Meagher M M, Tao B Y, Chow J M, Reilly P J
Department of Chemical Engineering, Iowa State University, Ames 50011.
Carbohydr Res. 1988 Mar 1;173(2):273-83. doi: 10.1016/s0008-6215(00)90823-1.
A previously described endo-(1----4)-beta-D-xylanase produced by Aspergillus niger was allowed to react with linear unlabeled and labeled D-xylo-oligosaccharides ranging from D-xylotriose to D-xylo-octaose. No evidence of multiple attack or of condensation and trans-D-xylosylation reactions was found. Maximum rates and Michaelis constants were measured at 40 degrees and pH 4.85. The former increased with increasing chain-length from D-xylotriose through D-xylohexaose to approximately 70% of that on soluble larchwood D-xylan, and then decreased slightly for D-xyloheptaose and D-xylo-octaose. Michaelis constants decreased monotonically with increasing chain-length. Bond-cleavage frequencies were highest near the reducing end of short substrates, with the locus of highest frequencies moving towards the middle of larger substrates. These data indicated that the endo-D-xylanase has five main subsites, with the catalytic site located between the third and fourth subsites, counting from the nonreducing end of the bound substrate. The subsite to the nonreducing side of the catalytic site strongly repels its corresponding D-xylosyl residue, while the two subsites farther towards the nonreducing end of the substrate strongly attract their corresponding residues. The subsite to the reducing side of the catalytic site moderately attracts D-xylosyl residues, while the next one towards the reducing end has a high affinity for them. The residual error of the numerical estimation was allocated largely to the Michaelis constants of the different D-xylo-oligosaccharides, whose calculated values were appreciably smaller than measured values, especially for shorter substrates. This suggests that the subsite model cannot fully account for the experimental data. Estimated and measured values of maximum rates, bond-cleavage frequencies, and dissociation constant when the active site is fully occupied by substrate agreed more closely with each other.
使黑曲霉产生的一种先前已描述的内切 -(1→4)-β -D-木聚糖酶与线性未标记和标记的D-木寡糖(范围从D-木三糖到D-木八糖)发生反应。未发现多次攻击或缩合及转D-木糖基化反应的证据。在40℃和pH 4.85下测量了最大反应速率和米氏常数。前者从D-木三糖到D-木六糖随着链长增加而增加,达到可溶性落叶松木D-木聚糖上反应速率的约70%,然后对于D-木七糖和D-木八糖略有下降。米氏常数随着链长增加而单调降低。键断裂频率在短底物的还原端附近最高,随着底物变大,最高频率位点向中间移动。这些数据表明该内切D-木聚糖酶有五个主要亚位点,催化位点位于从结合底物的非还原端开始计数的第三和第四亚位点之间。催化位点非还原侧的亚位点强烈排斥其相应的D-木糖基残基,而底物非还原端更远的两个亚位点强烈吸引其相应残基。催化位点还原侧的亚位点适度吸引D-木糖基残基,而靠近还原端的下一个亚位点对它们有高亲和力。数值估计的残余误差主要归因于不同D-木寡糖的米氏常数,其计算值明显小于测量值,特别是对于较短的底物。这表明亚位点模型不能完全解释实验数据。当活性位点被底物完全占据时,最大反应速率、键断裂频率和解离常数的估计值和测量值彼此更接近。