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dc.contributor.authorChamoli S.-
dc.contributor.authorYadav E.-
dc.contributor.authorHemansi H.-
dc.contributor.authorSaini J.K.-
dc.contributor.authorVerma A.K.-
dc.contributor.authorNavani, Naveen Kumar-
dc.contributor.authorKumar P.-
dc.date.accessioned2020-09-30T11:33:03Z-
dc.date.available2020-09-30T11:33:03Z-
dc.date.issued2020-
dc.identifier.citationInternational Journal of Biological Macromolecules (2020), 164(): 1729-1736-
dc.identifier.issn1418130-
dc.identifier.other32800958-
dc.identifier.urihttps://doi.org/10.1016/j.ijbiomac.2020.08.102-
dc.identifier.urihttp://repository.iitr.ac.in/handle/123456789/1182-
dc.description.abstractThis study reports covalent immobilization of β-glucosidase (BGL) from Bacillus subtilis PS on magnetically recyclable iron nanoparticles for enhancing robustness, facile recovery and reuse of enzyme. Immobilized BGL iron nanoparticles (BGL-INPs) were characterized by various biophysical techniques viz. TEM, DLS, FTIR and CD spectroscopy. The efficiency and yield of immobilization were 89.78 and 84.80%, respectively. After immobilization, optimum pH remained 6.0 whereas optimum temperature upraised to 70 °C whereas apparent Km and Vmax shifted from 0.819 mM to 0.941 mM and 54.46 to 57.67 μmole/min/mg, respectively. Immobilization conferred lower activation energy and improved pH and thermal stabilities. The BGL-INPs retained 85% activity up to 10th cycle of reuse and hydrolyzed more than 90% of cellobiose to glucose within 30 min. Conclusively, improved pH, thermal stability and excellent reusability over free enzyme make BGL-INPs a promising candidate for sustainable bioethanol production and other industrial applications. © 2020 Elsevier B.V.-
dc.language.isoen_US-
dc.publisherElsevier B.V.-
dc.relation.ispartofInternational Journal of Biological Macromolecules-
dc.subjectBacillus subtilis-
dc.subjectCellobiose hydrolysis-
dc.subjectCovalent immobilization-
dc.subjectIron nanoparticles-
dc.subjectβ-Glucosidase-
dc.titleMagnetically recyclable catalytic nanoparticles grafted with Bacillus subtilis β-glucosidase for efficient cellobiose hydrolysis-
dc.typeArticle-
dc.scopusid55557730300-
dc.scopusid57216942262-
dc.scopusid57218550707-
dc.scopusid55513166000-
dc.scopusid55574182650-
dc.scopusid6507073924-
dc.scopusid57216399468-
dc.affiliationChamoli, S., Department of Biochemistry, C.B.S.H., Govind Ballabh Pant University of Agriculture and Technology PantnagarUttarakhand 263145, India, Deen Dayal Upadhyay Kaushal Kendra, Central University of Haryana, Mahendergarh, Haryana 123031, India-
dc.affiliationYadav, E., Department of Biochemistry, Central University of Haryana, Mahendergarh, Haryana 123031, India-
dc.affiliationHemansi, H., Department of Microbiology, Central University of Haryana, Mahendergarh, Haryana 123031, India-
dc.affiliationSaini, J.K., Department of Microbiology, Central University of Haryana, Mahendergarh, Haryana 123031, India-
dc.affiliationVerma, A.K., Department of Biochemistry, C.B.S.H., Govind Ballabh Pant University of Agriculture and Technology PantnagarUttarakhand 263145, India-
dc.affiliationNavani, N.K., Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India-
dc.affiliationKumar, P., Department of Biochemistry, Central University of Haryana, Mahendergarh, Haryana 123031, India, Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India-
dc.description.fundingSC is thankful to Directorate of Experiment Station (DES), Pantnagar, India for providing fellowship support. SC, PK and JKS would like to thank Central University of Haryana for infrastructural support.-
dc.description.correspondingauthorKumar, P.; Department of Biochemistry, Central University of HaryanaIndia; email: piyushkalra22@gmail.com-
Appears in Collections:Journal Publications [BT]

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