Ashby G A, Thorneley R N
AFRC Unit of Nitrogen Fixation, University of Sussex, Falmer, Brighton, U.K.
Biochem J. 1987 Sep 1;246(2):455-65. doi: 10.1042/bj2460455.
The kinetics of reduction of indigocarmine-dye-oxidized Fe protein of nitrogenase from Klebsiella pneumoniae (Kp2ox) by sodium dithionite in the presence and absence of MgADP were studied by stopped-flow spectrophotometry at 23 degrees C and at pH 7.4. Highly co-operative binding of 2MgADP (composite K greater than 4 X 10(10) M-2) to Kp2ox induced a rapid conformation change which caused the redox-active 4Fe-4S centre to be reduced by SO2-.(formed by the predissociation of dithionite ion) with k = 3 X 10(6) M-1.s-1. This rate constant is at least 30 times lower than that for the reduction of free Kp2ox (k greater than 10(8) M-1.s-1). Two mechanisms have been considered and limits obtained for the rate constants for MgADP binding/dissociation and a protein conformation change. Both mechanisms give rate constants (e.g. MgADP binding 3 X 10(5) less than k less than 3 X 10(6) M-1.s-1 and protein conformation change 6 X 10(2) less than k less than 6 X 10(3) s-1) that are similar to those reported for creatine kinase (EC 2.7.3.2). The kinetics also show that in the catalytic cycle of nitrogenase with sodium dithionite as reductant replacement of 2MgADP by 2MgATP occurs on reduced and not oxidized Kp2. Although the Kp2ox was reduced stoichiometrically by SO2-. and bound two equivalents of MgADP with complete conversion into the less-reactive conformation, it was only 45% active with respect to its ability to effect MgATP-dependent electron transfer to the MoFe protein.
在23℃和pH 7.4条件下,利用停流分光光度法研究了在有和没有MgADP存在的情况下,连二亚硫酸钠对肺炎克雷伯菌(Kp2ox)固氮酶的靛蓝胭脂红染料氧化型铁蛋白(Kp2ox)的还原动力学。2MgADP(复合K大于4×10¹⁰ M⁻²)与Kp2ox的高度协同结合诱导了快速构象变化,导致氧化还原活性的4Fe-4S中心被SO₂⁻(由连二亚硫酸根离子预解离形成)还原,k = 3×10⁶ M⁻¹·s⁻¹。该速率常数至少比游离Kp2ox还原的速率常数低30倍(k大于10⁸ M⁻¹·s⁻¹)。已经考虑了两种机制,并获得了MgADP结合/解离和蛋白质构象变化的速率常数的极限值。两种机制给出的速率常数(例如,MgADP结合3×10⁵<k<3×10⁶ M⁻¹·s⁻¹和蛋白质构象变化6×10²<k<6×10³ s⁻¹)与肌酸激酶(EC 2.7.3.2)报道的相似。动力学还表明,在以连二亚硫酸钠为还原剂的固氮酶催化循环中,2MgATP取代2MgADP发生在还原态而非氧化态的Kp2上。尽管Kp2ox被SO₂⁻化学计量还原,并结合了两当量的MgADP,完全转化为反应性较低的构象,但就其实现MgATP依赖性电子转移至钼铁蛋白的能力而言,其活性仅为45%。