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首页> 外文期刊>Analytical Sciences >Bioluminescence Inhibition of Bacterial Luciferase by Aliphatic Alcohol, Amine and Carboxylic Acid: Inhibition Potency and Mechanism
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Bioluminescence Inhibition of Bacterial Luciferase by Aliphatic Alcohol, Amine and Carboxylic Acid: Inhibition Potency and Mechanism

机译:脂肪醇,胺和羧酸对细菌萤光素酶的生物发光抑制作用:抑制作用及其机理

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摘要

The inhibitory effects of hydrophobic molecules on the bacterial luciferase, BL, luminescence reaction were analyzed using an electrochemically-controlled BL luminescence system. The inhibition potency of alkyl amines, CnNH2, and fatty acids, CmCOOH (m = n – 1), on the BL reaction increased with an increase in the alkyl chain-length of these aliphatic compounds. CmCOOH showed lower inhibition potency than CnNH2 and alkyl alcohols, CnOH, data for which have been previously reported. To make clear the inhibition mechanisms of the aliphatic compounds on the BL reaction, the initial rate of the BL reaction was measured and analyzed using the Dixon plot and Cornish–Bowden plot. The C12OH inhibited the BL reaction in competition with the substrate C11CHO, while C12NH2 and C11COOH inhibited in an uncompetitive manner with the C11CHO. These results suggest that the alkyl chain-length and the terminal unit of the aliphatic compound determine the inhibition potency and the inhibition mechanism, respectively.
机译:使用电化学控制的BL发光系统分析了疏水分子对细菌荧光素酶BL的抑制作用。随着这些脂肪族化合物烷基链长度的增加,烷基胺CnNH2和脂肪酸CmCOOH(m = n – 1)的抑制力也随之增加。 CmCOOH显示出比CnNH2和烷基醇CnOH更低的抑制能力,有关数据先前已有报道。为了阐明脂族化合物对BL反应的抑制机理,使用Dixon图和Cornish-Bowden图测量并分析了BL反应的初始速率。 C12OH与底物C11CHO竞争抑制了BL反应,而C12NH2和C11COOH与C11CHO竞争地抑制了反应。这些结果表明,脂族化合物的烷基链长和末端单元分别决定了抑制能力和抑制机理。

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