کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
16900 42621 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A high performance Trichoderma reesei strain that reveals the importance of xylanase III in cellulosic biomass conversion
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی بیو مهندسی (مهندسی زیستی)
پیش نمایش صفحه اول مقاله
A high performance Trichoderma reesei strain that reveals the importance of xylanase III in cellulosic biomass conversion
چکیده انگلیسی


• T. reesei X3AB1 extracts supplemented with two xylanases were evaluated.
• Supplemental experiment showed that XYN III is important in biomass conversion.
• Recombinant T. reesei strain with intact endogenous XYN III was constructed.
• Enzyme from T. reesei E1AB1 is 20–30% more effective than recent commercial enzymes.

The ability of the Trichoderma reesei X3AB1strain enzyme preparations to convert cellulosic biomass into fermentable sugars is enhanced by the replacement of xyn3 by Aspergillus aculeatus β-glucosidase 1 gene (aabg1), as shown in our previous study.However, subsequent experiments using T. reesei extracts supplemented with the glycoside hydrolase (GH) family 10 xylanase III (XYN III) and GH Family 11 XYN II showed increased conversion of alkaline treated cellulosic biomass, which is rich in xylan, underscoring the importance of XYN III.To attain optimal saccharifying potential in T. reesei, we constructed two new strains, C1AB1 and E1AB1, in which aabg1 was expressed heterologously by means of the cbh1 or egl1 promoters, respectively, so that the endogenous XYN III synthesis remained intact. Due to the presence of wild-type xyn3 in T. reesei E1AB1, enzymes prepared from this strain were 20–30% more effective in the saccharification of alkaline-pretreated rice straw than enzyme extracts from X3AB1, and also outperformed recent commercial cellulase preparations. Our results demonstrate the importance of XYN III in the conversion of alkaline-pretreated cellulosic biomass by T. reesei.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Enzyme and Microbial Technology - Volume 82, January 2016, Pages 89–95
نویسندگان
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