Department of Biochemistry & Cellular and Molecular Biology, University of Tennessee, 1311 Cumberland Avenue, Knoxville, Tennessee 37996-1939, United States.
Department of Systems and Computational Biology, School of Life Sciences, University of Hyderabad, Prof. C. R. Rao Road, Gachibowli, Hyderabad 500046, Telangana, India.
J Chem Inf Model. 2022 Dec 26;62(24):6628-6638. doi: 10.1021/acs.jcim.2c00239. Epub 2022 Jun 1.
Bacterial cellulase enzymes are potent candidates for the efficient production of bioethanol, a promising alternative to fossil fuels, from cellulosic biomass. These enzymes catalyze the breakdown of cellulose in plant biomass into simple sugars and then to bioethanol. In the absence of the enzyme, the cellulosic biomass is recalcitrant to decomposition due to fermentation-resistant lignin and pectin coatings on the cellulose surface, which make them inaccessible for hydrolysis. Cellobiohydrolase CelS is a microbial enzyme that binds to cellulose fiber and efficiently cleaves it into a simple sugar (cellobiose) by a repeated processive chopping mechanism. The two contributing factors to the catalytic reaction rate and the yield of cellobiose are the efficient product expulsion from the product binding site of CelS and the movement of the substrate or cellulose chain into the active site. Despite progress in understanding product expulsion in other cellulases, much remains to be understood about the molecular mechanism of processive action of these enzymes. Here, nonequilibrium molecular dynamics simulations using suitable reaction coordinates are carried out to investigate the energetics and mechanism of the substrate dynamics and product expulsion in CelS. The calculated free energy barrier for the product expulsion is three times lower than that for the processive action indicating that product removal is relatively easier and faster than the sliding of the substrate to the catalytic active site. The water traffic near the active site in response to the product expulsion and the processive action is also explored.
细菌纤维素酶是高效生产生物乙醇的有力候选者,生物乙醇是一种有前途的化石燃料替代品,可从纤维素生物质中获得。这些酶能催化植物生物质中的纤维素分解为简单的糖,然后转化为生物乙醇。如果没有这种酶,由于纤维素表面的木质素和果胶涂层具有抗发酵性,使纤维素生物质难以分解,因此纤维素生物质难以分解。纤维二糖水解酶 CelS 是一种微生物酶,它能与纤维素纤维结合,并通过重复的连续切割机制有效地将其切割成简单的糖(纤维二糖)。催化反应速率和纤维二糖产率的两个贡献因素是 CelS 的产物从产物结合位点的有效排出以及底物或纤维素链向活性位点的移动。尽管在理解其他纤维素酶的产物排出方面取得了进展,但这些酶的连续作用的分子机制仍有许多需要了解。在这里,使用合适的反应坐标进行了非平衡分子动力学模拟,以研究 CelS 中底物动力学和产物排出的能量学和机制。计算出的产物排出的自由能势垒比连续作用的自由能势垒低三倍,这表明产物的去除比底物滑向催化活性位点相对更容易和更快。还探讨了活性位点附近水的流动对产物排出和连续作用的响应。