Biovalorization of the raw agro-industrial waste rice husk through directed production of xylanase by Thermomyces lanuginosus strain A3-1 DSM 105773: a statistical sequential model
| Autor: | Amira A. Matrawy, H. S. Marey, Amira M. Embaby, A. I. Khalil |
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| Rok vydání: | 2020 |
| Předmět: |
Ammonium sulfate
Thermomyces lanuginosus Strain (chemistry) Renewable Energy Sustainability and the Environment 020209 energy 02 engineering and technology 010501 environmental sciences Pulp and paper industry 01 natural sciences Husk Industrial waste chemistry.chemical_compound chemistry 0202 electrical engineering electronic engineering information engineering Xylanase Production (economics) Fermentation 0105 earth and related environmental sciences |
| Zdroj: | Biomass Conversion and Biorefinery. 11:2177-2189 |
| ISSN: | 2190-6823 2190-6815 |
| DOI: | 10.1007/s13399-020-00824-9 |
| Popis: | The current work addresses a statistically optimized, economic, and efficient approach for the professional valorization of the massively accumulated non-efficiently utilized, raw agro-industrial waste rice husk (RH). Thermomyces lanuginosus strain A3-1 DSM 105773, a locally isolated strain, was employed for directed production of xylanase, an industrially important enzyme upon growing on RH-based medium. A three-step empirical sequential, statistical approach—one variable at a time (OVAT), Plackett–Burman design (PBD), and Box–Behnken design (BBD)—was employed to optimize the xylanase production through liquid-state fermentation of rice husk. Incubation temperature (50 °C) and ammonium sulfate concentration as an inorganic nitrogen source were the most appropriate parameters triggering the production of xylanase, deduced from OVAT. The three key determinants RH concentration, initial pH of the production medium, and incubation time did exhibit significant influences (P ≤ 0.001) on the production of xylanase, deduced from PBD. By the end of the optimization process, the optimal levels of RH, initial pH of the production medium, and incubation time were 3.8% (w/v), 4.5, and 8 days, respectively, with an agitation speed of 120 rpm to achieve a maximal xylanase level of 0.8344 U/mL with a fivefold enhancement deduced from the estimated ridge of the canonical path. Present data would reinforce the scaling up of xylanase production using the present powerful and reproducible approach for the simultaneous and proficient valorization of RH and production of xylanase for further exploitation in food, pharmaceutical, and textile industries. |
| Databáze: | OpenAIRE |
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