Ameyama M, Nonobe M, Shinagawa E, Matsushita K, Adachi O
Anal Biochem. 1985 Dec;151(2):263-7. doi: 10.1016/0003-2697(85)90174-5.
An improved enzymatic method for the determination of pyrroloquinoline quinone, a novel prosthetic group of some important oxidoreductases, has been developed with cytoplasmic membrane of Escherichia coli K-12, in which D-glucose dehydrogenase (EC 1.1.99.17) was completely resolved to apo-enzyme by EDTA treatment. Incubation of the EDTA-treated membrane with exogenous pyrroloquinoline quinone in the presence of magnesium ions gave a quantitative determination of pyrroloquinoline quinone by assaying the restored D-glucose dehydrogenase activity. This novel enzymatic method was confirmed to be highly reproducible up to 10 ng of pyrroloquinoline quinone and could be applied to a routine assay of pyrroloquinoline quinone.
一种改进的酶法已被开发出来,用于测定吡咯喹啉醌,它是一些重要氧化还原酶的新型辅基,该方法使用大肠杆菌K-12的细胞质膜,其中通过EDTA处理将D-葡萄糖脱氢酶(EC 1.1.99.17)完全转化为脱辅基酶。在镁离子存在下,将经EDTA处理的膜与外源吡咯喹啉醌一起温育,通过测定恢复的D-葡萄糖脱氢酶活性来定量测定吡咯喹啉醌。这种新的酶法被证实,对于高达10 ng的吡咯喹啉醌具有高度的可重复性,并且可应用于吡咯喹啉醌的常规测定。