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谢平会, 杨征武, 刘鹰. 用伏安型生物传感器检测酵母菌细胞的研究[J]. 中国公共卫生, 2001, 17(9): 849-850. DOI: 10.11847/zgggws2001-17-09-61
引用本文: 谢平会, 杨征武, 刘鹰. 用伏安型生物传感器检测酵母菌细胞的研究[J]. 中国公共卫生, 2001, 17(9): 849-850. DOI: 10.11847/zgggws2001-17-09-61
XIE Ping-hui, . Study on Detection of S.cerevisiae by a Voltammetric Biosensor[J]. Chinese Journal of Public Health, 2001, 17(9): 849-850. DOI: 10.11847/zgggws2001-17-09-61
Citation: XIE Ping-hui, . Study on Detection of S.cerevisiae by a Voltammetric Biosensor[J]. Chinese Journal of Public Health, 2001, 17(9): 849-850. DOI: 10.11847/zgggws2001-17-09-61

用伏安型生物传感器检测酵母菌细胞的研究

Study on Detection of S.cerevisiae by a Voltammetric Biosensor

  • 摘要: 目的 研究一种利用伏安型生物传感器检测(计数)微生物细胞(啤酒酵母菌)的新方法.方法 该传感器由一个平面热解石墨电极、铂电极及Ag/AgCl电极的三电极系统组成.将阻留啤酒酵母菌细胞的滤膜紧附在工作电极表面,然后在工作电极与对极间施加一扫描电压,进行半微分循环伏安扫描,记录伏安图谱,依据峰电流计数微生物.结果 本实验选用啤酒酵母菌为实验菌种,探讨了啤酒酵母菌浓度与峰电流的关系.发现膜上细胞数在5×106~2.5×107范围内与峰电流呈线性关系.相关系数为0.9901,直线回归方程为Y=0.66+0.56X(×107),检测下限为2.8×106cells.结论 提示我们可利用峰电流进行微生物活细胞的快速计数.

     

    Abstract: Objective To study the method of the detection of microbial cell by a voltammetric Biosensor.Method An electro-chemical method for detection of microbial cells was developed by appling semi-differential cyclic voltammetry to microbial cells.A modified basal plane pyrolytic graphite electrod was empolyed as a working electrod.Applying a sweep voltage between a working electrod and a counter electrod while the microbial cells on a membrane filter were brought into contact with the working electrod.Then measure the gener ated cur rent between the electrodes in phosphate buffered soline.Results The anodic peak potential of S.cerevisiae was 0.75V(vs Ag/AgCl electrod).The relationship between the peak current and the cell concentration of S.Cerevisiae was studied.The anodic peak current was proportional to the cell numbers on the membrane filter in a range of(0.5-2.5)×107 cells.Regression equation Y=0166+0.56X(×107 ),correlation coefficient 0.9901.The minimum detectable cell number was 2.8×106 cells.Conclusion Cell numbers of microbial cells could be determined from the anodic peak current of semi-differential cyclic voltammetry.

     

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