Academic Journal

Bioprospecting of novel thermostable β-glucosidase from Bacillus subtilis RA10 and its application in biomass hydrolysis

التفاصيل البيبلوغرافية
العنوان: Bioprospecting of novel thermostable β-glucosidase from Bacillus subtilis RA10 and its application in biomass hydrolysis
المؤلفون: Rameshwar Tiwari, Puneet Kumar Singh, Surender Singh, Pawan K. S. Nain, Lata Nain, Pratyoosh Shukla
المصدر: Biotechnology for Biofuels, Vol 10, Iss 1, Pp 1-18 (2017)
بيانات النشر: BMC, 2017.
سنة النشر: 2017
المجموعة: LCC:Fuel
LCC:Biotechnology
مصطلحات موضوعية: Thermotolerant, Thermostable β-glucosidase, Saccharification, Cloning and expression, Molecular modelling, Fuel, TP315-360, Biotechnology, TP248.13-248.65
الوصف: Abstract Background Saccharification is the most crucial and cost-intensive process in second generation biofuel production. The deficiency of β-glucosidase in commercial enzyme leads to incomplete biomass hydrolysis. The decomposition of biomass at high temperature environments leads us to isolate thermotolerant microbes with β-glucosidase production potential. Results A total of 11 isolates were obtained from compost and cow dung samples that were able to grow at 50 °C. On the basis of qualitative and quantitative estimation of β-glucosidase enzyme production, Bacillus subtilis RA10 was selected for further studies. The medium components and growth conditions were optimized and β-glucosidase enzyme production was enhanced up to 19.8-fold. The β-glucosidase from B. subtilis RA10 retained 78% of activity at 80 °C temperature and 68.32% of enzyme activity was stable even at 50 °C after 48 h of incubation. The supplementation of β-glucosidase from B. subtilis RA10 into commercial cellulase enzyme resulted in 1.34-fold higher glucose release. Furthermore, β-glucosidase was also functionally elucidated by cloning and overexpression of full length GH1 family β-glucosidase gene from B. subtilis RA10. The purified protein was characterized as thermostable β-glucosidase enzyme. Conclusions The thermostable β-glucosidase enzyme from B. subtilis RA10 would facilitate efficient saccharification of cellulosic biomass into fermentable sugar. Consequently, after saccharification, thermostable β-glucosidase enzyme would be recovered and reused to reduce the cost of overall bioethanol production process.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1754-6834
84076933
Relation: http://link.springer.com/article/10.1186/s13068-017-0932-8; https://doaj.org/toc/1754-6834
DOI: 10.1186/s13068-017-0932-8
URL الوصول: https://doaj.org/article/33d13d967bd84076933557486646e8dd
رقم الانضمام: edsdoj.33d13d967bd84076933557486646e8dd
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17546834
84076933
DOI:10.1186/s13068-017-0932-8