Chirico W J, Brown R D
Eur J Biochem. 1987 Jun 1;165(2):343-51. doi: 10.1111/j.1432-1033.1987.tb11447.x.
To determine the mode of action of the beta-glucosidase from Trichoderma reesei a method was developed for synthesizing [1-3H]cello-oligosaccharides with specific radioactivities of approximately 3000 Ci/mol. The beta-glucosidase removed glucosyl residues from the non-reducing end of the [1-3H]cello-oligosaccharides in a multiple attack mode with little tendency to attack the substrates repetitively. Values of Km were lower for longer cello-oligosaccharides, whereas values of V remained essentially constant. A subsite map, constructed using values of V/Km for the cello-oligosaccharides, showed that the substrate-binding region comprises primarily three subsites.
为了确定里氏木霉β-葡萄糖苷酶的作用模式,开发了一种合成比放射性约为3000 Ci/mol的[1-³H]纤维寡糖的方法。β-葡萄糖苷酶以多次攻击模式从[1-³H]纤维寡糖的非还原端去除葡萄糖基残基,几乎没有重复攻击底物的倾向。较长的纤维寡糖的Km值较低,而V值基本保持恒定。使用纤维寡糖的V/Km值构建的亚位点图谱表明,底物结合区域主要由三个亚位点组成。