Nakanishi K, Ikebukuro K, Karube I
Research Center for Advanced Science and Technology, University of Tokyo, Japan.
Appl Biochem Biotechnol. 1996 Aug;60(2):97-106. doi: 10.1007/BF02788064.
A microbial cyanide sensor was prepared, consisting of immobilized Saccharomyces cerevisiae and an oxygen electrode. When the electrode was inserted into a solution containing glucose, the respiration activity of the microorganisms increased. The change in the respiration activity is monitored with the oxygen electrode. When cyanide is added to the sample solution, the electron transport chain reaction of the respiration system in the mitochondria is inhibited, resulting in a decrease in respiration. The inhibition is caused by cyanide binding with respiration enzymes such as the cytochrome oxidase complex in the mitochondrial inner membrane. Therefore, the cyanide concentration can be measured from the change in the respiration rate. When the sensor was applied to a batch system at pH 8.0 and 30 degrees C, the cyanide calibration curve showed linearity in the concentration range between 0.3 microM and 150 microM CN-.
制备了一种微生物氰化物传感器,它由固定化的酿酒酵母和一个氧电极组成。当将电极插入含有葡萄糖的溶液中时,微生物的呼吸活性会增加。呼吸活性的变化通过氧电极进行监测。当向样品溶液中添加氰化物时,线粒体中呼吸系统的电子传递链反应受到抑制,导致呼吸作用减弱。这种抑制是由氰化物与线粒体内膜中的呼吸酶(如细胞色素氧化酶复合物)结合引起的。因此,可以根据呼吸速率的变化来测量氰化物浓度。当该传感器应用于pH值为8.0、温度为30℃的间歇系统时,氰化物校准曲线在0.3微摩尔至150微摩尔CN-的浓度范围内呈线性。