Wang W, Hou Z, Honzatko R B, Fromm H J
Department of Biochemistry and Biophysics, Iowa State University, Ames, Iowa 50011, USA.
J Biol Chem. 1997 Jul 4;272(27):16911-6. doi: 10.1074/jbc.272.27.16911.
Gln34, Gln224, Leu228, and Ser240 are conserved residues in the vicinity of bound IMP in the crystal structure of Escherichia coli adenylosuccinate synthetase. Directed mutations were carried out, and wild-type and mutant enzymes were purified to homogeneity. Circular dichroism spectroscopy indicated no difference in secondary structure between the mutants and the wild-type enzyme in the absence of substrates. Mutants L228A and S240A exhibited modest changes in their initial rate kinetics relative to the wild-type enzyme, suggesting that neither Leu228 nor Ser240 play essential roles in substrate binding or catalysis. The mutants Q224M and Q224E exhibited no significant change in KmGTP and KmASP and modest changes in KmIMP relative to the wild-type enzyme. However, kcat decreased 13-fold for the Q224M mutant and 10(4)-fold for the Q224E mutant relative to the wild-type enzyme. Furthermore, the Q224E mutant showed an optimum pH at 6.2, which is 1.5 pH units lower than that of the wild-type enzyme. Tryptophan emission fluorescence spectra of Q224M, Q224E, and wild-type proteins under denaturing conditions indicate comparable stabilities. Mutant Q34E exhibits a 60-fold decrease in kcat compared with that of the wild-type enzyme, which is attributed to the disruption of the Gln34 to Gln224 hydrogen bond observed in crystal structures. Presented here is a mechanism for the synthetase, whereby Gln224 works in concert with Asp13 to stabilize the 6-oxyanion of IMP.
在大肠杆菌腺苷酸琥珀酸合成酶的晶体结构中,Gln34、Gln224、Leu228和Ser240是结合IMP附近的保守残基。进行了定向突变,并将野生型和突变型酶纯化至同质。圆二色光谱表明,在没有底物的情况下,突变体和野生型酶的二级结构没有差异。相对于野生型酶,突变体L228A和S240A在其初始速率动力学上表现出适度变化,这表明Leu228和Ser240在底物结合或催化中均不发挥关键作用。相对于野生型酶,突变体Q224M和Q224E在KmGTP和KmASP上没有显著变化,而在KmIMP上有适度变化。然而,相对于野生型酶,Q224M突变体的kcat降低了13倍,Q224E突变体的kcat降低了10^4倍。此外,Q224E突变体在pH 6.2时表现出最佳活性,比野生型酶低1.5个pH单位。在变性条件下,Q224M、Q224E和野生型蛋白的色氨酸发射荧光光谱表明它们具有相当的稳定性。与野生型酶相比,突变体Q34E的kcat降低了60倍,这归因于在晶体结构中观察到的Gln34与Gln224之间氢键的破坏。本文提出了一种合成酶的机制,即Gln224与Asp13协同作用以稳定IMP的6-氧阴离子。