Reactive Sulphydryl Groups in Horse Carbonmonoxyhaemoglobin

O. Omotosho, F. Iheagwam, P. E. Imion, E. Idowu, P. Chinonyere, Shalom Nwodo Chinedu
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Abstract

Background and Objective: Reactive sulphydryl groups in haemoglobin has been related with oxygen binding. In this study, the researchers analyzed the reactive sulphydryl groups in horse (Equus ferus caballus) carbonmonoxyhaemoglobin. Materials and Methods: Hemolysate gotten from fresh horse blood was converted to yield the carbonmonoxy derivative. It was then separated via carboxymethylcellulose into major and minor fractions of haemoglobin. These fractions were titrated with Ellmanʼs reagent (DTNB) and p-hydroxymercuri(II)benzoate (p-MB) stock solutions in increasing volumes. Results: Results showed that two sulphydryl groups reacted with DTNB and p-MB in both major and minor haemoglobin fractions. p-MB is known to be more reactive with thiols than DTNB, on the other hand the reactivity is the same with horse carbonmonoxyhaemoglobin. Conclusion: This study will enable a better understanding as regards the kinetics and equilibrium behind this reaction.
马碳氧血红蛋白中的活性巯基
背景与目的:血红蛋白中的活性巯基与氧结合有关。在这项研究中,研究人员分析了马(Equus ferus caballus)碳氧血红蛋白中的活性巯基。材料与方法:将新鲜马血的溶血液转化为羰基衍生物。然后通过羧甲基纤维素将其分离成血红蛋白的主要部分和次要部分。这些馏分用Ellman试剂(DTNB)和对羟基汞(II)苯甲酸酯(p-MB)原液逐渐滴定。结果:两个巯基与DTNB和p-MB在主要和次要血红蛋白组分中均发生反应。已知p-MB比DTNB与硫醇反应性更强,另一方面与马碳氧血红蛋白的反应性相同。结论:本研究将使人们对该反应背后的动力学和平衡有更好的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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