Roskilde University, NSM, Research Unit for Biomaterials, Roskilde, Denmark.
FEBS J. 2011 May;278(9):1547-60. doi: 10.1111/j.1742-4658.2011.08078.x. Epub 2011 Mar 28.
Cellobiohydrolases (exocellulases) hydrolyze cellulose processively, i.e. by sequential cleaving of soluble sugars from one end of a cellulose strand. Their activity generally shows an initial burst, followed by a pronounced slowdown, even when substrate is abundant and product accumulation is negligible. Here, we propose an explicit kinetic model for this behavior, which uses classical burst phase theory as the starting point. The model is tested against calorimetric measurements of the activity of the cellobiohydrolase Cel7A from Trichoderma reesei on amorphous cellulose. A simple version of the model, which can be solved analytically, shows that the burst and slowdown can be explained by the relative rates of the sequential reactions in the hydrolysis process and the occurrence of obstacles for the processive movement along the cellulose strand. More specifically, the maximum enzyme activity reflects a balance between a rapid processive movement, on the one hand, and a slow release of enzyme which is stalled by obstacles, on the other. This model only partially accounts for the experimental data, and we therefore also test a modified version that takes into account random enzyme inactivation. This approach generally accounts well for the initial time course (approximately 1 h) of the hydrolysis. We suggest that the models will be useful in attempts to rationalize the initial kinetics of processive cellulases, and demonstrate their application to some open questions, including the effect of repeated enzyme dosages and the 'double exponential decay' in the rate of cellulolysis.
纤维二糖水解酶(外切纤维素酶)可从纤维素链的一端连续切割可溶性糖,从而逐步水解纤维素。其活性通常表现为初始爆发,随后明显减速,即使底物丰富且产物积累可忽略不计。在此,我们提出了一个明确的动力学模型来解释这一行为,该模型以经典爆发阶段理论为起点。我们根据 Trichoderma reesei 来源的纤维二糖水解酶 Cel7A 在无定形纤维素上的活性量热测量对模型进行了检验。该模型的一个简单版本可以进行解析求解,表明爆发和减速可以通过水解过程中连续反应的相对速率和沿纤维素链进行连续运动的障碍物的出现来解释。更具体地说,最大酶活性反映了快速连续运动和因障碍物而停滞的酶缓慢释放之间的平衡。该模型仅部分解释了实验数据,因此我们还测试了一个考虑随机酶失活的修改版本。该方法通常可以很好地解释水解的初始时程(约 1 h)。我们建议这些模型将有助于尝试使连续纤维素酶的初始动力学合理化,并展示其在一些悬而未决的问题上的应用,包括重复酶剂量的影响和纤维素分解率的“双指数衰减”。