Mattiasson B, Mosbach K
Biotechnol Bioeng. 1977 Nov;19(11):1643-51. doi: 10.1002/bit.260191104.
The application of the enzyme thermistor in the analysis of cyanide in standard solutions as well as in blast furnace waste water is described. The heat signal is generated in the conversion of cyanide, catalyzed by the immobilized enzymes rhodanese (E.C. 2.8.1.1) and injectase (E.C. 4.4.19). Using the combination of cyanide-metabolizing enzymes and the enzyme thermistor unit, assays down to 20 microM cyanide can be carried out. Linear relationships were obtained at 20-600 microM cyanide for injectase and 20-1000 microM for rhodanese. The stability at 27 degrees C of the heat response was initially decreased, but soon stabilized at about 80% of the initial value and remained so for at least 200 hr. The technique was easily adapted to continuous analysis, applicable to environmental control (e.g., a "cyanide guard") with a response time at present within 2-3 min after a sudden change in cyanide concentration has appeared.
本文描述了酶热敏电阻在标准溶液以及高炉废水中氰化物分析中的应用。固定化酶硫氰酸酶(E.C. 2.8.1.1)和注射酶(E.C. 4.4.19)催化氰化物转化时会产生热信号。使用氰化物代谢酶和酶热敏电阻单元的组合,可对低至20微摩尔的氰化物进行测定。对于注射酶,在20 - 600微摩尔氰化物浓度范围内呈线性关系;对于硫氰酸酶,在20 - 1000微摩尔氰化物浓度范围内呈线性关系。热响应在27℃下的稳定性最初有所下降,但很快稳定在初始值的约80%,并至少保持200小时。该技术易于适应连续分析,适用于环境控制(例如“氰化物防护器”),目前在氰化物浓度突然变化后2 - 3分钟内即可响应。