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Rapid and direct spectrophotometric method for kinetics studies and routine assay of peroxidase based on aniline diazo substrates

机译:基于苯胺Diazo基材的过氧化物酶的动力学研究和常规测定的快速和直接分光光度法

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摘要

Peroxidases are ubiquitous enzymes that play an important role in living organisms. Current spectrophotometrically based peroxidase assay methods are based on the production of chromophoric substances at the end of the enzymatic reaction. The ambiguity regarding the formation and identity of the final chromophoric product and its possible reactions with other molecules have raised concerns about the accuracy of these methods. This can be of serious concern in inhibition studies. A novel spectrophotometric assay for peroxidase, based on direct measurement of a soluble aniline diazo substrate, is introduced. In addition to the routine assays, this method can be used in comprehensive kinetics studies. 4-[(4-Sulfophenyl)azo]aniline (lambda max - 390 nm, epsilon - 32 880 M-1 cm(-1) at pH 4.5 to 9) was introduced for routine assay of peroxidase. This compound is commercially available and is indexed as a food dye. Using this method, a detection limit of 0.05 nmol mL(-1) was achieved for peroxidase.
机译:过氧化物酶是普遍存在的酶,其在生物体中起重要作用。电流分光光度法基于过氧化物酶测定方法基于酶促反应结束时的发色物质的产生。关于最终发色产品的形成和身份的模糊性及其与其他分子的可能反应已经提出了对这些方法的准确性的担忧。这可能是抑制研究的严重关注。引入了过氧化物酶的新型分光光度法,基于直接测量可溶性苯胺二佐底物的直接测量。除了常规测定外,该方法还可用于综合动力学研究。 4 - [(4-磺基)偶氮]苯胺(Lambda Max-390nm,PH 4.5至9的ε-22880m-1cm(-1)用于过氧化物酶的常规测定。该化合物可商购获得,并以食品染料分析。使用该方法,对过氧化物酶实现0.05nmol ml(-1)的检出限。

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