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Biokemistri
Nigerian Society for Experimental Biology
ISSN: 0795-8080
Vol. 26, No. 2, 2014, pp. 36-42
Bioline Code: bk14007
Full paper language: English
Document type: Research Article
Document available free of charge

Biokemistri, Vol. 26, No. 2, 2014, pp. 36-42

 en Catalytic cofactors (Mg2+ and Zn2+ ions) influence the pattern of vanadate Inhibition of the monoesterase activity of calf intestinal alkaline phosphatase
Igunnu, Adedoyin; Arise, Rotimi O.; Adebayo, Joseph O.; Olorunniji, Femi J. & Malomo, Sylvia O.

Abstract

The mechanism of modulation of vanadate inhibition of alkaline phosphatase activity by catalytic cofactors has not been fully characterized. We investigated the effect of the interaction of catalytic cofactors (Mg2+ and Zn2+) and vanadate (an active site inhibitor) on the rate of hydrolysis of para-nitrophenyl phosphate (pNPP) (monoesterase reaction) by calf intestinal alkaline phosphatase (CIAP). The results showed that vanadate significantly inhibited ‘cofactor-free’ CIAP, and the inhibition was relieved by the presence of the catalytic cofactors in the reaction. Our results show that the absence of the cofactors did not significantly alter the Km of the reaction, but caused a decrease in the Vmax. Kinetic analyses showed that vanadate inhibited CIAP-catalyzed hydrolysis of pNPP by decreasing the Vmax and increasing the Km of the reaction. The presence of cofactors in the reaction alleviated the effect of vanadate by increasing the Vmax and decreasing the Km. The activity of the dialyzed CIAP was increased by the addition of catalytic cofactors to vanadate-inhibited enzyme. This study provides preliminary data that reversible inhibition of CIAP is subject to the influence of catalytic cofactors. Further studies will reveal detailed mechanistic aspects of this observation and its significance in the biological system.

Keywords
alkaline phosphatase; monoesterase reaction; vanadate inhibition; catalytic cofactors

 
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