Some characteristics of nitrate reductase from sugar beet leaves shown in this paper were as follows:The nitrate reductase from sugar beet leaves required NADH as an electron donor.Accordingly,the nitrate reductase wa...Some characteristics of nitrate reductase from sugar beet leaves shown in this paper were as follows:The nitrate reductase from sugar beet leaves required NADH as an electron donor.Accordingly,the nitrate reductase was classified as NADH-dependent(E.C.1 .6.6.1).The Km value of the nitrate reductase for NADH and NO-3 were 0.86 m mol and 0.18μp mol respectively.The optimum pH in reaction mixture solution for nitrate reduction activity was 7.5.The effect of variable concentrations of inorganic phosphorus in the reaction buffer on nitratereductase activity was investigated.When the inorganic phosphorus concentration was below35 mmol,the nitrate reductase activity was increased with increase of inorganic phosphorus concentration.Conversely,when the inorganic phosphorus concentration was Over 35 mmol.the nitrate reductase activity was inhibited.The nitrate reductase activity assayed in vitro was 3.2 and 5.6 times of that assayed in vivo under the condition of exogenous and endogenous ground substance respectively.展开更多
文摘Some characteristics of nitrate reductase from sugar beet leaves shown in this paper were as follows:The nitrate reductase from sugar beet leaves required NADH as an electron donor.Accordingly,the nitrate reductase was classified as NADH-dependent(E.C.1 .6.6.1).The Km value of the nitrate reductase for NADH and NO-3 were 0.86 m mol and 0.18μp mol respectively.The optimum pH in reaction mixture solution for nitrate reduction activity was 7.5.The effect of variable concentrations of inorganic phosphorus in the reaction buffer on nitratereductase activity was investigated.When the inorganic phosphorus concentration was below35 mmol,the nitrate reductase activity was increased with increase of inorganic phosphorus concentration.Conversely,when the inorganic phosphorus concentration was Over 35 mmol.the nitrate reductase activity was inhibited.The nitrate reductase activity assayed in vitro was 3.2 and 5.6 times of that assayed in vivo under the condition of exogenous and endogenous ground substance respectively.
