Publication:
Robust Peroxidase From Bacillus mojavensis TH309: Immobilization on Walnut Shell Hydrochar and Evaluation of Its Potential in Dye Decolorization

dc.authorscopusid57190686688
dc.authorscopusid55644648500
dc.authorscopusid57544790100
dc.authorscopusid59246061900
dc.authorscopusid58489067900
dc.authorwosidYabalak, Erdal/G-3095-2015
dc.authorwosidAdigüzel, Ali/H-5850-2017
dc.contributor.authorAdiguzel, Ali Osman
dc.contributor.authorYabalak, Erdal
dc.contributor.authorCilmeli, Sumeyye
dc.contributor.authorDurgun, Recep Tayyip
dc.contributor.authorKaya, Nisa Gul
dc.contributor.authorIDDurgun, Recep Tayyip/0009-0007-7952-2344
dc.contributor.authorIDKaya, Nisa Gül/0000-0003-2911-9876
dc.date.accessioned2025-12-11T01:18:46Z
dc.date.issued2024
dc.departmentOndokuz Mayıs Üniversitesien_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, Turkiyeen_US
dc.descriptionDurgun, Recep Tayyip/0009-0007-7952-2344; Kaya, Nisa Gül/0000-0003-2911-9876en_US
dc.description.abstractPeroxidases 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.sponsorshipScientific Research Projects Unit of Ondokuz Mayis University (Turkey) [PYO. FEN.1901.23.003]en_US
dc.description.sponsorshipThis work was supported by Scientific Research Projects Unit of Ondokuz Mayis University (Turkey) . Project number: PYO. FEN.1901.23.003.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1016/j.ijbiomac.2024.134525
dc.identifier.issn0141-8130
dc.identifier.issn1879-0003
dc.identifier.pmid39111491
dc.identifier.scopus2-s2.0-85200337269
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.ijbiomac.2024.134525
dc.identifier.urihttps://hdl.handle.net/20.500.12712/42755
dc.identifier.volume277en_US
dc.identifier.wosWOS:001291463600001
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofInternational Journal of Biological Macromoleculesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBacillus mojavensisen_US
dc.subjectPeroxidaseen_US
dc.subjectImmobilizationen_US
dc.subjectWalnut Shell Hydrocharen_US
dc.subjectDecolorizationen_US
dc.titleRobust Peroxidase From Bacillus mojavensis TH309: Immobilization on Walnut Shell Hydrochar and Evaluation of Its Potential in Dye Decolorizationen_US
dc.typeArticleen_US
dspace.entity.typePublication

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