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反硝化微球菌形成的铁色素的鉴定与生物合成。

The identification and biosynthesis of siderochromes formed by Micrococcus denitrificans.

作者信息

Tait G H

出版信息

Biochem J. 1975 Jan;146(1):191-204. doi: 10.1042/bj1460191.

Abstract
  1. Micrococcus denitrificans excretes three catechol-containing compounds, which can bind iron, when grown aerobically and anaerobically in media deficient in iron, and anaerobically in medium with a high concentration of Ca2+. 2. One of these compounds was identified as 2,3-dihydroxybenzoic acid (compound I), and the other two were tentatively identified as N1N8-bis-(2,3-dihydroxybenzoyl)spermidine (compound II) and 2-hydroxybenzoyl-N-L-threonyl-N4[N1N8-bis-(2,3-dihydroxybenzoyl)]spermidine (compound III). 3. The equimolar ferric complex of compound III was prepared; compound III also forms complexes with Al3+, Cr3+ and Co2+ ions. 4. Cell-free extracts from iron-deficient organisms catalyse the formation of compound II from 2,3-dihydroxybenzoic acid and spermidine, and of compound III from compound II, L-threonine and 2-hydroxybenzoic acid; both reactions require ATP and dithiothreitol, and Mg2+ stimulates activity. The enzyme system catalysing the formation of compound II has optimum activity at pH 8.8 Fe2+ (35muM), Fe3+ (35muM) and Al3+ (65muM) inhibit the reaction by 50 percent. The enzyme system forming compound III has optimum activity at pH 8.6. Fe2+ (110 muM), Fe3+ (110 muM) and Al3+ (135 muM) inhibit the reaction by 50 percent. 5. At least two proteins are required for the formation of compound II, and another two proteins for its conversion into compound III. 6. The changes in the activities of these two systems were followed after cultures became deficient in iron. 7. Ferrous 1,10-phenanthroline is formed when a cell-free extract from iron-deficient cells is incubated with the ferric complex of compound III, succinate, NADH and 1,10-phenanthroline under N2.
摘要
  1. 脱氮微球菌在缺铁培养基中好氧和厌氧生长时,以及在高浓度Ca2+培养基中厌氧生长时,会分泌三种含儿茶酚的化合物,这些化合物能结合铁。2. 其中一种化合物被鉴定为2,3 - 二羟基苯甲酸(化合物I),另外两种被初步鉴定为N1N8 - 双 -(2,3 - 二羟基苯甲酰基)亚精胺(化合物II)和2 - 羟基苯甲酰基 - N - L - 苏氨酰基 - N4 [N1N8 - 双 -(2,3 - 二羟基苯甲酰基)]亚精胺(化合物III)。3. 制备了化合物III的等摩尔铁络合物;化合物III还能与Al3 +、Cr3 +和Co2 +离子形成络合物。4. 缺铁生物体的无细胞提取物催化由2,3 - 二羟基苯甲酸和亚精胺形成化合物II,以及由化合物II、L - 苏氨酸和2 - 羟基苯甲酸形成化合物III;这两个反应都需要ATP和二硫苏糖醇,Mg2 +能刺激活性。催化形成化合物II的酶系统在pH 8.8时具有最佳活性。Fe2 +(35μM)、Fe3 +(35μM)和Al3 +(65μM)可使反应受到50%的抑制。形成化合物III的酶系统在pH 8.6时具有最佳活性。Fe2 +(110μM)、FeFe3 +(110μM)和Al3 +(135μM)可使反应受到50%的抑制。5. 形成化合物II至少需要两种蛋白质,将其转化为化合物III还需要另外两种蛋白质。6. 在培养物缺铁后,跟踪这两个系统活性的变化。7. 当缺铁细胞的无细胞提取物与化合物III 的铁络合物、琥珀酸、NADH和1,10 - 菲咯啉在N2 下孵育时,会形成亚铁1,10 - 菲咯啉。

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