Moody M D, Dailey H A
J Bacteriol. 1985 Sep;163(3):1120-5. doi: 10.1128/jb.163.3.1120-1125.1985.
Ferric iron reductase activity was examined in the facultative photosynthetic bacterium Rhodopseudomonas sphaeroides. The specific activities of extracts from cells grown under phototrophic and aerobic conditions were similar and not affected by the concentration of iron in the growth media. The activity was resolved by ion-exchange column chromatography into two fractions, designated iron reductase A and iron reductase B, with molecular weights of 41,000 and 32,000, respectively. Both of these soluble cytoplasmic enzymes required the presence of flavin mononucleotide for activity and utilized NADH to reduce iron supplied as ferric citrate. Iron reductase B was responsible for the majority of activity in crude extracts and was purified 556-fold by conventional protein purification techniques. The apparent Km values of iron reductase B for NADH, Fe3+, and flavin mononucleotide were determined to be 18.2, 8.3, and 3.2 microM, respectively.
在兼性光合细菌球形红假单胞菌中检测了铁还原酶活性。在光养和好氧条件下生长的细胞提取物的比活性相似,且不受生长培养基中铁浓度的影响。通过离子交换柱色谱将该活性分离为两个组分,分别命名为铁还原酶A和铁还原酶B,分子量分别为41,000和32,000。这两种可溶性细胞质酶都需要黄素单核苷酸才能发挥活性,并利用NADH还原以柠檬酸铁形式提供的铁。铁还原酶B在粗提取物中占大部分活性,并通过传统蛋白质纯化技术纯化了556倍。铁还原酶B对NADH、Fe3+和黄素单核苷酸的表观Km值分别测定为18.2、8.3和3.2 microM。