Cellulase enzyme: Homology modeling, binding site identification and molecular docking

• DOI: 10.1016/j.molstruc.2017.08.067
• Publication Date: 2017-08-22T09:15:15Z
• Authors: K. Selvam; D. Senbagam; T. Selvankumar; C. Sudhakar; S. Kamala-Kannan; B. Senthilkumar; M. Govarthanan
• Keywords: 0301 basic medicine; 03 medical and health sciences

Abstract Cellulase is an enzyme that degrades the linear polysaccharide like cellulose into glucose by breaking the β-1,4- glycosidic bonds. These enzymes are the third largest enzymes with a great potential towards the ethanol production and play a vital role in degrading the biomass. The production of ethanol depends upon the ability of the cellulose to utilize the wide range of substrates. In this study, the 3D structure of cellulase from Acinetobacter sp. was modeled by using Modeler 9v9 and validated by Ramachandran plot. The accuracy of the predicted 3D structure was checked using Ramachandran plot analysis showed that 81.1% in the favored region, compatibility of an atomic model (3D) with amino acid sequence (1D) for the model was observed as 78.21% and 49.395% for Verify 3D and ERRAT at SAVES server. As the binding efficacy with the substrate might suggests the choice of the substrate as carbon and nitrogen sources, the cellobiose, cellotetraose, cellotetriose and laminaribiose were employed in the docking studies. The docking of cellobiose, cellotetraose, cellotetriose and laminaribiose with cellulase exhibited the binding energy of −6.1523 kJ/mol, −7.8759 kJ/mol,-6.1590 kJ/mol and −6.7185 kJ/mol, respectively. These docking studies revealed that cellulase has the greater potential towards the cellotetraose as a substrate for the high yield of ethanol.