首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Enzymatic detection of mercuric ions in ground-water from vegetable wastes by immobilizing pumpkin (Cucumis melo) urease in calcium alginate beads
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Enzymatic detection of mercuric ions in ground-water from vegetable wastes by immobilizing pumpkin (Cucumis melo) urease in calcium alginate beads

机译:通过固定藻酸钙珠粒中的南瓜(Cucumis melo)脲酶的酶法检测蔬菜废物中的地下水中的汞离子

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Present report describes a quick and simple test based on enzyme inhibition for the detection of mercury in aqueous medium by urease immobilized in alginate beads. Urease was extracted from the discarded seeds of pumpkin (Cucumis melo) and was purified to apparent homogeneity (5.2-fold) by heat treatment at 48 +/- 0.1 degrees C and gel filtration through Sephadex G-200. the homogeneous enzyme preparation (Sp activity 353 U/mg protein, A(280)/A(260) = 1.12) was immobilized in 3.5% alginate leading to 86% immobilization. Effect of mercuric ion on the activity of soluble as well as immobilized enzyme was investigated. Hg2+ exhibited a concentration-dependent inhibition both in the presence and absence of the substrate. The alginate immobilized enzyme showed less inhibition. There was no leaching of the enzyme over a period of 15 days at 4 degrees C. The inhibition was non-competitive and the K-i was found to be. 1.26 x 10(-1) mu M. Time-dependent interaction of urease with Hg2+ exhibited a biphasic inhibition behavior in which approximately half of the initial activity was lost rapidly (within 10 min) and reminder in a slow phase. Binding of Hg2+ with the enzyme was largely irreversible, as the activity could not be restored by dialysis. The significance of the observations is discussed. (c) 2007 Elsevier Ltd. All rights reserved.
机译:本报告描述了一种基于酶抑制作用的快速简便的测试,用于通过固定在藻酸盐珠粒中的脲酶检测水性介质中的汞。从废弃的南瓜种子(Cucumis melo)中提取脲酶,并通过在48 +/- 0.1摄氏度下进行热处理并通过Sephadex G-200进行凝胶过滤将其纯化至表观均匀性(5.2倍)。将同质酶制剂(Sp活性353 U / mg蛋白,A(280)/ A(260)= 1.12)固定在3.5%藻酸盐中,导致86%固定。研究了汞离子对可溶性酶和固定化酶活性的影响。在存在和不存在底物的情况下,Hg2 +均表现出浓度依赖性抑制作用。藻酸盐固定化酶显示较少的抑制作用。在4摄氏度下经过15天的时间,没有酶的浸出。抑制作用是非竞争性的,发现K-i是。 1.26 x 10(-1)μM。脲酶与Hg2 +的时间依赖性相互作用表现出双相抑制行为,其中大约一半的初始活性迅速消失(在1​​0分钟内),并在缓慢的阶段提醒。 Hg2 +与酶的结合在很大程度上是不可逆的,因为不能通过透析恢复其活性。讨论了观察的意义。 (c)2007 Elsevier Ltd.保留所有权利。

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