89.6 ± 0.5 55.2 ± 0.1 132.7 ± 2.1
OSGlu a 94.9 ± 0.2 47.6 ± 0.1 84.6 ± 0.6 90.3 ± 1.1 39.8 ± 0.1 96.4 ± 0.6
OSEpx b 96.7 ± 0.8 56.1 ± 0.1 101.5 ± 1.6 88.0 ± 0.9 5.3 ± 1.2 12.6 ± 0.2
OSGlx c 95.5 ± 0.6 33.9 ± 0.2 60.7 ± 1.6 90.3 ± 1.4 6.0 ± 1.0 14.6 ± 0.2

a 25 °C, pH 7.0 (10 mM sodium phosphate buffer) for 6 h. b 25 °C, pH 7.0 (10 mM sodium phosphate buffer), followed by incubating at pH 10.0 (100 mM sodium carbonate buffer) for 3 h—Remaining epoxy groups were blocked with 3 M glycine solution (25 °C for 1 h). c 25 °C, pH 7.0 (10 mM sodium phosphate buffer), followed by incubating at pH 10.0 (100 mM sodium carbonate buffer) for 3 h—Remaining free aldehydes and Schiff’s bases were reduced with sodium borohydride (1 mg/mL, 25 °C for 1 h). d Immobilization yield. e Recovered activity. f Apparent hydrolytic activity.