Biotechnology Research Center and Department of Biotechnology, Toyama Prefectural University, 5180 Kurokawa, Imizu, Toyama 939-0398, Japan; Asano Active Enzyme Molecule Project, ERATO, JST, 5180 Kurokawa, Imizu, Toyama 939-0398, Japan.
Asano Active Enzyme Molecule Project, ERATO, JST, 5180 Kurokawa, Imizu, Toyama 939-0398, Japan; Research Center of Smart Molecules, Rikkyo University, Nishi-ikebukuro, Toshimaku, Tokyo 171-8501, Japan.
J Biol Chem. 2014 Apr 11;289(15):10445-10454. doi: 10.1074/jbc.M113.540773. Epub 2014 Feb 20.
Crystal structures of short chain dehydrogenase-like L-threonine dehydrogenase from Cupriavidus necator (CnThrDH) in the apo and holo forms were determined at 2.25 and 2.5 Å, respectively. Structural comparison between the apo and holo forms revealed that four regions of CnThrDH adopted flexible conformations when neither NAD(+) nor L-Thr were bound: residues 38-59, residues 77-87, residues 180-186, and the catalytic domain. Molecular dynamics simulations performed at the 50-ns time scale revealed that three of these regions remained flexible when NAD(+) was bound to CnThrDH: residues 80-87, residues 180-186, and the catalytic domain. Molecular dynamics simulations also indicated that the structure of CnThrDH changed from a closed form to an open form upon NAD(+) binding. The newly formed cleft in the open form may function as a conduit for substrate entry and product exit. These computational results led us to hypothesize that the CnThrDH reaction progresses by switching between the closed and open forms. Enzyme kinetics parameters of the L80G, G184A, and T186N variants also supported this prediction: the kcat/Km, L-Thr value of the variants was >330-fold lower than that of the wild type; this decrease suggested that the variants mostly adopt the open form when L-Thr is bound to the active site. These results are summarized in a schematic model of the stepwise changes in flexibility and structure that occur in CnThrDH upon binding of NAD(+) and L-Thr. This demonstrates that the dynamical structural changes of short chain dehydrogenase-like L-threonine dehydrogenase are important for the reactivity and specificity of the enzyme.
铜绿假单胞菌(Cupriavidus necator)中短链脱氢酶样 L-苏氨酸脱氢酶(CnThrDH)的 apo 和 holo 形式的晶体结构分别在 2.25 和 2.5 Å分辨率下确定。apo 和 holo 形式的结构比较表明,当既没有 NAD(+)也没有 L-Thr 结合时,CnThrDH 的四个区域采用了灵活的构象:残基 38-59、残基 77-87、残基 180-186 和催化域。在 50-ns 时间尺度上进行的分子动力学模拟表明,当 NAD(+)与 CnThrDH 结合时,其中三个区域仍然保持灵活:残基 80-87、残基 180-186 和催化域。分子动力学模拟还表明,CnThrDH 的结构在 NAD(+)结合后从闭合形式转变为开放形式。在开放形式中形成的新裂缝可能作为底物进入和产物退出的通道。这些计算结果使我们假设 CnThrDH 的反应通过在闭合和开放形式之间切换来进行。L80G、G184A 和 T186N 变体的酶动力学参数也支持了这一预测:变体的 kcat/Km、L-Thr 值比野生型低>330 倍;这种减少表明,当 L-Thr 结合到活性位点时,变体主要采用开放形式。这些结果总结在一个示意图模型中,该模型描述了 CnThrDH 在结合 NAD(+)和 L-Thr 时灵活性和结构的逐步变化。这表明短链脱氢酶样 L-苏氨酸脱氢酶的动态结构变化对于酶的反应性和特异性很重要。