Colorimetric determination of pure Mg(2+)-dependent phosphatidate phosphatase activity |
| |
Authors: | Havriluk Tara Lozy Fred Siniossoglou Symeon Carman George M |
| |
Affiliation: | Department of Food Science and Rutgers Center for Lipid Research, Rutgers University, New Brunswick, NJ 08901, U.S.A. |
| |
Abstract: | The malachite green-molybdate reagent was used for a colorimetric assay of pure Mg2(+)-dependent phosphatidate phosphatase activity. This enzyme plays a major role in fat metabolism. Enzyme activity was linear with time and protein concentration, and with the concentration of water-soluble dioctanoyl phosphatidate. The colorimetric assay was used to examine enzyme inhibition by phenylglyoxal, propranolol, and dimethyl sulfoxide. Pure enzyme and a water-soluble phosphatidate substrate were required for the assay, which should be applicable to a well-defined large-scale screen of Mg2(+)-dependent phosphatidate phosphatise inhibitors (or activators). |
| |
Keywords: | |
本文献已被 ScienceDirect PubMed 等数据库收录! |
|