Optimization of medium composition for alkali-stable xylanase production by Aspergillus fischeri Fxn 1 in solid-state fermentation using central composite rotary design
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Senthilkumar, SR
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机构:Madurai Kamaraj Univ, Sch Biol Sci, Dept Microbial Technol, Ctr Excellence Genom Sci, Madurai 625021, Tamil Nadu, India
Senthilkumar, SR
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Ashokkumar, B
Raj, KC
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机构:Madurai Kamaraj Univ, Sch Biol Sci, Dept Microbial Technol, Ctr Excellence Genom Sci, Madurai 625021, Tamil Nadu, India
Raj, KC
Gunasekaran, P
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Madurai Kamaraj Univ, Sch Biol Sci, Dept Microbial Technol, Ctr Excellence Genom Sci, Madurai 625021, Tamil Nadu, IndiaMadurai Kamaraj Univ, Sch Biol Sci, Dept Microbial Technol, Ctr Excellence Genom Sci, Madurai 625021, Tamil Nadu, India
Gunasekaran, P
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机构:
[1] Madurai Kamaraj Univ, Sch Biol Sci, Dept Microbial Technol, Ctr Excellence Genom Sci, Madurai 625021, Tamil Nadu, India
[2] Indian Inst Technol, Dept Biotechnol, Madras 600036, Tamil Nadu, India
Response surface methodology and central composite rotary design (CCRD) was employed to optimize a fermentation medium for the production of alkali-stable cellulase-free xylanase by Aspergillus fischeri in solid-state fermentation at pH 9.0 with wheat bran as substrate. The four variables involved in this study were sodium nitrite, potassium dihydrogen phosphate, magnesium sulphate and yeast extract. The statistical analysis of the results showed that, in the range studied, only sodium nitrite had a significant effect on xylanase production. The optimized medium containing (in g/l) NaNO2-7.0, K2HPO4-1.0, MgSO4-0.5 and yeast extract-5.0 resulted in 1.9-fold increased level of alkali-stable xylanase (1024 U/g wheat bran) production compared to initial level (540 U/g) after 72 h of fermentation, whereas its value predicted by the quadratic model was 931 U/g. The level of protease activity was considerably decreased in optimized medium, thus helping to preserve the xylanase activity and demonstrating another advantage of applying statistical experimental design. (c) 2005 Published by Elsevier Ltd.