Department of Chemistry, P.O. Box 30012, Texas A&M University, College Station, Texas 77843-3012, United States.
Biochemistry. 2011 Mar 22;50(11):1917-27. doi: 10.1021/bi101788n. Epub 2011 Feb 4.
Adenine deaminase (ADE) catalyzes the conversion of adenine to hypoxanthine and ammonia. The enzyme isolated from Escherichia coli using standard expression conditions was low for the deamination of adenine (k(cat) = 2.0 s(-1); k(cat)/K(m) = 2.5 × 10(3) M(-1) s(-1)). However, when iron was sequestered with a metal chelator and the growth medium was supplemented with Mn(2+) prior to induction, the purified enzyme was substantially more active for the deamination of adenine with k(cat) and k(cat)/K(m) values of 200 s(-1) and 5 × 10(5) M(-1) s(-1), respectively. The apoenzyme was prepared and reconstituted with Fe(2+), Zn(2+), or Mn(2+). In each case, two enzyme equivalents of metal were necessary for reconstitution of the deaminase activity. This work provides the first example of any member of the deaminase subfamily of the amidohydrolase superfamily to utilize a binuclear metal center for the catalysis of a deamination reaction. [Fe(II)/Fe(II)]-ADE was oxidized to [Fe(III)/Fe(III)]-ADE with ferricyanide with inactivation of the deaminase activity. Reducing [Fe(III)/Fe(III)]-ADE with dithionite restored the deaminase activity, and thus, the diferrous form of the enzyme is essential for catalytic activity. No evidence of spin coupling between metal ions was evident by electron paramagnetic resonance or Mössbauer spectroscopy. The three-dimensional structure of adenine deaminase from Agrobacterium tumefaciens (Atu4426) was determined by X-ray crystallography at 2.2 Å resolution, and adenine was modeled into the active site on the basis of homology to other members of the amidohydrolase superfamily. On the basis of the model of the adenine-ADE complex and subsequent mutagenesis experiments, the roles for each of the highly conserved residues were proposed. Solvent isotope effects, pH-rate profiles, and solvent viscosity were utilized to propose a chemical reaction mechanism and the identity of the rate-limiting steps.
腺嘌呤脱氨酶(ADE)催化腺嘌呤转化为次黄嘌呤和氨。使用标准表达条件从大肠杆菌中分离的酶对腺嘌呤的脱氨活性较低(kcat = 2.0 s-1;kcat/Km = 2.5 × 103 M-1 s-1)。然而,当用金属螯合剂螯合铁并在诱导前用 Mn2+补充生长培养基时,纯化的酶对腺嘌呤的脱氨活性大大提高,kcat 和 kcat/Km 值分别为 200 s-1 和 5 × 105 M-1 s-1。制备了脱辅基酶并与 Fe2+、Zn2+或 Mn2+重组。在每种情况下,都需要两个酶当量的金属来重新形成脱氨酶活性。这项工作提供了酰胺水解酶超家族的脱氨酶亚家族的第一个成员利用双核金属中心催化脱氨反应的例子。[Fe(II)/Fe(II)]-ADE 用铁氰化物氧化为[Fe(III)/Fe(III)]-ADE,导致脱氨酶活性失活。用连二亚硫酸钠还原[Fe(III)/Fe(III)]-ADE 可恢复脱氨酶活性,因此,酶的二价形式对催化活性至关重要。电子顺磁共振或穆斯堡尔谱没有显示金属离子之间存在自旋偶合的证据。根据与酰胺水解酶超家族其他成员的同源性,在 2.2 Å 分辨率下通过 X 射线晶体学确定了来自根癌农杆菌(Agrobacterium tumefaciens)的腺嘌呤脱氨酶的三维结构,并根据该结构将腺嘌呤模型构建到活性部位。根据腺嘌呤-ADE 复合物的模型和随后的突变实验,提出了每个高度保守残基的作用。利用溶剂同位素效应、pH 速率曲线和溶剂粘度提出了一个化学反应机制和限速步骤的身份。