@article{ref1,
title="Suicide-peroxide inactivation of microperoxidase-11: a kinetic study",
journal="Journal of enzyme inhibition and medicinal chemistry",
year="2007",
author="Khosraneh, M. and Mahmoudi, A. and Rahimi, H. and Nazari, K. and Moosavi-Movahedi, A. A.",
volume="22",
number="6",
pages="677-684",
abstract="The kinetics of microperoxidase-11 (MP-11) in the oxidation reaction of guaiacol (AH) by hydrogen peroxide was studied, taking into account the inactivation of enzyme during reaction by its suicide substrate, H2O2. Concentrations of substrates were so selected that: 1) the reaction was first-order in relation to benign substrate, AH and 2) high ratio of suicide substrate to the benign substrate, [H2O2] >> [AH]. Validation and reliability of the obtained kinetic equations were evaluated in various nonlinear and linear forms. Fitting of experimental data into the obtained integrated equation showed a close match between the kinetic model and the experimental results. Indeed, a similar mechanism to horseradish peroxidase was found for the suicide-peroxide inactivation of MP-11. Kinetic parameters of inactivation including the intact activity of MP-11, alphai, and the apparent inactivation rate constant, ki, were obtained as 0.282 +/- 0.006 min(-1) and 0.497 +/- 0.013(-1) min at [H2O2] = 1.0 mM, 27 degrees C, phosphate buffer 5.0 mM, pH = 7.0. <br><br>RESULTS showed that inactivation of microperoxidase as a peroxidase model enzyme can occur even at low concentrations of hydrogen peroxide (0.4 mM).<p /><p>Language: en</p>",
language="en",
issn="1475-6366",
doi="10.1080/14756360701270683",
url="http://dx.doi.org/10.1080/14756360701270683"
}