Improved thermodynamic stability of subtilisin Carlsberg by covalent modification.

Enzyme and Microbial Technology; 2006; 39; 301–307.

Abstract: The present work is aimed at improving the kinetic, thermal and thermodynamic stability of subtilisin Carlsberg (SCB) obtained from Bacillus licheniformis by means of simple, inexpensive but effective covalent coupling to oxidized sucrose polymers (OSP) of varying sizes (OSP400 and OSP70) as well as polyglutaraldehyde (PGA). In the presence of 10mM calcium the half-life of the enzyme at 60 ? C increased by 6.06-fold, 5.20-fold and 2.92-fold when coupled with OSP400, OSP70 and PGA, respectively. Even in the absence of added calcium the stability against thermal inactivation was found to be greater for the modified enzymes as evident from the increase in the energy of activation for the inactivation process ( E ai ). Guanidium thiocyanate-induced unfolding indicated C m values of 1.3 M, 1.8 M, 1.5 M and 1.4 Mfor the native and enzymes modified with OSP400, OSP70 and PGA, respectively. Thermally induced unfolding was delayed for the modified enzymes as evident from the shift in T m of 8.45 ? C, 5.91 ? C and 4.66 ? C for OSP400, OSP70 and PGA modified enzymes. The results indicate that among the modifiers used OSP400 was most effective in stabilizing the enzyme and interestingly the increase in stability reported here is comparable to the most stabilized subtilisin variants obtained by site-directed mutagenesis.

Keywords: Carbohydrates; Chemical modification; Conformational stability; Heat inactivation; Subtilisin

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