Robust peroxidase from Bacillus mojavensis TH309: Immobilization on walnut shell hydrochar and evaluation of its potential in dye decolorization

被引:4
作者
Adiguzel, Ali Osman [1 ]
Yabalak, Erdal [2 ,3 ]
Cilmeli, Sumeyye [1 ]
Durgun, Recep Tayyip [1 ]
Kaya, Nisa Gul [1 ]
机构
[1] Ondokuz Mayis Univ, Sci Fac, Dept Mol Biol & Genet, Samsun, Turkiye
[2] Mersin Univ, Dept Nanotechnol & Adv Mat, Mersin, Turkiye
[3] Mersin Univ, Tech Sci Vocat Sch, Dept Chem & Chem Proc Technol, TR-33343 Mersin, Turkiye
关键词
Bacillus mojavensis; Peroxidase; Immobilization; Walnut shell hydrochar; Decolorization; HORSERADISH-PEROXIDASE; PHOTOCATALYTIC DEGRADATION; TEXTILE DYE; PURIFICATION; DECOLORATION; CHITOSAN; TIO2;
D O I
10.1016/j.ijbiomac.2024.134525
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
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页数:11
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