Université de Lyon, Laboratoire des Sciences Analytiques, Université Claude Bernard, Lyon 1, 43 Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex, France.
Biosens Bioelectron. 2011 Oct 15;28(1):105-11. doi: 10.1016/j.bios.2011.07.005. Epub 2011 Jul 13.
Amperometric and impedimetric biosensor for detecting trimethylamine (TMA) which represents good parameters for estimating fish freshness has been developed. The biosensor is based on a conducting polypyrrole substituted with ferrocenyl, where flavin-containing monooxygenase 3 (FMO3) enzyme was immobilised by covalent bonding. FMO3 catalyzes the monooxygenation TMA to trimethylamine N-oxide (TMO). For catalysis FMO require flavin adenine (FAD) as a prosthetic group, NADPH as a cofactor and molecular oxygen as cosubstrate. Ferrocenyl group substituted on the polypyrrole matrix will serve as redox probe for monitoring the response of the biosensor to TMA. The construction of the biosensor was characterized by FT-IR, cyclic voltammetry and impedance measurements. Detection is done through the analysis of the current of oxidation signal of the ferrocenyl groups and compared to the measurement of impedance related to the electrical properties of the layers. Amperometric and impedimetric response were measured as a function of TMA concentration in range of 0.4 μgm L(-1)-80 μgm L(-1) (6.5 μmol L(-1)-1.5 mmol L(-1)). Amperometric measurements show a decrease in current response which is in correlation with the increase of the charge transfer resistance demonstrated by impedance. Calibration curve obtained by impedance spectroscopy shows a high sensitivity with a dynamic range from (0.4 μgm L(-1) to 80 μgm L(-1)). We demonstrated, using ferrocene as redox probe for catalytic reaction of FMO3, that high sensitivity and dynamic range was obtained. The biosensor was stable during 16 days. The biosensor shows high selectivity and its sensitivity to TMA in real samples was evaluated using fish extract after deterioration during storage.
已开发出一种用于检测三甲胺(TMA)的安培和阻抗生物传感器,TMA 是评估鱼类新鲜度的良好参数。该生物传感器基于掺杂有二茂铁的导电聚吡咯,其中黄素单加氧酶 3(FMO3)通过共价键固定。FMO3 催化 TMA 单加氧生成三甲胺 N-氧化物(TMO)。FMO 催化需要黄素腺嘌呤二核苷酸(FAD)作为辅基、NADPH 作为辅酶和分子氧作为共底物。掺杂在聚吡咯基质上的二茂铁基团将作为氧化还原探针,用于监测生物传感器对 TMA 的响应。生物传感器的构建通过傅里叶变换红外光谱(FT-IR)、循环伏安法和阻抗测量进行了表征。检测是通过分析二茂铁基团的氧化信号电流与与电特性相关的阻抗测量值来进行的。在 0.4 μgm L(-1)-80 μgm L(-1)(6.5 μmol L(-1)-1.5 mmol L(-1))范围内,通过安培和阻抗测量法测量了 TMA 浓度的响应。安培测量显示电流响应下降,这与阻抗显示的电荷转移电阻增加相关。阻抗光谱法获得的校准曲线显示出高灵敏度,动态范围从(0.4 μgm L(-1)到 80 μgm L(-1))。我们使用二茂铁作为 FMO3 催化反应的氧化还原探针证明,获得了高灵敏度和动态范围。在 16 天内,生物传感器保持稳定。生物传感器具有高选择性,并使用储存过程中变质的鱼提取物评估了其对真实样品中 TMA 的灵敏度。