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用于精胺和亚精胺测定的基于胺氧化酶的生物传感器。

Amine oxidase-based biosensors for spermine and spermidine determination.

作者信息

Boffi Alberto, Favero Gabriele, Federico Rodolfo, Macone Alberto, Antiochia Riccarda, Tortolini Cristina, Sanzó Gabriella, Mazzei Franco

机构信息

Department of Biochemical Sciences, Sapienza University of Rome, P.le Aldo Moro 5, 00185, Rome, Italy.

出版信息

Anal Bioanal Chem. 2015 Feb;407(4):1131-7. doi: 10.1007/s00216-014-8324-4. Epub 2014 Nov 19.

Abstract

The present work describes the development and optimization of electrochemical biosensors for specific determination of the biogenic polyamine spermine (Spm) and spermidine (Spmd) whose assessment represents a novel important analytical tool in food analysis and human diagnostics. These biosensors have been prepared using novel engineered enzymes: polyamine oxidase (PAO) endowed with selectivity towards Spm and Spmd and spermine oxidase (SMO) characterized by strict specificity towards Spm. The current design entails biosensors in which the enzymes were entrapped in poly(vinyl alcohol) bearing styrylpyridinium groups (PVA-SbQ), a photocrosslinkable gel, onto an electrode surface. Screen-printed electrodes (SPEs) were used as electrochemical transducers for enzymatically produced hydrogen peroxide, operating at different potential vs Ag/AgCl according to the material of the working electrode (WE): +700 mV for graphite (GP) or -100 mV for Prussian blue (PB)-modified SPE, respectively. Biosensor performances were evaluated by means of flow injection amperometric (FIA) measurements. The modified electrodes showed good sensitivity, long-term stability and reproducibility. Under optimal conditions, the PAO biosensor showed a linear range 0.003-0.3 mM for Spm and 0.01-0.4 mM for Spmd, while with the SMO biosensor, a linear range of 0.004-0.5 mM for Spm has been obtained. The main kinetic parameters apparent Michaelis constant (K M), turnover number (K cat) and steady-state current (I max) were determined. The proposed device was then applied to the determination of biogenic amines in blood samples. The results obtained were in good agreement with those obtained with the GC-MS reference method.

摘要

本工作描述了用于特异性测定生物胺精胺(Spm)和亚精胺(Spmd)的电化学生物传感器的开发与优化,对它们的评估是食品分析和人体诊断中一种新型重要的分析工具。这些生物传感器是使用新型工程酶制备的:对Spm和Spmd具有选择性的多胺氧化酶(PAO)以及对Spm具有严格特异性的精胺氧化酶(SMO)。当前的设计包括将酶包埋在带有苯乙烯基吡啶鎓基团的聚乙烯醇(PVA-SbQ)(一种可光交联凝胶)中的生物传感器,该凝胶位于电极表面。丝网印刷电极(SPEs)用作酶促产生过氧化氢的电化学换能器,根据工作电极(WE)的材料在相对于Ag/AgCl的不同电位下工作:石墨(GP)工作电极时为+700 mV,普鲁士蓝(PB)修饰SPE时为-100 mV。通过流动注射安培法(FIA)测量评估生物传感器性能。修饰电极表现出良好的灵敏度、长期稳定性和重现性。在最佳条件下,PAO生物传感器对Spm的线性范围为0.003 - 0.3 mM,对Spmd的线性范围为0.01 - 0.4 mM,而对于SMO生物传感器,已获得对Spm的线性范围为0.004 - 0.5 mM。测定了主要动力学参数表观米氏常数(K M)、周转数(K cat)和稳态电流(I max)。然后将所提出的装置应用于血液样本中生物胺的测定。获得的结果与气相色谱 - 质谱(GC-MS)参考方法获得的结果高度一致。

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