Wan Chin-Feng, Chen Wei-Hong, Chen Cheng-Ta, Chang Margaret Dah-Tsyr, Lo Lee-Chiang, Li Yaw-Kuen
Department of Applied Chemistry, National Chiao Tung University, Hsinchu, Taiwan.
Biochem J. 2007 Jan 15;401(2):551-8. doi: 10.1042/BJ20060717.
A GH (glycoside hydrolase) family 54 alpha-L-arabinofuranosidase from Trichoderma koningii G-39 (termed Abf) was successfully expressed in Pichia pastoris and purified to near homogeneity by cation-exchange chromatography. To determine the amino acid residues essential for the catalytic activity of Abf, extensive mutagenesis of 24 conserved glutamate and aspartate residues was performed. Among the mutants, D221N, E223Q and D299N were found to decrease catalytic activity significantly. The kcat values of the D221N and D299N mutants were 7000- and 1300-fold lower respectively, than that of the wild-type Abf. E223Q was nearly inactive. These results are consistent with observations obtained from the Aspergillus kawachii alpha-L-arabinofuranosidase three-dimensional structure. This structure indicates that Asp221 of T. koningii Abf is significant for substrate binding and that Glu223 as well as Asp299 function as a nucleophile and a general acid/base catalyst for the enzymatic reaction respectively. The catalytic mechanism of wild-type Abf was further investigated by NMR spectroscopy and kinetic analysis. The results showed that Abf is a retaining enzyme. It catalyses the hydrolysis of various substrates via the formation of a common intermediate that is probably an arabinosyl-enzyme intermediate. A two-step, double-displacement mechanism involving first the formation, and then the breakdown, of an arabinosyl-enzyme intermediate was proposed. Based on the kcat values of a series of aryl-alpha-L-arabinofuranosides catalytically hydrolysed by wild-type Abf, a relatively small Brønsted constant, beta(lg)=-0.18, was obtained, suggesting that the rate-limiting step of the enzymatic reaction is the dearabinosylation step. Further kinetic studies with the D299G mutant revealed that the catalytic activity of this mutant depended largely on the pK(a) values (>6) of leaving phenols, with beta(lg)=-1.3, indicating that the rate-limiting step of the reaction becomes the arabinosylation step. This kinetic outcome supports the idea that Asp299 is the general acid/base residue. The pH activity profile of D299N provided further evidence strengthening this suggestion.
来自康宁木霉G-39的一种糖基水解酶(GH)家族54的α-L-阿拉伯呋喃糖苷酶(称为Abf)在毕赤酵母中成功表达,并通过阳离子交换色谱纯化至接近均一。为了确定对Abf催化活性至关重要的氨基酸残基,对24个保守的谷氨酸和天冬氨酸残基进行了广泛的诱变。在这些突变体中,发现D221N、E223Q和D299N显著降低催化活性。D221N和D299N突变体的kcat值分别比野生型Abf低7000倍和1300倍。E223Q几乎没有活性。这些结果与从泡盛曲霉α-L-阿拉伯呋喃糖苷酶三维结构获得的观察结果一致。该结构表明,康宁木霉Abf的天冬氨酸221对底物结合很重要,谷氨酸223和天冬氨酸299分别作为酶促反应的亲核试剂和广义酸碱催化剂发挥作用。通过核磁共振光谱和动力学分析进一步研究了野生型Abf的催化机制。结果表明,Abf是一种保留型酶。它通过形成一种可能是阿拉伯糖基-酶中间体的共同中间体来催化各种底物的水解。提出了一种两步双置换机制,首先形成阿拉伯糖基-酶中间体,然后将其分解。基于野生型Abf催化水解的一系列芳基-α-L-阿拉伯呋喃糖苷的kcat值,获得了一个相对较小的布仑斯惕常数,β(lg)=-0.18,这表明酶促反应的限速步骤是脱阿拉伯糖基步骤。对D299G突变体的进一步动力学研究表明,该突变体的催化活性很大程度上取决于离去酚的pK(a)值(>6),β(lg)=-1.3,这表明反应的限速步骤变成了阿拉伯糖基化步骤。这一动力学结果支持了天冬氨酸299是广义酸碱残基的观点。D299N的pH活性曲线提供了进一步的证据支持这一观点。