کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
69623 48782 2013 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Immobilization of β-glucosidase on mercaptopropyl-functionalized mesoporous titanium dioxide
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Immobilization of β-glucosidase on mercaptopropyl-functionalized mesoporous titanium dioxide
چکیده انگلیسی


• Mesoporous TiO2 (M-TiO2) and mercaptopropyl-functionalized M-TiO2 (SH-M-TiO2) as the carriers of β-glucosidase (BG).
• High BG activity recovery, 92.8%, was achieved of the BG immobilized on SH-M-TiO2 (BG-SH-M-TiO2).
• The conversion rates of cellobiose in 10 batches were around 90% by BG-SH-M-TiO2.

Mesoporous titanium dioxide (M-TiO2) and mercaptopropyl-functionalized M-TiO2 (SH-M-TiO2) were prepared as carriers for immobilization of β-glucosidase (BG). Analyses suggested that in SH-M-TiO2 the grafted mercaptopropyl groups attributed to about 3.5% of the total weight of the matrices. For the immobilization of BG, SH-M-TiO2 or M-TiO2 powder was added with free BG solution and stirred at 4 °C for 8 h, followed by centrifugation and washing. BG was effectively immobilized on SH-M-TiO2 with an enzyme activity of 10.9 U/g, which was 92.8% of the total enzyme activity in the starting solution of free BG. BG immobilized on SH-M-TiO2 (BG-SH-M-TiO2) was more stable in pH, thermal, and storage tests than BG on M-TiO2 or free BG in solution. The Km and vmax of BG-SH-M-TiO2 were similar to values for free BG in solution. Batch hydrolysis of cellobiose-containing substrate by BG-SH-M-TiO2 was conducted. Conversion rates of cellobiose in 10 batches were consistently around 90%. Although the residual enzyme activity of BG-SH-M-TiO2 decreased gradually, only a small amount of BG activity was detected in supernatants. This indicated effective adsorption of enzyme molecules to SH-M-TiO2 matrices.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Catalysis B: Enzymatic - Volume 97, 15 December 2013, Pages 303–310
نویسندگان
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