首页> 外文期刊>Pesticide Biochemistry and Physiology >Inhibitory effects of Schiff analogs of salicylidene aniline on phenoloxidase from Pieris rapae L. (Lepidoptera: Pieridae)
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Inhibitory effects of Schiff analogs of salicylidene aniline on phenoloxidase from Pieris rapae L. (Lepidoptera: Pieridae)

机译:水杨基苯胺的席夫类似物对菜青虫(Pieris rapae L。)(鳞翅目:Pieridae)的酚氧化酶的抑制作用。

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In order to gain insight into the development of insecticides with novel modes of action, the effects of salicylidene aniline (a), salicylidene-4-chloroaniline (b), salicylidene-4-bromoaniline (c), and salicylidene-4-nitroaniline (d) on partially purified phenoloxidase (PO) from Pieris rapae L. were investigated. The results showed that the 4 compounds could inhibit PO activity, and the inhibitor concentrations leading to a loss of 50% activity (IC50) were estimated to be 0.025 mmol L-1, 0.732 mmol L-1, 0.471 mmol L-1, and 0.675 mmol L-1, respectively. Meanwhile, all the inhibitors showed reversible competitive inhibition, except (d), which showed reversible mixed inhibition. The K(I) values were determined as 0.106 mmol L-1, 10.059 mmol L-1, 8.390 mmol L-1, and 20.198 mmol L-1 for the four compounds, respectively. The UV-vis spectra of (a) and (d) in the presence of copper ions and the enzyme showed that (a) could directly chelate the copper ions of PO; however, (d) could neither chelate the additional copper ions nor the copper ions of PO.
机译:为了深入了解具有新作用方式的杀虫剂的开发,对水杨基苯胺(a),水杨基-4-氯苯胺(b),水杨基-4-溴苯胺(c)和水杨基-4-硝基苯胺( d)在来自Pieris rapae L.的部分纯化的酚氧化酶(PO)上进行了研究。结果表明这4种化合物可以抑制PO活性,导致50%活性降低的抑制剂浓度(IC50)估计为0.025 mmol L-1、0.732 mmol L-1、0.471 mmol L-1和分别为0.675 mmol L-1。同时,除(d)显示可逆的混合抑制外,所有抑制剂均显示出可逆的竞争抑制。四种化合物的K(I)值分别确定为0.106 mmol L-1、10.059 mmol L-1、8.390 mmol L-1和20.198 mmol L-1。 (a)和(d)在铜离子和酶存在下的紫外-可见光谱表明,(a)可以直接螯合PO的铜离子;但是,(d)既不能螯合额外的铜离子也不能螯合PO的铜离子。

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