Title of article :
Chemical modification and immobilisation of lipase B from Candida antarctica onto mesoporous silicates
Author/Authors :
Forde، نويسنده , , Jessica and Vakurov، نويسنده , , Alex M. Gibson، نويسنده , , Tim D. and Millner، نويسنده , , Paul and Whelehan، نويسنده , , M?che?l and Marison، نويسنده , , Ian W. and ?’F?g?in، نويسنده , , Ciar?n، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2010
Pages :
7
From page :
203
To page :
209
Abstract :
The chemical modification and immobilisation of lipase B from Candida antarctica (CalB) onto three different types of mesoporous silicate (MPS) were undertaken. Soluble CalB was modified by two bifunctional reagents, ethylene glycol bis(succinimidyl succinate) (EGNHS) and glutaraldehyde, and by the monofunctional citraconic anhydride. Both chemically modified and untreated enzyme were then immobilised onto SBA-15-, CNS- and MCM-type MPS by adsorption. Thermal stabilities of chemically modified CalB in solution and of the immobilised preparations were evaluated and compared. Citraconic anhydride dramatically reduced the stability of CalB whereas both bifunctionals yielded an eightfold increase in stability over the native free CalB at 70 °C. Following immobilisation of the EGNHS-treated preparation onto CNS-MPS, the stability gain increased to over 60-fold and this combination proved to be the most effective stabilisation strategy. CalB also showed a preference for MPS with larger pores, namely SBA-15. Immobilisation of CalB in alginate beads was also stabilising.
Keywords :
stabilisation , Candida antarctica lipase B , Chemical modification , Bifunctional reagents , Mesoporous silicate
Journal title :
Journal of Molecular Catalysis B Enzymatic
Serial Year :
2010
Journal title :
Journal of Molecular Catalysis B Enzymatic
Record number :
1714757
Link To Document :
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