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Bioresource Technology
Volume 97, Issue 15, October 2006, Pages 1902-1906
 
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doi:10.1016/j.biortech.2005.08.013    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2005 Elsevier Ltd All rights reserved.

Statistical optimization of thermo-tolerant xylanase activity from Amazon isolated Bacillus circulans on solid-state cultivation

Júlio Xandro Hecka, Simone Hickmann Flôresa, Plinho Francisco Hertza and Marco Antônio Záchia AyubCorresponding Author Contact Information, a, E-mail The Corresponding Author

aFood Science and Technology Institute, Federal University of Rio Grande do Sul State, Av. Bento Gonçalves, 9500, P.O. Box 15090, ZC 91501-970, Porto Alegre, RS, Brazil

Received 11 May 2004; 
revised 26 July 2005; 
accepted 19 August 2005. 
Available online 7 October 2005.

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Abstract

A 22 factorial design was performed to find the best conditions of pH and temperature for xylanolytic activity of Bacillus circulans BL53 isolated from the Amazon environment. Solid-state cultivation was carried out on an inexpensive, abundant agro-industrial soybean residue. The central composite design (CCD) used for the analysis of treatment combinations showed that a second-order polynomial regression model was in good agreement with experimental results, with R2 = 0.9369 (P < 0.05). The maximum activity was obtained at a high temperature (80 °C) and over a large pH range (4.0–7.0). Enzymatic activity was maintained in heated extracts up to 50 °C, suggesting that the xylanases of B. circulans BL53 are thermo-tolerant biocatalysts, being of interest for industrial processes. The crude enzyme extract hydrolyzed rice straw, sugar cane bagasse and soybean fiber and its activity was stimulated by Co2+, Fe3+, and β-mercaptoethanol but inhibited by Mn2+, Cu2+, Ca2+, Zn2+, Ba2+, Mg2+ and by EDTA.

Keywords: Xylanase; Enzyme technology; Optimization; Bioconversion; Solid-state cultivation; Bioprocess design; Biodiversity

Article Outline

1. Introduction
2. Methods
2.1. Microorganism
2.2. Substrate, medium and pre-inoculum
2.3. Bioreactor and cultivation conditions
2.4. Enzyme extraction
2.5. Xylanase activity assay
2.6. Protein determination
2.7. Thermal stability of the enzyme extract
2.8. Effects of inhibitors on enzyme activity
2.9. Experimental design
3. Results and discussion
3.1. Xylanase activity optimization
3.2. Effect of various additives on xylanase extract activities
3.3. Thermal stability of enzymes
4. Conclusions
Acknowledgements
References



Bioresource Technology
Volume 97, Issue 15, October 2006, Pages 1902-1906
 
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