کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
34339 45018 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A potential cellulose microfibril swelling enzyme isolated from Bacillus sp. AY8 enhances cellulose hydrolysis
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی بیو مهندسی (مهندسی زیستی)
پیش نمایش صفحه اول مقاله
A potential cellulose microfibril swelling enzyme isolated from Bacillus sp. AY8 enhances cellulose hydrolysis
چکیده انگلیسی


• We isolate and identify a potential cellulose microfibril swelling enzyme (Cms) producing strain, Bacillus sp. AY8.
• Purified Cms disrupts cellulose intra-chain, inter-chain, and inter-sheet H-bonds.
• The biochemical characterization of Cms was conducted using Congo red colorimetric method.
• The Cms serves as a potential source for the maximum sugar production from saccharification.

An enzyme of 16.8 ± 0.5 kDa, designated the potential cellulose microfibril swelling enzyme (Cms), was purified from newly isolated Bacillus sp. AY8 culture filtrate. The Cms-treated cotton cellulose hydrogen (H) bond intensity at approximately 3000–4000 cm−1 decreased, and consequently, the crystalline index declined by 2.07%, as shown by Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD), respectively. In addition, carbon atoms shifted the resonance up- or downfield, as shown by nuclear magnetic resonance (NMR). These results indicate that the Cms caused swelling of the cotton by weakening the cellulose intra-chain, inter-chain, and inter-sheet H-bonds. The optimum pH and temperature of the Cms were 7 and 37 °C, respectively. The activity of the Cms was enhanced by 2.24-fold in the presence of Cu2+ ions. The Cms-treated avicel yielded a 1.58-fold greater reducing sugar than that of the untreated avicel after 48 h of saccharification. This study revealed a potential cellulose swelling enzyme found in nature that may have significant applications in the bioethanol industry.

Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Process Biochemistry - Volume 50, Issue 5, May 2015, Pages 807–815
نویسندگان
, , , , ,