Imamura I, Maeyama K, Watanabe T, Wada H
Anal Biochem. 1984 Jun;139(2):444-7. doi: 10.1016/0003-2697(84)90032-0.
A simple nonradioisotopic fluorescent method for assay of histamine N-methyltransferase (HMT) activity was developed. After termination of the HMT reaction, the remaining excess substrate, histamine, was degraded by Pauly 's diazo reagent, whereas the product, N tau-methylhistamine (N- MeHA ), was not degraded by the reagent. Then the mixture was applied to high-performance liquid chromatography under conditions in which N- MeHA was not separated from histamine, and N- MeHA was measured fluorometrically by condensation with o-phthalaldehyde. The method would be convenient for measurement of HMT activity during enzyme purification.
开发了一种用于测定组胺N-甲基转移酶(HMT)活性的简单非放射性荧光方法。在HMT反应终止后,剩余的过量底物组胺被保利重氮试剂降解,而产物N-τ-甲基组胺(N-MeHA)不被该试剂降解。然后将混合物应用于高效液相色谱,在该条件下N-MeHA与组胺未分离,并且通过与邻苯二甲醛缩合以荧光法测定N-MeHA。该方法对于在酶纯化过程中测量HMT活性将是方便的。