Shumiantseva V V, Meshkov S V, Uvarov V Iu, Archakov A I
Izv Akad Nauk Ser Biol. 1996 Nov-Dec(6):749-53.
Interaction between phosphorus amino acids analogs, 1-aminoalkylphosphonous and 1-aminoalkylthiophosphonic acids, and microsomes from the liver of phenobarbital-induced rabbits was studied. The phosphorus amino acids analogs cause type I and reverse type I spectral changes, respectively. A new reaction in the microsomal monooxygenase system was revealed. In the presence of NADPH, 1-aminoalkylphosphonous acids can be transformed to the corresponding 1-aminoalkylphosphonic acids by the reaction P-H-->P-OH. The reaction was monitored by 1H-NMR spectroscopy. 1-Aminoalkylphosphonous acids also serve as substrates for the NADPH-dependent monooxygenase system. 31P-NMR has shown that the oxidative desulfuration produces 1-aminoalkylphosphonous acids according to the reaction P=S-->P=O. Neither 1-aminoalkylphosphonous nor 1-aminoalkylphosphonic acids are deaminated in the NADPH-dependent monooxygenase system as follows from 1H-NMR spectroscopy.
研究了磷氨基酸类似物(1-氨基烷基次膦酸和1-氨基烷基硫代膦酸)与苯巴比妥诱导的兔肝脏微粒体之间的相互作用。磷氨基酸类似物分别引起I型和逆向I型光谱变化。揭示了微粒体单加氧酶系统中的一种新反应。在NADPH存在下,1-氨基烷基次膦酸可通过P-H→P-OH反应转化为相应的1-氨基烷基膦酸。该反应通过1H-NMR光谱监测。1-氨基烷基次膦酸也是NADPH依赖的单加氧酶系统的底物。31P-NMR表明,氧化脱硫反应根据P=S→P=O反应生成1-氨基烷基次膦酸。根据1H-NMR光谱,在NADPH依赖的单加氧酶系统中,1-氨基烷基次膦酸和1-氨基烷基膦酸均不会脱氨基。