Rhee S G, Chock P B
Biochemistry. 1976 Apr 20;15(8):1755-60. doi: 10.1021/bi00653a025.
The kinetics of protein fluorescence change exhibited by ADP or orthophosphate addition to the Mg2+-or Mn2+-activated unadenylylated glutamine synthetase from Escherichia coli were studied. The kinetic patterns of these reactions are incompatible with a simple bimolecular binding process and a mechanism which required protein isomerization prior to substrate binding. They are consistent with a mechanism in which direct substrate binding is followed by a substrate-induced conformational change step, ES in equilibrium ES. At pH 7.0 and 15 degrees C, the association constants for the direct binding (K1) of ADP to MnE1.0 and of Pi to MnE1.0ADP are 3.9 X 10(4) and 2.28 X 10(2) M(-1), respectively. The association constant for the direct binding of ADP to MnE1.0Pi is 2.3 X 10(4) M(-1) at pH 7.0 and 19 degrees C. The deltaG degrees for the substrate-induced conformational step are -3.5 and -1.3 kcal mol(-1) due to ADP binding to MnE1.0Pi and MnE1.0, respectively, and -1.4 kcal mol(-1) due to Pi binding to MnE1.0ADP. Rate constants, k2 and k(-2), for the isomerization step are: 90 and 9.5 s(-1) for ADP binding to MnE1.0, 440 and 0.36 s(-1) for ADP binding to MnE1.0Pi, and 216 and 1.8 s(-1) for Pi binding to MnE1.0ADP. Due to low substrate affinity, the association constant for direct Pi binding to MnE1.0 was roughly estimated to be 230 M(-1) and k2 = 750 s(-1), k(-2) = 250 s(-1). At 9 degrees C and pH 7.0, the estimated association constants for the direct ADP binding to MgE1.0 and MgE1.0 Pi are 1.8 X 10(4) and 1.6 X 10(4) M(-1), respectively; and the rate constants for the isomerization step associated with the corresponding reaction are k2 = 550 s(-1), k(-2) = 500 s(-1), and k2 = 210 s(-1), k(-2) = 100 s(-1). From the kinetic analysis it is evident that the inability of Mn2+ to support biosynthetic activity of the unadenylylated enzyme is due to the slow rate of ADP release from the MnE1.0PiADP complex. In contrast the large k(-2) obtained for ADP release from the MgE1.0ADP or MgE1.0PiADP complex indicates that this step is not rate limiting in the biosynthesis of glutamine since the k catalysis obtained under the same conditions is 7.2 s(-1).
研究了向来自大肠杆菌的Mg2+或Mn2+激活的未腺苷酸化谷氨酰胺合成酶中添加ADP或正磷酸盐后所表现出的蛋白质荧光变化动力学。这些反应的动力学模式与简单的双分子结合过程以及在底物结合之前需要蛋白质异构化的机制不相符。它们与一种机制一致,即直接底物结合后接着是底物诱导的构象变化步骤,ES处于平衡状态ES。在pH 7.0和15℃下,ADP与MnE1.0的直接结合(K1)以及Pi与MnE1.0ADP的直接结合的缔合常数分别为3.9×10(4)和2.28×10(2) M(-1)。在pH 7.0和19℃下,ADP与MnE1.0Pi的直接结合的缔合常数为2.3×10(4) M(-1)。由于ADP分别与MnE1.0Pi和MnE1.0结合以及Pi与MnE1.0ADP结合,底物诱导的构象步骤的ΔG°分别为-3.5和-1.3 kcal mol(-1),以及-1.4 kcal mol(-1)。异构化步骤的速率常数k2和k(-2)为:ADP与MnE1.0结合时为90和9.5 s(-l),ADP与MnE1.0Pi结合时为440和0.36 s(-1),Pi与MnE1.0ADP结合时为216和1.8 s(-1)。由于底物亲和力低,Pi与MnE1.0的直接结合的缔合常数大致估计为230 M(-1),k2 = 750 s(-1),k(-2) = 250 s(-1)。在9℃和pH 7.0下,ADP与MgE1.0和MgE1.0 Pi的直接结合的估计缔合常数分别为1.8×10(4)和1.6×1×0(4) M(-1);与相应反应相关的异构化步骤的速率常数为k2 = 550 s(-1),k(-2) = 500 s(-1),以及k2 = 210 s(-1),k(-2) = 100 s(-1)。从动力学分析可以明显看出,Mn2+无法支持未腺苷酸化酶的生物合成活性是由于ADP从MnE1.0PiADP复合物中释放的速率缓慢。相比之下,从MgE1.0ADP或MgE1.0PiADP复合物中释放ADP所获得的较大k(-2)表明,这一步骤在谷氨酰胺生物合成中不是限速步骤,因为在相同条件下获得的k催化值为7.2 s(-1)。