Publication: Robust Peroxidase From Bacillus mojavensis TH309: Immobilization on Walnut Shell Hydrochar and Evaluation of Its Potential in Dye Decolorization
| dc.authorscopusid | 57190686688 | |
| dc.authorscopusid | 55644648500 | |
| dc.authorscopusid | 57544790100 | |
| dc.authorscopusid | 59246061900 | |
| dc.authorscopusid | 58489067900 | |
| dc.authorwosid | Yabalak, Erdal/G-3095-2015 | |
| dc.authorwosid | Adigüzel, Ali/H-5850-2017 | |
| dc.contributor.author | Adiguzel, Ali Osman | |
| dc.contributor.author | Yabalak, Erdal | |
| dc.contributor.author | Cilmeli, Sumeyye | |
| dc.contributor.author | Durgun, Recep Tayyip | |
| dc.contributor.author | Kaya, Nisa Gul | |
| dc.contributor.authorID | Durgun, Recep Tayyip/0009-0007-7952-2344 | |
| dc.contributor.authorID | Kaya, Nisa Gül/0000-0003-2911-9876 | |
| dc.date.accessioned | 2025-12-11T01:18:46Z | |
| dc.date.issued | 2024 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Adiguzel, Ali Osman; Cilmeli, Sumeyye; Durgun, Recep Tayyip; Kaya, Nisa Gul] Ondokuz Mayis Univ, Sci Fac, Dept Mol Biol & Genet, Samsun, Turkiye; [Yabalak, Erdal] Mersin Univ, Dept Nanotechnol & Adv Mat, Mersin, Turkiye; [Yabalak, Erdal] Mersin Univ, Tech Sci Vocat Sch, Dept Chem & Chem Proc Technol, TR-33343 Mersin, Turkiye | en_US |
| dc.description | Durgun, Recep Tayyip/0009-0007-7952-2344; Kaya, Nisa Gül/0000-0003-2911-9876 | en_US |
| dc.description.abstract | Peroxidases have received considerable attention as a cost-effective and environmentally friendly catalyst for bioremediation. Their rapid activity loss under harsh environmental conditions and inability to be used repetitively limit their exploitation in real-world wastewater treatment. First, a peroxidase was produced extracellularly by Bacillus mojavensis TH309 and purified 8.12-fold with a final yield of 47.10 % using Sephadex G-100 superfine resin. The pure peroxidase (BmPer) possessed a relatively low molecular weight of similar to 21 kDa and was active against L-DOPA on acrylamide gel after electrophoresis. BmPer was immobilized by adsorption functionalized walnut shell hydrochar (WsH) with 61.99 +/- 1.34 % efficiency and 37.07 +/- 4.16 % activity loss. BmPer and its immobilized form (WsH-BmPer) exhibited maximum activity at 50 degrees C and pH 9. WsH-BmPer exhibited 3.23-, 2.37-, 1.65-, and 2.25-fold longer half-life than BmPer at 50, 60, 70, and 80 degrees C, respectively. Immobilization significantly enhanced the stability of the enzyme under acidic conditions. BmPer and WsH-BmPer showed maximal activity in the presence of 1 % salt and retained more than 85 % of their activity even after pre-incubation with 2.5 M salt for 60 min at 50 degrees C. Their catalytic efficiency was significantly stimulated by pre-incubation with Triton X-100 (1 mM), Tween20 (1 mM), and Mg2+ (1 and 10 mM). Immobilization strongly reduced the loss of activity caused by inhibitors including Ba2+, Hg2+, and Cu2+. Moreover, both forms of the enzyme were compatible with solvents. The Michaelis constant (K-m) values of BmPer and WsH-BmPer were 0.88 and 2.66 mM for 2,4 DCP, respectively. WsH-BmPer peroxidase maintained about 82 % and 85 % of its activity when stored at 4 degrees C for 30 days and reused for up to 10 cycles, respectively. Furthermore, it decolorized Cibacron red (CR), Poly R-478 (PR), Remazol Brilliant Blue R (RBBR), and Methyl red (MR) dyes by 60.13 %, 91.34 %, 86.41 %, and 50.51 % within 60 min, respectively. | en_US |
| dc.description.sponsorship | Scientific Research Projects Unit of Ondokuz Mayis University (Turkey) [PYO. FEN.1901.23.003] | en_US |
| dc.description.sponsorship | This work was supported by Scientific Research Projects Unit of Ondokuz Mayis University (Turkey) . Project number: PYO. FEN.1901.23.003. | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded | |
| dc.identifier.doi | 10.1016/j.ijbiomac.2024.134525 | |
| dc.identifier.issn | 0141-8130 | |
| dc.identifier.issn | 1879-0003 | |
| dc.identifier.pmid | 39111491 | |
| dc.identifier.scopus | 2-s2.0-85200337269 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.uri | https://doi.org/10.1016/j.ijbiomac.2024.134525 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/42755 | |
| dc.identifier.volume | 277 | en_US |
| dc.identifier.wos | WOS:001291463600001 | |
| dc.identifier.wosquality | Q1 | |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier | en_US |
| dc.relation.ispartof | International Journal of Biological Macromolecules | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Bacillus mojavensis | en_US |
| dc.subject | Peroxidase | en_US |
| dc.subject | Immobilization | en_US |
| dc.subject | Walnut Shell Hydrochar | en_US |
| dc.subject | Decolorization | en_US |
| dc.title | Robust Peroxidase From Bacillus mojavensis TH309: Immobilization on Walnut Shell Hydrochar and Evaluation of Its Potential in Dye Decolorization | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
