Optimization of medium composition for alkali-stable xylanase production by Aspergillus fischeri Fxn 1 in solid-state fermentation using central composite rotary design

被引:151
作者
Senthilkumar, SR
Ashokkumar, B
Raj, KC
Gunasekaran, P [1 ]
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
关键词
xylanase; alkali-stable; Aspergillus fischeri; optimization; RSM; CCRD;
D O I
10.1016/j.biortech.2004.11.005
中图分类号
S2 [农业工程];
学科分类号
0828 [农业工程];
摘要
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.
引用
收藏
页码:1380 / 1386
页数:7
相关论文
共 18 条
[1]
High molecular weight cellulase-free xylanase from alkali-tolerant Aspergillus fumigatus AR1 [J].
Anthony, T ;
Raj, KC ;
Rajendran, A ;
Gunasekaran, P .
ENZYME AND MICROBIAL TECHNOLOGY, 2003, 32 (06) :647-654
[2]
INTERLABORATORY TESTING OF METHODS FOR ASSAY OF XYLANASE ACTIVITY [J].
BAILEY, MJ ;
BIELY, P ;
POUTANEN, K .
JOURNAL OF BIOTECHNOLOGY, 1992, 23 (03) :257-270
[3]
XYLANASE ACTIVE AT HIGH PH FROM AN ALKALOTOLERANT CEPHALOSPORIUM SPECIES [J].
BANSOD, SM ;
DUTTACHOUDHARY, M ;
SRINIVASAN, MC ;
RELE, MV .
BIOTECHNOLOGY LETTERS, 1993, 15 (09) :965-970
[4]
Optimization of xylanase production by Bacillus circulans D1 in submerged fermentation using response surface methodology [J].
Bocchini, DA ;
Alves-Prado, HF ;
Baida, LC ;
Roberto, IC ;
Gomes, E ;
Da Silva, R .
PROCESS BIOCHEMISTRY, 2002, 38 (05) :727-731
[5]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]
APPLICATION OF XYLANASES IN THE PULP AND PAPER-INDUSTRY [J].
BUCHERT, J ;
TENKANEN, M ;
KANTELINEN, A ;
VIIKARI, L .
BIORESOURCE TECHNOLOGY, 1994, 50 (01) :65-72
[7]
Production of Aspergillus terreus xylanase in solid-state cultures:: application of the Plackett-Burman experimental design to evaluate nutritional requirements [J].
Ghanem, NB ;
Yusef, HH ;
Mahrouse, HK .
BIORESOURCE TECHNOLOGY, 2000, 73 (02) :113-121
[8]
OPTIMIZATION OF A CULTURE-MEDIUM FOR INCREASED XYLANASE PRODUCTION BY A WILD STRAIN OF SCHIZOPHYLLUM-COMMUNE [J].
HALTRICH, D ;
PREISS, M ;
STEINER, W .
ENZYME AND MICROBIAL TECHNOLOGY, 1993, 15 (10) :854-860
[9]
USE OF DINITROSALICYLIC ACID REAGENT FOR DETERMINATION OF REDUCING SUGAR [J].
MILLER, GL .
ANALYTICAL CHEMISTRY, 1959, 31 (03) :426-428
[10]
Mitchell D. A., 1992, APPL BIOTECHNOLOGY S, P1