电化学生物传感器 2011

Optimization of 2,3-dihydroxybiphenyl 1,2-dioxygenase expression and its application for biosensor.

Bioresource technology Zhang Q, Qu Y, Zhou J, Zhang X, Zhou H, Ma Q, Li X
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组成图示

Optimization of 2,3-dihydroxybiphenyl... 传感器构成示意图

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传感器类型

电化学生物传感器

检测对象

儿茶酚(catechol)、3-甲基儿茶酚(3-methylcatechol)、4-甲基儿茶酚(4-methylcatechol);样品基质:PBS缓冲液(模拟环境水样)

检测原理

BphC_LA-4作为识别与催化元件,被PVA-SiO2溶胶-凝胶固定于玻璃碳电极表面。儿茶酚类底物扩散至酶层后,被BphC_LA-4催化发生meta开环氧化,使电极表面氧化还原状态改变。裸GCE上儿茶酚类化合物存在可逆氧化还原峰,而酶电极上还原峰消失、氧化峰正移,形成与底物相关的电化学响应。PVA-SiO2凝胶包埋酶并维持其活性,PBS提供离子导电环境;三电极体系通过循环伏安读取电流/电位变化。对4-甲基儿茶酚,游离酶催化弱但固定化电极响应良好,提示电催化与酶催化协同可能改变底物结合或电子转移过程。

检测灵敏度

原文未报告 LOD、线性范围、灵敏度斜率及相关系数。

效应效果

本研究未报告重现性、稳定性、实际样品回收率及与ELISA/HPLC/qPCR的定量对比。主要性能为酶表达优化后BphC_LA-4最大比活0.58 U/mg,较先前约提高3倍;SDS-PAGE显示约33.4 kDa目标蛋白条带清晰。PVA-SiO2/BphC_LA-4酶电极在0.4 mM儿茶酚、3-甲基儿茶酚、4-甲基儿茶酚的CV中均产生明显响应,且对4-甲基儿茶酚的响应优于游离酶,显示固定化与电催化协同可改善底物识别/电子转移。作者认为该酶电极具有用于儿茶酚类污染物检测的潜力,但定量分析性能尚需进一步研究。

传感器的构成

  • 工作电极基底:玻璃碳电极(GCE),提供导电表面与电子转导基础
  • 溶胶-凝胶固定化层:PVA–SiO2溶胶-凝胶(TEOS水解缩合SiO2与聚乙烯醇PVA,V:V=8:1),包埋并稳定酶
  • 酶识别/催化层:2,3-二羟基联苯1,2-双加氧酶BphC_LA-4粗提液,催化儿茶酚类底物开环氧化
  • 参比电极:饱和甘汞电极(SCE),提供稳定电位参考
  • 辅助电极:铂片电极(Pt),构成三电极电化学回路
  • 电解液:0.2 M磷酸盐缓冲液(PBS,pH 8.0),维持酶活性与离子导电

中文摘要

本研究采用Plackett–Burman设计(PBD)和响应面法(RSM)两种统计实验设计,提高2,3-二羟基联苯1,2-双加氧酶(BphC_LA-4)的表达,并将其用于构建儿茶酚生物传感器。PBD评价了10个重要因素,随后RSM优化4个显著参数。在适宜发酵条件下,以儿茶酚为底物时BphC_LA-4最大比活约为0.58 U/mg。同时,利用同源建模和分子对接帮助理解BphC_LA-4与儿茶酚类底物的相互作用,结果表明BphC_LA-4对4-甲基儿茶酚的结合亲和力低于3-甲基儿茶酚和儿茶酚。有趣的是,由SiO2溶胶-凝胶制备的BphC_LA-4酶电极对这三种儿茶酚类化合物均表现出良好响应。游离酶与固定化酶对4-甲基儿茶酚选择性的差异表明,引入电催化可能对酶催化过程产生影响。

英文摘要

In this study, two statistical experimental designs, Plackett-Burman design (PBD) and response surface methodology (RSM), were employed to enhance the expression of 2,3-dihydroxybiphenyl 1,2-dioxygenase (BphC_LA-4), which was subsequently used for the construction of catechol biosensor. Ten important factors were evaluated by PBD, and four significant parameters were then optimized by RSM. Under the favorable fermentation conditions, the maximal specific activity of BphC_LA-4 was about 0.58U/mg with catechol as substrate. Meanwhile, homology modeling and molecular docking were utilized to help understand the interaction between BphC_LA-4 and catecholic substrates, which illustrated that BphC_LA-4 presented lower binding affinity towards 4-methylcatechol in comparison with 3-methylcatechol and catechol. Interestingly, the BphC_LA-4 enzyme electrode prepared by SiO2 sol-gel showed good response to all these three catecholic compounds. The differences of selectivity to 4-methylcatechol between free and immobilized enzyme implied that the introduction of electro-catalysis might have an effect on the enzyme-catalysis process.