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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Development of sensors for direct detection of organophosphates. Part I: Immobilization, characterization and stabilization of acetylcholinesterase and organophosphate hydrolase on silica supports
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Development of sensors for direct detection of organophosphates. Part I: Immobilization, characterization and stabilization of acetylcholinesterase and organophosphate hydrolase on silica supports

机译:开发用于直接检测有机磷酸盐的传感器。第一部分:乙酰胆碱酯酶和有机磷酸水解酶在二氧化硅载体上的固定,表征和稳定

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摘要

Biosensors for organophosphates in solution may be constructed by monitoring the activity of acetylcholinesterase (AChE) or organophosphate hydrolase (OPH) immobilized to a variety of microsensor platforms. The area available for enzyme immobilization is small (<1 mm super(2)) for microsensors. In order to construct microsensors with increased surface area for enzyme immobilization, we used a sol-gel process to create highly porous and stable silica matrices. Surface porosity of sol-gel coated surfaces was characterized using scanning electron microscopy; pore structure was found to be very similar to that of commercially available porous silica supports. Based upon this analysis, porous and non-porous silica beads were used as model substrates of sol-gel coated and uncoated sensor surfaces. Two different covalent chemistries were used to immobilize AChE and OPH to these porous and non-porous silica beads. The first chemistry used amine-silanization of silica followed by enzyme attachment using the homobifunctional linker glutaraldehyde. The second chemistry used sulfhydryl-silanization followed by enzyme attachment using the heterobifunctional linker N- gamma -maleimidobutyryloxy succinimide ester (GMBS). Surfaces were characterized in terms of total enzyme immobilized, total and specific enzyme activity, and long term stability of enzyme activity. Amine derivitization followed by glutaraldehyde linking yielded supports with greater amounts of immobilized enzyme and activity. Use of porous supports not only yielded greater amounts of immobilized enzyme and activity, but also significantly improved long term stability of enzyme activity. Enzyme was also immobilized to sol-gel coated glass slides. The mass of immobilized enzyme increased linearly with thickness of coating. However, immobilized enzyme activity saturated at a porous silica thickness of approximately 800 nm.
机译:可以通过监测固定在各种微传感器平台上的乙酰胆碱酯酶(AChE)或有机磷酸水解酶(OPH)的活性来构建溶液中有机磷酸酯的生物传感器。对于微型传感器,可用于酶固定的区域很小(<1 mm super(2))。为了构建具有增加的表面积以固定化酶的微传感器,我们使用了溶胶-凝胶工艺来创建高度多孔和稳定的硅胶基质。溶胶-凝胶涂覆的表面的表面孔隙率用扫描电子显微镜表征。发现孔结构与可商购的多孔二氧化硅载体非常相似。基于此分析,将多孔和无孔二氧化硅微珠用作溶胶-凝胶涂层和未涂层​​传感器表面的模型基材。使用两种不同的共价化学将AChE和OPH固定在这些多孔和无孔二氧化硅微珠上。第一种化学方法是使用二氧化硅的胺硅烷化,然后使用同双功能接头戊二醛进行酶连接。第二种化学方法是使用巯基硅烷化,然后使用异双功能接头N-γ-马来酰亚胺基丁酰氧基琥珀酰亚胺酯(GMBS)进行酶连接。根据固定的总酶,总酶和比酶的活性以及酶活性的长期稳定性来表征表面。胺衍生化,然后戊二醛连接产生具有大量固定化酶和活性的载体。多孔载体的使用不仅产生更多的固定化酶和活性,而且显着改善了酶活性的长期稳定性。酶也固定在溶胶凝胶涂布的载玻片上。固定化酶的质量随涂层厚度的增加而线性增加。但是,固定的酶活性在约800 nm的多孔二氧化硅厚度处达到饱和。

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