Sussmane S, Koontz J
Department of Biochemistry, University of Tennessee, Knoxville 37996, USA.
Anal Biochem. 1995 Feb 10;225(1):109-12. doi: 10.1006/abio.1995.1115.
We have developed an assay for pyridoxal kinase which takes advantage of the intense fluorescence yield of the oxime of pyridoxal or pyridoxal-5'-phosphate and the substantial difference in the rates of formation of these two oximes. Evidence is presented which demonstrates that the assay is linear with respect to time and amount of protein and is applicable to the activity in crude cell extracts as well as purified enzyme.
我们开发了一种用于测定吡哆醛激酶的分析方法,该方法利用了吡哆醛或磷酸吡哆醛肟的强烈荧光产率以及这两种肟形成速率的显著差异。文中给出的证据表明,该分析方法在时间和蛋白量方面呈线性,适用于粗细胞提取物以及纯化酶中的活性测定。